Literature DB >> 15629598

Low BAX protein expression correlates with disease recurrence in preoperatively irradiated rectal carcinoma.

Oliver Nehls1, Thomas Okech, Chih-Jen Hsieh, Mario Sarbia, Franz Borchard, Hans-Helmut Gruenagel, Vera Gaco, Rainer Porschen, Michael Gregor, Bodo Klump.   

Abstract

PURPOSE: To determine the prognostic impact of BAX in correlation to its upstream effector p53 as well as clinicopathologic variables and patient outcome in preoperatively irradiated rectal carcinoma. METHODS AND MATERIALS: We investigated 92 rectal carcinoma patients treated by preoperative radiotherapy to a total dose of 30 Gy followed by surgery. Median follow-up was 71 months. Immunohistochemistry was performed on paraffin sections of pretreatment biopsy samples for BAX protein. Also, we considered the previously determined p53 expression data from this cohort.
RESULTS: BAX protein expression was classified as high and low in 63 (68.5%) and 29 (31.5%) tumors, respectively. Unlike clinicopathologic variables, high BAX expression was significantly associated with improved disease-free survival by univariate analysis (p = 0.048). Moreover, in multivariate analyses, high BAX expression was an independent prognostic indicator for both improved local recurrence-free interval and improved disease-free survival (p = 0.03 and 0.047, respectively). Concerning the p53/BAX pathway, subgroup analysis yielded no association between p53 immunonegative/BAX high vs. p53 immunopositive/BAX low expressing tumors with regard to overall, disease-free, or local recurrence-free survival in either univariate (p = 0.88, 0.54, and 0.16, respectively) or multivariate analysis.
CONCLUSIONS: This study demonstrates that BAX protein expression might help to predict disease recurrence in preoperatively irradiated rectal carcinoma, whereas determination of p53, the proposed upstream regulator of BAX-induced apoptosis, did not provide additional prognostic information.

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Year:  2005        PMID: 15629598     DOI: 10.1016/j.ijrobp.2004.05.023

Source DB:  PubMed          Journal:  Int J Radiat Oncol Biol Phys        ISSN: 0360-3016            Impact factor:   7.038


  7 in total

1.  Adjuvant therapy for rectal cancer.

Authors:  Smitha S Krishnamurthi; Yuji Seo; Timothy J Kinsella
Journal:  Clin Colon Rectal Surg       Date:  2007-08

2.  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

3.  Low Mmp 9 and VEGF levels predict good oncologic outcome in mid and low rectal cancer patients with neoadjuvant chemoradiation.

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Journal:  BMC Clin Pathol       Date:  2012-12-31

Review 4.  The prognostic value of the apoptosis pathway in colorectal cancer: a review of the literature on biomarkers identified by immunohistochemistry.

Authors:  Eliane C M Zeestraten; Anne Benard; Marlies S Reimers; Philip C Schouten; Gerrit J Liefers; Cornelis J H van de Velde; Peter J K Kuppen
Journal:  Biomark Cancer       Date:  2013-07-04

5.  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

6.  Studies on p53, BAX and Bcl-2 protein expression and microsatellite instability in stage III (UICC) colon cancer treated by adjuvant chemotherapy: major prognostic impact of proapoptotic BAX.

Authors:  O Nehls; T Okech; C-J Hsieh; T Enzinger; M Sarbia; F Borchard; H-H Gruenagel; V Gaco; H G Hass; H T Arkenau; J T Hartmann; R Porschen; M Gregor; B Klump
Journal:  Br J Cancer       Date:  2007-04-10       Impact factor: 7.640

7.  BG-4, a novel anticancer peptide from bitter gourd (Momordica charantia), promotes apoptosis in human colon cancer cells.

Authors:  Vermont P Dia; Hari B Krishnan
Journal:  Sci Rep       Date:  2016-09-15       Impact factor: 4.379

  7 in total

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