提吉特
癌症研究
癌症
骨髓
癌细胞
外体
间充质干细胞
癌症干细胞
CD8型
小RNA
化学
医学
微泡
病理
内科学
免疫学
免疫疗法
抗原
生物化学
基因
出处
期刊:Journal of Biomaterials and Tissue Engineering
[American Scientific Publishers]
日期:2022-01-13
卷期号:12 (5): 920-925
标识
DOI:10.1166/jbt.2022.2972
摘要
The BMSCs are one of the components of tumor micro-environment and participate in tumor evolution. Our study aimed to discuss the effect of exosome derived from BMSC on gastric cancer cells. Tumor and para-tumor tissues were isolated to measure miR-206 level by RT-PCR. Gastric cancer cell behaviors were analyzed using MTT assay and scratch test. Gastric cancer model was established and treated TIGIT inhibitor to assess its role in the tumor growth in vivo . The miR-206 in exosome from BMSCs in cancer tissue was detected. CD8 expression excreted by DC could be induced after miR-206 treatment possibly through regulating the signaling pathway of TIGIT/PVR. Inhibition of TIGIT decreased tumor growth, development and reversed tumor phenotype. In conclusion, miR-206 derived from BMSCs induces CD8 expression in gastric cancer through regulating the signaling pathway of TIGIT/PVR, indicating that it might be a novel target for the treatment of gastric cancer.
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