• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

整合素和金属蛋白酶-17抑制剂TNF484对肝癌细胞增殖、迁移和侵袭的抑制作用

Inhibition of hepatocellular carcinoma cell proliferation, migration, and invasion by a disintegrin and metalloproteinase-17 inhibitor TNF484.

作者信息

Xia Changhong, Zhang Dongsheng, Li Yanmei, Chen Jie, Zhou Haibo, Nie Long, Sun Yanyan, Guo Siyan, Cao Jianbiao, Zhou Fangzheng, Li Junlai

机构信息

Department of Ultrasound, Chinese People's Liberation Army General Hospital, Beijing, China.

Department of Oncology, Suizhou Hospital, Hubei University of Medicine, Suizhou, China.

出版信息

J Res Med Sci. 2019 Mar 25;24:26. doi: 10.4103/jrms.JRMS_129_17. eCollection 2019.

DOI:10.4103/jrms.JRMS_129_17
PMID:31007696
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6450222/
Abstract

BACKGROUND

The aim of this study was to test the effect of TNF484 on cell proliferation, migration, and invasion of hepatocellular carcinoma (HCC) cells.

MATERIALS AND METHODS

Various doses (0, 1, 10, 50, and 100 nM) of TNF484 were applied to the HepG2 and Bel7402 cells, and cell proliferation was measured by using 3-(4,5-dimethylthiazol-2-yl)-2,5 diphenyl tetrazolium bromide assay after 72 h. Cell migration rate was measured using the xCELLigence system, and the cell invasion ability was examined by the three-dimensional spheroid BME cell invasion assay. The expression level of ADAM17 was also measured with RT-PCR.

RESULTS

With the treatment of TNF484, the cell proliferation of HepG2 and Bel7402 cells was inhibited in a dose-dependent manner. Moreover, under TNF484 treatment, the cell migration rate as well as cell invasion ability of the HepG2 and Bel7402 cells were suppressed.

CONCLUSION

TNF484 could inhibit the cell proliferation, migration, and invasion of some HCC cell lines, making it a potential therapeutic option for liver cancer treatment.

摘要

背景

本研究旨在测试TNF484对肝癌(HCC)细胞增殖、迁移和侵袭的影响。

材料与方法

将不同剂量(0、1、10、50和100 nM)的TNF484应用于HepG2和Bel7402细胞,72小时后使用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐法测量细胞增殖。使用xCELLigence系统测量细胞迁移率,并通过三维球体BME细胞侵袭试验检测细胞侵袭能力。还通过RT-PCR测量ADAM17的表达水平。

结果

经TNF484处理后,HepG2和Bel7402细胞的增殖受到剂量依赖性抑制。此外,在TNF484处理下,HepG2和Bel7402细胞的迁移率和侵袭能力均受到抑制。

结论

TNF484可抑制某些肝癌细胞系的细胞增殖、迁移和侵袭,使其成为肝癌治疗的潜在选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06b8/6450222/31355d5a9b9e/JRMS-24-26-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06b8/6450222/f46aa6d1535b/JRMS-24-26-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06b8/6450222/e9fbf18436b2/JRMS-24-26-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06b8/6450222/eed82487fe43/JRMS-24-26-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06b8/6450222/31355d5a9b9e/JRMS-24-26-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06b8/6450222/f46aa6d1535b/JRMS-24-26-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06b8/6450222/e9fbf18436b2/JRMS-24-26-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06b8/6450222/eed82487fe43/JRMS-24-26-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06b8/6450222/31355d5a9b9e/JRMS-24-26-g004.jpg

相似文献

1
Inhibition of hepatocellular carcinoma cell proliferation, migration, and invasion by a disintegrin and metalloproteinase-17 inhibitor TNF484.整合素和金属蛋白酶-17抑制剂TNF484对肝癌细胞增殖、迁移和侵袭的抑制作用
J Res Med Sci. 2019 Mar 25;24:26. doi: 10.4103/jrms.JRMS_129_17. eCollection 2019.
2
Lowered HGK expression inhibits cell invasion and adhesion in hepatocellular carcinoma cell line HepG2.低表达 HGK 抑制肝癌细胞系 HepG2 中的细胞侵袭和黏附。
World J Gastroenterol. 2010 Sep 28;16(36):4541-8. doi: 10.3748/wjg.v16.i36.4541.
3
Restoration of miR-20a expression suppresses cell proliferation, migration, and invasion in HepG2 cells.miR-20a表达的恢复抑制了HepG2细胞的增殖、迁移和侵袭。
Onco Targets Ther. 2016 May 27;9:3067-76. doi: 10.2147/OTT.S96861. eCollection 2016.
4
MicroRNA-383 inhibits proliferation, migration, and invasion in hepatocellular carcinoma cells by targeting PHF8.MicroRNA-383 通过靶向 PHF8 抑制肝癌细胞的增殖、迁移和侵袭。
Mol Genet Genomic Med. 2020 Aug;8(8):e1272. doi: 10.1002/mgg3.1272. Epub 2020 May 22.
5
[The effects of microRNA-7 on proliferation and invasion of hepatocellular carcinoma HepG2 cells].[微小RNA-7对肝癌HepG2细胞增殖和侵袭的影响]
Zhonghua Zhong Liu Za Zhi. 2018 Jun 23;40(6):406-411. doi: 10.3760/cma.j.issn.0253-3766.2018.06.002.
6
MiR-451a suppresses cell proliferation, metastasis and EMT via targeting YWHAZ in hepatocellular carcinoma.微小RNA-451a通过靶向14-3-3ζ抑制肝癌细胞的增殖、转移和上皮-间质转化。
Eur Rev Med Pharmacol Sci. 2019 Jun;23(12):5158-5167. doi: 10.26355/eurrev_201906_18180.
7
Akebia trifoliata (Thunb.) Koidz Seed Extract inhibits human hepatocellular carcinoma cell migration and invasion in vitro.三叶木通(Thunb.)种子提取物抑制人肝癌细胞在体外的迁移和侵袭。
J Ethnopharmacol. 2019 Apr 24;234:204-215. doi: 10.1016/j.jep.2018.11.044. Epub 2018 Dec 7.
8
Propofol inhibits proliferation, migration, and invasion of hepatocellular carcinoma cells by downregulating Twist.异丙酚通过下调 Twist 抑制肝癌细胞的增殖、迁移和侵袭。
J Cell Biochem. 2019 Aug;120(8):12803-12809. doi: 10.1002/jcb.28551. Epub 2019 Mar 12.
9
Activation of PI3K/AKT is involved in TINAG-mediated promotion of proliferation, invasion and migration of hepatocellular carcinoma.PI3K/AKT 的激活参与了 TINAG 介导的促进肝癌细胞增殖、侵袭和迁移。
Cancer Biomark. 2018;23(1):33-43. doi: 10.3233/CBM-181277.
10
LncRNA SNHG14 aggravates invasion and migration as ceRNA via regulating miR-656-3p/SIRT5 pathway in hepatocellular carcinoma.长链非编码RNA SNHG14通过调控miR-656-3p/SIRT5通路作为竞争性内源RNA加重肝细胞癌的侵袭和迁移。
Mol Cell Biochem. 2020 Oct;473(1-2):143-153. doi: 10.1007/s11010-020-03815-6. Epub 2020 Jun 30.

引用本文的文献

1
ITGB1 Drives Hepatocellular Carcinoma Progression by Modulating Cell Cycle Process Through PXN/YWHAZ/AKT Pathways.整合素β1通过PXN/YWHAZ/AKT信号通路调控细胞周期进程,驱动肝细胞癌进展。
Front Cell Dev Biol. 2021 Dec 17;9:711149. doi: 10.3389/fcell.2021.711149. eCollection 2021.
2
Implications of ADAM17 activation for hyperglycaemia, obesity and type 2 diabetes.ADAM17 激活对高血糖、肥胖和 2 型糖尿病的影响。
Biosci Rep. 2021 May 28;41(5). doi: 10.1042/BSR20210029.
3
A Disintegrin and Metalloproteinase 9 (ADAM9) in Advanced Hepatocellular Carcinoma and Their Role as a Biomarker During Hepatocellular Carcinoma Immunotherapy.

本文引用的文献

1
ADAM17 is essential for ectodomain shedding of the EGF-receptor ligand amphiregulin.ADAM17对于表皮生长因子受体配体双调蛋白的胞外域脱落至关重要。
FEBS Open Bio. 2018 Mar 12;8(4):702-710. doi: 10.1002/2211-5463.12407. eCollection 2018 Apr.
2
Recent Advances in ADAM17 Research: A Promising Target for Cancer and Inflammation.ADAM17 研究的最新进展:癌症和炎症的有希望的靶点。
Mediators Inflamm. 2017;2017:9673537. doi: 10.1155/2017/9673537. Epub 2017 Nov 2.
3
The shedding protease ADAM17: Physiology and pathophysiology.脱落蛋白酶 ADAM17:生理学和病理生理学。
晚期肝细胞癌中的解整合素和金属蛋白酶9(ADAM9)及其在肝细胞癌免疫治疗期间作为生物标志物的作用。
Cancers (Basel). 2020 Mar 21;12(3):745. doi: 10.3390/cancers12030745.
4
Aberrant expression of ADAM9 in ovarian cancer and its clinical significance.ADAM9 在卵巢癌中的异常表达及其临床意义。
J Clin Lab Anal. 2020 Apr;34(4):e23136. doi: 10.1002/jcla.23136. Epub 2019 Dec 3.
Biochim Biophys Acta Mol Cell Res. 2017 Nov;1864(11 Pt B):2059-2070. doi: 10.1016/j.bbamcr.2017.07.001. Epub 2017 Jul 11.
4
Role of superoxide dismutase in hepatitis B virus-related hepatocellular carcinoma.超氧化物歧化酶在乙型肝炎病毒相关肝细胞癌中的作用。
J Res Med Sci. 2016 Oct 18;21:94. doi: 10.4103/1735-1995.192510. eCollection 2016.
5
The role of ADAM17 in tumorigenesis and progression of breast cancer.ADAM17在乳腺癌发生发展中的作用。
Tumour Biol. 2016 Dec;37:15359–15370. doi: 10.1007/s13277-016-5418-y. Epub 2016 Sep 22.
6
ADAM17 is a Tumor Promoter and Therapeutic Target in Western Diet-associated Colon Cancer.ADAM17是西方饮食相关结肠癌中的肿瘤促进因子和治疗靶点。
Clin Cancer Res. 2017 Jan 15;23(2):549-561. doi: 10.1158/1078-0432.CCR-15-3140. Epub 2016 Aug 3.
7
Targeting ADAM17 Sheddase Activity in Cancer.靶向癌症中的ADAM17蛋白酶活性
Curr Drug Targets. 2016;17(16):1908-1927. doi: 10.2174/1389450117666160727143618.
8
The ADAMs family of proteases as targets for the treatment of cancer.作为癌症治疗靶点的ADAMs蛋白酶家族。
Cancer Biol Ther. 2016 Aug 2;17(8):870-80. doi: 10.1080/15384047.2016.1177684. Epub 2016 Apr 26.
9
Role of ADAM17 in invasion and migration of CD133-expressing liver cancer stem cells after irradiation.ADAM17在放疗后表达CD133的肝癌干细胞侵袭和迁移中的作用
Oncotarget. 2016 Apr 26;7(17):23482-97. doi: 10.18632/oncotarget.8112.
10
SAR Studies of Exosite-Binding Substrate-Selective Inhibitors of A Disintegrin And Metalloprotease 17 (ADAM17) and Application as Selective in Vitro Probes.去整合素和金属蛋白酶17(ADAM17)的外位点结合底物选择性抑制剂的构效关系研究及其作为选择性体外探针的应用
J Med Chem. 2015 Aug 13;58(15):5808-24. doi: 10.1021/acs.jmedchem.5b00354. Epub 2015 Aug 4.