中华临床营养杂志
中華臨床營養雜誌
중화림상영양잡지
CHINESE JOURNAL OF CLINICAL NUTRITION
2011年
5期
307-311
,共5页
游离脂肪酸%PTEN%乳腺癌%凋亡%侵袭
遊離脂肪痠%PTEN%乳腺癌%凋亡%侵襲
유리지방산%PTEN%유선암%조망%침습
Free fatty acids%PTEN%Breast cancer%Apoptosis%Invasion
目的探讨不同游离脂肪酸(FFAs)对MDA-MB-231人乳腺癌细胞凋亡和迁移的影响.方法用50、200、500 umol/L三种不同浓度的油酸(0A)和棕榈酸(PA)分别刺激MDA-MB-231细胞,采用实时定量PCR分析细胞中PTEN的mRNA含量,蛋白免疫印迹法检测PTEN和Bcl-2的蛋白表达,原位末端标记法(TUNEL)观察细胞的凋亡情况,小室迁移实验测定细胞的迁移能力.结果OA使MDA-MB-231细胞中PTEN的mRNA和蛋白表达水平降低,Bcl-2蛋白表达升高(P均<0.05);PA则使PTEN的mRNA和蛋白表达水平上升,Bcl-2蛋白表达下降(P均<0.05).显微镜下观察到PA刺激后的MDA-MB-231细胞凋亡增加.迁移实验显示OA和PA都能使乳腺癌细胞侵袭能力增强.结论PA可能通过上调PTEN的表达促进MDA-MB-231人乳腺癌细胞凋亡,但同时也增强细胞的侵袭能力.OA也可增强癌细胞侵袭能力.
目的探討不同遊離脂肪痠(FFAs)對MDA-MB-231人乳腺癌細胞凋亡和遷移的影響.方法用50、200、500 umol/L三種不同濃度的油痠(0A)和棕櫚痠(PA)分彆刺激MDA-MB-231細胞,採用實時定量PCR分析細胞中PTEN的mRNA含量,蛋白免疫印跡法檢測PTEN和Bcl-2的蛋白錶達,原位末耑標記法(TUNEL)觀察細胞的凋亡情況,小室遷移實驗測定細胞的遷移能力.結果OA使MDA-MB-231細胞中PTEN的mRNA和蛋白錶達水平降低,Bcl-2蛋白錶達升高(P均<0.05);PA則使PTEN的mRNA和蛋白錶達水平上升,Bcl-2蛋白錶達下降(P均<0.05).顯微鏡下觀察到PA刺激後的MDA-MB-231細胞凋亡增加.遷移實驗顯示OA和PA都能使乳腺癌細胞侵襲能力增彊.結論PA可能通過上調PTEN的錶達促進MDA-MB-231人乳腺癌細胞凋亡,但同時也增彊細胞的侵襲能力.OA也可增彊癌細胞侵襲能力.
목적탐토불동유리지방산(FFAs)대MDA-MB-231인유선암세포조망화천이적영향.방법용50、200、500 umol/L삼충불동농도적유산(0A)화종려산(PA)분별자격MDA-MB-231세포,채용실시정량PCR분석세포중PTEN적mRNA함량,단백면역인적법검측PTEN화Bcl-2적단백표체,원위말단표기법(TUNEL)관찰세포적조망정황,소실천이실험측정세포적천이능력.결과OA사MDA-MB-231세포중PTEN적mRNA화단백표체수평강저,Bcl-2단백표체승고(P균<0.05);PA칙사PTEN적mRNA화단백표체수평상승,Bcl-2단백표체하강(P균<0.05).현미경하관찰도PA자격후적MDA-MB-231세포조망증가.천이실험현시OA화PA도능사유선암세포침습능력증강.결론PA가능통과상조PTEN적표체촉진MDA-MB-231인유선암세포조망,단동시야증강세포적침습능력.OA야가증강암세포침습능력.
Objective To observe the effects of free fatty aids (FFAs) on the apoptosis and migration of human breast cancer cells ( MDA-MB-231 ).Methods Breast cancer cells were exposed to oleic acid (OA) and palmitic acid (PA) with different concentrations (50,200,and 500 umol/L).Quantity RT-PCR was conducted to detect mRNA expression of PTEN,and Western blot to detect protein expression of PTEN and Bcl-2.Cell apoptosis was measured with TUNEL method,and migration measured with transwell method.Results The mRNA and protein expressions of PTEN in MDA-MB-231 cells were down-regulated after OA stimulation,but up-regulated after PA stimulation ( all P < 0.05 ).The protein expression of Bcl-2 increased after OA stimulation and decreased after PA stimulation ( both P < 0.05 ).PA increased the apoptosis,and both OA and PA enhanced the invasion of MDA-MB-231 cells.Conclusions PA may promote apoptosis of MDA-MB-231 cells through changing the expression of the tumor suppressor PTEN,but also increases the invasion of the cancer cells.The invasion of cancer cells could be enhanced by OA stimulation as well.