海南医学
海南醫學
해남의학
HAINAN MEDICAL JOURNAL
2015年
8期
1108-1110,1111
,共4页
肝细胞癌%肿瘤干细胞%金雀异黄素%多药耐药
肝細胞癌%腫瘤榦細胞%金雀異黃素%多藥耐藥
간세포암%종류간세포%금작이황소%다약내약
Liver cancer%Cancer stem cells%Genistein%Multidrug resistance
目的:研究金雀异黄素对SMMC-7721细胞系肝癌干细胞样细胞特性以及氟尿嘧啶敏感性的影响。方法不同浓度金雀异黄素处理SMMC-7721细胞系球形成细胞。肿瘤球形成法检测自我更新能力。MTT比色法测定氟尿嘧啶药物敏感性。Western blot分析干细胞标志物CD133、CD44、Gli1和ABCG2蛋白表达。结果金雀异黄素显著抑制SMMC-7721细胞肿瘤球形成,并优先抑制球形成细胞增殖活性(P<0.05)。金雀异黄素(10μmol/L)有效逆转球形成细胞对氟尿嘧啶的耐药性。金雀异黄素降低CD133、CD44、Gli1和ABCG2蛋白表达水平。结论金雀异黄素抑制肝癌干细胞样细胞特性和氟尿嘧啶耐药性,其作用机制与抑制干细胞标志物蛋白表达和阻断Hedgehog信号传导有关。
目的:研究金雀異黃素對SMMC-7721細胞繫肝癌榦細胞樣細胞特性以及氟尿嘧啶敏感性的影響。方法不同濃度金雀異黃素處理SMMC-7721細胞繫毬形成細胞。腫瘤毬形成法檢測自我更新能力。MTT比色法測定氟尿嘧啶藥物敏感性。Western blot分析榦細胞標誌物CD133、CD44、Gli1和ABCG2蛋白錶達。結果金雀異黃素顯著抑製SMMC-7721細胞腫瘤毬形成,併優先抑製毬形成細胞增殖活性(P<0.05)。金雀異黃素(10μmol/L)有效逆轉毬形成細胞對氟尿嘧啶的耐藥性。金雀異黃素降低CD133、CD44、Gli1和ABCG2蛋白錶達水平。結論金雀異黃素抑製肝癌榦細胞樣細胞特性和氟尿嘧啶耐藥性,其作用機製與抑製榦細胞標誌物蛋白錶達和阻斷Hedgehog信號傳導有關。
목적:연구금작이황소대SMMC-7721세포계간암간세포양세포특성이급불뇨밀정민감성적영향。방법불동농도금작이황소처리SMMC-7721세포계구형성세포。종류구형성법검측자아경신능력。MTT비색법측정불뇨밀정약물민감성。Western blot분석간세포표지물CD133、CD44、Gli1화ABCG2단백표체。결과금작이황소현저억제SMMC-7721세포종류구형성,병우선억제구형성세포증식활성(P<0.05)。금작이황소(10μmol/L)유효역전구형성세포대불뇨밀정적내약성。금작이황소강저CD133、CD44、Gli1화ABCG2단백표체수평。결론금작이황소억제간암간세포양세포특성화불뇨밀정내약성,기작용궤제여억제간세포표지물단백표체화조단Hedgehog신호전도유관。
Objective To investigate the effects of genistein on the characteristics of liver cancer stem-like cells (LCSLCs) derived from SMMC-7721 cell line and the sensitivity to fluorouracil. Methods Sphere-forming cells (SFCs) from SMMC-7721 cell line were treated with various concentrations of genistein. The capability of self-renewal was tested using tumor sphere-forming assay. The sensitivity to fluorouracil was determined by MTT as-say. And the protein expression of stem cell markers CD133, CD44, Hedgehog (Hh) signal effector Gli1 and its target molecule ABCG2 was analyzed using Western blot. Results Genistein significantly inhibited the capability of sphere-forming in SMMC-7721 SFCs and relative selectively suppressed the proliferation activity of SFCs (P<0.05). Genistein (10 μmol/L) could effectively reverse the resistance of SFCs to fluorouracil. And genistein could also down-regulate the protein expression of CD133, CD44, Gli1 and ABCG2. Conclusion Genistein inhibits characteristics of liver cancer stem cells and resistance to Fluorouracil, and its mechanism is likely involved in inhibiting protein ex-pression of stem cell markers and obstructing Hh signal pathway.