Literature DB >> 29807045

Androgen blockade based clinical trials landscape in triple negative breast cancer.

Yaqin Shi1, Fang Yang1, Doudou Huang1, Xiaoxiang Guan2.   

Abstract

Androgen receptor (AR) targeted treatment has shown promising preliminary results in triple negative breast cancer (TNBC). Identification of AR-associated signaling pathways is of great significance for in-depth understanding of their roles in pathogenesis of TNBC. To meet this objective, preclinical and clinical studies were conducted to clarify the biological interactions of AR signaling and combination strategies based on AR-targeted therapy. Biologically, AR signaling in TNBC which not only interacts with a network of key pathways, involving PI3K/AKT/mTOR, cell cycle, and DNA damage repair pathways, but mediates pivotal processes of tumor initiation and immunogenic modulation, may present an opportunity to overcome the insensitivity of single AR-targeted therapy. Research in investigating androgen-blockade based combination therapy in this aggressive tumor has demonstrated promising benefit in preclinical studies, and comparable clinical trials of combined strategies with CDK4/6 inhibitors, PI3K inhibition, chemotherapy, and immunotherapy, are ongoing. Accordingly, clinical interpretation of AR-related biological interactions, aiming at combined blockade of the signaling pathways may pave a new way for endocrine-based therapy in the treatment of TNBC.
Copyright © 2018 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Androgen; Breast; Combination; Receptor; Triple

Mesh:

Substances:

Year:  2018        PMID: 29807045     DOI: 10.1016/j.bbcan.2018.05.004

Source DB:  PubMed          Journal:  Biochim Biophys Acta Rev Cancer        ISSN: 0304-419X            Impact factor:   10.680


  6 in total

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Authors:  Hanane Mansouri; Lindsay B Alcaraz; Caroline Mollevi; Aude Mallavialle; William Jacot; Florence Boissière-Michot; Joelle Simony-Lafontaine; Valérie Laurent-Matha; Pascal Roger; Emmanuelle Liaudet-Coopman; Séverine Guiu
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3.  Germline TP53 and MSH6 mutations implicated in sporadic triple-negative breast cancer (TNBC): a preliminary study.

Authors:  Dandan Yi; Lei Xu; Jiaqi Luo; Xiaobin You; Tao Huang; Yi Zi; Xiaoting Li; Ru Wang; Zaixuan Zhong; Xiaoqiao Tang; Ang Li; Yujian Shi; Jianmei Rao; Yifen Zhang; Jianfeng Sang
Journal:  Hum Genomics       Date:  2019-01-10       Impact factor: 4.639

Review 4.  Recent advances of therapeutic targets based on the molecular signature in breast cancer: genetic mutations and implications for current treatment paradigms.

Authors:  Zeinab Safarpour Lima; Mostafa Ghadamzadeh; Farzad Tahmasebi Arashloo; Ghazaleh Amjad; Mohammad Reza Ebadi; Ladan Younesi
Journal:  J Hematol Oncol       Date:  2019-04-11       Impact factor: 17.388

5.  A Phase II Clinical Trial of Pembrolizumab and Enobosarm in Patients with Androgen Receptor-Positive Metastatic Triple-Negative Breast Cancer.

Authors:  Yuan Yuan; Jin Sun Lee; Susan E Yost; Paul H Frankel; Christopher Ruel; Colt A Egelston; Weihua Guo; John D Gillece; Megan Folkerts; Lauren Reining; Sarah K Highlander; Kim Robinson; Simran Padam; Norma Martinez; Aileen Tang; Daniel Schmolze; James Waisman; Mina Sedrak; Peter P Lee; Joanne Mortimer
Journal:  Oncologist       Date:  2020-11-24       Impact factor: 5.837

6.  Expression and clinical significance of MAPK and EGFR in triple-negative breast cancer.

Authors:  Weihua Jiang; Xiaowen Wang; Chenguang Zhang; Laiti Xue; Liang Yang
Journal:  Oncol Lett       Date:  2020-01-09       Impact factor: 2.967

  6 in total

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