Evidence map›Paper›PMID 12644821›Full record

ArticleBritish journal of cancer2003

Evaluation of clinical significance of TP53, BCL-2, BAX and MEK1 expression in 229 ovarian carcinomas treated with platinum-based regimen.

J Kupryjańczyk, T Szymańska, R Madry, A Timorek, J Stelmachów, G Karpińska, A Rembiszewska, I Ziółkowska, E Kraszewska, J Debniak and 12 more

Open access · hybridAbstract readEvaluation Study
In one paragraph

Article in British journal of cancer, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

29 citing papers in PubMed, 81 citations in OpenAlex.

  1. Lack of Bax expression is associated with irinotecan-based treatment activity in advanced colorectal cancer patients.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2013
    Trial
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  6. The Clinical Significance ofInternational journal of molecular sciences · 2024
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  13. Review
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  19. Role of BAX for outcome prediction in gastrointestinal malignancies.Medical oncology (Northwood, London, England) · 2013
    Review
  20. Article
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

22 authors at 6 institutions in 2 countries.

J KupryjańczykDepartment of Molecular Pathology, Institute of Oncology, Roentgena 5, Warsaw, Poland. jolantak@coi.waw.pl
T Szymańska
R Madry
A Timorek
J Stelmachów
G Karpińska
A Rembiszewska
I Ziółkowska
E Kraszewska
J Debniak
J Emerich
M Ułańska
A Płuzańska
M Jedryka
M Goluda
A Chudecka-Głaz
I Rzepka-Górska
M Klimek
K Urbański
J Breborowicz
J Zieliński
J Markowska
Institute of Psychiatry and Neurology · PLPoznan University of Medical Sciences · PLGdańsk Medical University · PLMedical University of Lodz · PLNational Institute of Oncology · HUSzczecin Academy of Arts · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In cell line studies, BCL-2, BAX, as well as novel MEK1 protein levels have strong influence on ovarian cancer response to cisplatin-based chemotherapy. However, such associations have not been demonstrated clinically. We evaluated prognostic/predictive significance of these proteins with regard to TP53 status. Immunohistochemical analysis was performed on 229 ovarian carcinomas FIGO stage IIB-IV treated with platinum-based chemotherapy; the results were analysed by the Cox and logistic regression models. Clinical parameters (residual tumour size, patient age, FIGO stage) were the only indicators of overall survival (OS) and the strongest predictors of complete remission (CR). On the other hand, BAX expression was the strongest (P=0.005) or the only (in FIGO IIIC, P=0.02) prognostic indicator of disease-free survival (DFS) in the TP53(+) group. TP53(+) and TP53(-) ovarian carcinomas differed in clinical and molecular prognostic and predictive factors. Another novel finding is that CR was negatively influenced by high BAX expression in all patients group (P=0.047) and by BCL2 expression in the TP53(-) group (P=0.05). High MEK1 expression was associated with endometrioid and clear cell carcinomas (P=0.049); its loss was found with advancing FIGO stage (P=0.002). Our results suggest that binomial TP53 status divides ovarian carcinomas into two biologically distinct groups. BAX expression is an important factor of DFS in the TP53(+) group. BCL-2 and BAX, but not MEK1 expressions have predictive value in ovarian cancer patients treated with platinum-based chemotherapy.

Indexed as

Gene Expression Regulation, NeoplasticAdultAgedAntineoplastic Combined Chemotherapy Protocolsbcl-2-Associated X ProteinBiomarkers, TumorCisplatinDisease-Free SurvivalFemaleHumansImmunohistochemistryMAP Kinase Kinase 1Middle AgedMitogen-Activated Protein Kinase KinasesNeoplasm StagingOvarian NeoplasmsBAX protein, humanbcl-2-Associated X ProteinBiomarkers, TumorCisplatinMAP2K1 protein, humanMAP Kinase Kinase 1Mitogen-Activated Protein Kinase KinasesProtein Serine-Threonine KinasesProto-Oncogene ProteinsProto-Oncogene Proteins c-bcl-2Tumor Suppressor Protein p53

Identifiers

PMID12644821
PMCPMC2377076
OpenAlexW1988436289

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.