临床外科杂志 ›› 2025, Vol. 33 ›› Issue (6): 596-601.doi: 10.3969/j.issn.1005-6483.20240399

• 论著 • 上一篇    下一篇

舒芬太尼调节AMPK-SIRT1-PGC-1α信号通路对甲状腺癌细胞增殖、侵袭迁移和凋亡的影响

马涛 李欣鑫 戚娟 张爱容   

  1. 061000 河北沧州,沧州市人民医院麻醉科
  • 收稿日期:2024-03-22 出版日期:2025-06-20 发布日期:2025-06-20
  • 通讯作者: 张爱容,Email:q46lya@163.com
  • 基金资助:
    河北省卫生健康委员会资助项目(20241252)

Effects of sufentanil on proliferation invasion migration and apoptosis of thyroid 〖JP2〗cancer cells by regulating the AMPK-SIRT1-PGC-1α signaling pathway

MA Tao,LI Xinxin,QI Juan,ZHANG Airong   

  1. Department of Anesthesiology,Cangzhou People’s Hospital,Cangzhou 061000,China
  • Received:2024-03-22 Online:2025-06-20 Published:2025-06-20

摘要: 目的 探讨舒芬太尼对甲状腺癌细胞增殖、侵袭迁移和凋亡的影响及其与AMP依赖蛋白激酶(AMPK)-沉默信息调节因子1(SIRT1)-过氧化物酶体增殖活化受体γ共激活因子1α(PGC-1α)信号通路的关系。方法 将人甲状腺癌细胞株(TPC-1)分为对照组、L、M、H-舒芬太尼组、H-舒芬太尼+AICAR组。TPC-1细胞活性、细胞凋亡、侵袭、迁移及蛋白表达分别利用CCK-8法、流式细胞仪、Transwell法、划痕实验以及Western blot检测。结果 与对照组比较,L、M、H-舒芬太尼组吸光值、侵袭数量、划痕愈合率、cleaved-Caspase-3、细胞程序性死亡-配体1、B淋巴细胞瘤-2、p-AMPK/AMPK、SIRT1、PGC-1α水平降低,凋亡率、Bax蛋白水平升高(P<0.05);AICAR处理逆转了H-舒芬太尼对上述指标的影响(P<0.05)。结论 舒芬太尼可能抑制AMPK-SIRT1-PGC-1α信号通路,进而抑制甲状腺癌细胞增殖、侵袭和迁移,促进细胞凋亡。

关键词: 舒芬太尼; AMPK-SIRT1-PGC-1α信号通路; 甲状腺癌; 增殖; 迁移; 侵袭; 凋亡

Abstract: Objective To investigate the effects of sufentanil on proliferation,invasion,migration,and apoptosis of thyroid cancer cells,and analyze whether its mechanism is related to the AMP-activated protein kinase(AMPK) -silent information regulator 1(SIRT1) -peroxisome proliferator activator receptor gamma coactivator 1α(PGC-1α) signaling pathway.Methods The human thyroid cancer cell line(TPC-1) was separated into a control group,L,M,H-sufentanil groups,and H-sufentanil+AICAR group.TPC-1 cell activity,apoptosis,invasion,migration,and expression of proteins were detected using CCK-8 assay,flow cytometry,Transwell assay,scratch assay,and Western blot,respectively.〖WTHZ〗ResultsCompared with the control group,the absorbance value,invasion number,scratch healing rate,cleaved-Caspase-3,programmed cell death 1 ligand 1,B lymphoblastoma-2,p-AMPK/AMPK,SIRT1,and PGC-1α protein levels in L,M,and H-sufentanil groups were reduced;the apoptosis rate and Bax protein level were increased(P<0.05).AICAR treatment reversed the effect of H-sufentanil on the above indicators(P<0.05).Conclusion Sufentanil may inhibit the AMPK-SIRT1-PGC-1α signaling pathway,thereby inhibiting the proliferation and invasion migration of thyroid cancer cells,and promoting cell apoptosis.

Key words: sufentanil;AMPK-SIRT1-PGC-1α signaling pathway;thyroid cancer;proliferation;migration;invasion;apoptosis

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