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中国临床药理学与治疗学 ›› 2024, Vol. 29 ›› Issue (3): 270-276.doi: 10.12092/j.issn.1009-2501.2024.03.004

• 基础研究 • 上一篇    下一篇

皖南蝮蛇毒抑瘤组分-Ⅰ对胃癌MKN-28细胞增殖、迁移及凋亡的影响

黄小梅1,支慧1,陈浩1,卢林明1,朱晓群1,王丽珍1,周珏1,庞金金2,许金亮2   

  1. 1皖南医学院 病理解剖学教研室,芜湖  241002,安徽;2皖南医学院 临床医学院,芜湖  241002,安徽

  • 收稿日期:2023-05-23 修回日期:2023-07-13 出版日期:2024-03-26 发布日期:2024-02-29
  • 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。 E-mail: Ilm7172@sina.com
  • 作者简介:黄小梅,女,硕士,副教授,研究方向:肿瘤分子病理学。 E-mail: 1256608319@qq.com
  • 基金资助:
    安徽省教育厅自然科学研究重点项目(KJ2020A0611);皖南医学院大学生科研资助金项目(WK2020S01);活性生物大分子研究安徽省重点实验室自主研究课题(LAB202004);安徽省高等学校质量工程项目(S202010368107)

Effects of the proliferation, migration and apoptosis of AHVAC-Ⅰ on gastric cancer MKN-28 cells

HUANG Xiaomei1, ZHI Hui1, CHEN Hao1, LU Linming1, ZHU Xiaoqun1, WANG Lizhen1, ZHOU Jue1, PANG Jinjin2, XU Jinliang2   

  1. 1 Department of Pathology, Wannan Medical College, Wuhu 241002, Anhui, China; 2 Clinical Medicine of Wannan Medical College, Wuhu 241002, Anhui, China
  • Received:2023-05-23 Revised:2023-07-13 Online:2024-03-26 Published:2024-02-29

摘要:

目的:探讨皖南蝮蛇毒抑瘤组分-Ⅰ(agkis-trodon halys venom antitumor component Ⅰ,AHVAC-Ⅰ)对胃癌MKN-28细胞生物学行为的影响作用。方法:不同实验浓度(5、10 和15 μg/mL)AHAVC-Ⅰ处理胃癌细胞MKN-28 24 h后,采用细胞增殖和毒性检测(cell counting kit-8,CCK-8)法检测细胞增殖活力;划痕实验和Tanswell小室检测细胞迁移能力;激光共聚焦显微镜(annexin V-mCherry/DAPI 双染)和流式细胞术(annexin V-FITC/PI 双染)检测细胞凋亡;Western blot检测细胞凋亡相关蛋白Caspease-3的表达水平。结果:AHVAC-Ⅰ各浓度组分别与正常对照组相比结果显示,随着AHVAC-Ⅰ浓度的增加,MKN-28细胞增殖活力逐渐下降(P<0.01),细胞迁移能力逐渐被抑制(P<0.01),细胞凋亡率增高(P<0.05),凋亡相关蛋白Caspease-3表达上调(P<0.01)。结论:AHVAC-Ⅰ抑制胃癌细胞MKN-28增殖和迁移,诱导其凋亡。

关键词: AHVAC-Ⅰ, 胃癌, 细胞增殖, 细胞迁移, 细胞凋亡

Abstract:

AIM: To investigate the effects of agkis-trodon halys venom anti-tumor component Ⅰ (AHVAC-Ⅰ) on the biological behavior of gastric cancer MKN-28 cells. METHODS: Gastric cancer MKN-28 cells were treated with the experimental concentrations (5, 10, 15 μg/mL) of AHAVC-Ⅰ for 24 h.Cell proliferation and toxicity assay (cell counting kit-8, CCK-8) was used to detect the inhibition rates of the cells in different concentrations of AHVAC-Ⅰ. The migration ability of the cells was evaluated by wound-healing and Transwell assay. The apoptosis were observed by laser confocal microscopy with annexin V-mCherry/DAPI double staining, and the apoptosis rates were analyzed by flow cytometry with annexin V-FITC/PI double fluorescence staining. The protein level of Caspease-3 was determined by Western blot. RESULTS: Compared with normal control group, the results of AHVAC-Ⅰ concentration groups showed that with the increase of AHVAC-Ⅰ concentration, the proliferative activity of MN-28 cells decreased gradually (P<0.01), the cell migration ability decreased gradually (P<0.01), and the cell apoptosis rate increased (P<0.05). The expression of apoptosis-related protein Caspease-3 was up-regulated (P<0.01). CONCLUSION: AHVAC-Ⅰ inhibits proliferation and migration of gastric cancer MSN-28 cells and induces apoptosis.

Key words: agkis-trodon halys venom antitumor component-Ⅰ (AHVAC-Ⅰ), gastric cancer, cell proliferation, cell migration, cell apoptosis

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