中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Ropivacaine suppresses tumor biological characteristics of human hepatocellular carcinoma via inhibiting IGF-1R/PI3K/AKT/mTOR signaling axis

文献类型:期刊论文

作者Zhang, Runze1,2; Lian, Yanhong1,2; Xie, Kangjie1,2; Cai, Yunfang1,2; Pan, Yafei1,2; Zhu, Yuntian1,2
刊名BIOENGINEERED
出版日期2021-12-20
卷号12
关键词Ropivacaine hepatocellular carcinoma IGF-1R IGF1R-PI3K-AKT-mTOR signaling cell cycle epithelial-mesenchymal transition
ISSN号2165-5979
DOI10.1080/21655979.2021.1995103
通讯作者Zhu, Yuntian(zhuyt@zjcc.org.cn)
英文摘要Ropivacaine, a common local anesthetic in the clinic, has anti-proliferative and pro-apoptotic effects in numerous cancers, however, the underlying regulatory mechanism of ropivacaine in hepatocellular carcinoma remains unclear. In the current study, human HepG2 cells were stimulated with different ropivacaine concentrations. Cell Counting Kit-8 assay, cell colony formation, and cell cycle were used to monitor cell viability. Cell apoptosis, migration, and invasion were determined by flow cytometry and transwell assays. Tumor xenograft experiments were performed to prove the anti-cancer effect of ropivacaine in vivo. A high dose of ropivacaine inhibited proliferation and promoted apoptosis of HepG2 cells in a dose-dependent manner. Ropivacaine challenge also arrested cells in the G2 phase, followed by a decline in the protein expression of cyclin D1 and cyclin-dependent kinase 2, and an increase in p27 levels in HepG2 cells. Additionally, different ropivacaine doses suppressed cell migration and invasion by upregulating E-cadherin expression and downregulating N-cadherin expression. Mechanically, ropivacaine challenge gradually restrained insulin-like growth factor-1 receptor (IGF-1 R) expression and the activities of phosphorylated-PI3K, AKT, and mTOR in HepG2 cells with increased ropivacaine doses. In the tumor xenograft experiment, ropivacaine was confirmed to inhibit tumor growth, accompanied by inhibition of the IGF-1 R/PI3K/AKT/mTOR signaling axis. In conclusion, ropivacaine suppressed tumor biological characteristics and promoted apoptosis, resulting in the suppression of hepatocellular carcinoma progression by targeting the IGF-1 R/PI3K/AKT/mTOR signaling pathway. It is possible that ropivacaine-mediated local anesthesia may be developed as a novel surgical adjuvant drug for treating hepatocellular carcinoma.
WOS关键词LOCAL-ANESTHETICS ; CANCER-CELLS ; WOUND INFILTRATION ; GASTRIC-CANCER ; STEM-CELLS ; APOPTOSIS ; BUPIVACAINE ; LIDOCAINE ; GROWTH ; MIGRATION
资助项目Zhejiang Province Medical Science and Technology Project[2019KY042] ; Zhejiang Province Medical Science and Technology Project[2020KY485] ; Zhejiang Province Medical Science and Technology Project[2021KY089]
WOS研究方向Biotechnology & Applied Microbiology
语种英语
WOS记录号WOS:000721087600001
出版者TAYLOR & FRANCIS INC
资助机构Zhejiang Province Medical Science and Technology Project
源URL[http://ir.hfcas.ac.cn:8080/handle/334002/126692]  
专题中国科学院合肥物质科学研究院
通讯作者Zhu, Yuntian
作者单位1.Univ Chinese Acad Sci, Dept Anesthesiol, Canc Hosp, Zhejiang Canc Hosp, Hangzhou, Zhejiang, Peoples R China
2.Chinese Acad Sci, Inst Basic Med & Canc IBMC, Dept Anesthesiol, Hangzhou, Zhejiang, Peoples R China
推荐引用方式
GB/T 7714
Zhang, Runze,Lian, Yanhong,Xie, Kangjie,et al. Ropivacaine suppresses tumor biological characteristics of human hepatocellular carcinoma via inhibiting IGF-1R/PI3K/AKT/mTOR signaling axis[J]. BIOENGINEERED,2021,12.
APA Zhang, Runze,Lian, Yanhong,Xie, Kangjie,Cai, Yunfang,Pan, Yafei,&Zhu, Yuntian.(2021).Ropivacaine suppresses tumor biological characteristics of human hepatocellular carcinoma via inhibiting IGF-1R/PI3K/AKT/mTOR signaling axis.BIOENGINEERED,12.
MLA Zhang, Runze,et al."Ropivacaine suppresses tumor biological characteristics of human hepatocellular carcinoma via inhibiting IGF-1R/PI3K/AKT/mTOR signaling axis".BIOENGINEERED 12(2021).

入库方式: OAI收割

来源:合肥物质科学研究院

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