首页|杠柳毒苷通过诱导细胞自噬抑制前列腺癌细胞增殖

杠柳毒苷通过诱导细胞自噬抑制前列腺癌细胞增殖

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检测杠柳毒苷(periplocin,PP)对前列腺癌细胞(prostate cancer,PCa)增殖的抑制作用并探讨其分子机制.体外培养前列腺癌DU145和PC3细胞,CCK8实验、克隆形成、3D基质胶侵袭实验检测杠柳毒苷对前列腺癌细胞增殖、克隆形成、迁移侵袭等作用;流式细胞术、Hoechst 33258染色、Western blot实验确定杠柳毒苷诱导前列腺癌细胞凋亡、诱导凋亡小体形成及细胞凋亡相关蛋白表达水平;RNA-Seq转录组测序检测杠柳毒苷对前列腺癌细胞基因表达谱影响;DCFH-DA荧光探针检测杠柳毒苷对细胞内活性氧(reactive oxygen species,ROS)水平影响;Western blot、EG-FP-LC3B融合蛋白表达细胞检测杠柳毒苷对细胞自噬相关蛋白表达及对细胞自噬体形成的影响;构建裸鼠荷瘤模型检测杠柳毒苷对前列腺癌细胞体内生长抑制作用.研究结果表明,杠柳毒苷可浓度依赖性抑制前列腺癌细胞增殖、克隆形成能力及迁移侵袭能力;诱导细胞凋亡小体产生及凋亡相关蛋白表达;改变前列腺癌细胞基因表达谱;浓度依赖性提高前列腺癌细胞内ROS水平,上调自噬标志蛋白LC3B和Beclin-1表达,下调自噬降解标志蛋白p62表达;抑制前列腺癌细胞在裸鼠体内生长.本研究发现PP可抑制PCa细胞增殖并诱导细胞凋亡,其分子机制可能为PP诱导前列腺癌细胞自噬最终导致细胞死亡.
Periplocin inhibits proliferation of prostate cancer cells by inducing autophagy
This study investigated the effect of periplocin(PP)on prostate cancer(PCa)cells and explored the molecular mechanisms.CCK8 assay,colony formation and 3D matrix gel invasion assay were applied on in vitro cultured DU145 and PC3 cells to evaluate the effect of PP on cell growth,colony formation,migration and invasion of PCa cells;Flow cytometry,Hoechst 33258 staining and Western blot were used to measure the ability of PP induced cell apoptosis,apoptotic body forma-tion and apoptotic proteins expression;RNA-Seq was carried out to figure out the PP-induced transcriptome expression regula-tion in PCa cells;DCFH-DA fluorescent probe was used to detect the effect of PP on intracellular reactive oxygen species(ROS)level;Western blot and cells expressing EGFP-LC3B fusion protein were used to detect the effect of PP on autophagy related proteins expression and autophagosome formation;A nude mouse tumor bearing model was established to detect the in-hibitory effect of PP on the in vivo growth of PCa cells.The results showed that PP could inhibit the proliferation,colony for-mation,migration and invasion of PCa cells in a concentration dependent manner;PP could induce apoptosis,apoptotic body formation and apoptosis-related protein expression in PCa cells.The results of RNA-Seq indicated that PP treatment could al-ter gene expression profile of PCa cells,and the differential expression genes were mainly enriched in autophagy related signa-ling pathways.PP could increase the cellular ROS of PCa cells in a concentration dependent manner,up-regulate the expres-sion of autophagy marker proteins LC3B and Beclin-1,and down-regulate the expression of autophagy degradation marker pro-tein p62.PP could inhibit the growth of prostate cancer cells in vivo.This study suggests that PP inhibited the proliferation of PCa cells and induced apoptosis.The molecular mechanism may be that PP induced PCa cells autophagy and eventually led to cell death.

prostate cancerperiplocinapoptosisRNA-Seqautophagy

王建良、付生军、李兰兰、李喜香

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甘肃省中医院药学部,兰州 730035

兰州大学第二医院甘肃省泌尿系统疾病研究重点实验室,兰州 730030

前列腺癌 杠柳毒苷 细胞凋亡 RNA-Seq 细胞自噬

甘肃省中医药管理局科研课题甘肃省科技计划自然科学基金甘肃省科技计划自然科学基金2021年度省级重点人才项目

GZKP-2020-2922JR5RA97321JR11RA1102021-17

2024

天然产物研究与开发
中国科学院成都文献情报中心

天然产物研究与开发

CSTPCD北大核心
影响因子:0.783
ISSN:1001-6880
年,卷(期):2024.36(7)