Literature DB >> 19008097

What is triple-negative breast cancer?

William J Irvin1, Lisa A Carey.   

Abstract

Triple-negative (ER-negative, PR-negative, HER2/neu not overexpressed) breast cancer has distinct clinical and pathologic features, and is a clinical problem because of its relatively poor prognosis, aggressive behaviour and lack of targeted therapies, leaving chemotherapy as the mainstay of treatment. Most triple-negative tumours fall into the basal-like molecular subtype of breast cancer, but the terms are not completely synonymous. Among the intriguing characteristics of triple-negative breast cancer is its association with cancers arising in BRCA1 mutation carriers, in young women and in African-American women. The reasons for these associations are unclear but may ultimately provide avenues for prevention and targeted therapy. This review discusses the definitions and characteristics of as well as current and evolving therapies for triple-negative and basal-like breast cancer.

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Year:  2008        PMID: 19008097     DOI: 10.1016/j.ejca.2008.09.034

Source DB:  PubMed          Journal:  Eur J Cancer        ISSN: 0959-8049            Impact factor:   9.162


  112 in total

Review 1.  Triple-negative breast cancer: present challenges and new perspectives.

Authors:  Franca Podo; Lutgarde M C Buydens; Hadassa Degani; Riet Hilhorst; Edda Klipp; Ingrid S Gribbestad; Sabine Van Huffel; Hanneke W M van Laarhoven; Jan Luts; Daniel Monleon; Geert J Postma; Nicole Schneiderhan-Marra; Filippo Santoro; Hans Wouters; Hege G Russnes; Therese Sørlie; Elda Tagliabue; Anne-Lise Børresen-Dale
Journal:  Mol Oncol       Date:  2010-04-24       Impact factor: 6.603

2.  Downregulation of antigen presentation-associated pathway proteins is linked to poor outcome in triple-negative breast cancer patient tumors.

Authors:  Martin H Pedersen; Brian L Hood; Hans Christian Beck; Thomas P Conrads; Henrik J Ditzel; Rikke Leth-Larsen
Journal:  Oncoimmunology       Date:  2017-03-16       Impact factor: 8.110

3.  Bcl-2 expression and triple negative profile in breast carcinoma.

Authors:  Imen Kallel-Bayoudh; Hanen Ben Hassen; Abdelmajid Khabir; Noureddine Boujelbene; Jamel Daoud; Mounir Frikha; Tahia Sallemi-Boudawara; Sami Aifa; Ahmed Rebaï
Journal:  Med Oncol       Date:  2010-10-02       Impact factor: 3.064

4.  Clinicopathologic features and outcomes of metaplastic breast carcinoma: comparison with invasive ductal carcinoma of the breast.

Authors:  Hyung Seok Park; Seho Park; Joo Hee Kim; Ju-Hyun Lee; So-Young Choi; Byeong-Woo Park; Kyong-Sik Lee
Journal:  Yonsei Med J       Date:  2010-11       Impact factor: 2.759

5.  A chimeric SERM-histone deacetylase inhibitor approach to breast cancer therapy.

Authors:  Hitisha K Patel; Marton I Siklos; Hazem Abdelkarim; Emma L Mendonca; Aditya Vaidya; Pavel A Petukhov; Gregory R J Thatcher
Journal:  ChemMedChem       Date:  2013-08-16       Impact factor: 3.466

6.  Characteristics of triple-negative breast cancer in patients with a BRCA1 mutation: results from a population-based study of young women.

Authors:  Eunjung Lee; Roberta McKean-Cowdin; Huiyan Ma; Darcy V Spicer; David Van Den Berg; Leslie Bernstein; Giske Ursin
Journal:  J Clin Oncol       Date:  2011-10-17       Impact factor: 44.544

Review 7.  Targeting apoptosis pathway with natural terpenoids: implications for treatment of breast and prostate cancer.

Authors:  Huanjie Yang; Q Ping Dou
Journal:  Curr Drug Targets       Date:  2010-06       Impact factor: 3.465

8.  Emerging trends in the treatment of triple-negative breast cancer in Canada: a survey.

Authors:  S Verma; L Provencher; R Dent
Journal:  Curr Oncol       Date:  2011-08       Impact factor: 3.677

9.  Blocking LLT1 (CLEC2D, OCIL)-NKRP1A (CD161) interaction enhances natural killer cell-mediated lysis of triple-negative breast cancer cells.

Authors:  Armando M Marrufo; Stephen O Mathew; Pankaj Chaudhary; Joseph D Malaer; Jamboor K Vishwanatha; Porunelloor A Mathew
Journal:  Am J Cancer Res       Date:  2018-06-01       Impact factor: 6.166

10.  Targeting BCL-xL improves the efficacy of bromodomain and extra-terminal protein inhibitors in triple-negative breast cancer by eliciting the death of senescent cells.

Authors:  Sylvia S Gayle; Jennifer M Sahni; Bryan M Webb; Kristen L Weber-Bonk; Melyssa S Shively; Raffaella Spina; Eli E Bar; Mathew K Summers; Ruth A Keri
Journal:  J Biol Chem       Date:  2018-11-27       Impact factor: 5.157

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