Evidence map›Paper›PMID 21466612›Full record

ArticleCancer science2011

An integrative approach to identify YB-1-interacting proteins required for cisplatin resistance in MCF7 and MDA-MB-231 breast cancer cells.

Chantal Garand, David Guay, Chris Sereduk, Donald Chow, Serges P Tsofack, Mathieu Langlois, Eve Perreault, Hongwei H Yin, Michel Lebel

Open access · bronzeAbstract read
In one paragraph

Article in Cancer science, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

22 citing papers in PubMed, 37 citations in OpenAlex.

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  13. Polysaccharide fromIranian journal of basic medical sciences · 2016
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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

9 authors at 3 institutions in 2 countries.

Chantal GarandDepartment of Molecular Biology, Medical Biochemistry, and Pathology, Laval University Quebec City, Québec, Canada.
David Guay
Chris Sereduk
Donald Chow
Serges P Tsofack
Mathieu Langlois
Eve Perreault
Hongwei H Yin
Michel Lebel
Université Laval · CATranslational Genomics Research Institute · USFeldan (Canada) · CA

Funding

Canadian Institutes of Health Research
6 · The paper itself

Abstract

The Y-box binding protein 1 (YB-1) is a multifunctional protein that affects transcription, splicing, and translation. Overexpression of YB-1 in breast cancers causes cisplatin resistance. The exact mechanism by which YB-1 confers cisplatin resistance is unknown. The aim of the present study was to identify, using mass spectrometry, proteins that interact with YB-1 that are important for cisplatin resistance in two breast cancer cell lines, namely MCF7 and MDA-MB-231. A tagged YB-1 construct was used to identify proteins interacting directly with YB-1 in breast cancer cells. We then focused on proteins that are potentially involved in breast cancer progression based on the ONCOMINE public microarray database. Genes encoding for these YB-1-interacting proteins were examined in the public NCBI comparative genomic hybridization database to determine whether they are localized to regions of chromosomes that are rearranged in breast cancer tissues. From these analyses, we generated a list of proteins potentially involved in cisplatin resistance. Cisplatin dose-response curves were constructed in MCF7 and MDA-MB-231 transfected with four siRNA corresponding to each of these YB-1 interactors to identify proteins significantly affecting cisplatin sensitivity upon gene silencing. Depletion of only the X-linked ribosomal protein S4 (RPS4X) resulted in consistent resistance to cisplatin in both cell lines with at least three different siRNA sequences against RPS4X. Further analyses indicated that the knock down of RPS4X decreased DNA synthesis, induced cisplatin resistance, and is equivalent to the overexpression of YB-1 in both MCF7 and MDA-MB-231 cells. These results suggest that the RPS4X/YB-1 complex is a significant potential target to counteract cisplatin resistance in breast cancer.

Indexed as

Antineoplastic AgentsBreast NeoplasmsBromodeoxyuridineCell Line, TumorCisplatinDNA-Binding ProteinsDose-Response Relationship, DrugDrug ResistanceFemaleHumansNuclear ProteinsRibosomal ProteinsRNA, Small InterferingY-Box-Binding Protein 1Antineoplastic AgentsBromodeoxyuridineCisplatinDNA-Binding ProteinsNuclear ProteinsRibosomal ProteinsRNA, Small InterferingY-Box-Binding Protein 1YBX1 protein, human

Identifiers

PMID21466612
PMCPMC11159804
OpenAlexW2052780159

What OpenQuestion holds

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Registered trials

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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.