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无蹼壁虎抗肿瘤活性成分对HepG2细胞增殖、迁移及凋亡的影响
引用本文:谢斌,高志芹,石剑飞,于文静,连波,张仕状,刘顺梅. 无蹼壁虎抗肿瘤活性成分对HepG2细胞增殖、迁移及凋亡的影响[J]. 中国药理学通报, 2012, 28(1): 101-105. DOI: 10.3969/j.issn.1001-1978.2012.024.
作者姓名:谢斌  高志芹  石剑飞  于文静  连波  张仕状  刘顺梅
作者单位:1. 潍坊医学院,细胞生物学教研室,山东,潍坊,261053
2. 潍坊医学院,生物技术专业实验室,山东,潍坊,261053
3. 潍坊医学院,附属医院影像中心,山东,潍坊,261053
基金项目:国家自然科学基金资助项目(No 30772716)
摘    要:目的观察无蹼壁虎抗肿瘤活性成分(Gekko Swinhonisanti-neoplasm active component,GSAAC)对人肝癌HepG2细胞增殖、迁移及凋亡的影响。方法 GSAAC与体外培养的人肝癌HepG2细胞共培养,分别以MTT法和Transwell小室检测其对细胞增殖及迁移、侵袭的影响;免疫组化法检测PCNA的表达;Hochest33342荧光染色法、TUNEL法观察GSAAC对HepG2细胞的作用;流式细胞术检测细胞周期及早期凋亡率。结果 GSAAC(25~400 mg.L-1)可明显抑制HepG2细胞的增殖、迁移和侵袭能力,呈浓度依赖性;Ho-chest33342、TUNEL染色及流式细胞术结果显示,GSAAC可诱导细胞发生早期凋亡,阻滞HepG2细胞从S期进入G2期。结论 GSAAC可能通过影响细胞周期进而抑制HepG2细胞增殖和迁移并诱导细胞发生凋亡,进而实现抑制肿瘤的作用。

关 键 词:HepG2  无蹼壁虎抗肿瘤活性成分  增殖  凋亡  迁移  流式细胞术

Effects of the Gekko Swinhonis anti-neoplasm active component on the proliferation,migration and apoptosis of HepG2 cells
XIE Bin,GAO Zhi-qin,SHI Jian-fei,YU Wen-jing,LIAN Bo,ZHANG Shi-zhuang,LIU Shun-mei. Effects of the Gekko Swinhonis anti-neoplasm active component on the proliferation,migration and apoptosis of HepG2 cells[J]. Chinese Pharmacological Bulletin, 2012, 28(1): 101-105. DOI: 10.3969/j.issn.1001-1978.2012.024.
Authors:XIE Bin  GAO Zhi-qin  SHI Jian-fei  YU Wen-jing  LIAN Bo  ZHANG Shi-zhuang  LIU Shun-mei
Affiliation:1.Dept of Cytobiology,Weifang Medical University;2.Biotechnology Laboratory,Weifang Medical University;3.Medical Image Center,the Affiliated Hospital of Weifang Medical University,Weifang Shandong 261053,China)
Abstract:Aim To investigate the effects of the Gekko Swinhonis anti-neoplasm active component(GSAAC) on the proliferation,migration and apoptosis of HepG2 cells.Methods HepG2 cells were treated with GSAAC.Cell proliferation and migration were determined by MTT and Transwell assay after treatment.The expression of PCNA was detected by immunohistochemistry.Hochest33342 fluorescence staining and TUNEL staining were used to observe the morphological changes of HepG2 cells.Early apoptosis and cell cycle distribution were assessed by flow cytometry.Results GSAAC significantly inhibited the proliferation,migration and induced the early apoptosis of HepG2 cells;GSAAC blocked HepG2 cells to go to G2 phase from S phase.Conclusion The intrinsic mechanism of GSAAC might relate to the blockage of HepG2 cells to go to G2 phase from S phase thus to inhibit the proliferation,migration and induce the early apoptosis of HepG2 cells.
Keywords:HepG2  the Gekko Swinhonis anti-neoplasm active component  proliferation  apoptosis  migration  flow cytometry
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