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The Role of Interleukin 17 in Tumour Proliferation, Angiogenesis, and Metastasis

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inferredcites →https://doi.org/10.1002/art.21749openalex-snapshot
Synovial membrane cytokine expression is predictive of joint damage progression in rheumatoid arthritis: A two‐year prospective study (the DAMAGE study cohort)
inferredcites →https://doi.org/10.1002/art.30278openalex-snapshot
Interleukin‐17–induced proliferation of fibroblast‐like synovial cells is mTOR dependent
inferredcites →https://doi.org/10.1002/eji.200737409openalex-snapshot
IL‐23 and the Th17 pathway promote inflammation and impair antifungal immune resistance
inferredcites →https://doi.org/10.1002/eji.200940157openalex-snapshot
Tumor‐infiltrating IL‐17‐producing γδ T cells support the progression of tumor by promoting angiogenesis
inferredcites →https://doi.org/10.1002/eji.201040707openalex-snapshot
Promoting angiogenesis within the tumor microenvironment: The secret life of murine lymphoid IL‐17‐producing γδ T cells
inferredcites →https://doi.org/10.1002/ibd.20339openalex-snapshot
Role of the novel Th17 cytokine IL-17F in inflammatory bowel disease (IBD): Upregulated colonic IL-17F expression in active Crohnʼs disease and analysis of the IL17F p.His161Arg polymorphism in IBD
inferredcites →https://doi.org/10.1002/ibd.21248openalex-snapshot
IL-23/IL-17 axis in IBD
inferredcites →https://doi.org/10.1002/iub.1216openalex-snapshot
Lactate dehydrogenase a in cancer: A promising target for diagnosis and therapy
inferredcites →https://doi.org/10.1002/jmri.21787openalex-snapshot
Relaxation times of skeletal muscle metabolites at 7T
inferredcites →https://doi.org/10.1006/bbrc.2001.4618openalex-snapshot
Expression of IL-17 mRNA in Ovarian Cancer
inferredcites →https://doi.org/10.1007/s00109-004-0555-yopenalex-snapshot
Nuclear factor-?B: its role in health and disease
inferredcites →https://doi.org/10.1007/s00262-011-1054-yopenalex-snapshot
Th17 and Th17-stimulated CD8+ T cells play a distinct role in Th17-induced preventive and therapeutic antitumor immunity
inferredcites →https://doi.org/10.1007/s00432-013-1441-1openalex-snapshot
High IL-17-positive tumor immune cell infiltration is indicative for chemosensitivity of ovarian carcinoma
inferredcites →https://doi.org/10.1007/s10875-012-9847-0openalex-snapshot
Cancer-Related Inflammation
inferredcites →https://doi.org/10.1007/s12026-013-8483-yopenalex-snapshot
Th17 cell expansion in gastric cancer may contribute to cancer development and metastasis
inferredcites →https://doi.org/10.1007/s12032-013-0795-1openalex-snapshot
Prediction of local recurrence in cervical cancer by a Cox model comprised of lymph node status, lymph-vascular space invasion, and intratumoral Th17 cell-infiltration
inferredcites →https://doi.org/10.1007/s13277-013-1220-2openalex-snapshot
Diagnostic value of pleural interleukin 17 and carcinoembryonic antigen in lung cancer patients with malignant pleural effusions
inferredcites →https://doi.org/10.1016/j.addr.2011.05.014openalex-snapshot
Role of the lymphatics in cancer metastasis and chemotherapy applications
inferredcites →https://doi.org/10.1016/j.bbrc.2011.03.021openalex-snapshot
IL-17 is associated with poor prognosis and promotes angiogenesis via stimulating VEGF production of cancer cells in colorectal carcinoma
inferredcites →https://doi.org/10.1016/j.ccr.2004.09.028openalex-snapshot
Ras-induced interleukin-8 expression plays a critical role in tumor growth and angiogenesis
inferredcites →https://doi.org/10.1016/j.ccr.2009.06.017openalex-snapshot
Polarization of Tumor-Associated Neutrophil Phenotype by TGF-β: “N1” versus “N2” TAN
inferredcites →https://doi.org/10.1016/j.ccr.2009.08.014openalex-snapshot
The Yin-Yang of Tumor-Associated Neutrophils
inferredcites →https://doi.org/10.1016/j.ceb.2008.12.012openalex-snapshot
VEGFs and receptors involved in angiogenesis versus lymphangiogenesis
inferredcites →https://doi.org/10.1016/j.cell.2010.01.045openalex-snapshot
Lymphangiogenesis: Molecular Mechanisms and Future Promise
inferredcites →https://doi.org/10.1016/j.cellimm.2011.10.015openalex-snapshot
Increased IL-17-producing CD4+ T cells in patients with esophageal cancer
inferredcites →https://doi.org/10.1016/j.cellimm.2013.06.001openalex-snapshot
Correlation between Th17 cells and tumor microenvironment
inferredcites →https://doi.org/10.1016/j.clinthera.2006.11.015openalex-snapshot
Bevacizumab: An angiogenesis inhibitor for the treatment of solid malignancies
inferredcites →https://doi.org/10.1016/j.cyto.2011.08.036openalex-snapshot
TH1 and TH17 interactions in untreated inflamed mucosa of inflammatory bowel disease, and their potential to mediate the inflammation
inferredcites →https://doi.org/10.1016/j.cyto.2013.06.296openalex-snapshot
293
inferredcites →https://doi.org/10.1016/j.cyto.2013.06.299openalex-snapshot
296
inferredcites →https://doi.org/10.1016/j.cytogfr.2005.04.007openalex-snapshot
CXC chemokines in angiogenesis
inferredcites →https://doi.org/10.1016/j.cytogfr.2009.11.005openalex-snapshot
Dangerous liaisons: STAT3 and NF-κB collaboration and crosstalk in cancer
inferredcites →https://doi.org/10.1016/j.cytogfr.2012.08.009openalex-snapshot
The emerging role of T cell cytokines in non-small cell lung cancer
inferredcites →https://doi.org/10.1016/j.ejso.2007.02.020openalex-snapshot
Evaluation of VEGF A expression and microvascular density as prognostic factors in extrahepatic cholangiocarcinoma
inferredcites →https://doi.org/10.1016/j.imlet.2004.01.014openalex-snapshot
Interleukin-17 augments tumor necrosis factor-α-induced elaboration of proangiogenic factors from fibroblasts
inferredcites →https://doi.org/10.1016/j.imlet.2012.10.011openalex-snapshot
IL-17 promoted metastasis of non-small-cell lung cancer cells
inferredcites →https://doi.org/10.1016/j.immuni.2004.08.018openalex-snapshot
Interleukin-17 Family Members and Inflammation
inferredcites →https://doi.org/10.1016/j.immuni.2008.03.004openalex-snapshot
The Biological Functions of T Helper 17 Cell Effector Cytokines in Inflammation
inferredcites →https://doi.org/10.1016/j.immuni.2009.09.014openalex-snapshot
T Helper 17 Cells Promote Cytotoxic T Cell Activation in Tumor Immunity
inferredcites →https://doi.org/10.1016/j.it.2004.05.003openalex-snapshot
Lymphatic vasculature: development, molecular regulation and role in tumor metastasis and inflammation
inferredcites →https://doi.org/10.1016/j.jhep.2008.12.033openalex-snapshot
Increased intratumoral IL-17-producing cells correlate with poor survival in hepatocellular carcinoma patients
inferredcites →https://doi.org/10.1016/j.joca.2005.10.004openalex-snapshot
Interleukin-17, a regulator of angiogenic factor release by synovial fibroblasts
inferredcites →https://doi.org/10.1016/j.leukres.2013.06.022openalex-snapshot
Expression levels of IL-27 and IL-17 in multiple myeloma patients: A higher ratio of IL-27:IL-17 in bone marrow was associated with a superior progression-free survival
inferredcites →https://doi.org/10.1016/j.lungcan.2009.11.013openalex-snapshot
Increased IL-17-producing cells correlate with poor survival and lymphangiogenesis in NSCLC patients
inferredcites →https://doi.org/10.1016/j.micinf.2009.04.003openalex-snapshot
IL-17 and Th17 cells in human inflammatory diseases
inferredcites →https://doi.org/10.1016/j.molmed.2012.09.007openalex-snapshot
Controversies on the role of Th17 in cancer: a TGF-β-dependent immunosuppressive activity?
inferredcites →https://doi.org/10.1016/j.mpdhp.2010.03.011openalex-snapshot
The biological significance of lymphangiogenesis in human tumours
inferredcites →https://doi.org/10.1016/j.mvr.2007.08.006openalex-snapshot
Potential therapeutic strategies for lymphatic metastasis
inferredcites →https://doi.org/10.1016/j.rmed.2003.10.011openalex-snapshot
Differential diagnosis of pleural effusions by fuzzy-logic-based analysis of cytokines
inferredcites →https://doi.org/10.1016/s0092-8674(00)80108-7openalex-snapshot
Patterns and Emerging Mechanisms of the Angiogenic Switch during Tumorigenesis
inferredcites →https://doi.org/10.1016/s0140-6736(13)61134-4openalex-snapshot
Anti-interleukin-17A monoclonal antibody secukinumab in treatment of ankylosing spondylitis: a randomised, double-blind, placebo-controlled trial
inferredcites →https://doi.org/10.1016/s0165-5728(99)00111-3openalex-snapshot
Interleukin-17 stimulates the expression of IκBα mRNA and the secretion of IL-6 and IL-8 in glioblastoma cell lines
inferredcites →https://doi.org/10.1016/s1471-4906(02)02302-5openalex-snapshot
Macrophage polarization: tumor-associated macrophages as a paradigm for polarized M2 mononuclear phagocytes
inferredcites →https://doi.org/10.1023/a:1009284305061openalex-snapshot
CXC chemokines mechanism of action in regulating tumor angiogenesis
inferredcites →https://doi.org/10.1038/cdd.2009.74openalex-snapshot
IL-17 stimulates the proliferation and differentiation of human mesenchymal stem cells: implications for bone remodeling
inferredcites →https://doi.org/10.1038/nature04870openalex-snapshot
Nuclear factor-κB in cancer development and progression
inferredcites →https://doi.org/10.1038/nature06764openalex-snapshot
Impaired TH17 cell differentiation in subjects with autosomal dominant hyper-IgE syndrome
inferredcites →https://doi.org/10.1038/nature07021openalex-snapshot
IL-21 and TGF-β are required for differentiation of human TH17 cells
inferredcites →https://doi.org/10.1038/nature07205openalex-snapshot
Cancer-related inflammation
inferredcites →https://doi.org/10.1038/ncomms1609openalex-snapshot
A role for T-bet-mediated tumour immune surveillance in anti-IL-17A treatment of lung cancer
inferredcites →https://doi.org/10.1038/ni.1610openalex-snapshot
The differentiation of human TH-17 cells requires transforming growth factor-β and induction of the nuclear receptor RORγt
inferredcites →https://doi.org/10.1038/nm.2015openalex-snapshot
A human colonic commensal promotes colon tumorigenesis via activation of T helper type 17 T cell responses
inferredcites →https://doi.org/10.1038/nm.3291openalex-snapshot
An interleukin-17–mediated paracrine network promotes tumor resistance to anti-angiogenic therapy
inferredcites →https://doi.org/10.1038/nm.3333openalex-snapshot
IL-17 mediates resistance to anti-VEGF therapy
inferredcites →https://doi.org/10.1038/nm.3432openalex-snapshot
Pathogenic conversion of Foxp3+ T cells into TH17 cells in autoimmune arthritis
inferredcites →https://doi.org/10.1038/npre.2008.2632.1openalex-snapshot
Breast Cancer Associated Metastasis is Significantly Increased in a Model of Autoimmune Arthritis
inferredcites →https://doi.org/10.1038/nrc1275openalex-snapshot
The STATs of cancer — new molecular targets come of age
inferredcites →https://doi.org/10.1038/nrc2734openalex-snapshot
STATs in cancer inflammation and immunity: a leading role for STAT3
inferredcites →https://doi.org/10.1038/nri2506openalex-snapshot
Myeloid-derived suppressor cells as regulators of the immune system
inferredcites →https://doi.org/10.1038/nri2742openalex-snapshot
TH17 cells in tumour immunity and immunotherapy
inferredcites →https://doi.org/10.1038/nrrheum.2013.213openalex-snapshot
Tipping the balance: conversion of Foxp3+ T cells to TH17 cells is crucial in autoimmune arthritis
inferredcites →https://doi.org/10.1038/onc.2010.367openalex-snapshot
Up for Mischief? IL-17/Th17 in the tumour microenvironment
inferredcites →https://doi.org/10.1038/onc.2013.268openalex-snapshot
Autocrine/paracrine mechanism of interleukin-17B receptor promotes breast tumorigenesis through NF-κB-mediated antiapoptotic pathway
inferredcites →https://doi.org/10.1038/srep03456openalex-snapshot
IL-17A is produced by breast cancer TILs and promotes chemoresistance and proliferation through ERK1/2
inferredcites →https://doi.org/10.1056/nejm199704103361506openalex-snapshot
Nuclear Factor-κB — A Pivotal Transcription Factor in Chronic Inflammatory Diseases
inferredcites →https://doi.org/10.1056/nejmra0707449openalex-snapshot
Interleukin-17 and Type 17 Helper T Cells
inferredcites →https://doi.org/10.1073/pnas.0712185105openalex-snapshot
Role of Bv8 in neutrophil-dependent angiogenesis in a transgenic model of cancer progression
inferredcites →https://doi.org/10.1073/pnas.0912675107openalex-snapshot
Ablation of IL-17A abrogates progression of spontaneous intestinal tumorigenesis
inferredcites →https://doi.org/10.1084/jem.169.4.1199openalex-snapshot
Site-restricted persistent cytomegalovirus infection after selective long-term depletion of CD4+ T lymphocytes.
inferredcites →https://doi.org/10.1084/jem.181.1.435openalex-snapshot
Inhibition of tumor growth by elimination of granulocytes.
inferredcites →https://doi.org/10.1084/jem.184.3.981openalex-snapshot
Interferon-gamma-inducible protein 10 (IP-10) is an angiostatic factor that inhibits human non-small cell lung cancer (NSCLC) tumorigenesis and spontaneous metastases.
inferredcites →https://doi.org/10.1084/jem.194.4.519openalex-snapshot
Requirement of Interleukin 17 Receptor Signaling for Lung Cxc Chemokine and Granulocyte Colony-Stimulating Factor Expression, Neutrophil Recruitment, and Host Defense
inferredcites →https://doi.org/10.1084/jem.20061775openalex-snapshot
Th17 functions as an osteoclastogenic helper T cell subset that links T cell activation and bone destruction
inferredcites →https://doi.org/10.1084/jem.20080218openalex-snapshot
Deficiency of Th17 cells in hyper IgE syndrome due to mutations in STAT3
inferredcites →https://doi.org/10.1084/jem.20090207openalex-snapshot
IL-17 can promote tumor growth through an IL-6–Stat3 signaling pathway
inferredcites →https://doi.org/10.1084/jem.20122308openalex-snapshot
Innate lymphoid cells sustain colon cancer through production of interleukin-22 in a mouse model
inferredcites →https://doi.org/10.1086/422329openalex-snapshot
Requirement of Interleukin‐17A for Systemic Anti– Candida albicans Host Defense in Mice
inferredcites →https://doi.org/10.1093/intimm/dxq455openalex-snapshot
IL-23-dependent and -independent enhancement pathways of IL-17A production by lactic acid
inferredcites →https://doi.org/10.1097/01.mib.0000218764.06959.91openalex-snapshot
Critical role of IL-17 receptor signaling in acute TNBS-induced colitis
inferredcites →https://doi.org/10.1097/cji.0000000000000005openalex-snapshot
Association of Myeloid-derived Suppressor Cells and Efficacy of Cytokine-induced Killer Cell Immunotherapy in Metastatic Renal Cell Carcinoma Patients
inferredcites →https://doi.org/10.1101/cshperspect.a006593openalex-snapshot
The VEGF Pathway in Cancer and Disease: Responses, Resistance, and the Path Forward
inferredcites →https://doi.org/10.1111/bjd.12025openalex-snapshot
Brodalumab and ixekizumab, anti-interleukin-17-receptor antibodies for psoriasis: a critical appraisal
inferredcites →https://doi.org/10.1111/bjd.12110openalex-snapshot
Efficacy and safety of secukinumab in the treatment of moderate-to-severe plaque psoriasis: a randomized, double-blind, placebo-controlled phase II dose-ranging study
inferredcites →https://doi.org/10.1111/bjd.12112openalex-snapshot
Secukinumab induction and maintenance therapy in moderate-to-severe plaque psoriasis: a randomized, double-blind, placebo-controlled, phase II regimen-finding study
inferredcites →https://doi.org/10.1111/j.1365-2893.2006.00782.xopenalex-snapshot
Increased expression of vascular endothelial growth factor in small hepatocellular carcinoma
inferredcites →https://doi.org/10.1111/j.1440-1843.2007.01154.xopenalex-snapshot
Diagnosis and management of malignant pleural effusions
inferredcites →https://doi.org/10.1111/j.1582-4934.2009.00834.xopenalex-snapshot
Lymphangiogenesis and cancer metastasis
inferredcites →https://doi.org/10.1128/iai.73.1.617-621.2005openalex-snapshot
Interleukin-17/Interleukin-17 Receptor-Mediated Signaling Is Important for Generation of an Optimal Polymorphonuclear Response againstToxoplasma gondiiInfection
inferredcites →https://doi.org/10.1136/annrheumdis-2012-202646openalex-snapshot
Efficacy and safety of secukinumab, a fully human anti-interleukin-17A monoclonal antibody, in patients with moderate-to-severe psoriatic arthritis: a 24-week, randomised, double-blind, placebo-controlled, phase II proof-of-concept trial
inferredcites →https://doi.org/10.1136/gut.2009.182170openalex-snapshot
Differential regulation of interleukin 17 and interferon production in inflammatory bowel disease
inferredcites →https://doi.org/10.1136/gut.52.1.65openalex-snapshot
Increased expression of interleukin 17 in inflammatory bowel disease
inferredcites →https://doi.org/10.1146/annurev.immunol.021908.132710openalex-snapshot
IL-17 and Th17 Cells
inferredcites →https://doi.org/10.1146/annurev.med.57.121304.131306openalex-snapshot
Angiogenesis
inferredcites →https://doi.org/10.1158/0008-5472.465.65.2openalex-snapshot
CXCL12 and Vascular Endothelial Growth Factor Synergistically Induce Neoangiogenesis in Human Ovarian Cancers
inferredcites →https://doi.org/10.1158/0008-5472.can-11-3795openalex-snapshot
Interleukin-17 Promotes Formation and Growth of Prostate Adenocarcinoma in Mouse Models
inferredcites →https://doi.org/10.1158/1078-0432.ccr-07-4843openalex-snapshot
The Interleukin-8 Pathway in Cancer
inferredcites →https://doi.org/10.1182/blood-2002-05-1461openalex-snapshot
Interleukin-17 promotes angiogenesis and tumor growth
inferredcites →https://doi.org/10.1182/blood-2007-09-113878openalex-snapshot
Angiostatic activity of the antitumor cytokine interleukin-21
inferredcites →https://doi.org/10.1182/blood-2007-11-120998openalex-snapshot
Tumor-specific Th17-polarized cells eradicate large established melanoma
inferredcites →https://doi.org/10.1182/blood-2008-03-143222openalex-snapshot
Dendritic cells mediate the induction of polyfunctional human IL17-producing cells (Th17-1 cells) enriched in the bone marrow of patients with myeloma
inferredcites →https://doi.org/10.1182/blood-2008-09-177360openalex-snapshot
Endogenous IL-17 contributes to reduced tumor growth and metastasis
inferredcites →https://doi.org/10.1182/blood-2009-03-208249openalex-snapshot
Phenotype, distribution, generation, and functional and clinical relevance of Th17 cells in the human tumor environments
inferredcites →https://doi.org/10.1182/blood-2009-10-246660openalex-snapshot
Elevated IL-17 produced by Th17 cells promotes myeloma cell growth and inhibits immune function in multiple myeloma
inferredcites →https://doi.org/10.1182/blood-2010-05-283895openalex-snapshot
A novel role of IL-17–producing lymphocytes in mediating lytic bone disease in multiple myeloma
inferredcites →https://doi.org/10.1182/blood-2011-01-332049openalex-snapshot
A novel pro-lymphangiogenic function for Th17/IL-17
inferredcites →https://doi.org/10.1182/blood.v99.6.2114openalex-snapshot
Interleukin-17 inhibits tumor cell growth by means of a T-cell–dependent mechanism
inferredcites →https://doi.org/10.1186/1475-2867-11-33openalex-snapshot
IFN-γ, IL-17 and TGF-β involvement in shaping the tumor microenvironment: The significance of modulating such cytokines in treating malignant solid tumors
inferredcites →https://doi.org/10.1186/1476-4598-12-78openalex-snapshot
TNFα and IL-17 cooperatively stimulate glucose metabolism and growth factor production in human colorectal cancer cells
inferredcites →https://doi.org/10.1186/1749-8090-7-104openalex-snapshot
Elevated levels of anti inflammatory IL-10 and pro inflammatory IL-17 in malignant pleural effusions
inferredcites →https://doi.org/10.1189/jlb.0806517openalex-snapshot
Mechanisms underlying TGF-β1-induced expression of VEGF and Flk-1 in mouse macrophages and their implications for angiogenesis
inferredcites →https://doi.org/10.12659/msm.882204openalex-snapshot
The role of Interleukin-17A and Interleukin-17E in multiple myeloma patients
inferredcites →https://doi.org/10.1309/l29k-7656-2310-428xopenalex-snapshot
Endoglin (CD105) and Vascular Endothelial Growth Factor as Prognostic Markers in Prostatic Adenocarcinoma
inferredcites →https://doi.org/10.1309/lm7t43aqziupiowzopenalex-snapshot
Advanced Colorectal Cancer Is Associated With Enhanced IL-23 and IL-10 Serum Levels
inferredcites →https://doi.org/10.1371/journal.pone.0034959openalex-snapshot
A Protective Role by Interleukin-17F in Colon Tumorigenesis
inferredcites →https://doi.org/10.1542/peds.22.2.413openalex-snapshot
Annual Review of Medicine , Vol. 8
inferredcites →https://doi.org/10.1593/neo.09988openalex-snapshot
The Chemokine CCL2 Increases Prostate Tumor Growth and Bone Metastasis through Macrophage and Osteoclast Recruitment
inferredcites →https://doi.org/10.2217/fon.11.45openalex-snapshot
Diagnostic Molecular Biomarkers for Malignant Pleural Effusions
inferredcites →https://doi.org/10.2353/ajpath.2007.060835openalex-snapshot
Distinct Roles of Vascular Endothelial Growth Factor-D in Lymphangiogenesis and Metastasis
inferredcites →https://doi.org/10.2741/1093openalex-snapshot
Regulation of stromal proliferation growth arrest differentiation and apoptosis in benign prostatic hyperplasia by TGF beta
inferredcites →https://doi.org/10.3109/07357900903287030openalex-snapshot
Interleukin-17F Suppresses Hepatocarcinoma Cell Growth via Inhibition of Tumor Angiogenesis
inferredcites →https://doi.org/10.3322/caac.21166openalex-snapshot
Cancer statistics, 2013
inferredcites →https://doi.org/10.3390/ijms12117424openalex-snapshot
Distribution and Clinical Significance of Th17 Cells in the Tumor Microenvironment and Peripheral Blood of Pancreatic Cancer Patients
inferredcites →https://doi.org/10.3892/or.2011.1201openalex-snapshot
Tumor-infiltrating CD4+ Th17 cells produce IL-17 in tumor microenvironment and promote tumor progression in human gastric cancer
inferredcites →https://doi.org/10.4049/jimmunol.0901017openalex-snapshot
Protumor vs Antitumor Functions of IL-17
inferredcites →https://doi.org/10.4049/jimmunol.0902574openalex-snapshot
IL-17 Promotes Tumor Development through the Induction of Tumor Promoting Microenvironments at Tumor Sites and Myeloid-Derived Suppressor Cells
inferredcites →https://doi.org/10.4049/jimmunol.0903271openalex-snapshot
IL-17 Contributes to Angiogenesis in Rheumatoid Arthritis
inferredcites →https://doi.org/10.4049/jimmunol.1003251openalex-snapshot
IL-17+ Regulatory T Cells in the Microenvironments of Chronic Inflammation and Cancer
inferredcites →https://doi.org/10.4049/jimmunol.166.4.2276openalex-snapshot
IFN-γ-Dependent Inhibition of Tumor Angiogenesis by Tumor-Infiltrating CD4+ T Cells Requires Tumor Responsiveness to IFN-γ
inferredcites →https://doi.org/10.4049/jimmunol.167.8.4137openalex-snapshot
Cutting Edge: IL-17F, a Novel Cytokine Selectively Expressed in Activated T Cells and Monocytes, Regulates Angiogenesis and Endothelial Cell Cytokine Production
inferredcites →https://doi.org/10.4049/jimmunol.175.9.6177openalex-snapshot
IL-17 Enhances the Net Angiogenic Activity and In Vivo Growth of Human Non-Small Cell Lung Cancer in SCID Mice through Promoting CXCR-2-Dependent Angiogenesis
inferredcites →https://doi.org/10.4049/jimmunol.180.11.7175openalex-snapshot
Tumor-Secreted Lactic Acid Promotes IL-23/IL-17 Proinflammatory Pathway
inferredcites →https://doi.org/10.4049/jimmunol.181.9.6536openalex-snapshot
Differential Regulation of Chemokines by IL-17 in Colonic Epithelial Cells
inferredcites →https://doi.org/10.4161/onci.19735openalex-snapshot
IL-17A is a central regulator of lung tumor growth
inferredcites →https://doi.org/10.5402/2012/578149openalex-snapshot
Interleukin-17 Expression in the Barrett’s Metaplasia-Dysplasia-Adenocarcinoma Sequence

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Inflammation and Cancer
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Inflammation and Cancer
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Exploring the Vasculitis‐Tumors Link: Epidemiological Patterns, Mechanistic Insights, and Clinical Implications
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IL‐17 and IL‐22 in immunity: Driving protection and pathology
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Pre‐operative predictors of early recurrence/mortality including the role of inflammatory indices in patients undergoing partial hepatectomy for spontaneously ruptured hepatocellular carcinoma
inferred← citeshttps://doi.org/10.1002/mco2.104openalex-snapshot
NF‐κB signaling in inflammation and cancer
inferred← citeshttps://doi.org/10.1002/mco2.70078openalex-snapshot
CD25 downregulation by tumor exosomal microRNA‐15a promotes interleukin‐17‐producing γδ‐T‐cells‐mediated radioresistance in nasopharyngeal carcinoma
inferred← citeshttps://doi.org/10.1007/978-3-030-36214-0_2openalex-snapshot
Gastric Tumor Microenvironment
inferred← citeshttps://doi.org/10.1007/978-3-031-06566-8_5openalex-snapshot
PHLPP Signaling in Immune Cells
inferred← citeshttps://doi.org/10.1007/978-3-319-28140-7_27openalex-snapshot
Interleukins
inferred← citeshttps://doi.org/10.1007/978-94-024-0921-5_7openalex-snapshot
Regulation of Interleukin-17 Production
inferred← citeshttps://doi.org/10.1007/978-981-13-1879-5_8openalex-snapshot
Zebrafish Angiogenesis and Valve Morphogenesis: Insights from Development and Disease Models
inferred← citeshttps://doi.org/10.1007/978-981-15-2017-4_7openalex-snapshot
Understanding Colorectal Cancer: The Basics
inferred← citeshttps://doi.org/10.1007/s00251-021-01205-wopenalex-snapshot
Rs-10889677 variant in interleukin-23 receptor may contribute to creating an inflammatory milieu more susceptible to bladder tumourigenesis: report and meta-analysis
inferred← citeshttps://doi.org/10.1007/s00251-023-01318-4openalex-snapshot
Increased circulating Th17 cell populations in patients with pancreatic ductal adenocarcinoma
inferred← citeshttps://doi.org/10.1007/s00262-018-2196-yopenalex-snapshot
Levels of peripheral blood polymorphonuclear myeloid-derived suppressor cells and selected cytokines are potentially prognostic of disease progression for patients with non-small cell lung cancer
inferred← citeshttps://doi.org/10.1007/s00262-022-03255-9openalex-snapshot
A Fc-VEGF chimeric fusion enhances PD-L1 immunotherapy via inducing immune reprogramming and infiltration in the immunosuppressive tumor microenvironment
inferred← citeshttps://doi.org/10.1007/s00520-019-04793-2openalex-snapshot
The use of crevicular fluid to assess markers of inflammation and angiogenesis, IL-17 and VEGF, in patients with solid tumors receiving zoledronic acid and/or bevacizumab
inferred← citeshttps://doi.org/10.1007/s10549-020-05540-6openalex-snapshot
Increased number of intratumoral IL-17+ cells, a harbinger of the adverse prognosis of triple-negative breast cancer
inferred← citeshttps://doi.org/10.1007/s10620-020-06700-wopenalex-snapshot
Inflammation, Tumoral Markers and Interleukin-17, -10, and -6 Profiles in Pancreatic Adenocarcinoma and Chronic Pancreatitis
inferred← citeshttps://doi.org/10.1007/s12029-026-01520-zopenalex-snapshot
Inflammation and RNA-Related Polymorphisms in Resected Cholangiocarcinoma: Prognostic Associations in Intrahepatic and Perihilar Tumors
inferred← citeshttps://doi.org/10.1007/s12035-017-0445-2openalex-snapshot
Anti-inflammatory Effects of Atorvastatin by Suppressing TRAF3IP2 and IL-17RA in Human Glioblastoma Spheroids Cultured in a Three-dimensional Model: Possible Relevance to Glioblastoma Treatment
inferred← citeshttps://doi.org/10.1007/s12253-020-00820-4openalex-snapshot
Loss of Interleukin-17RA Expression is Associated with Tumour Progression in Colorectal Carcinoma
inferred← citeshttps://doi.org/10.1007/s13277-016-5397-zopenalex-snapshot
Dysregulation of TTP and HuR plays an important role in cancers
inferred← citeshttps://doi.org/10.1007/s13555-025-01515-xopenalex-snapshot
Strategies for Optimal Use of Biological Therapies in Managing Psoriasis: Focus on Secukinumab
inferred← citeshttps://doi.org/10.1016/b978-0-443-18696-7.00009-9openalex-snapshot
Role of Tumor-associated neutrophils in the breast tumor microenvironment
inferred← citeshttps://doi.org/10.1016/bs.adgen.2024.05.002openalex-snapshot
Microbiota-associated mechanisms in colorectal cancer
inferred← citeshttps://doi.org/10.1016/bs.pmbts.2022.07.007openalex-snapshot
An overview of cancer and the human microbiome
inferred← citeshttps://doi.org/10.1016/j.bbcan.2020.188393openalex-snapshot
PERP-ing into diverse mechanisms of cancer pathogenesis: Regulation and role of the p53/p63 effector PERP
inferred← citeshttps://doi.org/10.1016/j.bbrc.2015.02.003openalex-snapshot
Transgene-derived overexpression of miR-17-92 in CD8+ T-cells confers enhanced cytotoxic activity
inferred← citeshttps://doi.org/10.1016/j.biopha.2022.112949openalex-snapshot
Hyperprogression, a challenge of PD-1/PD-L1 inhibitors treatments: potential mechanisms and coping strategies
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2020.126170openalex-snapshot
Enhanced morphological transformation of human lung epithelial cells by continuous exposure to cellulose nanocrystals
inferred← citeshttps://doi.org/10.1016/j.clcc.2017.10.003openalex-snapshot
Monoclonal Antibodies Targeting the IL-17/IL-17RA Axis: An Opportunity to Improve the Efficiency of Anti-VEGF Therapy in Fighting Metastatic Colorectal Cancer?
inferred← citeshttps://doi.org/10.1016/j.clim.2020.108343openalex-snapshot
The increased IL-17-producing γδT cells promote tumor cell proliferation and migration in neuroblastoma
inferred← citeshttps://doi.org/10.1016/j.ctrv.2023.102629openalex-snapshot
Regulatory T cells in gastric cancer: Key controllers from pathogenesis to therapy
inferred← citeshttps://doi.org/10.1016/j.cyto.2018.12.021openalex-snapshot
IL-17 and colorectal cancer: From carcinogenesis to treatment
inferred← citeshttps://doi.org/10.1016/j.ebiom.2019.08.076openalex-snapshot
Impact of the microbiome on checkpoint inhibitor treatment in patients with non-small cell lung cancer and melanoma
inferred← citeshttps://doi.org/10.1016/j.fbio.2025.107309openalex-snapshot
A comprehensive review of the anti-angiogenic potential of edible and medicinal mushrooms: bioactive compounds, mechanisms of action and clinical status
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e27480openalex-snapshot
Innate immune cells: Key players of orchestra in modulating tumor microenvironment (TME)
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e41483openalex-snapshot
Molecular mechanisms of mTOR-mediated cisplatin response in tumor cells
inferred← citeshttps://doi.org/10.1016/j.humimm.2023.110748openalex-snapshot
Elevated levels of peripheral Th17 cells and Th17-related cytokines in patients with periampullary adenocarcinoma
inferred← citeshttps://doi.org/10.1016/j.immuni.2014.12.004openalex-snapshot
IL-17 Cuts to the Chase in Colon Cancer
inferred← citeshttps://doi.org/10.1016/j.intimp.2021.108402openalex-snapshot
The role of IL-17 and anti-IL-17 agents in the immunopathogenesis and management of autoimmune and inflammatory diseases
inferred← citeshttps://doi.org/10.1016/j.jksus.2022.102493openalex-snapshot
Assessment of the relationships between IL-17A polymorphisms and the risk to acute lymphoblastic leukemia in Saudi population
inferred← citeshttps://doi.org/10.1016/j.mgene.2019.100605openalex-snapshot
Association of the IL-17A rs2275913 and MIF rs755622 polymorphisms with the risk of gastric and colorectal cancer
inferred← citeshttps://doi.org/10.1016/j.retram.2025.103527openalex-snapshot
The immunobiological functions and therapeutic applications of interleukin-17 family in cancer
inferred← citeshttps://doi.org/10.1016/j.tice.2017.12.008openalex-snapshot
Nintedanib effects on delaying cancer progression and decreasing COX-2 and IL-17 in the prostate anterior lobe in TRAMP mice
inferred← citeshttps://doi.org/10.1016/j.virusres.2020.198226openalex-snapshot
Interleukin-17 haplotyping predicts hepatocellular carcinoma in sofosbuvir, pegylated interferon-alpha-2a & ribavirin treated chronic hepatitis C patients
inferred← citeshttps://doi.org/10.1017/s0022215117000573openalex-snapshot
Serum cytokine profile of laryngeal squamous cell carcinoma patients
inferred← citeshttps://doi.org/10.1038/nri.2017.142openalex-snapshot
NF-κB, inflammation, immunity and cancer: coming of age
inferred← citeshttps://doi.org/10.1038/s41417-020-0172-0openalex-snapshot
MicroRNA binding site polymorphism in inflammatory genes associated with colorectal cancer: literature review and bioinformatics analysis
inferred← citeshttps://doi.org/10.1038/s41417-024-00811-6openalex-snapshot
NF-κB role on tumor proliferation, migration, invasion and immune escape
inferred← citeshttps://doi.org/10.1038/s41434-022-00362-1openalex-snapshot
Design, construction and in vivo functional assessment of a hinge truncated sFLT01
inferred← citeshttps://doi.org/10.1038/s41573-021-00155-yopenalex-snapshot
Beyond immune checkpoint blockade: emerging immunological strategies
inferred← citeshttps://doi.org/10.1038/s41590-020-0620-xopenalex-snapshot
PD-L1 engagement on T cells promotes self-tolerance and suppression of neighboring macrophages and effector T cells in cancer
inferred← citeshttps://doi.org/10.1038/s41598-017-03278-8openalex-snapshot
Association of increased Treg and Th17 with pathogenesis of moyamoya disease
inferred← citeshttps://doi.org/10.1038/srep11874openalex-snapshot
IL-17A and its homologs IL-25/IL-17E recruit the c-RAF/S6 kinase pathway and the generation of pro-oncogenic LMW-E in breast cancer cells
inferred← citeshttps://doi.org/10.1042/bsr20193308openalex-snapshot
Genomic analysis and clinical implications of immune cell infiltration in gastric cancer
inferred← citeshttps://doi.org/10.1080/2162402x.2016.1234573openalex-snapshot
Functional impairment of infiltrating T cells in human colorectal cancer
inferred← citeshttps://doi.org/10.1101/2023.05.08.23289655openalex-snapshot
Immunomodulatory Effects of Atractylodes Lancea in Healthy Volunteers with Dosage Prediction for Cholangiocarcinoma Therapy: a modelling approach
inferred← citeshttps://doi.org/10.1101/869776openalex-snapshot
Prognostic significances of interleukin-17-producing cells and Th17 cells in malignant cancers: a meta-analysis of the literatures
inferred← citeshttps://doi.org/10.1111/cei.12758openalex-snapshot
The role of high-mobility group box protein 1 in collagen antibody-induced arthritis is dependent on vascular endothelial growth factor
inferred← citeshttps://doi.org/10.1111/dth.15716openalex-snapshot
Successful treatment of cabozantinib‐induced pyoderma gangrenosum with ixekizumab therapy: A case report
inferred← citeshttps://doi.org/10.1111/imm.12571openalex-snapshot
Interleukin‐17A neutralization alleviated ocular neovascularization by promoting M2 and mitigating M1 macrophage polarization
inferred← citeshttps://doi.org/10.1111/jop.12762openalex-snapshot
Immunohistochemical analysis of neutrophils, interleukin‐17, matrix metalloproteinase‐9, and neoformed vessels in oral squamous cell carcinoma
inferred← citeshttps://doi.org/10.1111/odi.14083openalex-snapshot
METTL3/14 and IL‐17 signaling contribute to CEBPA‐DT enhanced oral cancer cisplatin resistance
inferred← citeshttps://doi.org/10.1134/s1990750820010047openalex-snapshot
Assessment of the Cytokine-Producing Resource of Tumor Biopsy Samples from Patients with Invasive Carcinoma of No Special Type and with Non-Malignant Breast Diseases
inferred← citeshttps://doi.org/10.1146/annurev-immunol-101819-092536openalex-snapshot
IL-17 in the Pathogenesis of Disease: Good Intentions Gone Awry
inferred← citeshttps://doi.org/10.1152/physrev.00018.2019openalex-snapshot
Immunity, Hypoxia, and Metabolism–the Ménage à Trois of Cancer: Implications for Immunotherapy
inferred← citeshttps://doi.org/10.1155/2017/7685142openalex-snapshot
S1P Lyase Regulation of Thymic Egress and Oncogenic Inflammatory Signaling
inferred← citeshttps://doi.org/10.1155/2017/9294018openalex-snapshot
Inflammation and Cancer: Extra- and Intracellular Determinants of Tumor-Associated Macrophages as Tumor Promoters
inferred← citeshttps://doi.org/10.1155/2022/2148240openalex-snapshot
[Retracted] Two Potential Biomarkers for the Diagnosis and Prognosis of Laryngeal Carcinoma: CCL20 and IL‐17A
inferred← citeshttps://doi.org/10.1155/2023/1248024openalex-snapshot
TNFSF15 and MIA Variant Associated with Immunotherapy and Prognostic Evaluation in Esophageal Cancer
inferred← citeshttps://doi.org/10.1158/1078-0432.ccr-18-3458openalex-snapshot
IL23-Producing Human Lung Cancer Cells Promote Tumor Growth via Conversion of Innate Lymphoid Cell 1 (ILC1) into ILC3
inferred← citeshttps://doi.org/10.1159/000446587openalex-snapshot
Association of Choroidal Interleukin-17-Producing T Lymphocytes and Macrophages with Geographic Atrophy
inferred← citeshttps://doi.org/10.1177/14703203261483503openalex-snapshot
Renin-angiotensin system imbalance is associated with immunometabolic reprogramming and tissue repair in COPD-lung cancer comorbidity
inferred← citeshttps://doi.org/10.1177/2397847318816617openalex-snapshot
Bronchioloalveolar lung tumors induced in “mice only” by non-genotoxic chemicals are not useful for quantitative assessment of pulmonary adenocarcinoma risk in humans
inferred← citeshttps://doi.org/10.1177/2397847319842845openalex-snapshot
Indirect oxidative stress from pulmonary inflammation exceeds direct oxidative stress from chemical damage to mitochondria
inferred← citeshttps://doi.org/10.1186/s12865-016-0164-xopenalex-snapshot
Capparis Spinosa L. promotes anti-inflammatory response in vitro through the control of cytokine gene expression in human peripheral blood mononuclear cells
inferred← citeshttps://doi.org/10.1186/s12885-017-3210-zopenalex-snapshot
A possible association of baseline serum IL-17A concentrations with progression-free survival of metastatic colorectal cancer patients treated with a bevacizumab-based regimen
inferred← citeshttps://doi.org/10.1186/s12885-021-08969-0openalex-snapshot
Variable roles of interleukin-17F in different cancers
inferred← citeshttps://doi.org/10.1186/s13578-021-00565-wopenalex-snapshot
In respond to commensal bacteria: γδT cells play a pleiotropic role in tumor immunity
inferred← citeshttps://doi.org/10.12677/acrem.2025.131012openalex-snapshot
The Diagnostic Value of Th17 Cells, Serum IL-17, and MMP2 Expression in the Lymph Node Metastasis in Gastric Cancer Patients
inferred← citeshttps://doi.org/10.12688/f1000research.172278.1openalex-snapshot
Assessment Levels of cytokines and chemokines parameters in Premenopausal and Postmenopausal Women with Breast Cancer
inferred← citeshttps://doi.org/10.1371/journal.ppat.1005852openalex-snapshot
Leishmaniavirus-Dependent Metastatic Leishmaniasis Is Prevented by Blocking IL-17A
inferred← citeshttps://doi.org/10.1517/14656566.2016.1109636openalex-snapshot
Novel systemic therapies for the treatment of psoriasis
inferred← citeshttps://doi.org/10.1530/erc-17-0303openalex-snapshot
RET-mediated modulation of tumor microenvironment and immune response in multiple endocrine neoplasia type 2 (MEN2)
inferred← citeshttps://doi.org/10.1620/tjem.247.87openalex-snapshot
Interleukin-17: The Role for Pathological Angiogenesis in Ocular Neovascular Diseases
inferred← citeshttps://doi.org/10.17116/onkolog20231204178openalex-snapshot
The significance of the tumor microenvironment and molecular biological parameters in assessing the prognosis of the disease in patients with early-stage gastric cancer
inferred← citeshttps://doi.org/10.18008/1816-5095-2022-3-557-564openalex-snapshot
Markers of Proliferative Diabetic Retinopathy
inferred← citeshttps://doi.org/10.18097/pbmc20196505418openalex-snapshot
Assessment of the cytokine-producing resource of tumor biopsy samples from patients with invasive carcinoma of no special type and with non-malignant breast diseases
inferred← citeshttps://doi.org/10.18097/pbmc20206606485openalex-snapshot
Influence of the HLDF differentiation factor on the production of cytokines by bio-tissues of breast tissue in its non-malignant diseases and in invasive carcinoma of a non-specific type
inferred← citeshttps://doi.org/10.18632/oncotarget.10655openalex-snapshot
IL-17A exacerbates cisplatin-based resistance of OVCA via upregulating the expression of ABCG2 and MDR1 through Gli1-mediated Hh signaling
inferred← citeshttps://doi.org/10.18632/oncotarget.10804openalex-snapshot
IL-17E synergizes with EGF and confersin vitroresistance to EGFR-targeted therapies in TNBC cells
inferred← citeshttps://doi.org/10.18632/oncotarget.25526openalex-snapshot
A bi-specific inhibitor targeting IL-17A and MMP-9 reduces invasion and motility in MDA-MB-231 cells
inferred← citeshttps://doi.org/10.18678/dtfd.1555362openalex-snapshot
Determination of Serum Interleukin-36 Alpha, Beta, Gamma, and Interleukin-17 Levels in Patients with Non-Hodgkin Lymphoma
inferred← citeshttps://doi.org/10.21203/rs.3.rs-3964228/v1openalex-snapshot
Prognostic role of plasma IL-17a expression and neoadjuvant therapy efficacy in breast cancer
inferred← citeshttps://doi.org/10.21203/rs.3.rs-637295/v1openalex-snapshot
Hub Genes Related to the Pathogenesis and Progression of Colorectal Cancer and Adenoma by Integrative Bioinformatics Approaches
inferred← citeshttps://doi.org/10.21315/mjms2020.27.4.2openalex-snapshot
The Mechanism of Bacteroides fragilis Toxin Contributes to Colon Cancer Formation
inferred← citeshttps://doi.org/10.2147/dddt.s86396openalex-snapshot
Inflammation, cytokines, the IL-17/IL-6/STAT3/NF-κB axis, and tumorigenesis
inferred← citeshttps://doi.org/10.2147/ott.s151129openalex-snapshot
Association between IL-17A G197A polymorphism and gastric cancer risk: an updated meta-analysis based on 6,624 cases and 7,631 controls
inferred← citeshttps://doi.org/10.21608/fsrt.2021.56346.1030openalex-snapshot
Tumour-associated macrophages (IL-23+CD14+ subset) levels during bladder cancer progression
inferred← citeshttps://doi.org/10.2174/0113892010338997241216053634openalex-snapshot
Potential Pathogens Associated with Colorectal Cancer
inferred← citeshttps://doi.org/10.22092/ari.2022.357801.2098openalex-snapshot
A Prognostic Impact of Interleukin 17 (IL-17) as an Immune-Marker in Patients with Bladder Cancer.
inferred← citeshttps://doi.org/10.3109/1354750x.2015.1068853openalex-snapshot
Interleukin-17 levels correlate with poor prognosis and vascular endothelial growth factor concentration in the serum of patients with non-small cell lung cancer
inferred← citeshttps://doi.org/10.32725/jab.2019.016openalex-snapshot
Correlation of adenosine deaminase operating under nitro-oxidative stress with tumor and vascularization in patients with advanced gallbladder carcinoma
inferred← citeshttps://doi.org/10.3389/fimmu.2015.00037openalex-snapshot
The Jekyll and Hyde story of IL17-Producing γδT Cells
inferred← citeshttps://doi.org/10.3389/fimmu.2018.00527openalex-snapshot
Contribution to Tumor Angiogenesis From Innate Immune Cells Within the Tumor Microenvironment: Implications for Immunotherapy
inferred← citeshttps://doi.org/10.3389/fimmu.2020.01691openalex-snapshot
Leveraging Public Single-Cell and Bulk Transcriptomic Datasets to Delineate MAIT Cell Roles and Phenotypic Characteristics in Human Malignancies
inferred← citeshttps://doi.org/10.3389/fimmu.2022.864497openalex-snapshot
Effector Memory T Cells and CD45RO+ Regulatory T Cells in Metastatic vs. Non-Metastatic Lymph Nodes in Lung Cancer Patients
inferred← citeshttps://doi.org/10.3389/fimmu.2023.1094823openalex-snapshot
The role of Th-17 cells and IL-17 in the metastatic spread of breast cancer: As a means of prognosis and therapeutic target
inferred← citeshttps://doi.org/10.3389/fimmu.2024.1479505openalex-snapshot
The role of interleukin-17 in inflammation-related cancers
inferred← citeshttps://doi.org/10.3389/fimmu.2025.1518664openalex-snapshot
NF-κB signaling and the tumor microenvironment in osteosarcoma: implications for immune evasion and therapeutic resistance
inferred← citeshttps://doi.org/10.3389/fimmu.2025.1575472openalex-snapshot
Hypercholesterolemia and the role of lipid metabolism gene CES1 in immune infiltration promote central nervous system relapse in acute myeloid leukemia
inferred← citeshttps://doi.org/10.3389/fonc.2021.731548openalex-snapshot
Re-Identification of Patient Subgroups in Uveal Melanoma
inferred← citeshttps://doi.org/10.3389/fonc.2022.1019247openalex-snapshot
Expression analysis of cytokines IL-5, IL-6, IL-8, IL-17 and VEGF in breast cancer patients
inferred← citeshttps://doi.org/10.3389/fonc.2022.893820openalex-snapshot
Targeting TRAF3IP2 inhibits angiogenesis in glioblastoma
inferred← citeshttps://doi.org/10.3389/fonc.2024.1325575openalex-snapshot
Th17/Treg cell balance in patients with papillary thyroid carcinoma: a new potential biomarker and therapeutic target
inferred← citeshttps://doi.org/10.3390/biology14040347openalex-snapshot
The Role of IL-23 in the Development of Inflammatory Diseases
inferred← citeshttps://doi.org/10.3390/biomedicines12040827openalex-snapshot
Decoding Tumor Angiogenesis for Therapeutic Advancements: Mechanistic Insights
inferred← citeshttps://doi.org/10.3390/biomedicines12040867openalex-snapshot
Potential Aspects of the Use of Cytokines in Atopic Dermatitis
inferred← citeshttps://doi.org/10.3390/cancers11040564openalex-snapshot
Tumor-Associated Neutrophils in Cancer: Going Pro
inferred← citeshttps://doi.org/10.3390/cancers12071760openalex-snapshot
MHC Class I Downregulation in Cancer: Underlying Mechanisms and Potential Targets for Cancer Immunotherapy
inferred← citeshttps://doi.org/10.3390/cancers13040734openalex-snapshot
Interplay between the Gut Microbiota and Inflammatory Mediators in the Development of Colorectal Cancer
inferred← citeshttps://doi.org/10.3390/cancers15010276openalex-snapshot
Tumor Microenvironment before and after Chemoradiation in Locally Advanced Rectal Cancer: Beyond PD-L1
inferred← citeshttps://doi.org/10.3390/cancers15030852openalex-snapshot
Head and Neck Cancer Immunotherapy: Molecular Biological Aspects of Preclinical and Clinical Research
inferred← citeshttps://doi.org/10.3390/cancers15133288openalex-snapshot
Sustaining the Activation of EGFR Signal by Inflammatory Cytokine IL17A Prompts Cell Proliferation and EGFR-TKI Resistance in Lung Cancer
inferred← citeshttps://doi.org/10.3390/cancers16244224openalex-snapshot
The Intersection of Psoriasis and Neoplasia: Risk Factors, Therapeutic Approaches, and Management Strategies
inferred← citeshttps://doi.org/10.3390/cells14020095openalex-snapshot
Gene–Environment Interaction: Small Deletions (DELs) and Transcriptomic Profiles in Non-Melanoma Skin Cancer (NMSC) and Potential Implications for Therapy
inferred← citeshttps://doi.org/10.3390/diagnostics12092068openalex-snapshot
The Urinary Microbiome: Role in Bladder Cancer and Treatment
inferred← citeshttps://doi.org/10.3390/ijms16011691openalex-snapshot
Mechanisms and Αpplications of Ιnterleukins in Cancer Immunotherapy
inferred← citeshttps://doi.org/10.3390/ijms19123880openalex-snapshot
The Interleukin-17 Family of Cytokines in Breast Cancer
inferred← citeshttps://doi.org/10.3390/ijms26199600openalex-snapshot
Co-Targeting PD-1 and IL-33/ST2 Pathways for Enhanced Acquired Anti-Tumor Immunity in Breast Cancer
inferred← citeshttps://doi.org/10.3390/jcm10194572openalex-snapshot
IL-17 Promotes Nitric Oxide Production in Non-Small-Cell Lung Cancer
inferred← citeshttps://doi.org/10.3390/jcm11174973openalex-snapshot
Interleukin 17 and Its Involvement in Renal Cell Carcinoma
inferred← citeshttps://doi.org/10.3390/ph18020198openalex-snapshot
Immunomodulatory Effects of Atractylodes lancea in Healthy Volunteers with Dosage Prediction for Cholangiocarcinoma Therapy: A Modelling Approach
inferred← citeshttps://doi.org/10.37897/rjr.2019.4.6openalex-snapshot
Connections between rheumatology and oncology – discussions based on a case report
inferred← citeshttps://doi.org/10.3892/mmr.2015.4694openalex-snapshot
Interleukin-17 potently increases non-small cell lung cancer growth
inferred← citeshttps://doi.org/10.3892/mmr.2019.10310openalex-snapshot
IL‑17A promotes CXCR2‑dependent angiogenesis in a mouse model of liver cancer
inferred← citeshttps://doi.org/10.3892/ol.2017.5638openalex-snapshot
High IL-17 expression is associated with an unfavorable prognosis in thyroid cancer
inferred← citeshttps://doi.org/10.3892/ol.2018.8716openalex-snapshot
Interplay between inflammatory tumor microenvironment and cancer stem cells (Review)
inferred← citeshttps://doi.org/10.3892/ol.2018.9645openalex-snapshot
Interleukin‑17 promotes the development of cisplatin resistance in colorectal cancer
inferred← citeshttps://doi.org/10.3892/ol.2019.10425openalex-snapshot
Cervical carcinoma high‑expressed long non‑coding RNA 1 may promote growth of colon adenocarcinoma through interleukin‑17A
inferred← citeshttps://doi.org/10.3892/or.2015.4246openalex-snapshot
IL-17A-producing T cells and associated cytokines are involved in the progression of gastric cancer
inferred← citeshttps://doi.org/10.3892/or.2016.4547openalex-snapshot
A matrix metalloproteinase inhibitor enhances anti-cytotoxic T lymphocyte antigen-4 antibody immunotherapy in breast cancer by reprogramming the tumor microenvironment
inferred← citeshttps://doi.org/10.3892/or.2016.4837openalex-snapshot
IL-17A-producing T cells are associated with the progression of lung adenocarcinoma
inferred← citeshttps://doi.org/10.3978/j.issn.2218-676x.2015.10.06openalex-snapshot
Sphingosine-1-phosphate in inflammatory bowel disease and colitis-associated colon cancer: the fat's in the fire.
inferred← citeshttps://doi.org/10.4103/0973-1482.157321openalex-snapshot
Anesthesia and cancer recurrences
inferred← citeshttps://doi.org/10.4110/in.2020.20.e6openalex-snapshot
IL-17-Producing Cells in Tumor Immunity: Friends or Foes?
inferred← citeshttps://doi.org/10.4238/gmr16038826openalex-snapshot
Research Article Role of IL17A rs2275913 and rs3748067 polymorphisms in the risk cervical cancer.
inferred← citeshttps://doi.org/10.46718/jbgsr.2020.05.000118openalex-snapshot
The Involvement of IL-17 – ACE-ACE2 System Connections in the Pathogenesis of Cancer
inferred← citeshttps://doi.org/10.5114/dr.2021.113155openalex-snapshot
The significance of secukinumab in the treatment of plaque psoriasis
inferred← citeshttps://doi.org/10.5114/wo.2016.61562openalex-snapshot
The inflammatory cytokine interleukin-23 is elevated in lung cancer, particularly small cell type
inferred← citeshttps://doi.org/10.54254/2753-8818/2024.18947openalex-snapshot
Impact of MR1 on lung cancer in the proliferation of MAIT cells, and production of cytokine and perforin
inferred← citeshttps://doi.org/10.5772/intechopen.100950openalex-snapshot
Chemokines Updates
inferred← citeshttps://doi.org/10.5772/intechopen.102893openalex-snapshot
Modulators of Tumor Angiogenesis: Insights into the Role of Galectin-3 and IL-17 Signaling
inferred← citeshttps://doi.org/10.5772/intechopen.105049openalex-snapshot
Glance on the Critical Role of IL-23 Receptor Gene Variations in Inflammation-Induced Carcinogenesis
inferred← citeshttps://doi.org/10.5772/intechopen.95139openalex-snapshot
Tumor Angiogenesis and Modulators
inferred← citeshttps://doi.org/10.5772/intechopen.96422openalex-snapshot
IL-17 Biological Effects and Signaling Mechanisms in Human Leukemia U937 Cells
inferred← citeshttps://doi.org/10.5812/gct.84483openalex-snapshot
Association Study of rs763780T>C IL-17F and rs2275913G>A IL-17A Polymorphisms with Breast Cancer Risk in East Azerbaijan-Iran
inferred← citeshttps://doi.org/10.70675/0f728c2fzfbb3z4cd8z9c09zad87af4858daopenalex-snapshot
Cancers du sein et immunité anti-tumorale
inferred← citeshttps://doi.org/10.70675/2c5fccd5z6a86z47cezbb48z8aabe5736cb6openalex-snapshot
MUC/EGFR/IL17 et l’autophagie sont associés à la résistance de la chimiothérapie ou des thérapies ciblées dans les cancers du sein triple négatif.
inferred← citeshttps://doi.org/10.70675/8ad0de1ezeb55z4983z9084z94cc8799b353openalex-snapshot
Analyse du rôle de l’IL-17 dans la progression du cancer du sein chez différents sous-groupes moléculaires de patientes : effet sur l’expression de PD-L1, sur la prolifération des cellules cancéreuses et sur la survie des patientes
inferred← citeshttps://doi.org/10.70675/93867442zef10z413bz8ac0z49dbe1889857openalex-snapshot
Influence de la réponse IL-17 dans la physiopathologie du foie
inferred← citeshttps://doi.org/10.70675/c5448d83z840cz458dz90d0za870d8188f29openalex-snapshot
Les cytokines inflammatoires et les canaux ioniques dans la tumorigénèse du cancer colorectal : rôle du TNF et modulation du KCa3.1
inferred← citeshttps://doi.org/10.70675/d7437ea2z8f5cz4c07za74dz1ada27505ca9openalex-snapshot
Thérapie des cancers du sein : efficacité thérapeutique et mécanisme d’action d’anticorps anti-cathepsine D dans des modèles de souris immunocompétentes
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