欢迎访问《中国临床药理学与治疗学》杂志官方网站,今天是

中国临床药理学与治疗学 ›› 2021, Vol. 26 ›› Issue (4): 389-394.doi: 10.12092/j.issn.1009-2501.2021.04.005

• 基础研究 • 上一篇    下一篇

皖南蝮蛇毒抑瘤组分-I逆转原代胃癌相关成纤维细胞促癌作用

江玉华,支慧,卢林明,田大皓,王晓庆,葛钰,谢尚富,王琪   

  1. 皖南医学院病理解剖教研室,芜湖 241002,安徽
  • 收稿日期:2020-12-17 修回日期:2021-01-21 出版日期:2021-04-26 发布日期:2021-05-11
  • 通讯作者: 卢林明,男,副教授,硕士生导师,研究方向:肿瘤分子病理学。 Tel: 13855383399 E-mail: llm7172@sina.com
  • 作者简介:江玉华,女,硕士研究生,研究方向:肿瘤分子病理学。 Tel: 13004068522 E-mail: 1248930347@qq.com

AHVAC-I reverses tumor growth of cancer-associated fibroblasats in gastric cancer

JIANG Yuhua, ZHI Hui, LU Linming, TIAN Dahao, WANG Xiaoqing, GE Yu, XIE Shangfu, WANG Qi   

  1. Department of Pathology, Wannan Medical College, Wuhu 241000, Anhui, China
  • Received:2020-12-17 Revised:2021-01-21 Online:2021-04-26 Published:2021-05-11

摘要: 目的:探讨皖南蝮蛇毒抑瘤组分-I(agkistrodon halys venom antitumor component-I, AHVAC-I)抑制胃癌细胞迁移的生物学活性。方法:组织块培养法和胰酶消化法分离培养人原代胃癌相关成纤维细胞(GCAFs);CCK8实验根据半数抑制浓度(IC50)确定AHVAC-I实验浓度;收集AHVAC-I作用GCAFs后的上清液(GCAFs-CMAHVAC-I),划痕实验法和Transwell检测GCAFs-CMAHVAC-I抑制胃癌细胞株MKN-28迁移的能力;用ELISA、RT-PCR检测AHVAC-I作用后GCAFs分泌产生的趋化因子CXCL12。结果:AHVAC-I可显著抑制人原代GCAFs分泌的CXCL12(P<0.05),AHVAC-I作用后生成的GCAFs-CMAHVAC-I明显抑制了胃癌细胞MKN-28的迁移能力(P<0.05)。 结论:AHVAC-I能够通过抑制GCAFs分泌生成的CXCL12抑制胃癌细胞MKN-28的迁移能力,逆转胃癌肿瘤微环境中的GCAFs的促进胃癌细胞转移的作用。

关键词: 皖南蝮蛇毒抑瘤组分-I, 胃癌相关成纤维细胞, 胃癌细胞迁移, 趋化因子

Abstract: AIM: To explore whether Agkistrodon Halys venom antitumor component-I (AHVAC-I) affects the migration of gastric cancer cells by human primary gastric cancer-associated fibroblast (GCAFs).  METHODS: Tissue block culture and trypsin digestion were used to separate and culture human primary gastric cancer-associated fibroblasts (GCAFs);  the GCAFs-CMAHVAC-I  was collected after AHVAC-I treatment to culture the MKN28 cells. Migration was evaluated by wound-healing and Transwell assay. ELISA and RT-PCR were used to verify wether AHVAC-I can play a role in the production of CXCL12 from GCAFs.RESULTS: AHVAC-I can decrease the CXCL12 production from GCAFs (P<0.05). Cultured with GCAFs-CMAHVAC-I , the migration of MKN28 cells were significantly inhibited (P<0.05). CONCLUSION: AHVAC-I can inhibit the migration ability of gastric cancer cells MKN-28 by decreasing CXCL12 production from GCAFs, and is valuable for gastric cancer therapy.

Key words: agkistrodon halys venom antitumor component-I, gastric cancer-associated fibroblast, gastric cancer cell migration, chemokine CXCL12

中图分类号: