Literature DB >> 25698149

p53 status identifies triple-negative breast cancer patients who do not respond to adjuvant chemotherapy.

Danila Coradini1, Elia Biganzoli2, Ilaria Ardoino3, Federico Ambrogi3, Patrizia Boracchi3, Romano Demicheli4, Maria Grazia Daidone5, Angela Moliterni6.   

Abstract

Genomic analysis and protein expression assimilate triple-negative breast cancers (TNBC) with basal-like breast tumors. TNBCs, however, have proved to encompass also tumors with normal-like phenotype and known to have favorable prognosis and to respond to chemotherapy. In a recent paper, we have provided evidence that p53 status is able to subdivide TNBCs into two distinct subgroups with different outcome, and consistent with basal- and normal-like phenotypes. Based on this finding, we explored the contribution of p53 status in predicting the response to adjuvant CMF or CMF followed doxorubicin chemotherapy of a group of TNBC patients. Results indicated that TNBC patients with a p53-positive tumor had a shorter relapse-free and overall survival than patients carrying a p53-negative TNBC, corroborating our hypothesis about the relationship between TNBC phenotype (basal-like versus normal-like) and p53 status as predictor of response to anthracycline/CMF-based chemotherapy.
Copyright © 2015 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Adjuvant chemotherapy; Breast cancer; Triple negative; p53 status

Mesh:

Substances:

Year:  2015        PMID: 25698149     DOI: 10.1016/j.breast.2015.01.007

Source DB:  PubMed          Journal:  Breast        ISSN: 0960-9776            Impact factor:   4.380


  8 in total

1.  Constitutively activated ERK sensitizes cancer cells to doxorubicin: Involvement of p53-EGFR-ERK pathway.

Authors:  Ratna Kumari; Surbhi Chouhan; Snahlata Singh; Rishi Raj Chhipa; Amrendra Kumar Ajay; Manoj Kumar Bhat
Journal:  J Biosci       Date:  2017-03       Impact factor: 1.826

2.  A combination of novel NSC small molecule inhibitor along with doxorubicin inhibits proliferation of triple-negative breast cancer through metabolic reprogramming.

Authors:  Hassan Yousefi; Maninder Khosla; Lothar Lauterboeck; Samuel C Okpechi; David Worthylake; Jone Garai; Jovanny Zabaleta; Jessie Guidry; Mohammad Amin Zarandi; Dorota Wyczechowska; Janarthanan Jayawickramarajah; Qinglin Yang; Joseph Kissil; Suresh K Alahari
Journal:  Oncogene       Date:  2022-10-15       Impact factor: 8.756

Review 3.  Breast cancer classification and prognostication through diverse systems along with recent emerging findings in this respect; the dawn of new perspectives in the clinical applications.

Authors:  Vida Pourteimoor; Samira Mohammadi-Yeganeh; Mahdi Paryan
Journal:  Tumour Biol       Date:  2016-09-20

Review 4.  Potentiating Therapeutic Effects of Epidermal Growth Factor Receptor Inhibition in Triple-Negative Breast Cancer.

Authors:  Kyu Sic You; Yong Weon Yi; Jeonghee Cho; Jeong-Soo Park; Yeon-Sun Seong
Journal:  Pharmaceuticals (Basel)       Date:  2021-06-18

5.  Double-positive in triple-negative? How significant is basal cytokeratin expression in breast cancer?

Authors:  Anusree Majumder; Rajat Jagani; Atoshi Basu
Journal:  Med J Armed Forces India       Date:  2019-02-26

Review 6.  Aberrant calcium signalling downstream of mutations in TP53 and the PI3K/AKT pathway genes promotes disease progression and therapy resistance in triple negative breast cancer.

Authors:  Alex J Eustace; Min Jie Lee; Grace Colley; Jack Roban; Tim Downing; Paul J Buchanan
Journal:  Cancer Drug Resist       Date:  2022-06-21

7.  Profiling molecular regulators of recurrence in chemorefractory triple-negative breast cancers.

Authors:  Bradley A Hancock; Yu-Hsiang Chen; Jeffrey P Solzak; Mufti N Ahmad; David C Wedge; Dumitru Brinza; Charles Scafe; James Veitch; Rajesh Gottimukkala; Walt Short; Rutuja V Atale; Mircea Ivan; Sunil S Badve; Bryan P Schneider; Xiongbin Lu; Kathy D Miller; Milan Radovich
Journal:  Breast Cancer Res       Date:  2019-08-05       Impact factor: 6.466

8.  miRNome and Functional Network Analysis of PGRMC1 Regulated miRNA Target Genes Identify Pathways and Biological Functions Associated With Triple Negative Breast Cancer.

Authors:  Diego A Pedroza; Matthew Ramirez; Venkatesh Rajamanickam; Ramadevi Subramani; Victoria Margolis; Tugba Gurbuz; Adriana Estrada; Rajkumar Lakshmanaswamy
Journal:  Front Oncol       Date:  2021-07-19       Impact factor: 6.244

  8 in total

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