Significant value of p53 accumulated in Invasive Ductal Breast Carcinoma

Author:

Baccouche Sami1,Rebai Ahmed1,Frikha Mounir2,Daoud Jamel2,Jlidi Rachid3,Gargouri Ali1

Affiliation:

1. Université de Sfax

2. CHU Habib Bourguiba Sfax

3. Centre medical ElBassatine

Abstract

Abstract Background The presence of a functional p53 protein is a key factor for the appropriate suppression of cancer development. The tumor suppressor p53 accumulates under stressful conditions, such as DNA damage, heat shock, hypoxia, and/or proto-oncogene activation, although conflicting reports exist on its transcriptional activity. A loss of p53 activity, by mutations or inhibition, is often associated with human malignancies. This work investigated the significant value of p53 accumulated in IDBC (Invasive Ductal Breast Carcinoma) and at the same time tries to arise different supports of this value. Results: To ensure this objective, we referred to two types of statistical analysis, the chi-square and logistic regression analysis. They confirmed the poor prognosis of p53 accumulated in IDBC (β* = -0.456 with p=0.00001) and showed that the independent variables (MDM2, BCL2, BAX and ER) formed an interesting model to explain the significant value of p53 accumulated in the IDBC. The predictive value of the model including the four biomarkers is AUC=93.5%, showing that if we take the expression status of the four biomarkers, we can deduce the status of p53 with a reliability of 93.5%. The residual term, representing 6,5% and involved in this significant value, corresponds to intrinsic modifications of p53: alterations of the TP53 gene, p53-oncoprotein interaction or cytoplasmic sequestration. In fact, following the IHC results of three different antibodies that recognize wild type or mutant p53, we examined the status of polymorphism 72, which may inform LOH (loss of heterozygozity). We found LOH associated with TP53 mutations in the context of down-regulated p53 target genes revealed by IHC. Although wild type in some cases, p53 loses its transcriptional activity; this may be due to oxidation of cysteine residues in the core domain, either iSAPP interaction or its cytoplasmic sequestration. Conclusion: P53 accumulated in IDBC had a significant value and the etiological factors of this value should be target for effective therapy.

Publisher

Research Square Platform LLC

Reference94 articles.

1. Lilia Ben Yaacoub, Mohamed Tahar Yaacoubi, Sihem Hmissa. Breast cancer in Tunisia: clinical and pathological findings;Nabiha Missaoui L;Asian Pac J Cancer Prev,2011

2. The dual role model for p53 in maintaining genomic integrity;Janus F;Cell Mol Life Sci,1999

3. p53, the cellular gatekeeper for growth and division;Levine AJ;Cell,1997

4. El-Deiry WS, Kern SE, Pietenpol JA, Kinzler KW, Vogelstein B (1992) Nat Genet 1:45–49

5. The first 30 years of p53: growing ever more complex;Levine AJ;Nat Rev Cancer,2009

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3