Literature DB >> 21778571

Clinical trials in triple negative breast cancer.

Katherine E Reeder-Hayes1, Lisa A Carey, William M Sikov.   

Abstract

Triple negative breast cancer (TNBC) is an aggressive subtype of the disease against which targeted therapies that significantly improve the prognosis for hormone receptor-positive and HER2-overexpressing breast cancers are ineffective. This article summarizes our current understanding of the biology of TNBC as it relates to the efficacy of standard and investigational therapies. It reviews promising preliminary results that have been achieved with chemotherapeutic agents including the platinum analogs and agents that inhibit DNA repair by targeting poly ADP-ribose polymerase (PARP), while anti-angiogenic therapies and those that target the epidermal growth factor receptor (EGFR) have had more limited success. Agents that target a number of other pathways which appear to influence the biologic aggressiveness of TNBC, including src and PI3K, are in early stage clinical trials. As we learn more about TNBC, and which of its characteristics determine treatment response and resistance, we should become better able to select appropriate therapies for biologically defined patient subgroups, and reduce the clinical burden of this disease.

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Year:  2010        PMID: 21778571     DOI: 10.3233/BD-2010-0310

Source DB:  PubMed          Journal:  Breast Dis        ISSN: 0888-6008


  10 in total

1.  Pharmacological profiling of kinase dependency in cell lines across triple-negative breast cancer subtypes.

Authors:  Lauren S Fink; Alexander Beatty; Karthik Devarajan; Suraj Peri; Jeffrey R Peterson
Journal:  Mol Cancer Ther       Date:  2014-10-24       Impact factor: 6.261

2.  Aminoflavone-loaded EGFR-targeted unimolecular micelle nanoparticles exhibit anti-cancer effects in triple negative breast cancer.

Authors:  Ashley M Brinkman; Guojun Chen; Yidan Wang; Curtis J Hedman; Nathan M Sherer; Thomas C Havighurst; Shaoqin Gong; Wei Xu
Journal:  Biomaterials       Date:  2016-05-27       Impact factor: 12.479

3.  Defining the expressed breast cancer kinome.

Authors:  Alicia A Midland; Martin C Whittle; James S Duncan; Amy N Abell; Kazuhiro Nakamura; Jon S Zawistowski; Lisa A Carey; H Shelton Earp; Lee M Graves; Shawn M Gomez; Gary L Johnson
Journal:  Cell Res       Date:  2012-02-07       Impact factor: 25.617

4.  Yiqi formula enhances the antitumor effects of erlotinib for treatment of triple-negative breast cancer xenografts.

Authors:  Ming-Juan Liao; Mei-Na Ye; Rui-Juan Zhou; Jia-Yu Sheng; Hong-Feng Chen
Journal:  Evid Based Complement Alternat Med       Date:  2014-10-19       Impact factor: 2.629

5.  Reduction in breast cancer susceptibility due to XbaI gene polymorphism of alpha estrogen receptor gene in Jordanians.

Authors:  Manar Fayiz Atoum; Foad Alzoughool
Journal:  Breast Cancer (Dove Med Press)       Date:  2017-01-24

6.  Candidate tumor suppressor gene IRF6 is involved in human breast cancer pathogenesis via modulating PI3K-regulatory subunit PIK3R2 expression.

Authors:  Hong-Fa Xu; Tie-Jun Huang; Qin Yang; Liang Xu; Fen Lin; Yan-Hong Lang; Hao Hu; Li-Xia Peng; Dong-Fang Meng; Yu-Jie Xie; Li Tan; Chao-Nan Qian; Bi-Jun Huang
Journal:  Cancer Manag Res       Date:  2019-06-21       Impact factor: 3.989

7.  Network pharmacology modeling identifies synergistic Aurora B and ZAK interaction in triple-negative breast cancer.

Authors:  Prson Gautam; Abhishekh Gupta; Jing Tang; Liye He; Sanna Timonen; Yevhen Akimov; Wenyu Wang; Agnieszka Szwajda; Alok Jaiswal; Denes Turei; Bhagwan Yadav; Matti Kankainen; Jani Saarela; Julio Saez-Rodriguez; Krister Wennerberg; Tero Aittokallio
Journal:  NPJ Syst Biol Appl       Date:  2019-07-08

8.  Nestin positively regulates the Wnt/β-catenin pathway and the proliferation, survival and invasiveness of breast cancer stem cells.

Authors:  Zuowei Zhao; Ping Lu; Hao Zhang; Huanming Xu; Ningning Gao; Man Li; Caigang Liu
Journal:  Breast Cancer Res       Date:  2014-07-24       Impact factor: 6.466

9.  Clinical implications of the coexpression of SRC1 and NANOG in HER-2-overexpressing breast cancers.

Authors:  Chengyan Jin; Xingyi Zhang; Mei Sun; Yifan Zhang; Guangxin Zhang; Bin Wang
Journal:  Onco Targets Ther       Date:  2016-09-06       Impact factor: 4.147

10.  Complement-Mediated Selective Tumor Cell Lysis Enabled by Bi-Functional RNA Aptamers.

Authors:  Prabhat K Mallik; Kimi Nishikawa; Pramit Mallik; Hua Shi
Journal:  Genes (Basel)       Date:  2021-12-29       Impact factor: 4.096

  10 in total

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