Evidence map›Paper›PMID 21080034›Full record

ArticleMolecular and cellular biochemistry2011

Proteomic analysis of cisplatin resistance in human ovarian cancer using 2-DE method.

Fengming Gong, Xingchen Peng, Zhi Zeng, Ming Yu, Yuwei Zhao, Aiping Tong

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Article in Molecular and cellular biochemistry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

18 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Fengming GongState Key Laboratory of Biotherapy and Cancer Center, West China Hospital, West China Medical School, Sichuan University, Chengdu, People's Republic of China.
Xingchen Peng
Zhi Zeng
Ming Yu
Yuwei Zhao
Aiping Tong

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Platinum-based chemotherapy, such as cisplatin, is the primary treatment for human ovarian cancer. However, overcoming drug resistance has become an important issue in cancer chemotherapy. In this study, we performed 2-DE and ESI-Q-TOF MS/MS analysis to identify differential proteins expression between cisplatin-sensitive (A2780S) and cisplatin-resistant (A2780-CP) ovarian cancer cell lines. Of the 14 spots identified as differentially expressed (±over twofold, P < 0.05) between the two cell lines, ten spots (corresponding to ten unique proteins) were positively identified by ESI-Q-TOF MS/MS analysis. These proteins include capsid glycoprotein, fructose-bisphosphate aldolase C, heterogeneous nuclear ribonucleoproteins A2/B1, putative RNA-binding protein 3, Ran-specific GTPase-activating protein, ubiquitin carboxyl-terminal hydrolase isozyme L1, stathmin, ATPSH protein, chromobox protein homolog3 and phosphoglycerate kinase 1. The proteins identified in this study would be useful in revealing the mechanisms underlying cisplatin resistance and also provide some clues for further research.

Indexed as

Drug Resistance, NeoplasmElectrophoresis, Gel, Two-DimensionalAmino Acid SequenceAntineoplastic AgentsBiomarkers, TumorBlotting, WesternCell Line, TumorCisplatinFemaleHumansMolecular Sequence DataNeoplasm ProteinsOvarian NeoplasmsProteomicsReproducibility of ResultsSpectrometry, Mass, Electrospray IonizationAntineoplastic AgentsBiomarkers, TumorCisplatinNeoplasm Proteins

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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.