Literature DB >> 21199790

p53 status identifies two subgroups of triple-negative breast cancers with distinct biological features.

Elia Biganzoli1, Danila Coradini, Federico Ambrogi, Jonhatan M Garibaldi, Paulo Lisboa, Daniele Soria, Andrew R Green, Massimo Pedriali, Mauro Piantelli, Patrizia Querzoli, Romano Demicheli, Patrizia Boracchi, Italo Nenci, Ian O Ellis, Saverio Alberti.   

Abstract

OBJECTIVE: Despite the clinical similarities triple-negative and basal-like breast cancer are not synonymous. Indeed, not all basal-like cancers are negative for estrogen receptor, progesterone receptor and HER2 expression while triple-negative also encompasses other cancer types. P53 protein appears heterogeneously expressed in triple-negative breast cancers, suggesting that it may be associated with specific biological subgroups with a different outcome.
METHODS: We comparatively analyzed p53 expression in triple-negative tumors from two independent breast cancer case series (633 cases from the University of Ferrara and 1076 cases from the University of Nottingham).
RESULTS: In both case series, p53 protein expression was able to subdivide the triple-negative cases into two distinct subsets consistent with a different outcome. In fact, triple-negative patients with a p53 expressing tumor showed worse overall and event-free survival.
CONCLUSIONS: The immunohistochemical evaluation of p53 expression may help in taming the currently stormy relationship between pathological (triple-negative tumors) and biological (basal breast cancers) classifications and in selecting patient subgroups with different biological features providing a potentially powerful prognostic contribution in triple-negative breast cancers.

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Year:  2011        PMID: 21199790     DOI: 10.1093/jjco/hyq227

Source DB:  PubMed          Journal:  Jpn J Clin Oncol        ISSN: 0368-2811            Impact factor:   3.019


  25 in total

1.  New insight on the biological role of p53 protein as a tumor suppressor: re-evaluation of its clinical significance in triple-negative breast cancer.

Authors:  Min-Sun Jin; In Ae Park; Ji Young Kim; Yul Ri Chung; Seock-Ah Im; Kyung-Hun Lee; Hyeong-Gon Moon; Wonshik Han; Dong-Young Noh; Han Suk Ryu
Journal:  Tumour Biol       Date:  2016-02-19

2.  Outcome of triple-negative breast cancer in patients with or without markers regulating cell cycle and cell death.

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Review 4.  Biomarkers in triple negative breast cancer: A review.

Authors:  Budhi S Yadav; Priyanka Chanana; Swaty Jhamb
Journal:  World J Clin Oncol       Date:  2015-12-10

5.  A phase II trial to assess efficacy and safety of afatinib in extensively pretreated patients with HER2-negative metastatic breast cancer.

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Journal:  Breast Cancer Res Treat       Date:  2012-07-05       Impact factor: 4.872

6.  TP53 mutation, epithelial-mesenchymal transition, and stemlike features in breast cancer subtypes.

Authors:  Danila Coradini; Marco Fornili; Federico Ambrogi; Patrizia Boracchi; Elia Biganzoli
Journal:  J Biomed Biotechnol       Date:  2012-07-30

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8.  Calpain system protein expression in basal-like and triple-negative invasive breast cancer.

Authors:  S J Storr; K W Lee; C M Woolston; S Safuan; A R Green; R D Macmillan; A Benhasouna; T Parr; I O Ellis; S G Martin
Journal:  Ann Oncol       Date:  2012-06-27       Impact factor: 32.976

9.  mTrop1/Epcam knockout mice develop congenital tufting enteropathy through dysregulation of intestinal E-cadherin/β-catenin.

Authors:  Emanuela Guerra; Rossano Lattanzio; Rossana La Sorda; Francesca Dini; Gian Mario Tiboni; Mauro Piantelli; Saverio Alberti
Journal:  PLoS One       Date:  2012-11-28       Impact factor: 3.240

10.  An Integrative Genomics Approach for Associating GWAS Information with Triple-Negative Breast Cancer.

Authors:  Chindo Hicks; Ranjit Kumar; Antonio Pannuti; Kandis Backus; Alexandra Brown; Jesus Monico; Lucio Miele
Journal:  Cancer Inform       Date:  2013-01-29
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