Evidence map›Paper›PMID 21685373›Full record

ArticleBlood2011

G-CSF supplementation with chemotherapy can promote revascularization and subsequent tumor regrowth: prevention by a CXCR4 antagonist.

Tali Voloshin, Svetlana Gingis-Velitski, Rotem Bril, Liat Benayoun, Michal Munster, Chloe Milsom, Shan Man, Robert S Kerbel, Yuval Shaked

Abstract read
In one paragraph

Article in Blood, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
2.1field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

40 citing papers in PubMed, 68 citations in OpenAlex.

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  20. Neutrophil Maturity in Cancer.Frontiers in immunology · 2019
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 2 countries.

Tali VoloshinDepartment of Molecular Pharmacology, Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel.
Svetlana Gingis-Velitski
Rotem Bril
Liat Benayoun
Michal Munster
Chloe Milsom
Shan Man
Robert S Kerbel
Yuval Shaked
Technion – Israel Institute of Technology · ILHealth Sciences Centre · CASunnybrook Health Science Centre · CAUniversity of Toronto · CA

Funding

TUMOR-HOST INTERACTIONS IN HUMAN MELANOMA METASTASISR01CA041233 · NCI · TORONTO-SUNNYBROOK REGIONAL CANCER CTR · PI KERBEL, ROBERT S · 1986 to 2013
$2.4M
NCI NIH HHS R01 CA041233NCI NIH HHS R01-CA-41233
6 · The paper itself

Abstract

Recombinant granulocyte colony-stimulating factor (G-CSF) is used to accelerate recovery from chemotherapy-induced myelosuppression. G-CSF has been recently shown to stimulate angiogenesis mediated by several types of bone marrow-derived cell populations. To investigate whether G-CSF may alter tumor response to therapy, we studied Lewis lung and EMT/6 breast carcinomas in mice treated with paclitaxel (PTX) chemotherapy in combination with G-CSF. We compared the results obtained to mice treated with PTX and AMD3100, a small-molecule drug antagonist of CXCR4 which, like G-CSF, can be used to mobilize hematopoietic cells. We show that PTX combined with G-CSF treatment facilitates revascularization, leading to an improvement in blood perfusion in LLC tumors, and a decrease in hypoxia in EMT/6 tumors, thus enhancing tumor growth in comparison to PTX or PTX and AMD3100 therapies. We found that hemangiocytes but not Gr-1(+) CD11b(+) cells colonize EMT/6 tumors after treatment with PTX and G-CSF, but not PTX and AMD3100, and therefore may contribute to angiogenesis. However, increases in hemangiocyte colonization were not observed in LLC PTX and G-CSF-treated tumors, suggesting distinct mechanisms of tumor revascularization after G-CSF. Overall, our observations suggest that despite its known considerable clinical benefits, G-CSF might contribute to tumor revascularization by various mechanisms, and diminish the antitumor activity of chemotherapy, an effect that can be prevented by AMD3100.

Indexed as

Heterocyclic CompoundsNeovascularization, PathologicAnimalsAntineoplastic AgentsBenzylaminesCarcinoma, Lewis LungCell Line, TumorCell ProliferationCell SurvivalCyclamsDrug CombinationsFemaleFlow CytometryGranulocyte Colony-Stimulating FactorHumansImmunohistochemistryAntineoplastic AgentsBenzylaminesCyclamsDrug CombinationsGranulocyte Colony-Stimulating FactorHeterocyclic CompoundsMatrix Metalloproteinase 2Mmp2 protein, mousePaclitaxelplerixaforReceptors, CXCR4Vascular Endothelial Growth Factor A

Identifiers

PMID21685373
PMCPMC3179406
OpenAlexW2086046468

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.