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Traditional Chinese Medicine CFF‐1 induced cell growth inhibition autophagy and apoptosis via inhibiting EGFR‐related pathways in prostate cancer

机译:中药CFF-1通过抑制EGFR相关途径诱导前列腺癌的细胞生长抑制自噬和凋亡

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摘要

Traditional Chinese medicine (TCM) has a combined therapeutic result in cancer treatment by integrating holistic and local therapeutical effects, by which TCM can enhance the curative effect and reduce the side effect. In this study, we analyzed the effect of CFF‐1 (alcohol extract from an anticancer compound Chinese medicine) on prostate cancer (PCa) cell lines and studied in detail the mechanism of cell death induced by CFF‐1 in vitro and in vivo. From our data, we found for the first time that CFF‐1 obviously arrested cell cycle in G1 phase, decreased cell viability and then increased nuclear rupture in a dose‐dependent manner and finally resulted in apoptosis in prostate cancer cells. In molecular level, our data showed that CFF‐1 induced inhibition of EGFR auto‐phosphorylation and inactivation of EGFR. Disruption of EGFR activity in turn suppressed downstream PI3K/AKT and Raf/Erk signal pathways, resulted in the decrease of p‐FOXO1 (Ser256) and regulated the expression of apoptosis‐related and cycle‐related genes. Moreover, CFF‐1 markedly induced cell autophagy through inhibiting PI3K/AKT/ style="fixed-case">mTOR pathway and then up‐regulating Beclin‐1 and style="fixed-case">LC‐3 style="fixed-case">II and down‐regulating phosphorylation of p70S6K. In vivo, style="fixed-case">CFF‐1‐treated group exhibited a significant decrease in tumor volume compared with the negative control group in subcutaneous xenograft tumor in nude mice via inhibiting style="fixed-case">EGFR‐related signal pathways. Thus, bio‐functions of Chinese medicine style="fixed-case">CFF‐1 in inducing style="fixed-case">PCa cell growth inhibition, autophagy, and apoptosis suggested that style="fixed-case">CFF‐1 had the clinical potential to treat patients with prostate cancer.
机译:中医通过综合整体和局部治疗作用,在癌症治疗中具有综合的治疗效果,中医可以提高疗效,减少副作用。在这项研究中,我们分析了CFF-1(一种抗癌中药的酒精提取物)对前列腺癌(PCa)细胞系的作用,并详细研究了CFF-1在体内和体外诱导的细胞死亡机制。从我们的数据中,我们首次发现CFF-1明显阻止了G1期的细胞周期,降低了细胞活力,然后以剂量依赖的方式增加了核破裂,最终导致前列腺癌细胞的凋亡。在分子水平上,我们的数据显示CFF-1诱导了EGFR自磷酸化的抑制和EGFR的失活。 EGFR活性的破坏反过来抑制了下游PI3K / AKT和Raf / Erk信号通路,导致p-FOXO1(Ser256)的减少,并调控了凋亡相关基因和周期相关基因的表达。此外,CFF-1通过抑制PI3K / AKT / style =“ fixed-case”> mTOR 途径,然后上调Beclin-1和 style =“ fixed-case”>来显着诱导细胞自噬。 LC ‐3 style =“ fixed-case”> II 和下调p70S6K的磷酸化。在体内,通过抑制 style =“,与阴性对照组相比, style =” fixed-case“> CFF -1治疗组在裸鼠皮下异种移植肿瘤中的肿瘤体积明显低于阴性对照组。固定病例“> EGFR 相关信号通路。因此,中药 style =“ fixed-case”> CFF -1的生物功能诱导 style =“ fixed-case”> PC a细胞生长抑制,自噬和细胞凋亡表明 style =“ fixed-case”> CFF -1具有治疗前列腺癌患者的临床潜力。

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