The implication and potential applications of high-mobility group box 1 protein in breast cancer

被引:35
作者
Sohun, Moonindranath [1 ]
Shen, Huiling [1 ]
机构
[1] Jiangsu Univ, Affiliated Peoples Hosp, Dept Oncol, Zhenjiang 212013, Peoples R China
基金
中国国家自然科学基金;
关键词
Breast cancer; high-mobility group box 1 protein (HMGB1); amphoterin; GLYCATION END-PRODUCTS; HMG-DOMAIN PROTEINS; TUMOR-CELLS; ESTROGEN-RECEPTOR; ANTICANCER CHEMOTHERAPY; IMMUNE-SYSTEM; GROUP B1; EXPRESSION; BINDING; RELEASE;
D O I
10.21037/atm.2016.05.36
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
High-mobility group box 1 protein (HMGB1) is a highly conserved, non-histone and ubiquitous chromosomal protein found enriched in active chromatin forming part of the high mobility group family of proteins and is encoded by the HMGB1 gene (13q12) in human beings. It has various intranuclear and extracellular functions. It plays an important role in the pathogenesis of many diseases including cancer. In 2012, there was approximately 1.67 million new breast cancer cases diagnosed which makes it the second most frequent cancer in the world after lung cancer (25% of all cancers) and the commonest cancer among women. Both pre-clinical and clinical studies have suggested that HMGB1 might be a useful target in the management of breast cancer. This review summarises the structure and functions of HMGB1 and its dual role in carcinogenesis both as a pro-tumorigenic and anti-tumorigenic factor. It also sums up evidence from in vitro and in vivo studies using breast cancer cell lines and samples which demonstrate its influence in radiotherapy, chemotherapy and hormonal therapy in breast cancer. It may have particular importance in HER2 positive and metastatic breast cancer. It might pave the way for new breast cancer treatments through development of novel drugs, use of microRNAs (miRNAs), targeting breast cancer stem cells (CSCs) and breast cancer immunotherapy. It may also play a role in determining breast cancer prognosis. Thus HMGB1 may open up novel avenues in breast cancer management.
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页数:13
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共 90 条
[71]  
Tiago M, 2014, TISSUE ENG PT A, V20, P2412, DOI [10.1089/ten.tea.2013.0473, 10.1089/ten.TEA.2013.0473]
[72]   The nuclear factor HMGB1 mediates hepatic injury after murine liver ischemia-reperfusion [J].
Tsung, A ;
Sahai, R ;
Tanaka, H ;
Nakao, A ;
Fink, MP ;
Lotze, MT ;
Yang, H ;
Li, JH ;
Tracey, KJ ;
Geller, DA ;
Billiar, TR .
JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 201 (07) :1135-1143
[73]   High-mobility group box 1 (HMGB1) protein: Friend and foe [J].
Ulloa, Luis ;
Messmer, Davorka .
CYTOKINE & GROWTH FACTOR REVIEWS, 2006, 17 (03) :189-201
[74]   Physical interaction of tumour suppressor p53/p73 with CCAAT-binding transcription factor 2 (CTF2) and differential regulation of human high-mobility group 1 (HMG1) gene expression [J].
Uramoto, H ;
Izumi, H ;
Nagatani, G ;
Ohmori, H ;
Nagasue, N ;
Ise, T ;
Yoshida, T ;
Yasumoto, K ;
Kohno, K .
BIOCHEMICAL JOURNAL, 2003, 371 :301-310
[75]   Opinion - Inflammation and necrosis promote tumour growth [J].
Vakkila, J ;
Lotze, MT .
NATURE REVIEWS IMMUNOLOGY, 2004, 4 (08) :641-648
[76]   Tumor angiogenesis is enforced by autocrine regulation of high-mobility group box 1 [J].
van Beijnum, J. R. ;
Nowak-Sliwinska, P. ;
van den Boezem, E. ;
Hautvast, P. ;
Buurman, W. A. ;
Griffioen, A. W. .
ONCOGENE, 2013, 32 (03) :363-374
[77]   Convergence and amplification of toll-like receptor (TLR) and receptor for advanced glycation end products (RAGE) signaling pathways via high mobility group B1 (HMGB1) [J].
van Beijnum, Judy R. ;
Buurman, Wim A. ;
Griffioen, Arjan W. .
ANGIOGENESIS, 2008, 11 (01) :91-99
[78]   Gene expression of tumor angiogenesis dissected: specific targeting of colon cancer angiogenic vasculature [J].
van Beijnum, Judy R. ;
Dings, Ruud P. ;
van der Linden, Edith ;
Zwaans, Bernadette M. M. ;
Ramaekers, Frans C. S. ;
Mayo, Kevin H. ;
Griffioen, Arjan W. .
BLOOD, 2006, 108 (07) :2339-2348
[79]   High-mobility group (HMG) protein HMG-1 and TATA-binding protein-associated factor TAF(II)30 affect estrogen receptor-mediated transcriptional activation [J].
Verrier, CS ;
Roodi, N ;
Yee, CJ ;
Bailey, LR ;
Jensen, RA ;
Bustin, M ;
Parl, FF .
MOLECULAR ENDOCRINOLOGY, 1997, 11 (08) :1009-1019
[80]  
VONHOFF DD, 1979, CANCER TREAT REP, V63, P1527