Role of Runx2 in breast cancer-mediated bone metastasis

被引:56
作者
Vishal, M. [1 ]
Swetha, R. [1 ]
Thejaswini, G. [1 ]
Arumugam, B. [1 ]
Selvamurugan, N. [1 ]
机构
[1] SRM Univ, Sch Bioengn, Dept Biotechnol, Kattankulathur 603203, Tamil Nadu, India
关键词
Breast cancer; Metastasis; Bone; Runx2; MicroRNA; TRANSCRIPTION FACTOR RUNX2; MAMMARY EPITHELIAL-CELLS; LONG NONCODING RNAS; CARCINOMA IN-SITU; OSTEOBLAST DIFFERENTIATION; EXTRACELLULAR-MATRIX; RISK-FACTORS; KAPPA-B; GENE; EXPRESSION;
D O I
10.1016/j.ijbiomac.2017.03.021
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Breast cancer is one of the most prevalent forms of cancer in women. The currently available treatment for breast cancer is mostly curative except when it becomes metastatic. One of the major sites for metastasis of breast cancer is the bone. Homing of the circulating tumor cells is tightly regulated including a number of factors present in the cells and their microenvironment. Runx2, a transcription factor plays an important role in osteogenesis and breast cancer mediated bone metastases. One of the recent advances in molecular therapy includes the discovery of the small, non-coding microRNAs (miRNAs) and they target specific genes to reduce their expression at the post-transcriptional level. This review provides an outline of breast cancer mediated bone metastasis and summarizes the recent development on the regulation of Runx2 expression by miRNAs which can lead to novel molecular therapeutics for the same. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:608 / 614
页数:7
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