On the public citation graph
A Review on How Neutrophils Are Related With Cancer Metastasis
0 signed · 42 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/s00018-014-1683-3openalex-extracted
Neutrophil extracellular traps in cancer progression
inferredcites →https://doi.org/10.1007/s00441-017-2777-7openalex-extracted
The complex interplay between neutrophils and cancer
inferredcites →https://doi.org/10.1007/s10555-015-9586-9openalex-extracted
The challenge of targeting metastasis
inferredcites →https://doi.org/10.1007/s10555-015-9594-9openalex-extracted
Neutrophils: important contributors to tumor progression and metastasis
inferredcites →https://doi.org/10.1007/s12307-014-0147-5openalex-extracted
The Multifaceted Roles Neutrophils Play in the Tumor Microenvironment
inferredcites →https://doi.org/10.1016/j.amjsurg.2017.08.003openalex-extracted
Cancer-promoting mechanisms of tumor-associated neutrophils
inferredcites →https://doi.org/10.1016/j.bbrc.2018.04.144openalex-extracted
ShRNA-mediated knock-down of CXCL8 inhibits tumor growth in colorectal liver metastasis
inferredcites →https://doi.org/10.1016/j.critrevonc.2004.09.004openalex-extracted
Hepatocyte growth factor, its receptor, and their potential value in cancer therapies
inferredcites →https://doi.org/10.1016/j.imbio.2013.06.003openalex-extracted
Tumor associated macrophages and neutrophils in cancer
inferredcites →https://doi.org/10.1038/bjc.2017.386openalex-extracted
Neutrophils: driving progression and poor prognosis in hepatocellular carcinoma?
inferredcites →https://doi.org/10.1038/cr.2015.62openalex-extracted
Promoting metastasis: neutrophils and T cells join forces
inferredcites →https://doi.org/10.1038/nature16140openalex-extracted
Neutrophils support lung colonization of metastasis-initiating breast cancer cells
inferredcites →https://doi.org/10.1038/nri1964openalex-extracted
Tuning inflammation and immunity by chemokine sequestration: decoys and more
inferredcites →https://doi.org/10.1038/onc.2016.406openalex-extracted
Neutrophil extracellular traps: protagonists of cancer progression?
inferredcites →https://doi.org/10.1038/s41571-019-0222-4openalex-extracted
Tumour-associated neutrophils in patients with cancer
inferredcites →https://doi.org/10.1074/jbc.m109.033472openalex-extracted
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/10.1093/carcin/bgs123openalex-extracted
Tumor-associated neutrophils: friend or foe?
inferredcites →https://doi.org/10.1093/rheumatology/ken028openalex-extracted
T lymphocytes in patients with primary vasculitis: expansion of CD8+ T cells with the propensity to activate polymorphonuclear neutrophils
inferredcites →https://doi.org/10.1097/pap.0000000000000219openalex-extracted
Paget’s “Seed and Soil” Theory of Cancer Metastasis: An Idea Whose Time has Come
inferredcites →https://doi.org/10.1111/febs.14206openalex-extracted
Neutrophils, G‐ CSF and their contribution to breast cancer metastasis
inferredcites →https://doi.org/10.1111/febs.14524openalex-extracted
Cancer‐related circulating and tumor‐associated neutrophils – subtypes, sources and function
inferredcites →https://doi.org/10.1111/imr.12459openalex-extracted
Neutrophils in the tumor microenvironment: trying to heal the wound that cannot heal
inferredcites →https://doi.org/10.1111/j.1440-1746.2004.03575.xopenalex-extracted
Neutrophils enhance invasion activity of human cholangiocellular carcinoma and hepatocellular carcinoma cells: An in vitro study
inferredcites →https://doi.org/10.1126/scitranslmed.aag0367openalex-extracted
Autoimmune manifestations in aged mice arise from early-life immune dysregulation
inferredcites →https://doi.org/10.1126/scitranslmed.aag1711openalex-extracted
Cancer cells induce metastasis-supporting neutrophil extracellular DNA traps
inferredcites →https://doi.org/10.1155/2014/971409openalex-extracted
Neutrophil Cathepsin G, but Not Elastase, Induces Aggregation of MCF-7 Mammary Carcinoma Cells by a Protease Activity-Dependent Cell-Oriented Mechanism
inferredcites →https://doi.org/10.1155/2015/983698openalex-extracted
Neutrophils in Cancer: Two Sides of the Same Coin
inferredcites →https://doi.org/10.1155/2019/6252138openalex-extracted
Influence of Interleukin-8 and Neutrophil Extracellular Trap (NET) Formation in the Tumor Microenvironment: Is There a Pathogenic Role?
inferredcites →https://doi.org/10.1158/0008-5472.can-05-1734openalex-extracted
Breast Cancer Cells Stimulate Neutrophils to Produce Oncostatin M: Potential Implications for Tumor Progression
inferredcites →https://doi.org/10.1158/0008-5472.can-09-4442openalex-extracted
Transiently Entrapped Circulating Tumor Cells Interact with Neutrophils to Facilitate Lung Metastasis Development
inferredcites →https://doi.org/10.1158/2159-8290.cd-15-1157openalex-extracted
Neutrophils Suppress Intraluminal NK Cell–Mediated Tumor Cell Clearance and Enhance Extravasation of Disseminated Carcinoma Cells
inferredcites →https://doi.org/10.1158/2326-6066.cir-15-0313openalex-extracted
The Complex Role of Neutrophils in Tumor Angiogenesis and Metastasis
inferredcites →https://doi.org/10.1172/jci37223openalex-extracted
Neutrophils responsive to endogenous IFN-β regulate tumor angiogenesis and growth in a mouse tumor model
inferredcites →https://doi.org/10.1189/jlb.1109737openalex-extracted
Exocytosis of azurophil and arginase 1-containing granules by activated polymorphonuclear neutrophils is required to inhibit T lymphocyte proliferation
inferredcites →https://doi.org/10.17305/bjbms.2017.1908openalex-extracted
Cancer metastasis - tricks of the trade
inferredcites →https://doi.org/10.21037/tlcr.2016.06.07openalex-extracted
Non-small cell lung cancer: current treatment and future advances
inferredcites →https://doi.org/10.3389/fphys.2018.00113openalex-extracted
Neutrophil: A Cell with Many Roles in Inflammation or Several Cell Types?
inferredcites →https://doi.org/10.3390/ijms20030529openalex-extracted
The Role of Tumor-Associated Neutrophils in Colorectal Cancer
inferredcites →https://doi.org/10.3892/ijo.2016.3616openalex-extracted
Neutrophils in cancer development and progression: Roles, mechanisms, and implications (Review)
inferredcites →https://doi.org/10.4161/cc.8.20.9699openalex-extracted
Inflammation: A driving force speeds cancer metastasis
inferredcites →https://doi.org/10.4161/onci.1.1.17938openalex-extracted
Trial Watch: Monoclonal antibodies in cancer therapy
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.