Evidence map›Paper›PMID 16788846›Full record

ArticleJournal of cancer research and clinical oncology2006

Role of glutathione-S-transferase and codon 72 of P53 genotypes in epithelial ovarian cancer patients.

Elaine Cristina Morari, Andre Bacellar Costa Lima, Natassia Elena Bufalo, Janaina Luisa Leite, Fabiana Granja, Laura Sterian Ward

Open access · greenAbstract readComparative Study
In one paragraph

Article in Journal of cancer research and clinical oncology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 7 pooled it
2.6field-weighted citation impact, top 11% 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, 7 syntheses or guidelines pooled it, 52 citations in OpenAlex.

  1. Pooled it
  2. Individual effects ofFrontiers in genetics · 2022
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  6. Association between glutathione S-transferase M 1 null genotype and risk of ovarian cancer: a meta-analysis.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2013
    Pooled it
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  9. Frontiers in oncology · 2021
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  11. No association betweenOncotarget · 2017
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  14. Association of GSTO2 (N142D) Genetic Polymorphism and Acute Rejection of Liver.International journal of organ transplantation medicine · 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

6 authors at 1 institution in 1 country.

Elaine Cristina MorariLaboratory of Cancer Molecular Genetics, Department of Medicine, Medical Sciences Faculty, State University of Campinas-UNICAMP, Tessalia Vieira de Camargo 126, 13084-970, Campinas, São Paulo, Brazil.
Andre Bacellar Costa Lima
Natassia Elena Bufalo
Janaina Luisa Leite
Fabiana Granja
Laura Sterian Ward
Universidade Estadual de Campinas (UNICAMP) · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeA series of polymorphisms in germ-line DNA have been investigated in an effort to delineate polygenic models of cancer susceptibility and prognosis. As low-penetrance susceptibility genes may combine additively or multiplicatively and contribute to cancer incidence and to the response to chemotherapy, we studied GSTT1, GSTM1, GSTO2, GSTP1 and codon 72 of p53 genotype profiles in ovarian cancer patients.

methodsWe compared 69 ovarian cancer patients with 222 control healthy women paired for ethnic and life-style characteristics. Outcome was evaluated in 29 stage III and IV patients submitted to a platinum-based chemotherapy followed-up for 6-29 months (17 +/- 9 months).

resultsGSTT1, GSTM1, GSTO2 and GSTP1 genes presented a similar genotype distribution, but codon 72 of p53 gene wild-type variant was less frequent in ovarian cancer patients than in controls (chi(2); P = 0.0004).

conclusionsWe were unable to demonstrate any association between the GST genotypes studied and the risk of ovarian cancer but the inheritance of a heterozygous Arg/Pro genotype of p53 increased the risk of ovarian cancer more than 2.5 times (OR = 2.571; 95% CI = 1.453-4.550). There was no association of the studied genes to any clinical or pathological feature of the patients or to their response to chemotherapy.

Indexed as

CodonGenes, p53AdultAgedAntineoplastic Combined Chemotherapy ProtocolsArginineDisease SusceptibilityFemaleGenotypeGlutathione S-Transferase piGlutathione TransferaseHumansLife StyleMiddle AgedNeoplasm StagingOdds RatioArginineCodonGlutathione S-Transferase piglutathione S-transferase T1Glutathione TransferaseGSTO2 protein, humanGSTP1 protein, humanProline

Identifiers

PMID16788846
PMCPMC12161103
OpenAlexW1977956216

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.