About this Biochemistry, Genetics and Molecular Biology article
MicroRNA-196b enhances the radiosensitivity of SNU-638 gastric cancer cells by targeting RAD23B by Shen, Yan Nan; Bae, In-Seon; Park, Gil Hong; Choi, Hwa Sik; Lee, Kee-Ho; Kim, Sang Hoon is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.
Gastric cancer is characterized by resistance to ionizing radiation. The development of resistance to radiotherapy in gastric cancer patients is one of the obstacles to effective radiotherapy. MicroRNAs are small well-conserved non-coding RNA species that regulate post-transcriptional activation. Our study aimed to investigate the role of miR-196b in radiation-induced gastric cancer. In the present study, we found that miR-196b expression was significantly reduced following radiation. The ectopic miR-196b expression sensitized SNU-638 gastric cancer cells and increased γ-H2AX foci upon radiation treatment. Bioinformatics analysis suggested that the DNA repair protein RAD23B was a putative target gene of miR-196b. Overexpression of miR-196b suppressed RAD23B expression in SNU-638 cells. Reporter assays further showed that miR-196b inhibited RAD23B 3'-UTR luciferase activity. Knockdown of RAD23B by small interfering RNA transfection closely mimicked the outcomes of miR-196b transfection, leading to impaired DNA damage repair in gastric cancer cells. Our results show that miR-196b improved radiosensitivity of SNU-638 cells by targeting RAD23B. Our data indicate that miR-196b is a pote
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- Author
- Shen, Yan Nan; Bae, In-Seon; Park, Gil Hong; Choi, Hwa Sik; Lee, Kee-Ho; Kim, Sang Hoon
- Publisher
- Elsevier Science; Elsevier ; Elsevier Masson; Elsevier BV (ISSN 0753-3322)
- Published
- 2018
- Language
- EN
- Field
- Biochemistry, Genetics and Molecular Biology (Life Sciences)