Evidence map›Paper›PMID 28031236›Full record

ArticleCancer genomics & proteomics2017

Proteomics Analysis of Ovarian Cancer Cell Lines and Tissues Reveals Drug Resistance-associated Proteins.

Isa N Cruz, Helen M Coley, Holger B Kramer, Thumuluru Kavitah Madhuri, Nur A M Safuwan, Ana Rita Angelino, Min Yang

Open access · diamondAbstract read
In one paragraph

Article in Cancer genomics & proteomics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 8% 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

44 citing papers in PubMed, 1 synthesis or guideline pooled it, 62 citations in OpenAlex.

  1. Biomarkers of tumor invasiveness in proteomics (Review).International journal of oncology · 2020
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  19. Research progress of omics technology in the field of tumor resistance: From singleZhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2021
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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

7 authors at 4 institutions in 2 countries.

Isa N CruzDepartment of Pharmaceutical & Biological Chemistry, UCL School of Pharmacy, London, U.K.
Helen M ColeyFaculty of Health and Medical Sciences, University of Surrey, Guildford, Surrey, U.K.
Holger B KramerDepartment of Physiology, Anatomy and Genetic, University of Oxford, South Parks Road, Oxford, U.K.
Thumuluru Kavitah MadhuriFaculty of Health and Medical Sciences, University of Surrey, Guildford, Surrey, U.K.
Nur A M SafuwanFaculty of Health and Medical Sciences, University of Surrey, Guildford, Surrey, U.K.
Ana Rita AngelinoDepartment of Pharmaceutical & Biological Chemistry, UCL School of Pharmacy, London, U.K.
Min YangDepartment of Pharmaceutical & Biological Chemistry, UCL School of Pharmacy, London, U.K. min.yang@ucl.ac.uk.
Royal Pharmaceutical Society · GBUniversity of Surrey · GBRoyal Surrey County Hospital · GBUniversity of Oxford · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCarboplatin and paclitaxel form the cornerstone of chemotherapy for epithelial ovarian cancer, however, drug resistance to these agents continues to present challenges. Despite extensive research, the mechanisms underlying this resistance remain unclear. MATERIALS AND

methodsA 2D-gel proteomics method was used to analyze protein expression levels of three human ovarian cancer cell lines and five biopsy samples. Representative proteins identified were validated via western immunoblotting. Ingenuity pathway analysis revealed metabolomic pathway changes.

resultsA total of 189 proteins were identified with restricted criteria. Combined treatment targeting the proteasome-ubiquitin pathway resulted in re-sensitisation of drug-resistant cells. In addition, examination of five surgical biopsies of ovarian tissues revealed α-enolase (ENOA), elongation factor Tu, mitochondrial (EFTU), glyceraldehyde-3-phosphate dehydrogenase (G3P), stress-70 protein, mitochondrial (GRP75), apolipoprotein A-1 (APOA1), peroxiredoxin (PRDX2) and annexin A (ANXA) as candidate biomarkers of drug-resistant disease.

conclusionProteomics combined with pathway analysis provided information for an effective combined treatment approach overcoming drug resistance. Analysis of cell lines and tissues revealed potential prognostic biomarkers for ovarian cancer.

Indexed as

Drug Resistance, NeoplasmProteomeProteomicsAntineoplastic AgentsAntineoplastic Combined Chemotherapy ProtocolsBiomarkersCell Line, TumorCell SurvivalCombined Modality TherapyComputational BiologyFemaleHumansNeoplasm StagingOvarian NeoplasmsProtein Interaction MappingSignal TransductionAntineoplastic AgentsBiomarkersProteome2D-gel proteomicsbiomarkerdrug resistance targetsOvarian cancertissue biopsies

Identifiers

PMID28031236
PMCPMC5267499
OpenAlexW2566723548

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.