Dysregulation of microRNAs in metal-induced angiogenesis and carcinogenesis

被引:17
|
作者
Wang, Lin [1 ,2 ]
Liu, Ling-Zhi [3 ]
Jiang, Bing-Hua [2 ]
机构
[1] Zhengzhou Univ, Acad Med Sci, Zhengzhou 450000, Henan, Peoples R China
[2] Thomas Jefferson Univ, Dept Pathol Anat & Cell Biol, Philadelphia, PA 19107 USA
[3] Thomas Jefferson Univ, Dept Med Oncol, Philadelphia, PA 19107 USA
关键词
Arsenic; Chromium; Nickel; Cadmium; microRNA; Cell transformation; Carcinogenesis; Angiogenesis; EPITHELIAL-MESENCHYMAL TRANSITION; CHRONIC ARSENIC EXPOSURE; MALIGNANT-TRANSFORMATION; CANCER-CELLS; NEOPLASTIC TRANSFORMATION; OXIDATIVE STRESS; GENE-EXPRESSION; DOWN-REGULATION; CELLULAR MECHANISMS; HUMAN KERATINOCYTES;
D O I
10.1016/j.semcancer.2021.08.009
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNAs (miRNAs) are small endogenous non-coding RNAs that regulate cancer initiation, development, angiogenesis, and therapeutic resistance. Metal exposure widely occurs through air, water, soil, food, and industrial contaminants. Hundreds of millions of people may have metal exposure associated with toxicity, serious health problems, and cancer occurrence. Metal exposure is found to induce oxidative stress, DNA damage and repair, and activation of multiple signaling pathways. However, molecular mechanisms of metal-induced carcinogenesis remain to be elucidated. Recent studies demonstrated that the exposure of metals such as arsenic, hexavalent chromium, cadmium, and nickel caused dysregulation of microRNAs that are implicated to play an important role in cell transformation, tumor growth and angiogenesis. This review focuses on the recent studies that show metal-induced miRNA dysregulation and underlined mechanisms in cell malignant transformation, angiogenesis and tumor growth.
引用
收藏
页码:279 / 286
页数:8
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