Suppr超能文献

重楼苷 II 通过抑制 PI3K/AKT/mTOR 和 STAT3 信号通路诱导结直肠癌细胞保护性自噬和凋亡。

Polyphyllin II Induces Protective Autophagy and Apoptosis via Inhibiting PI3K/AKT/mTOR and STAT3 Signaling in Colorectal Cancer Cells.

机构信息

Department of Biology, Hong Kong Baptist University (HKBU), Hong Kong 999077, China.

Golden Meditech Center for Neuro-Regeneration Sciences (GMCNS), HKBU, Hong Kong 999077, China.

出版信息

Int J Mol Sci. 2022 Oct 6;23(19):11890. doi: 10.3390/ijms231911890.

Abstract

Polyphyllin II (PPII) is a natural steroidal saponin occurring in . It has been demonstrated to exhibit anti-cancer activity against a variety of cancer cells. However, the anti-colorectal cancer (CRC) effects and mechanism of action of PPII are rarely reported. In the present study, we showed that PPII inhibited the proliferation of HCT116 and SW620 cells. Moreover, PPII induced G2/M-phase cell cycle arrest and apoptosis, as well as protective autophagy, in CRC cells. We found that PPII-induced autophagy was associated with the inhibition of PI3K/AKT/mTOR signaling. Western blotting results further revealed that PPII lowered the protein levels of phospho-Src (Tyr416), phospho-JAK2 (Tyr1007/1008), phospho-STAT3 (Tyr705), and STAT3-targeted molecules in CRC cells. The overactivation of STAT3 attenuated the cytotoxicity of PPII against HCT116 cells, indicating the involvement of STAT3 inhibition in the anti-CRC effects of PPII. PPII (0.5 mg/kg or 1 mg/kg, i.p. once every 3 days) suppressed HCT116 tumor growth in nude mice. In alignment with the in vitro results, PPII inhibited proliferation, induced apoptosis, and lowered the protein levels of phospho-STAT3, phospho-AKT, and phospho-mTOR in xenografts. These data suggest that PPII could be a potent therapeutic agent for the treatment of CRC.

摘要

重楼皂苷 II (PPII) 是一种天然甾体皂甙,存在于 中。已证实其对多种癌细胞具有抗癌活性。然而,PPII 对结直肠癌 (CRC) 的作用机制和抗癌效果鲜有报道。在本研究中,我们表明 PPII 抑制了 HCT116 和 SW620 细胞的增殖。此外,PPII 诱导 CRC 细胞发生 G2/M 期细胞周期阻滞和细胞凋亡,并诱导保护性自噬。我们发现,PPII 诱导的自噬与 PI3K/AKT/mTOR 信号通路的抑制有关。Western blot 结果进一步表明,PPII 降低了 CRC 细胞中磷酸化Src(Tyr416)、磷酸化 JAK2(Tyr1007/1008)、磷酸化 STAT3(Tyr705)和 STAT3 靶向分子的蛋白水平。STAT3 的过度激活削弱了 PPII 对 HCT116 细胞的细胞毒性,表明 STAT3 抑制参与了 PPII 的抗 CRC 作用。PPII(腹腔注射,0.5mg/kg 或 1mg/kg,每 3 天一次)抑制裸鼠 HCT116 肿瘤生长。与体外结果一致,PPII 抑制了异种移植物的增殖,诱导了细胞凋亡,并降低了磷酸化 STAT3、磷酸化 AKT 和磷酸化 mTOR 的蛋白水平。这些数据表明,PPII 可能是治疗 CRC 的有效治疗剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85be/9570434/4a5e83dc20a9/ijms-23-11890-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验