饱和脂肪酸和不饱和脂肪酸对肺癌细胞增殖与自噬的影响

目的 研究饱和脂肪酸和不饱和脂肪酸对肺癌细胞增殖与自噬的影响。方法 用0、30、60、120、240μmol/L硬脂酸(饱和脂肪酸)和DHA(不饱和脂肪酸)分别处理肺癌细胞A549,绘制细胞生长曲线并计算克隆形成率以检测细胞增殖。采用硬脂酸和DHA分别处理A549细胞24h后,采用激光共聚焦显微镜从形态学方面观察细胞自噬情况。采用硬脂酸和DHA分别处理A549细胞12、24、36h后,用Western blotting检测细胞自噬相关蛋白的表达。结果30~240μmol/L硬脂酸和DHA均有抑制A549细胞增殖的作用(P<0.05),硬脂酸、DHA处理A549细胞24h后均检测到...

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Published inJie fang jun yi xue za zhi Vol. 42; no. 8; pp. 668 - 673
Main Author 李慧敏 伍俊 吴尚 余华军 汪亚君 熊禹真 兰柳波 张海涛
Format Journal Article
LanguageChinese
Published Beijing People's Military Medical Press 2017
524001 广东湛江 广东医科大学附属医院呼吸内科
524023,广东湛江 广东医科大学生物化学与分子生物学教研室%524001,广东湛江 广东医科大学附属医院呼吸内科%524023 广东湛江 广东医科大学生物化学与分子生物学教研室
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ISSN0577-7402
DOI10.11855/j.issn.0577-7402.2017.08.02

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Abstract 目的 研究饱和脂肪酸和不饱和脂肪酸对肺癌细胞增殖与自噬的影响。方法 用0、30、60、120、240μmol/L硬脂酸(饱和脂肪酸)和DHA(不饱和脂肪酸)分别处理肺癌细胞A549,绘制细胞生长曲线并计算克隆形成率以检测细胞增殖。采用硬脂酸和DHA分别处理A549细胞24h后,采用激光共聚焦显微镜从形态学方面观察细胞自噬情况。采用硬脂酸和DHA分别处理A549细胞12、24、36h后,用Western blotting检测细胞自噬相关蛋白的表达。结果30~240μmol/L硬脂酸和DHA均有抑制A549细胞增殖的作用(P<0.05),硬脂酸、DHA处理A549细胞24h后均检测到细胞出现明显的自噬;Western blotting结果显示,硬脂酸、DHA分别处理A549细胞12、24、36h后,LC3Ⅱ/LC3Ⅰ比值升高(P<0.05),哺乳动物雷帕霉素靶蛋白(ser2481)磷酸化水平降低(P<0.05)。结论 饱和脂肪酸和不饱和脂肪酸均有抑制肺癌细胞增殖、诱导肺癌细胞自噬的作用,其机制可能与p-m TOR(ser2481)信号通路有关。
AbstractList R734.2; 目的 研究饱和脂肪酸和不饱和脂肪酸对肺癌细胞增殖与自噬的影响.方法 用0、30、60、120、240μmol/L硬脂酸(饱和脂肪酸)和DHA(不饱和脂肪酸)分别处理肺癌细胞A549,绘制细胞生长曲线并计算克隆形成率以检测细胞增殖.采用硬脂酸和DHA分别处理A549细胞24h后,采用激光共聚焦显微镜从形态学方面观察细胞自噬情况.采用硬脂酸和DHA分别处理A549细胞12、24、36h后,用Western blotting检测细胞自噬相关蛋白的表达.结果 30~240μmol/L硬脂酸和DHA均有抑制A549细胞增殖的作用(P<0.05),硬脂酸、DHA处理A549细胞24h后均检测到细胞出现明显的自噬;Western blotting结果 显示,硬脂酸、DHA分别处理A549细胞12、24、36h后,LC3Ⅱ/LC3Ⅰ比值升高(P<0.05),哺乳动物雷帕霉素靶蛋白(ser2481)磷酸化水平降低(P<0.05).结论 饱和脂肪酸和不饱和脂肪酸均有抑制肺癌细胞增殖、诱导肺癌细胞自噬的作用,其机制可能与p-mTOR(ser2481)信号通路有关.
目的 研究饱和脂肪酸和不饱和脂肪酸对肺癌细胞增殖与自噬的影响。方法 用0、30、60、120、240μmol/L硬脂酸(饱和脂肪酸)和DHA(不饱和脂肪酸)分别处理肺癌细胞A549,绘制细胞生长曲线并计算克隆形成率以检测细胞增殖。采用硬脂酸和DHA分别处理A549细胞24h后,采用激光共聚焦显微镜从形态学方面观察细胞自噬情况。采用硬脂酸和DHA分别处理A549细胞12、24、36h后,用Western blotting检测细胞自噬相关蛋白的表达。结果30~240μmol/L硬脂酸和DHA均有抑制A549细胞增殖的作用(P&lt;0.05),硬脂酸、DHA处理A549细胞24h后均检测到细胞出现明显的自噬;Western blotting结果显示,硬脂酸、DHA分别处理A549细胞12、24、36h后,LC3Ⅱ/LC3Ⅰ比值升高(P&lt;0.05),哺乳动物雷帕霉素靶蛋白(ser2481)磷酸化水平降低(P&lt;0.05)。结论 饱和脂肪酸和不饱和脂肪酸均有抑制肺癌细胞增殖、诱导肺癌细胞自噬的作用,其机制可能与p-m TOR(ser2481)信号通路有关。
Objective To investigate the effects of saturated fatty acids and unsaturated fatty acids on proliferation and autophagy of human lung cancer cells. Methods The lung cancer cells A549 were treated with stearic acid (saturated fatty acid) and doconexent (DHA, unsaturated fatty acid), respectively, in concentrations of 0, 30, 60, 120 and 240μmol/L. MTT test and cell clone formation assay were performed to detect the proliferation of A549 cells. The morphology of A549 autophagy was observed by confocal laser scanning microscopy after A549 cells were treated with stearic acid or DHA for 24 hours. Western blotting assay was used to detect the expression of autophagy-related protein after A549 cells were treated with stearic acid or DHA for 12, 24 and 36 hours, respectively. Results 30-240μmol/L stearic acid or DHA both inhibited the proliferation of A549 cells (P<0.05). Both stearic acid and DHA induced autophagy of A549 cells, meanwhile, down-regulated Phospho-mTOR (ser2481) and up-regulated LC3Ⅱ/LC3Ⅰ of A549 cel
Abstract_FL Objective To investigate the effects of saturated fatty acids and unsaturated fatty acids on proliferation and autophagy of human lung cancer cells. Methods The lung cancer cells A549 were treated with stearic acid (saturated fatty acid) and doconexent (DHA, unsaturated fatty acid), respectively, in concentrations of 0, 30, 60, 120 and 240μmol/L. MTT test and cell clone formation assay were performed to detect the proliferation of A549 cells. The morphology of A549 autophagy was observed by confocal laser scanning microscopy after A549 cells were treated with stearic acid or DHA for 24 hours. Western blotting assay was used to detect the expression of autophagy-related protein after A549 cells were treated with stearic acid or DHA for 12, 24 and 36 hours, respectively. Results 30-240μmol/L stearic acid or DHA both inhibited the proliferation of A549 cells (P<0.05). Both stearic acid and DHA induced autophagy of A549 cells, meanwhile, down-regulated Phospho-mTOR (ser2481) and up-regulated LC3Ⅱ/LC3Ⅰ of A549 cells (P<0.05). Conclusions Both saturated fatty acid and unsaturated fatty acid can inhibit the proliferation and induce autophagy of lung cancer cells. The mechanisms of autophagy may be related to Phospho-mTOR (ser2481) signaling pathway.
Author 李慧敏 伍俊 吴尚 余华军 汪亚君 熊禹真 兰柳波 张海涛
AuthorAffiliation 广东医科大学生物化学与分子生物学教研室;广东医科大学附属医院呼吸内科
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WU Jun
WANG Ya-jun
XIONG Yu-zhen
WU Shang
LAN Liu-bo
ZHANG Hai-tao
YU Hua-jun
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Keywords 自噬
stearic acids
mammalian target of rapamycin
autophagy
A549 cells
cell proliferation
docosahexaenoic acids
哺乳动物雷帕霉素靶蛋白
硬脂酸类
二十二碳六烯酸类
A549细胞
细胞增殖
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Snippet 目的 研究饱和脂肪酸和不饱和脂肪酸对肺癌细胞增殖与自噬的影响。方法...
Objective To investigate the effects of saturated fatty acids and unsaturated fatty acids on proliferation and autophagy of human lung cancer cells. Methods...
R734.2; 目的 研究饱和脂肪酸和不饱和脂肪酸对肺癌细胞增殖与自噬的影响.方法...
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SubjectTerms Autophagy
Fatty acids
Lung cancer
硬脂酸类;二十二碳六烯酸类;A549细胞;细胞增殖;自噬;哺乳动物雷帕霉素靶蛋白
Title 饱和脂肪酸和不饱和脂肪酸对肺癌细胞增殖与自噬的影响
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