台湾海峡
檯灣海峽
태만해협
JOURNAL OF OCEANOGRAPHY IN TAIWAN STRAIT
2009年
4期
472-476
,共5页
范成成%张剑%康劲翮%邱乒乒%韩鹏%李文岗%陈清西
範成成%張劍%康勁翮%邱乒乒%韓鵬%李文崗%陳清西
범성성%장검%강경핵%구핑핑%한붕%리문강%진청서
海洋生物学%细胞%文蛤多肽%抗癌%MTT比色法%凋亡
海洋生物學%細胞%文蛤多肽%抗癌%MTT比色法%凋亡
해양생물학%세포%문합다태%항암%MTT비색법%조망
marine biology%cell%Meretrix meretrix peptide%antitumor%MTT colorimetry%apoptosis
采用硫酸铵沉淀、有机溶剂分离、Sephadex G-25分子筛层析等实验方法,从文蛤肉中提取了一种低分子量的多肽,命名为Mer2.本文以溴化二苯偶氮盐(MTT)法检测Mer2对体外培养的癌细胞的抑制作用.结果表明Mer2对体外培养的人肝癌细胞株(HepG2)、宫颈癌细胞株(Hela)、胆管癌细胞株(QBC939)、肺癌细胞株(SPC-A-1和LTEP-a-2)的生长均有很强的抑制作用,且抑制效果随着Mer2含量的增高和处理时间的延长而增强,证明Mer2具有广谱的抗癌活性.其中Mer2对人肝癌HepG_2细胞株抑制作用最为显著,光学显微镜观察经Mer2细胞培养液处理后的细胞形态发生明显的改变,流式细胞仪实验的结果表明处理后的细胞周期发生明显的改变,并在G_0/G_1期前出现凋亡峰.
採用硫痠銨沉澱、有機溶劑分離、Sephadex G-25分子篩層析等實驗方法,從文蛤肉中提取瞭一種低分子量的多肽,命名為Mer2.本文以溴化二苯偶氮鹽(MTT)法檢測Mer2對體外培養的癌細胞的抑製作用.結果錶明Mer2對體外培養的人肝癌細胞株(HepG2)、宮頸癌細胞株(Hela)、膽管癌細胞株(QBC939)、肺癌細胞株(SPC-A-1和LTEP-a-2)的生長均有很彊的抑製作用,且抑製效果隨著Mer2含量的增高和處理時間的延長而增彊,證明Mer2具有廣譜的抗癌活性.其中Mer2對人肝癌HepG_2細胞株抑製作用最為顯著,光學顯微鏡觀察經Mer2細胞培養液處理後的細胞形態髮生明顯的改變,流式細胞儀實驗的結果錶明處理後的細胞週期髮生明顯的改變,併在G_0/G_1期前齣現凋亡峰.
채용류산안침정、유궤용제분리、Sephadex G-25분자사층석등실험방법,종문합육중제취료일충저분자량적다태,명명위Mer2.본문이추화이분우담염(MTT)법검측Mer2대체외배양적암세포적억제작용.결과표명Mer2대체외배양적인간암세포주(HepG2)、궁경암세포주(Hela)、담관암세포주(QBC939)、폐암세포주(SPC-A-1화LTEP-a-2)적생장균유흔강적억제작용,차억제효과수착Mer2함량적증고화처리시간적연장이증강,증명Mer2구유엄보적항암활성.기중Mer2대인간암HepG_2세포주억제작용최위현저,광학현미경관찰경Mer2세포배양액처리후적세포형태발생명현적개변,류식세포의실험적결과표명처리후적세포주기발생명현적개변,병재G_0/G_1기전출현조망봉.
An anti-cancer peptide was purified from Mercenaria(Meretrix meretrix)by methods of fragmentation,organic precipitation and column chromatogram (Sephadex G-25).Finally,the anticancer peptide was obtained and named as Mer2.The antitumor activity and stability of Mer2 were preliminarily determined by MTT method in vitro.It shows that Mer2 inhibited significantly the growth of human cancer cells including HepG_2,HeLa,QBC939,SPC-A-1 and LTEP-a-2 in a dose-dependent manner in vitro,and had a more remarkable inhibitory effect on liver cancer cell strain HepG_2.The cell morphology of HepG_2 treated by the peptide Mer2 was changed distinctly under the LM and the proliferation of HepG_2 cells through induced-apoptosis was changed clearly showed by flow cytometry.