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The Good, the Bad, and the Ugly: Neutrophils, Angiogenesis, and Cancer

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inferredcites →https://doi.org/10.1002/1878-0261.12630openalex-snapshot

Cancer‐associated V‐ATPase induces delayed apoptosis of protumorigenic neutrophils

inferredcites →https://doi.org/10.1002/hep.29088openalex-snapshot

Neutrophils promote hepatic metastasis growth through fibroblast growth factor 2–dependent angiogenesis in mice

inferredcites →https://doi.org/10.1002/ijc.24040openalex-snapshot

CXCL8/IL‐8 and CXCL12/SDF‐1α co‐operatively promote invasiveness and angiogenesis in pancreatic cancer

inferredcites →https://doi.org/10.1002/ijc.28551openalex-snapshot

CXCR2‐mediated tumor‐associated neutrophil recruitment is regulated by IFN‐β

inferredcites →https://doi.org/10.1002/ijc.28957openalex-snapshot

Delayed apoptosis of tumor associated neutrophils in the absence of endogenous IFN‐β

inferredcites →https://doi.org/10.1002/ijc.29444openalex-snapshot

The lack of type I interferon induces neutrophil-mediated pre-metastatic niche formation in the mouse lung

inferredcites →https://doi.org/10.1002/ijc.29519openalex-snapshot

HIF ‐1 at the crossroads of hypoxia, inflammation, and cancer

inferredcites →https://doi.org/10.1002/ijc.29945openalex-snapshot

Type I IFN s induce anti‐tumor polarization of tumor associated neutrophils in mice and human

inferredcites →https://doi.org/10.1002/ijc.30076openalex-snapshot

Occurrence and significance of tumor‐associated neutrophils in patients with colorectal cancer

inferredcites →https://doi.org/10.1002/ijc.31808openalex-snapshot

NAMPT signaling is critical for the proangiogenic activity of tumor‐associated neutrophils

inferredcites →https://doi.org/10.1002/ijc.33871openalex-snapshot

SIRT1 ‐mediated deacetylation of FOXO3a transcription factor supports pro‐angiogenic activity of interferon‐deficient tumor‐associated neutrophils

inferredcites →https://doi.org/10.1002/jcb.24438openalex-snapshot

HIFs, angiogenesis, and cancer

inferredcites →https://doi.org/10.1002/jlb.5hr0120-459ropenalex-snapshot

On the origin of low-density neutrophils

inferredcites →https://doi.org/10.1002/path.5449openalex-snapshot

Neutrophils expressing lysyl oxidase‐like 4 protein are present in colorectal cancer liver metastases resistant to anti‐angiogenic therapy

inferredcites →https://doi.org/10.1006/cyto.1997.0283openalex-snapshot

ONCOSTATIN M-SPECIFIC RECEPTOR EXPRESSION AND FUNCTION IN REGULATING CELL PROLIFERATION OF NORMAL AND MALIGNANT MAMMARY EPITHELIAL CELLS

inferredcites →https://doi.org/10.1006/scbi.2000.0365openalex-snapshot

Proteases in invasion: matrix metalloproteinases

inferredcites →https://doi.org/10.1007/s00018-019-03351-7openalex-snapshot

Tumor angiogenesis: causes, consequences, challenges and opportunities

inferredcites →https://doi.org/10.1007/s00262-008-0516-3openalex-snapshot

Pre-treatment neutrophil to lymphocyte ratio is elevated in epithelial ovarian cancer and predicts survival after treatment

inferredcites →https://doi.org/10.1007/s00262-013-1476-9openalex-snapshot

Tumor-associated neutrophils (TAN) develop pro-tumorigenic properties during tumor progression

inferredcites →https://doi.org/10.1007/s00441-003-0784-3openalex-snapshot

Vascular remodeling by intussusceptive angiogenesis

inferredcites →https://doi.org/10.1007/s00441-009-0908-5openalex-snapshot

Neutrophils promote inflammatory angiogenesis via release of preformed VEGF in an in vivo corneal model

inferredcites →https://doi.org/10.1007/s10147-018-1242-2openalex-snapshot

Interleukin-1 receptor antagonist inhibits angiogenesis in gastric cancer

inferredcites →https://doi.org/10.1007/s10585-021-10108-9openalex-snapshot

JUNB suppresses distant metastasis by influencing the initial metastatic stage

inferredcites →https://doi.org/10.1007/s12079-017-0433-3openalex-snapshot

Integration of pro- and anti-angiogenic signals by endothelial cells

inferredcites →https://doi.org/10.1007/s12272-020-01287-2openalex-snapshot

Pathological angiogenesis and inflammation in tissues

inferredcites →https://doi.org/10.1016/j.ajpath.2011.05.031openalex-snapshot

Tumor-Recruited Neutrophils and Neutrophil TIMP-Free MMP-9 Regulate Coordinately the Levels of Tumor Angiogenesis and Efficiency of Malignant Cell Intravasation

inferredcites →https://doi.org/10.1016/j.bbi.2020.12.012openalex-snapshot

Neutrophil dynamics, plasticity and function in acute neurodegeneration following neonatal hypoxia–ischemia

inferredcites →https://doi.org/10.1016/j.bcp.2006.05.017openalex-snapshot

S100A8 and S100A9 in inflammation and cancer

inferredcites →https://doi.org/10.1016/j.bjps.2012.05.006openalex-snapshot

EPO reverses defective wound repair in hypercholesterolaemic mice by increasing functional angiogenesis

inferredcites →https://doi.org/10.1016/j.canlet.2015.07.028openalex-snapshot

Classical and non-classical proangiogenic factors as a target of antiangiogenic therapy in tumor microenvironment

inferredcites →https://doi.org/10.1016/j.ccell.2015.11.005openalex-snapshot

Neutrophils Oppose Uterine Epithelial Carcinogenesis via Debridement of Hypoxic Tumor Cells

inferredcites →https://doi.org/10.1016/j.ccell.2016.06.001openalex-snapshot

Origin and Role of a Subset of Tumor-Associated Neutrophils with Antigen-Presenting Cell Features in Early-Stage Human Lung Cancer

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.cell.2011.08.039openalex-snapshot

Basic and Therapeutic Aspects of Angiogenesis

inferredcites →https://doi.org/10.1016/j.celrep.2014.12.039openalex-snapshot

Phenotypic Diversity and Plasticity in Circulating Neutrophil Subpopulations in Cancer

inferredcites →https://doi.org/10.1016/j.celrep.2021.109253openalex-snapshot

Tumor vessel co-option probed by single-cell analysis

inferredcites →https://doi.org/10.1016/j.it.2010.05.006openalex-snapshot

Neutrophil kinetics in health and disease

inferredcites →https://doi.org/10.1016/j.neo.2014.08.013openalex-snapshot

Tissue-Infiltrating Neutrophils Constitute the Major In Vivo Source of Angiogenesis-Inducing MMP-9 in the Tumor Microenvironment

inferredcites →https://doi.org/10.1016/j.scr.2020.102122openalex-snapshot

Exosomes from 3D culture of marrow stem cells enhances endothelial cell proliferation, migration, and angiogenesis via activation of the HMGB1/AKT pathway

inferredcites →https://doi.org/10.1016/j.smim.2021.101538openalex-snapshot

Versatile neutrophil functions in cancer

inferredcites →https://doi.org/10.1016/j.trecan.2016.12.006openalex-snapshot

Mouse versus Human Neutrophils in Cancer: A Major Knowledge Gap

inferredcites →https://doi.org/10.1016/s1074-7613(01)00101-7openalex-snapshot

STAT-3 Activation Is Required for Normal G-CSF-Dependent Proliferation and Granulocytic Differentiation

inferredcites →https://doi.org/10.1016/s1368-8375(01)00110-5openalex-snapshot

VEGF in the culture of PMN and the serum in oral cavity cancer patients

inferredcites →https://doi.org/10.1023/b:agen.0000029415.62384.baopenalex-snapshot

Platelets and Granulocytes, in Particular the Neutrophils, Form Important Compartments for Circulating Vascular Endothelial Growth Factor

inferredcites →https://doi.org/10.1023/b:neon.0000024241.05346.24openalex-snapshot

CXCL12 in Malignant Glial Tumors: A Possible Role in Angiogenesis and Cross-Talk between Endothelial and Tumoral Cells

inferredcites →https://doi.org/10.1038/bjc.2017.69openalex-snapshot

Personalising and targeting antiangiogenic resistance: a complex and multifactorial approach

inferredcites →https://doi.org/10.1038/nature06348openalex-snapshot

Bv8 regulates myeloid-cell-dependent tumour angiogenesis

inferredcites →https://doi.org/10.1038/nature14282openalex-snapshot

IL-17-producing γδ T cells and neutrophils conspire to promote breast cancer metastasis

inferredcites →https://doi.org/10.1038/nbt1323openalex-snapshot

Tumor refractoriness to anti-VEGF treatment is mediated by CD11b+Gr1+ myeloid cells

inferredcites →https://doi.org/10.1038/ncomms14381openalex-snapshot

Neutrophils dominate the immune cell composition in non-small cell lung cancer

inferredcites →https://doi.org/10.1038/nm0603-653openalex-snapshot

Angiogenesis in health and disease

inferredcites →https://doi.org/10.1038/nm1294openalex-snapshot

Induction of interleukin-8 preserves the angiogenic response in HIF-1α–deficient colon cancer cells

inferredcites →https://doi.org/10.1038/nnano.2014.84openalex-snapshot

In vivo endothelial siRNA delivery using polymeric nanoparticles with low molecular weight

inferredcites →https://doi.org/10.1038/nrc.2017.51openalex-snapshot

Microenvironmental regulation of tumour angiogenesis

inferredcites →https://doi.org/10.1038/nrc1093openalex-snapshot

Tumorigenesis and the angiogenic switch

inferredcites →https://doi.org/10.1038/nri1995openalex-snapshot

Crosstalk between cancer and immune cells: role of STAT3 in the tumour microenvironment

inferredcites →https://doi.org/10.1038/nri3024openalex-snapshot

Neutrophils in the activation and regulation of innate and adaptive immunity

inferredcites →https://doi.org/10.1038/nri3175openalex-snapshot

Coordinated regulation of myeloid cells by tumours

inferredcites →https://doi.org/10.1038/onc.2011.204openalex-snapshot

IL-3 is a novel target to interfere with tumor vasculature

inferredcites →https://doi.org/10.1038/onc.2012.201openalex-snapshot

Neutrophil chemokines secreted by tumor cells mount a lung antimetastatic response during renal cell carcinoma progression

inferredcites →https://doi.org/10.1038/s12276-020-00500-yopenalex-snapshot

Combination of anti-angiogenic therapy and immune checkpoint blockade normalizes vascular-immune crosstalk to potentiate cancer immunity

inferredcites →https://doi.org/10.1038/s41392-021-00658-5openalex-snapshot

Inflammation and tumor progression: signaling pathways and targeted intervention

inferredcites →https://doi.org/10.1038/s41416-018-0198-3openalex-snapshot

Tumour-infiltrating neutrophils counteract anti-VEGF therapy in metastatic colorectal cancer

inferredcites →https://doi.org/10.1038/s41419-018-0458-4openalex-snapshot

Cancer-associated fibroblasts induce PDL1+ neutrophils through the IL6-STAT3 pathway that foster immune suppression in hepatocellular carcinoma

inferredcites →https://doi.org/10.1038/s41568-020-0281-yopenalex-snapshot

Neutrophil diversity and plasticity in tumour progression and therapy

inferredcites →https://doi.org/10.1038/s41571-019-0222-4openalex-snapshot

Tumour-associated neutrophils in patients with cancer

inferredcites →https://doi.org/10.1038/s41577-019-0141-8openalex-snapshot

Heterogeneity of neutrophils

inferredcites →https://doi.org/10.1038/s41590-018-0229-5openalex-snapshot

Unique pattern of neutrophil migration and function during tumor progression

inferredcites →https://doi.org/10.1038/s41598-018-36855-6openalex-snapshot

Stem cell exosomes inhibit angiogenesis and tumor growth of oral squamous cell carcinoma

inferredcites →https://doi.org/10.1038/s41598-019-38643-2openalex-snapshot

CXCR4 signaling regulates metastatic onset by controlling neutrophil motility and response to malignant cells

inferredcites →https://doi.org/10.1038/srep31952openalex-snapshot

Enhanced angiogenesis, hypoxia and neutrophil recruitment during Myc-induced liver tumorigenesis in zebrafish

inferredcites →https://doi.org/10.1038/srep36865openalex-snapshot

Cancer derived peptide of vacuolar ATPase ‘a2’ isoform promotes neutrophil migration by autocrine secretion of IL-8

inferredcites →https://doi.org/10.1056/nejm197111182852108openalex-snapshot

Tumor Angiogenesis: Therapeutic Implications

inferredcites →https://doi.org/10.1056/nejm199101033240101openalex-snapshot

Tumor Angiogenesis and Metastasis — Correlation in Invasive Breast Carcinoma

inferredcites →https://doi.org/10.1073/pnas.0601807103openalex-snapshot

Infiltrating neutrophils mediate the initial angiogenic switch in a mouse model of multistage carcinogenesis

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.0902280106openalex-snapshot

G-CSF-initiated myeloid cell mobilization and angiogenesis mediate tumor refractoriness to anti-VEGF therapy in mouse models

inferredcites →https://doi.org/10.1073/pnas.1113744109openalex-snapshot

Origins of tumor-associated macrophages and neutrophils

inferredcites →https://doi.org/10.1073/pnas.1611944114openalex-snapshot

Neutrophils induce proangiogenic T cells with a regulatory phenotype in pregnancy

inferredcites →https://doi.org/10.1073/pnas.1710754114openalex-snapshot

Targeting CXCR4-dependent immunosuppressive Ly6C low monocytes improves antiangiogenic therapy in colorectal cancer

inferredcites →https://doi.org/10.1073/pnas.1913373116openalex-snapshot

Pericytes enable effective angiogenesis in the presence of proinflammatory signals

inferredcites →https://doi.org/10.1073/pnas.2008112117openalex-snapshot

Suppressing neutrophil-dependent angiogenesis abrogates resistance to anti-VEGF antibody in a genetic model of colorectal cancer

inferredcites →https://doi.org/10.1073/pnas.83.24.9739openalex-snapshot

Oncostatin M: a growth regulator produced by differentiated histiocytic lymphoma cells.

inferredcites →https://doi.org/10.1074/jbc.m107348200openalex-snapshot

Vascular Endothelial Growth Factor Modulates Neutrophil Transendothelial Migration via Up-regulation of Interleukin-8 in Human Brain Microvascular Endothelial Cells

inferredcites →https://doi.org/10.1074/jbc.m109.033472openalex-snapshot

Neutrophil MMP-9 Proenzyme, Unencumbered by TIMP-1, Undergoes Efficient Activation in Vivo and Catalytically Induces Angiogenesis via a Basic Fibroblast Growth Factor (FGF-2)/FGFR-2 Pathway

inferredcites →https://doi.org/10.1074/jbc.m111.326801openalex-snapshot

Induction of Bv8 Expression by Granulocyte Colony-stimulating Factor in CD11b+Gr1+ Cells

inferredcites →https://doi.org/10.1080/01913120802636696openalex-snapshot

Ultrastructural Observations on Inflammatory Angiogenesis in Gastric Carcinomas with Massive Neutrophil Infiltration

inferredcites →https://doi.org/10.1080/16078454.2021.1965725openalex-snapshot

New insight into the mechanism of granulocyte colony-stimulating factor (G-CSF) that induces the mobilization of neutrophils

inferredcites →https://doi.org/10.1091/mbc.1.11.833openalex-snapshot

Heparanase activity expressed by platelets, neutrophils, and lymphoma cells releases active fibroblast growth factor from extracellular matrix.

inferredcites →https://doi.org/10.1093/annonc/mdx663.019openalex-snapshot

G-CSF induces production of Bv8 in murine bone marrow neutrophils and promotes tumor growth and angiogenesis of U14 murine cervical cancer cell line

inferredcites →https://doi.org/10.1093/carcin/bgs123openalex-snapshot

Tumor-associated neutrophils: friend or foe?

inferredcites →https://doi.org/10.1093/jnci/82.1.4openalex-snapshot

What Is the Evidence That Tumors Are Angiogenesis Dependent?

inferredcites →https://doi.org/10.1093/jnci/95.6.437openalex-snapshot

Effects of Interferon Alpha on Vascular Endothelial Growth Factor Gene Transcription and Tumor Angiogenesis

inferredcites →https://doi.org/10.1097/ppo.0000000000000138openalex-snapshot

The Contribution of Angiogenesis to the Process of Metastasis

inferredcites →https://doi.org/10.1111/bph.15303openalex-snapshot

Protection against light‐induced retinal degeneration via dual anti‐inflammatory and anti‐angiogenic functions of thrombospondin‐1

inferredcites →https://doi.org/10.1111/febs.14524openalex-snapshot

Cancer‐related circulating and tumor‐associated neutrophils – subtypes, sources and function

inferredcites →https://doi.org/10.1111/imm.12876openalex-snapshot

Endoplasmic reticulum stress induced LOX‐1+ CD 15+ polymorphonuclear myeloid‐derived suppressor cells in hepatocellular carcinoma

inferredcites →https://doi.org/10.1111/j.1365-2613.2009.00641.xopenalex-snapshot

Neutrophils: key mediators of tumour angiogenesis

inferredcites →https://doi.org/10.1111/jcmm.13232openalex-snapshot

Tumstatin regulates the angiogenic and inflammatory potential of airway smooth muscle extracellular matrix

inferredcites →https://doi.org/10.1126/sciimmunol.aaf8943openalex-snapshot

Lectin-type oxidized LDL receptor-1 distinguishes population of human polymorphonuclear myeloid-derived suppressor cells in cancer patients

inferredcites →https://doi.org/10.1136/ard.2009.127241openalex-snapshot

Interleukin 18 induces angiogenesis in vitro and in vivo via Src and Jnk kinases

inferredcites →https://doi.org/10.1136/gutjnl-2020-320608openalex-snapshot

Blocking VCAM-1 inhibits pancreatic tumour progression and cancer-associated thrombosis/thromboembolism

inferredcites →https://doi.org/10.1136/jitc-2020-001358openalex-snapshot

Deep immunophenotyping at the single-cell level identifies a combination of anti-IL-17 and checkpoint blockade as an effective treatment in a preclinical model of data-guided personalized immunotherapy

inferredcites →https://doi.org/10.1155/2015/701067openalex-snapshot

Distinct Functions of Neutrophil in Cancer and Its Regulation

inferredcites →https://doi.org/10.1155/2015/983698openalex-snapshot

Neutrophils in Cancer: Two Sides of the Same Coin

inferredcites →https://doi.org/10.1155/2016/6058147openalex-snapshot

Tumor-Associated Macrophages and Neutrophils in Tumor Microenvironment

inferredcites →https://doi.org/10.1155/2016/6530410openalex-snapshot

Tumor-Derived CXCL1 Promotes Lung Cancer Growth via Recruitment of Tumor-Associated Neutrophils

inferredcites →https://doi.org/10.1158/0008-5472.can-05-1734openalex-snapshot

Breast Cancer Cells Stimulate Neutrophils to Produce Oncostatin M: Potential Implications for Tumor Progression

inferredcites →https://doi.org/10.1158/0008-5472.can-05-3842openalex-snapshot

High Expression of Ligands for Chemokine Receptor CXCR2 in Alveolar Epithelial Neoplasia Induced by Oncogenic Kras

inferredcites →https://doi.org/10.1158/0008-5472.can-20-3941openalex-snapshot

TGFβ Signaling Activated by Cancer-Associated Fibroblasts Determines the Histological Signature of Lung Adenocarcinoma

inferredcites →https://doi.org/10.1158/1078-0432.ccr-08-1954openalex-snapshot

Characterization and Regulation of Bv8 in Human Blood Cells

inferredcites →https://doi.org/10.1158/1078-0432.ccr-16-0617openalex-snapshot

Interleukin-17–Producing Neutrophils Link Inflammatory Stimuli to Disease Progression by Promoting Angiogenesis in Gastric Cancer

inferredcites →https://doi.org/10.1158/1535-7163.mct-14-0836openalex-snapshot

Endostatin Has ATPase Activity, Which Mediates Its Antiangiogenic and Antitumor Activities

inferredcites →https://doi.org/10.1158/2326-6066.cir-15-0313openalex-snapshot

The Complex Role of Neutrophils in Tumor Angiogenesis and Metastasis

inferredcites →https://doi.org/10.1158/2326-6066.cir-17-0204openalex-snapshot

NK Cells Control Tumor-Promoting Function of Neutrophils in Mice

inferredcites →https://doi.org/10.1158/2326-6066.cir-18-0489openalex-snapshot

Immune-Checkpoint Protein VISTA Regulates Antitumor Immunity by Controlling Myeloid Cell–Mediated Inflammation and Immunosuppression

inferredcites →https://doi.org/10.1159/000338278openalex-snapshot

Intussusceptive Angiogenesis: A Biologically Relevant Form of Angiogenesis

inferredcites →https://doi.org/10.1159/000476017openalex-snapshot

Angiogenesis and Inflammation in Peritoneal Dialysis: The Role of Adipocytes

inferredcites →https://doi.org/10.1161/01.atv.0000154137.21230.80openalex-snapshot

Molecular Mechanisms Underlying the Proangiogenic Effect of Factor XIII

inferredcites →https://doi.org/10.1161/atvbaha.116.307634openalex-snapshot

Neutrophil Extracellular Traps Promote Angiogenesis

inferredcites →https://doi.org/10.1161/circresaha.120.316851openalex-snapshot

Basic and Therapeutic Aspects of Angiogenesis Updated

inferredcites →https://doi.org/10.1167/iovs.06-1234openalex-snapshot

Positive Feedback Regulation between MMP-9 and VEGF in Human RPE Cells

inferredcites →https://doi.org/10.1172/jci35213openalex-snapshot

Stat3 mediates myeloid cell–dependent tumor angiogenesis in mice

inferredcites →https://doi.org/10.1172/jci37223openalex-snapshot

Neutrophils responsive to endogenous IFN-β regulate tumor angiogenesis and growth in a mouse tumor model

inferredcites →https://doi.org/10.1172/jci39065openalex-snapshot

The tumor-promoting actions of TNF-α involve TNFR1 and IL-17 in ovarian cancer in mice and humans

inferredcites →https://doi.org/10.1172/jci77053openalex-snapshot

Tumor-associated neutrophils stimulate T cell responses in early-stage human lung cancer

inferredcites →https://doi.org/10.1172/jci93182openalex-snapshot

Ly6Clo monocytes drive immunosuppression and confer resistance to anti-VEGFR2 cancer therapy

inferredcites →https://doi.org/10.1177/1010428317706214openalex-snapshot

The prognostic value of pretreatment neutrophil-to-lymphocyte ratio in breast cancer: Deleterious or advantageous?

inferredcites →https://doi.org/10.1182/blood-2006-02-003012openalex-snapshot

STAT3 governs distinct pathways in emergency granulopoiesis and mature neutrophils

inferredcites →https://doi.org/10.1182/blood-2007-08-108597openalex-snapshot

TNF primes endothelial cells for angiogenic sprouting by inducing a tip cell phenotype

inferredcites →https://doi.org/10.1182/blood-2009-08-240317openalex-snapshot

STAT3 controls the neutrophil migratory response to CXCR2 ligands by direct activation of G-CSF–induced CXCR2 expression and via modulation of CXCR2 signal transduction

inferredcites →https://doi.org/10.1182/blood-2012-04-421040openalex-snapshot

VEGF-A recruits a proangiogenic MMP-9–delivering neutrophil subset that induces angiogenesis in transplanted hypoxic tissue

inferredcites →https://doi.org/10.1182/blood-2012-11-466532openalex-snapshot

Neutrophils contribute to inflammatory lymphangiogenesis by increasing VEGF-A bioavailability and secreting VEGF-D

inferredcites →https://doi.org/10.1182/blood-2015-03-631572openalex-snapshot

Identification and characterization of VEGF-A–responsive neutrophils expressing CD49d, VEGFR1, and CXCR4 in mice and humans

inferredcites →https://doi.org/10.1182/blood-2018-11-844548openalex-snapshot

Neutrophil plasticity in the tumor microenvironment

inferredcites →https://doi.org/10.1182/blood.v90.10.4153openalex-snapshot

Intracellular Pool of Vascular Endothelial Growth Factor in Human Neutrophils

inferredcites →https://doi.org/10.1182/blood.v99.8.2997openalex-snapshot

Presence of a mobilizable intracellular pool of hepatocyte growth factor in human polymorphonuclear neutrophils

inferredcites →https://doi.org/10.1186/bcr65openalex-snapshot

Metalloproteinases: role in breast carcinogenesis, invasion and metastasis

inferredcites →https://doi.org/10.1186/s12916-020-01817-1openalex-snapshot

Neutrophil to lymphocyte ratio and cancer prognosis: an umbrella review of systematic reviews and meta-analyses of observational studies

inferredcites →https://doi.org/10.1186/s12943-020-01258-7openalex-snapshot

Targeting STAT3 in Cancer Immunotherapy

inferredcites →https://doi.org/10.1186/s12964-020-0527-zopenalex-snapshot

Role of STAT3 signaling pathway in breast cancer

inferredcites →https://doi.org/10.1186/s13045-021-01187-yopenalex-snapshot

Neutrophils in cancer carcinogenesis and metastasis

inferredcites →https://doi.org/10.1186/s13046-015-0247-1openalex-snapshot

CXCR2–CXCL1 axis is correlated with neutrophil infiltration and predicts a poor prognosis in hepatocellular carcinoma

inferredcites →https://doi.org/10.1186/s13046-019-1384-8openalex-snapshot

Hypoxic exosomes facilitate angiogenesis and metastasis in esophageal squamous cell carcinoma through altering the phenotype and transcriptome of endothelial cells

inferredcites →https://doi.org/10.1189/jlb.3mr0117-015ropenalex-snapshot

Neutrophil, quo vadis?

inferredcites →https://doi.org/10.1371/journal.pcbi.1009081openalex-snapshot

Multiscale modeling of tumor growth and angiogenesis: Evaluation of tumor-targeted therapy

inferredcites →https://doi.org/10.1371/journal.pone.0007190openalex-snapshot

3D Multi-Cell Simulation of Tumor Growth and Angiogenesis

inferredcites →https://doi.org/10.1371/journal.pone.0200444openalex-snapshot

CD177-mediated nanoparticle targeting of human and mouse neutrophils

inferredcites →https://doi.org/10.1371/journal.pone.0216055openalex-snapshot

Cancer cell–induced neutrophil extracellular traps promote both hypercoagulability and cancer progression

inferredcites →https://doi.org/10.1371/journal.pone.0231137openalex-snapshot

A hybrid model of tumor growth and angiogenesis: In silico experiments

inferredcites →https://doi.org/10.18632/oncotarget.12289openalex-snapshot

IL-1 drives breast cancer growth and bone metastasisin vivo

inferredcites →https://doi.org/10.18632/oncotarget.16819openalex-snapshot

IL-35 induces N2 phenotype of neutrophils to promote tumor growth

inferredcites →https://doi.org/10.18632/oncotarget.5439openalex-snapshot

Breast cancer associated a2 isoform vacuolar ATPase immunomodulates neutrophils: potential role in tumor progression

inferredcites →https://doi.org/10.21037/tcr.2016.10.06openalex-snapshot

The emerging role of chemokine receptor CXCR2 in cancer progression

inferredcites →https://doi.org/10.2147/cmar.s147699openalex-snapshot

Interleukin-1 receptor antagonist inhibits angiogenesis via blockage IL-1α/PI3K/NF-κB pathway in human colon cancer cell

inferredcites →https://doi.org/10.2147/jir.s312605openalex-snapshot

Overexpression of Neutrophil MMP-9 and HIF-1α May Contribute to the Finger-Like Projections Formation and Histo-Pathogenesis in Nasal Inverted Papilloma

inferredcites →https://doi.org/10.2741/3504openalex-snapshot

Tumor angiogenesis and molecular targets for therapy

inferredcites →https://doi.org/10.3389/fimmu.2016.00629openalex-snapshot

The Essential Role of Type I Interferons in Differentiation and Activation of Tumor-Associated Neutrophils

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