miR-155 in cancer drug resistance and as target for miRNA-based therapeutics

被引:193
作者
Bayraktar, Recep [1 ]
Van Roosbroeck, Katrien [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Expt Therapeut, 1881 Holcombe Blvd,Unit 1950, Houston, TX 77054 USA
关键词
miR-155; miRNA; Cancer; Chemoresistance; Radioresistance; oncomiR; Therapy; CHRONIC LYMPHOCYTIC-LEUKEMIA; ACUTE MYELOID-LEUKEMIA; B-CELL LYMPHOMA; PROMOTES TUMOR-GROWTH; BREAST-CANCER; LUNG-CANCER; HEPATOCELLULAR-CARCINOMA; MICRORNA EXPRESSION; ONCOGENIC MICRORNA-155; TRANSCRIPTION FACTORS;
D O I
10.1007/s10555-017-9724-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Small non-coding microRNAs (miRNAs) are instrumental in physiological processes, such as proliferation, cell cycle, apoptosis, and differentiation, processes which are often disrupted in diseases like cancer. miR-155 is one of the best conserved and multifunctional miRNAs, which is mainly characterized by overexpression in multiple diseases including malignant tumors. Altered expression of miR-155 is found to be associated with various physiological and pathological processes, including hematopoietic lineage differentiation, immune response, inflammation, and tumorigenesis. Furthermore, miR-155 drives therapy resistance mechanisms in various tumor types. Therefore, miR-155-mediated signaling pathways became a potential target for the molecular treatment of cancer. In this review, we summarize the current findings of miR-155 in hematopoietic lineage differentiation, the immune response, inflammation, and cancer therapy resistance. Furthermore, we discuss the potential of miR-155-based therapeutic approaches for the treatment of cancer.
引用
收藏
页码:33 / 44
页数:12
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