The Role of miR-23b in Cancer and Autoimmune Disease

Author:

Guo Yu-Xin1ORCID,Wang Na2ORCID,Wu Wen-Cheng1ORCID,Li Cui-Qin1ORCID,Chen Rui-Heng3ORCID,Zhang Yuan1ORCID,Li Xing1ORCID

Affiliation:

1. National Engineering Laboratory for Resource Development of Endangered Crude Drugs in Northwest China, Key Laboratory of Medicinal Resources and Natural Pharmaceutical Chemistry (Shaanxi Normal University), The Ministry of Education, College of Life Sciences, Shaanxi Normal University, Xi’an, Shaanxi 710119, China

2. Surgical Oncology Department, The First People’s Hospital of Tianshui, Tianshui, Gansu 741000, China

3. The High School Affiliated to Shaanxi Normal University, Xi’an, Shaanxi 710119, China

Abstract

Short-stranded miRNAs are single-stranded RNA molecules involved in the regulation of gene expression. miRNAs are involved in a variety of cellular physiological processes, including cell proliferation, differentiation, and apoptosis. miR-23b have been identified to act both as oncogenes and as tumor suppressors. In addition, miR-23b is related to inflammation resistance to various autoimmune diseases and restrained inflammatory cell migration. The characterization of the specific alterations in the patterns of miR-23b expression in cancer and autoimmune disease has great potential for identifying biomarkers for early disease diagnosis, as well as for potential therapeutic intervention in various diseases. In this review, we summarize the ever-expanding role of miR-23b and its target genes in different models and offer insight into how this multifunctional miRNA modulates tumor cell proliferation and apoptosis or inflammatory cell activation, differentiation, and migration.

Funder

National Natural Science Foundation of China

Publisher

Hindawi Limited

Subject

Oncology

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