Evidence map›Paper›PMID 26797460›Full record

ArticleCancer letters2016

Induction of CXCR2 ligands, stem cell-like phenotype, and metastasis in chemotherapy-resistant breast cancer cells.

Bhawna Sharma, Michelle L Varney, Sugandha Saxena, Lingyun Wu, Rakesh K Singh

Abstract read
In one paragraph

Article in Cancer letters, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

31 citing papers in PubMed, 42 citations in OpenAlex.

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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

5 authors at 2 institutions in 1 country.

Bhawna SharmaDepartment of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, NE; Department of Medicine, University of Wisconsin Carbone Cancer Center, University of Wisconsin School of Medicine and Public Health, Madison, WI.
Michelle L VarneyDepartment of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, NE.
Sugandha SaxenaDepartment of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, NE.
Lingyun WuDepartment of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, NE.
Rakesh K SinghDepartment of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, NE; Department of Pathology and Microbiology, University of Nebraska Medical Center, 985900 Nebraska Medical Center, Omaha, NE. Electronic address: rsingh@unmc.edu.
University of Nebraska Medical Center · USUniversity of Wisconsin Carbone Cancer Center · US

Funding

UNMC/EPPLEY CANCER CENTER SUPPORT GRANTP30CA036727 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI Apar Kishor Ganti · 1985 to 2026
$55.0M
Role of N-Cadherin in Pancreatic Tumor MicroenvironmentU54CA163120 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI HOLLINGSWORTH, MICHAEL A. · 2011 to 2015
$4.2M
NCI NIH HHS P30 CA036727NCI NIH HHS P30CA036727NCI NIH HHS U54 CA163120NCI NIH HHS U54CA163120PHS HHS KG090860
6 · The paper itself

Abstract

CXCR2 and its ligands have been shown to play an important role in tumor angiogenesis, therapy resistance and progression. In this study, we investigated whether CXCR2 ligands are responsible for the survival advantage and metastasis of drug-resistant cells and examined the underlying mechanism(s) doxorubicin or paclitaxel resistant mammary tumor cells. Our results demonstrated that drug-resistant Cl66 cells upregulated CXCR2 ligands but downregulated expression of CXCR2. We observed delayed tumor growth but increased metastasis in mice using these drug-resistant cells. Furthermore, we observed differential upregulation of stem cell and mesenchymal markers in the doxorubicin and paclitaxel-resistant tumor cells. Abrogation of the CXCR2 signaling axis using CXCR2 ligand neutralization resulted in significant inhibition of drug-resistant cell growth. Together, our data suggest chemotherapy-specific differential regulation of CXCR2 ligands, stem cell-like and mesenchymal phenotypes, and enhanced metastasis in drug-resistant cells and targeting CXCR2 signaling, may help circumvent therapy resistance in breast cancer.

Indexed as

Drug Resistance, NeoplasmAdenocarcinomaAnimalsAntineoplastic AgentsBreast NeoplasmsCell Line, TumorCell ProliferationDose-Response Relationship, DrugDoxorubicinEpithelial-Mesenchymal TransitionFemaleGene Expression Regulation, NeoplasticLigandsMice, Inbred BALB CMice, NudeNeoplastic Stem CellsAntineoplastic AgentsDoxorubicinLigandsPaclitaxelReceptors, Interleukin-8BChemokinesCXCR2Stem cellTherapy resistance

Identifiers

PMID26797460
PMCPMC4821546
OpenAlexW2235860151

What OpenQuestion holds

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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.