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Prognostic significances of interleukin-17-producing cells and Th17 cells in malignant cancers: a meta-analysis of the literatures
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/cncr.24558openalex-snapshot
Radiation dose escalation for localized prostate cancer
inferredcites →https://doi.org/10.1002/ijc.30134openalex-snapshot
IL17 producing γδT cells induce angiogenesis and are associated with poor survival in gallbladder cancer patients
inferredcites →https://doi.org/10.1002/sim.1605openalex-snapshot
Extracting summary statistics to perform meta‐analysis of the published literature for survival endpoints
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Dose Escalation in Prostate Radiotherapy up to 82 Gy Using Simultaneous Integrated Boost
inferredcites →https://doi.org/10.1007/s00066-014-0806-yopenalex-snapshot
Comparing morbidity and cancer control after 3D-conformal (70/74 Gy) and intensity modulated radiotherapy (78/82 Gy) for prostate cancer
inferredcites →https://doi.org/10.1007/s00262-013-1460-4openalex-snapshot
Mast cells expressing interleukin 17 in the muscularis propria predict a favorable prognosis in esophageal squamous cell carcinoma
inferredcites →https://doi.org/10.1007/s00441-013-1567-0openalex-snapshot
High density of IL-17-producing cells is associated with improved prognosis for advanced epithelial ovarian cancer
inferredcites →https://doi.org/10.1007/s12032-013-0732-3openalex-snapshot
Prognostic value of Th17 cells in acute leukemia
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/s12032-014-0082-9openalex-snapshot
The effect of immune microenvironment on the progression and prognosis of colorectal cancer
inferredcites →https://doi.org/10.1007/s12094-014-1197-3openalex-snapshot
Interleukin-17 is a favorable prognostic marker for colorectal cancer
inferredcites →https://doi.org/10.1007/s40265-015-0359-0openalex-snapshot
Secukinumab: First Global Approval
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.2012.02.022openalex-snapshot
Accessories to the Crime: Functions of Cells Recruited to the Tumor Microenvironment
inferredcites →https://doi.org/10.1016/j.clim.2014.05.004openalex-snapshot
Emerging role of IL-17 and Th17 cells in systemic lupus erythematosus
inferredcites →https://doi.org/10.1016/j.coi.2007.07.020openalex-snapshot
Th17: the third member of the effector T cell trilogy
inferredcites →https://doi.org/10.1016/j.eururo.2011.08.006openalex-snapshot
Improved Toxicity Profile Following High-Dose Postprostatectomy Salvage Radiation Therapy With Intensity-Modulated Radiation Therapy
inferredcites →https://doi.org/10.1016/j.ijrobp.2005.02.050openalex-snapshot
Whole pelvic radiotherapy for prostate cancer using 3D conformal and intensity-modulated radiotherapy
inferredcites →https://doi.org/10.1016/j.ijrobp.2007.01.043openalex-snapshot
Analysis of Biochemical Control and Prognostic Factors in Patients Treated With Either Low-Dose Three-Dimensional Conformal Radiation Therapy or High-Dose Intensity-Modulated Radiotherapy for Localized Prostate Cancer
inferredcites →https://doi.org/10.1016/j.ijrobp.2014.12.017openalex-snapshot
Acute Toxicity After Image-Guided Intensity Modulated Radiation Therapy Compared to 3D Conformal Radiation Therapy in Prostate Cancer Patients
inferredcites →https://doi.org/10.1016/j.imlet.2004.11.012openalex-snapshot
Interleukin-17 enhances bFGF-, HGF- and VEGF-induced growth of vascular endothelial 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.2014.11.009openalex-snapshot
Interleukin-17 Receptor A Signaling in Transformed Enterocytes Promotes Early Colorectal Tumorigenesis
inferredcites →https://doi.org/10.1016/j.immuni.2014.12.004openalex-snapshot
IL-17 Cuts to the Chase in Colon Cancer
inferredcites →https://doi.org/10.1016/j.it.2017.01.006openalex-snapshot
IL-17 Signaling: The Yin and the Yang
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.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.radonc.2009.08.042openalex-snapshot
IMRT significantly reduces acute toxicity of whole-pelvis irradiation in patients treated with post-operative adjuvant or salvage radiotherapy after radical prostatectomy
inferredcites →https://doi.org/10.1016/s0090-4295(00)00890-6openalex-snapshot
Toxicity following high-dose three-dimensional conformal and intensity-modulated radiation therapy for clinically localized prostate cancer
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/s1359-6349(09)70517-8openalex-snapshot
2001 Acute toxicity of curative radiotherapy for intermediate risk localized prostate cancer in the EORTC trial 22991
inferredcites →https://doi.org/10.1038/nature07036openalex-snapshot
Induction and effector functions of TH17 cells
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.3394openalex-snapshot
Microenvironmental regulation of tumor progression and metastasis
inferredcites →https://doi.org/10.1038/nri2800openalex-snapshot
Innate IL-17-producing cells: the sentinels of the immune system
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/s41591-018-0014-xopenalex-snapshot
Understanding the tumor immune microenvironment (TIME) for effective therapy
inferredcites →https://doi.org/10.1093/annonc/mdy505openalex-snapshot
Intratumoral IL17-producing cells infiltration correlate with antitumor immune contexture and improved response to adjuvant chemotherapy in gastric cancer
inferredcites →https://doi.org/10.1093/carcin/bgr019openalex-snapshot
Th17 cells in cancer: help or hindrance?
inferredcites →https://doi.org/10.1111/apm.12725openalex-snapshot
Cytokine expression associated with Helicobacter pylori and Epstein‐Barr virus infection in gastric carcinogenesis
inferredcites →https://doi.org/10.1111/cas.12459openalex-snapshot
Th17 cells and interleukin‐17 increase with poor prognosis in patients with acute myeloid leukemia
inferredcites →https://doi.org/10.1111/cas.14068openalex-snapshot
Long‐term prognostic significance of interleukin‐17‐producing T cells in patients with non‐small cell lung cancer
inferredcites →https://doi.org/10.1111/his.12156openalex-snapshot
Interleukin‐17‐producing cell infiltration in the breast cancer tumour microenvironment is a poor prognostic factor
inferredcites →https://doi.org/10.1111/jgh.12418openalex-snapshot
Intrahepatic interleukin‐17+ T cells and F ox P 3+ regulatory T cells cooperate to promote development and affect the prognosis of hepatocellular carcinoma
inferredcites →https://doi.org/10.1111/sji.12109openalex-snapshot
Tumour‐Infiltrating FoxP3+ and IL ‐17‐Producing T Cells Affect the Progression and Prognosis of Gallbladder Carcinoma after Surgery
inferredcites →https://doi.org/10.1136/annrheumdis-2019-215386openalex-snapshot
A head-to-head comparison of the efficacy and safety of ixekizumab and adalimumab in biological-naïve patients with active psoriatic arthritis: 24-week results of a randomised, open-label, blinded-assessor trial
inferredcites →https://doi.org/10.1136/bmj.315.7109.629openalex-snapshot
Bias in meta-analysis detected by a simple, graphical test
inferredcites →https://doi.org/10.1155/2014/623759openalex-snapshot
The Role of Interleukin 17 in Tumour Proliferation, Angiogenesis, and Metastasis
inferredcites →https://doi.org/10.1158/0008-5472.can-10-2907openalex-snapshot
Clinical Impact of Different Classes of Infiltrating T Cytotoxic and Helper Cells (Th1, Th2, Treg, Th17) in Patients with Colorectal Cancer
inferredcites →https://doi.org/10.1158/0008-5472.can-15-0054openalex-snapshot
IL17 Promotes Mammary Tumor Progression by Changing the Behavior of Tumor Cells and Eliciting Tumorigenic Neutrophils Recruitment
inferredcites →https://doi.org/10.1158/0008-5472.can-15-3164openalex-snapshot
Accumulation of MDSC and Th17 Cells in Patients with Metastatic Colorectal Cancer Predicts the Efficacy of a FOLFOX–Bevacizumab Drug Treatment Regimen
inferredcites →https://doi.org/10.1177/153303460700600102openalex-snapshot
Influence of Intensity-Modulated Radiotherapy on Acute Genitourinary and Gastrointestinal Toxicity in the Treatment of Localized Prostate 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.v99.6.2114openalex-snapshot
Interleukin-17 inhibits tumor cell growth by means of a T-cell–dependent mechanism
inferredcites →https://doi.org/10.1186/1476-4598-10-150openalex-snapshot
IL-17 induces AKT-dependent IL-6/JAK2/STAT3 activation and tumor progression in hepatocellular carcinoma
inferredcites →https://doi.org/10.1186/1476-4598-9-4openalex-snapshot
Different subsets of tumor infiltrating lymphocytes correlate with NPC progression in different ways
inferredcites →https://doi.org/10.1186/1756-9966-32-3openalex-snapshot
High expression of IL-17 and IL-17RE associate with poor prognosis of hepatocellular carcinoma
inferredcites →https://doi.org/10.1186/s13046-018-1003-0openalex-snapshot
Tumor-associated neutrophils induce EMT by IL-17a to promote migration and invasion in gastric cancer cells
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/10.1245/s10434-012-2268-8openalex-snapshot
Intratumoral IL-17+ Cells and Neutrophils show Strong Prognostic Significance in Intrahepatic Cholangiocarcinoma
inferredcites →https://doi.org/10.1371/journal.pone.0018219openalex-snapshot
The Accumulation and Prognosis Value of Tumor Infiltrating IL-17 Producing Cells in Esophageal Squamous Cell Carcinoma
inferredcites →https://doi.org/10.1371/journal.pone.0021816openalex-snapshot
Interleukin 17A Promotes Hepatocellular Carcinoma Metastasis via NF-kB Induced Matrix Metalloproteinases 2 and 9 Expression
inferredcites →https://doi.org/10.1371/journal.pone.0096080openalex-snapshot
Prevalence and Clinical Relevance of T-Helper Cells, Th17 and Th1, in Hepatitis B Virus-Related Hepatocellular Carcinoma
inferredcites →https://doi.org/10.1371/journal.pone.0106834openalex-snapshot
Intratumor IL-17-Positive Mast Cells Are the Major Source of the IL-17 That Is Predictive of Survival in Gastric Cancer Patients
inferredcites →https://doi.org/10.1371/journal.pone.0118391openalex-snapshot
Human Papillomavirus Infection Correlates with Inflammatory Stat3 Signaling Activity and IL-17 Level in Patients with Colorectal Cancer
inferredcites →https://doi.org/10.1620/tjem.233.175openalex-snapshot
Colorectal Cancer Progression Is Associated with Accumulation of Th17 Lymphocytes in Tumor Tissues and Increased Serum Levels of Interleukin-6
inferredcites →https://doi.org/10.18632/oncotarget.14471openalex-snapshot
Th1high in tumor microenvironment is an indicator of poor prognosis for patients with NSCLC
inferredcites →https://doi.org/10.18632/oncotarget.23934openalex-snapshot
Interleukin 17 and peripheral IL-17-expressing T cells are negatively correlated with the overall survival of head and neck cancer patients
inferredcites →https://doi.org/10.2147/cmar.s174899openalex-snapshot
IL-17 induces macrophages to M2-like phenotype via NF-κB
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/10.3324/haematol.2011.047316openalex-snapshot
Th17 and non-Th17 interleukin-17-expressing cells in chronic lymphocytic leukemia: delineation, distribution, and clinical relevance
inferredcites →https://doi.org/10.3346/jkms.2009.24.5.894openalex-snapshot
Positional Reproducibility and Effects of a Rectal Balloon in Prostate Cancer Radiotherapy
inferredcites →https://doi.org/10.3892/ol.2017.5638openalex-snapshot
High IL-17 expression is associated with an unfavorable prognosis in thyroid cancer
inferredcites →https://doi.org/10.3892/ol.2018.9316openalex-snapshot
Recruitment and significance of Th22 cells and Th17 cells in malignant ascites
inferredcites →https://doi.org/10.4049/jimmunol.0901017openalex-snapshot
Protumor vs Antitumor Functions of IL-17
inferredcites →https://doi.org/10.4049/jimmunol.150.12.5445openalex-snapshot
CTLA-8, cloned from an activated T cell, bearing AU-rich messenger RNA instability sequences, and homologous to a herpesvirus saimiri gene
inferredcites →https://doi.org/10.4049/jimmunol.160.7.3513openalex-snapshot
IL-17 Stimulates the Production and Expression of Proinflammatory Cytokines, IL-β and TNF-α, by Human Macrophages
inferredcites →https://doi.org/10.4049/jimmunol.162.1.577openalex-snapshot
Evidence for a Role of IL-17 in Organ Allograft Rejection: IL-17 Promotes the Functional Differentiation of Dendritic Cell Progenitors
inferredcites →https://doi.org/10.4161/2162402x.2014.984547openalex-snapshot
The correlations between IL-17 vs. Th17 cells and cancer patient survival: a systematic review
inferredcites →https://doi.org/10.7150/ijbs.7.53openalex-snapshot
Intratumoral Expression of IL-17 and Its Prognostic Role in Gastric Adenocarcinoma Patients
inferredcites →https://doi.org/10.7314/apjcp.2012.13.8.3955openalex-snapshot
CD4+, IL17 and Foxp3 Expression in Different pTNM Stages of Operable Non-small Cell Lung Cancer and Effects on Disease Prognosis
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