Department of Colorectal Surgery, Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University, Hangzhou, P.R. China.
Key Laboratory of Biotherapy of Zhejiang Province, Sir Run Run Shaw Hospital, Hangzhou, P.R. China.
Anticancer Res. 2024 Mar;44(3):1193-1199. doi: 10.21873/anticanres.16914.
BACKGROUND/AIM: In earlier research, we demonstrated that pyrvinium pamoate (PP) can effectively inhibit the proliferation and migration of colorectal cancer (CRC) cells. In the current study, we further explore the possibility of PP, as a potential therapeutic drug in the treatment of CRC.
Hoechst 33258 staining, immunofluorescence, and western blotting were used to further investigate the connection between PP and CRC cell apoptosis and autophagy.
We found that PP promoted apoptosis and autophagy of CRC cells. At the protein level, the expression of proteins related to the PI3K/mTOR signaling pathway exhibited a negative correlation with the dosage of PP. PP may therefore induce apoptosis and autophagy by inhibiting the PI3K/mTOR signaling pathway.
Our in vitro experiments demonstrated that PP could inhibit the progression of colorectal cancer cells by inducing apoptosis and autophagy. The detailed mechanism needs further investigation.
背景/目的:在早期的研究中,我们证明了匹可硫酸钠(PP)能够有效地抑制结直肠癌细胞(CRC)的增殖和迁移。在本研究中,我们进一步探索了 PP 作为 CRC 治疗潜在治疗药物的可能性。
采用 Hoechst 33258 染色、免疫荧光和 Western blot 进一步研究了 PP 与 CRC 细胞凋亡和自噬之间的关系。
我们发现 PP 促进了 CRC 细胞的凋亡和自噬。在蛋白质水平上,与 PI3K/mTOR 信号通路相关的蛋白表达与 PP 的剂量呈负相关。因此,PP 可能通过抑制 PI3K/mTOR 信号通路诱导细胞凋亡和自噬。
我们的体外实验表明,PP 通过诱导细胞凋亡和自噬来抑制结直肠癌细胞的进展。其详细的作用机制需要进一步研究。