Literature DB >> 11992551

Analysis of p53/BAX in primary colorectal carcinoma: low BAX protein expression is a negative prognostic factor in UICC stage III tumors.

Katharina Schelwies1, Isrid Sturm, Patricia Grabowski, Hans Scherübl, Isabell Schindler, Sandra Hermann, Harald Stein, Heinz-Johannes Buhr, Ernst O Riecken, Martin Zeitz, Bernd Dörken, Peter T Daniel.   

Abstract

Deregulation of cell death pathways contributes to tumor development and to the clinical course of cancer disease. In patients with liver metastases of colorectal cancer, we have previously shown that an intact p53/BAX apoptotic pathway is a positive prognostic factor. Therefore, the purpose of our study was to determine the prognostic value of BAX protein expression and the mutational status of its upstream regulator p53 in primary colorectal adenocarcinoma. To this end, we analyzed retrospectively tumor samples of 116 patients who underwent surgery for colorectal adenocarcinoma and had a follow-up for a minimum of 5 years or until death (UICC Stage III: 59 patients, UICC Stage IV: 57 patients). Tumors were screened for p53 mutations and investigated for BAX protein expression. Overall median survival was 17 months. As expected, patients with UICC III tumors survived longer than patients with UICC IV tumors: 69 months vs. 8 months (p < 0.0001). UICC III tumors with high BAX expression were associated with a significantly better prognosis (p = 0.009) than BAX low expressing tumors. The combined p53/BAX pathway analysis for the UICC Stage III group revealed the worst outcome for patients with a disrupted p53/BAX pathway (i.e., BAX low/p53 mutated; p = 0.004). In contrast, no significant effect of the p53/BAX status on survival was found in UICC IV tumors. Our study in primary adenocarcinoma of the colorectum shows for the first time that a disrupted p53/BAX pathway is associated with a poor clinical outcome in UICC III tumors. These data also confirm our previous report on the relevance of an intact p53/BAX pathway in liver metastasis of colorectal cancer. Nevertheless, we were not able to confirm this finding in the heterogenous subgroup of UICC IV tumors of the colorectum. Our study therefore provides the basis for the analysis of defects in p53/BAX (and additional genes) in a prospective trial that is the logical basis for future risk-adapted therapies. Copyright 2002 Wiley-Liss, Inc.

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Year:  2002        PMID: 11992551     DOI: 10.1002/ijc.10380

Source DB:  PubMed          Journal:  Int J Cancer        ISSN: 0020-7136            Impact factor:   7.396


  15 in total

Review 1.  Role of BAX for outcome prediction in gastrointestinal malignancies.

Authors:  Filippo Pietrantonio; Pamela Biondani; Elisa Ciurlia; Giuseppe Fanetti; Anna Tessari; Gaia Bertarelli; Ilaria Bossi; Valeria Musella; Flavia Melotti; Maria Di Bartolomeo; Francesca Valvo; Alessandro Pellegrinelli; Massimo Milione; Federica Perrone; Filippo de Braud
Journal:  Med Oncol       Date:  2013-05-23       Impact factor: 3.064

2.  Bax expression is a candidate prognostic and predictive marker of colorectal cancer.

Authors:  Venkat R Katkoori; Catalina Suarez-Cuervo; Chandrakumar Shanmugam; Nirag C Jhala; Tom Callens; Ludwine Messiaen; James Posey; Harvey L Bumpers; Sreelatha Meleth; William E Grizzle; Upender Manne
Journal:  J Gastrointest Oncol       Date:  2010-12

3.  A novel mechanism for CTCF in the epigenetic regulation of Bax in breast cancer cells.

Authors:  Claudia Fabiola Méndez-Catalá; Svetlana Gretton; Alexander Vostrov; Elena Pugacheva; Dawn Farrar; Yoko Ito; France Docquier; Georgia-Xanthi Kita; Adele Murrell; Victor Lobanenkov; Elena Klenova
Journal:  Neoplasia       Date:  2013-08       Impact factor: 5.715

Review 4.  [Clinical, pathological and molecular prognostic factors in colorectal carcinomas].

Authors:  S E Baldus
Journal:  Pathologe       Date:  2003-01-21       Impact factor: 1.011

5.  Analysis of neuroendocrine differentiation and the p53/BAX pathway in UICC stage III colorectal carcinoma identifies patients with good prognosis.

Authors:  Patricia Grabowski; Isrid Sturm; Katharina Schelwies; Kerstin Maaser; Heinz-Johannes Buhr; Bernd Dörken; Martin Zeitz; Peter T Daniel; Hans Scherübl
Journal:  Int J Colorectal Dis       Date:  2005-06-14       Impact factor: 2.571

6.  Prognostic implications of BAX protein expression and microsatellite instability in all non-metastatic stages of primary colon cancer treated by surgery alone.

Authors:  Oliver Nehls; Holger G Hass; Thomas Okech; Silke Zenner; Chih-Jen Hsieh; Mario Sarbia; Franz Borchard; Hans-Helmut Gruenagel; Vera Gaco; Rainer Porschen; Michael Gregor; Bodo Klump
Journal:  Int J Colorectal Dis       Date:  2009-02-17       Impact factor: 2.571

7.  What's new in target volume definition for radiologists in ICRU Report 71? How can the ICRU volume definitions be integrated in clinical practice?

Authors:  Anne Kiil Berthelsen; Jane Dobbs; Elisabeth Kjellén; Torsten Landberg; Torgil R Möller; Per Nilsson; Lena Specht; André Wambersie
Journal:  Cancer Imaging       Date:  2007-06-11       Impact factor: 3.909

8.  Genetic dissection of apoptosis and cell cycle control in response of colorectal cancer treated with preoperative radiochemotherapy.

Authors:  Isrid Sturm; Beate Rau; Peter M Schlag; Peter Wust; Bert Hildebrandt; Hanno Riess; Steffen Hauptmann; Bernd Dörken; Peter T Daniel
Journal:  BMC Cancer       Date:  2006-05-10       Impact factor: 4.430

9.  Bax expression measured by AQUAnalysis is an independent prognostic marker in oral squamous cell carcinoma.

Authors:  Pinaki Bose; Alexander C Klimowicz; Elizabeth Kornaga; Stephanie K Petrillo; T Wayne Matthews; Shamir Chandarana; Anthony M Magliocco; Nigel T Brockton; Joseph C Dort
Journal:  BMC Cancer       Date:  2012-08-01       Impact factor: 4.430

10.  Gene expression profiling reveals two separate mechanisms regulating apoptosis in rectal carcinomas in vivo.

Authors:  Elza C de Bruin; Simone van de Pas; Cornelis J H van de Velde; J Han J M van Krieken; Lucy T C Peltenburg; Corrie A M Marijnen; Jan Paul Medema
Journal:  Apoptosis       Date:  2007-09       Impact factor: 4.677

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