Evidence map›Paper›PMID 27400751›Full record

ArticleBMC cancer2016

Osteopontin splice variants are differential predictors of breast cancer treatment responses.

Krzysztof Zduniak, Anil Agrawal, Siddarth Agrawal, Md Monir Hossain, Piotr Ziolkowski, Georg F Weber

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 15% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
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  7. Obesity and endocrine therapy resistance in breast cancer: Mechanistic insights and perspectives.Obesity reviews : an official journal of the International Association for the Study of Obesity · 2022
    Review
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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

6 authors at 3 institutions in 2 countries.

Krzysztof ZduniakDepartment of Pathology, Wroclaw Medical University, Wroclaw, Poland.
Anil AgrawalDepartment of General and Oncological Surgery, Wroclaw Medical University, Wroclaw, Poland.
Siddarth AgrawalDepartment of General and Oncological Surgery, Wroclaw Medical University, Wroclaw, Poland.
Md Monir HossainDivision of Biostatistics and Epidemilogy, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Piotr ZiolkowskiDepartment of Pathology, Wroclaw Medical University, Wroclaw, Poland. ziolkows@interia.pl.
Georg F WeberUniversity of Cincinnati Academic Health Center, College of Pharmacy, 3225 Eden Avenue, Cincinnati, OH, 45267-0004, USA. georg.weber@uc.edu.
Wroclaw Medical University · PLCincinnati Children's Hospital Medical Center · USUniversity of Cincinnati Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOsteopontin is a marker for breast cancer progression, which in previous studies has also been associated with resistance to certain anti-cancer therapies. It is not known which splice variants may mediate treatment resistance.

methodsHere we analyze the association of osteopontin variant expression before treatment, differentiated according to immunohistochemistry with antibodies to exon 4 and to the osteopontin-c splice junction respectively, with the ensuing therapy responses in 119 Polish breast cancer patients who presented between 1995 and 2008.

resultsWe found from Cox hazard models, logrank test and Wilcoxon test that osteopontin exon 4 was associated with a favorable response to tamoxifen, but a poor response to chemotherapy with CMF (cyclophosphamide, methotrexate, fluorouracil). Osteopontin-c is prognostic, but falls short of being a significant predictor for sensitivity to treatment.

conclusionsThe addition of osteopontin splice variant immunohistochemistry to standard pathology work-ups has the potential to aid decision making in breast cancer treatment.

Indexed as

Drug Resistance, NeoplasmAlternative SplicingAntineoplastic AgentsAntineoplastic Combined Chemotherapy ProtocolsBiomarkers, PharmacologicalBiopsyBreast NeoplasmsCyclophosphamideFemaleFluorouracilHumansImmunohistochemistryMethotrexateMiddle AgedOsteopontinPolandAntineoplastic AgentsBiomarkers, PharmacologicalCyclophosphamideFluorouracilMethotrexateOsteopontinProtein IsoformsSPP1 protein, humanTamoxifenBreast cancerChemotherapyHormone therapyImmunohistochemistryRadiation therapyTumor progression marker

Identifiers

PMID27400751
PMCPMC4940753
OpenAlexW2474404849

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.