中国癌症杂志
中國癌癥雜誌
중국암증잡지
CHINA ONCOLOGY
2014年
9期
641-645
,共5页
汪灵芝%彭建新%余美玲%黄焕森
汪靈芝%彭建新%餘美玲%黃煥森
왕령지%팽건신%여미령%황환삼
辛伐他汀%缝隙连接%肝癌
辛伐他汀%縫隙連接%肝癌
신벌타정%봉극련접%간암
Simvastatin%Gap junction%Hepatoma carcinoma
背景与目的:肝癌的发生、发展过程中伴随着细胞间缝隙连接(gap junction,GJ)功能的下降,恢复或增强肿瘤细胞间的GJ可以抑制肿瘤细胞的恶性转化和生长增殖。本研究拟通过观察辛伐他汀对肝癌细胞间GJ功能的影响,寻找能够增强GJ功能的药物,从而为肝癌的治疗提供新策略和新手段。方法:采用磺酰罗丹明B法观察辛伐他汀对大鼠肝癌细胞Hep3b的抑制作用;细胞接种荧光法和划痕标记/染料示踪技术观察辛伐他汀对GJ功能的影响。结果:1、5和10μmol/L辛伐他汀在24 h作用时间内均对细胞生长无抑制作用,将不影响GJ的数量;取5、10μmol/L辛伐他汀作用细胞4 h后,与对照组相比,GJ的荧光传递功能明显增强;与对照组相比,5、10μmol/L辛伐他汀作用细胞4 h后,荧光黄染料(lucifer yellow,Ly,Sigma)传输范围随着辛伐他汀浓度的升高逐渐增大。结论:辛伐他汀可以增强肝癌细胞GJ功能。
揹景與目的:肝癌的髮生、髮展過程中伴隨著細胞間縫隙連接(gap junction,GJ)功能的下降,恢複或增彊腫瘤細胞間的GJ可以抑製腫瘤細胞的噁性轉化和生長增殖。本研究擬通過觀察辛伐他汀對肝癌細胞間GJ功能的影響,尋找能夠增彊GJ功能的藥物,從而為肝癌的治療提供新策略和新手段。方法:採用磺酰囉丹明B法觀察辛伐他汀對大鼠肝癌細胞Hep3b的抑製作用;細胞接種熒光法和劃痕標記/染料示蹤技術觀察辛伐他汀對GJ功能的影響。結果:1、5和10μmol/L辛伐他汀在24 h作用時間內均對細胞生長無抑製作用,將不影響GJ的數量;取5、10μmol/L辛伐他汀作用細胞4 h後,與對照組相比,GJ的熒光傳遞功能明顯增彊;與對照組相比,5、10μmol/L辛伐他汀作用細胞4 h後,熒光黃染料(lucifer yellow,Ly,Sigma)傳輸範圍隨著辛伐他汀濃度的升高逐漸增大。結論:辛伐他汀可以增彊肝癌細胞GJ功能。
배경여목적:간암적발생、발전과정중반수착세포간봉극련접(gap junction,GJ)공능적하강,회복혹증강종류세포간적GJ가이억제종류세포적악성전화화생장증식。본연구의통과관찰신벌타정대간암세포간GJ공능적영향,심조능구증강GJ공능적약물,종이위간암적치료제공신책략화신수단。방법:채용광선라단명B법관찰신벌타정대대서간암세포Hep3b적억제작용;세포접충형광법화화흔표기/염료시종기술관찰신벌타정대GJ공능적영향。결과:1、5화10μmol/L신벌타정재24 h작용시간내균대세포생장무억제작용,장불영향GJ적수량;취5、10μmol/L신벌타정작용세포4 h후,여대조조상비,GJ적형광전체공능명현증강;여대조조상비,5、10μmol/L신벌타정작용세포4 h후,형광황염료(lucifer yellow,Ly,Sigma)전수범위수착신벌타정농도적승고축점증대。결론:신벌타정가이증강간암세포GJ공능。
Background and purpose:It has been reported that gap junctional (GJ) function was signiifcantly decreased in hepatocellular carcinoma (HCC) tissues and cell lines. However, the increased GJ suppress tumorigenesis and the development of liver cancer. This study therefore aimed to examine the effect of simvastatin on GJ function between Hep3b cells. Thus, the exploition of drugs to increase GJ function between liver cancer cells will provide an efifcient approach to ifght against liver tumor as well as increase cytotoxicity of antitumor agents.Methods:SRB was used to assay the toxicity of simvastatin. The effect of simvastatin on GJ function was determined by “Parachute” dye-coupling assay and scrape loading/dye transfer assay.Results:Pretreated Hep3b cells with simvastatin at the concentration of 1, 5 or 10 μmol/L for 24 h did not induce the cytotoxicity. So simvastatin at the concentration of 5 and 10 μmol/L would not reduce the amount of GJ on cell membranes. “Parachute” dye-coupling assay showed that the treatment with 5 and 10 μmol/L simvastatin for 4 h enhanced the dye spread through GJ in Hep3b cells. Similarly, scrape loading/dye transfer assay showed that simvastatin could induce the increasing spread of lucifer yellow (Ly, Sigma) around the scoifng cells with increasing concentrations.Conclusion:Simvastatin could increase the GJ function of Hep3b cells.