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Qianlongtong Inhibits Proliferation and Induces Apoptosis of Hyperplastic Prostate Cells

机译:乾隆通抑制增生性前列腺细胞增殖并诱导其凋亡

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摘要

Qianlongtong is a compound made from traditional Chinese herbs and it has proven to be very effective to treat patients with benign prostate hypertrophy. However, its mechanism is still unknown. This study is designed to investigate the effect of Qianlongtong on proliferation and apoptosis of hyperplastic prostate cells. Flow cytometry (FCM) and terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) were used to assess proliferation and apoptosis of hyperplastic prostate cells in the following groups: control group, tamoxifen group, and groups with low, moderate, and high dosage of Qianlongtong. Reverse transcription-polymerase chain reaction analysis was used to investigate the underlying mechanisms for increased apoptosis. Cells treated with Qianlongtong were mainly blocked in the G0/G1 phase. The apoptotic index of each group was significantly higher than that in the control group. The apoptotic index in the high- and moderate-dosage groups was similar to that in the tamoxifen group. The high- and moderate-dosage groups had lower Bcl-2 and higher Bax messenger RNA (mRNA) levels compared with the control group. Qianlongtong inhibits proliferation and promotes the apoptosis of hyperplastic prostate cells.
机译:乾隆通是由传统中草药制成的化合物,已被证明对治疗前列腺肥大的患者非常有效。但是,其机制仍然未知。本研究旨在研究乾隆通对增生性前列腺细胞增殖和凋亡的影响。流式细胞仪(FCM)和末端脱氧核苷酸转移酶dUTP缺口末端标记(TUNEL)用于评估以下组增生性前列腺细胞的增殖和凋亡:对照组,他莫昔芬组以及低,中,高剂量的乾隆通组。逆转录聚合酶链反应分析用于研究细胞凋亡增加的潜在机制。用乾隆通处理的细胞主要在G0 / G1期被阻滞。各组的细胞凋亡指数均显着高于对照组。高剂量和中剂量组的细胞凋亡指数与他莫昔芬组相似。与对照组相比,高剂量组和中等剂量组的Bcl-2水平较低,Bax信使RNA(mRNA)水平较高。乾隆通抑制增生性前列腺细胞的增殖并促进其凋亡。

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