• 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

胰腺星状细胞谷氨酸代谢诱导胰腺癌中自噬的功能特征。

Functional characteristics of autophagy in pancreatic cancer induced by glutamate metabolism in pancreatic stellate cells.

机构信息

Department of Gastroenterology, Shanghai Ninth People's Hospital, Shanghai Jiaotong University, Shanghai, China.

Department of Pulmonary, Longhua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, China.

出版信息

J Int Med Res. 2020 Apr;48(4):300060519865368. doi: 10.1177/0300060519865368. Epub 2019 Dec 19.

DOI:10.1177/0300060519865368
PMID:31856624
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7607760/
Abstract

OBJECTIVE

To observe the effects of glutaminase (GLS) inhibitors on autophagy and proliferation of pancreatic stellate cells, and to explore their functions in pancreatic cancer.

METHODS

Pancreatic cancer cells were divided into two groups. Group A was the control untreated group, and group B cells were treated with GLS inhibitors. Western blotting was used to detect the expression of Atg5, Bcl-2, Bax, and Bid proteins. The bromodeoxyuridine assay and scratch test were employed to investigate cell proliferation and invasion, respectively. The expression of E-cadherin, vimentin, cell adhesion molecule 2 (CADM2), and Snail protein was investigated by immunofluorescence.

RESULTS

The expression of Atg5, Bax, and Bid was higher in group A than in group B, while Bcl-2 expression was lower in group A than in group B. Group A cells demonstrated greater proliferation and invasion than group B cells. The expression of E-cadherin was lower in group A cells than group B cells, while vimentin, CADM2, and Snail were expressed at higher levels in group A than group B cells.

CONCLUSION

The inhibition of glutamine isozymes reduces autophagy and apoptosis in astrocytes, and inhibits pancreatic cancer cell proliferation and metastasis, while reducing their invasiveness.

摘要

目的

观察谷氨酰胺酶(GLS)抑制剂对胰腺星状细胞自噬和增殖的影响,并探讨其在胰腺癌中的作用。

方法

将胰腺癌细胞分为两组。A 组为对照组,未进行处理;B 组细胞用 GLS 抑制剂处理。采用 Western blot 法检测 Atg5、Bcl-2、Bax 和 Bid 蛋白的表达。采用溴脱氧尿苷检测法和划痕实验分别检测细胞增殖和侵袭情况。免疫荧光法检测 E-钙黏蛋白、波形蛋白、细胞黏附分子 2(CADM2)和 Snail 蛋白的表达。

结果

与 B 组相比,A 组 Atg5、Bax 和 Bid 的表达更高,而 Bcl-2 的表达更低。A 组细胞的增殖和侵袭能力均强于 B 组。与 B 组相比,A 组细胞中 E-钙黏蛋白的表达更低,而波形蛋白、CADM2 和 Snail 的表达更高。

结论

抑制谷氨酰胺同工酶可减少星形胶质细胞中的自噬和凋亡,抑制胰腺癌细胞的增殖和转移,同时降低其侵袭性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/225a/7607760/59d59c955998/10.1177_0300060519865368-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/225a/7607760/2aa433d26c4d/10.1177_0300060519865368-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/225a/7607760/bc8ab99ec3f2/10.1177_0300060519865368-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/225a/7607760/8adf6be48159/10.1177_0300060519865368-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/225a/7607760/2a3d86bb5316/10.1177_0300060519865368-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/225a/7607760/59d59c955998/10.1177_0300060519865368-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/225a/7607760/2aa433d26c4d/10.1177_0300060519865368-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/225a/7607760/bc8ab99ec3f2/10.1177_0300060519865368-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/225a/7607760/8adf6be48159/10.1177_0300060519865368-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/225a/7607760/2a3d86bb5316/10.1177_0300060519865368-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/225a/7607760/59d59c955998/10.1177_0300060519865368-fig5.jpg

相似文献

1
Functional characteristics of autophagy in pancreatic cancer induced by glutamate metabolism in pancreatic stellate cells.胰腺星状细胞谷氨酸代谢诱导胰腺癌中自噬的功能特征。
J Int Med Res. 2020 Apr;48(4):300060519865368. doi: 10.1177/0300060519865368. Epub 2019 Dec 19.
2
Inhibition of ERK1/2 in cancer-associated pancreatic stellate cells suppresses cancer-stromal interaction and metastasis.抑制癌相关胰腺星状细胞中的 ERK1/2 可抑制癌-基质相互作用和转移。
J Exp Clin Cancer Res. 2019 May 27;38(1):221. doi: 10.1186/s13046-019-1226-8.
3
Autophagy Is Required for Activation of Pancreatic Stellate Cells, Associated With Pancreatic Cancer Progression and Promotes Growth of Pancreatic Tumors in Mice.自噬对于胰腺星状细胞的激活是必需的,与胰腺癌的进展相关,并促进了小鼠胰腺肿瘤的生长。
Gastroenterology. 2017 May;152(6):1492-1506.e24. doi: 10.1053/j.gastro.2017.01.010. Epub 2017 Jan 23.
4
Hic-5 in pancreatic stellate cells affects proliferation, apoptosis, migration, invasion of pancreatic cancer cells and postoperative survival time of pancreatic cancer.Hic-5 在胰腺星状细胞中影响胰腺癌细胞的增殖、凋亡、迁移和侵袭以及胰腺癌患者的术后生存时间。
Biomed Pharmacother. 2020 Jan;121:109355. doi: 10.1016/j.biopha.2019.109355. Epub 2019 Nov 1.
5
Effects of microRNA-183 on epithelial-mesenchymal transition, proliferation, migration, invasion and apoptosis in human pancreatic cancer SW1900 cells by targeting MTA1.微小RNA-183通过靶向MTA1对人胰腺癌SW1900细胞上皮-间质转化、增殖、迁移、侵袭及凋亡的影响
Exp Mol Pathol. 2017 Jun;102(3):522-532. doi: 10.1016/j.yexmp.2017.05.009. Epub 2017 May 12.
6
Effects of ginsenoside Rh2 on growth and migration of pancreatic cancer cells.人参皂苷 Rh2 对胰腺癌细胞生长和迁移的影响。
World J Gastroenterol. 2013 Mar 14;19(10):1582-92. doi: 10.3748/wjg.v19.i10.1582.
7
Liraglutide suppresses the metastasis of PANC-1 co-cultured with pancreatic stellate cells through modulating intracellular calcium content.利拉鲁肽通过调节细胞内钙含量抑制与胰腺星状细胞共培养的 PANC-1 的转移。
Endocr J. 2019 Dec 25;66(12):1053-1062. doi: 10.1507/endocrj.EJ19-0215. Epub 2019 Aug 30.
8
Effect of PPM1H on malignant phenotype of human pancreatic cancer cells.PPM1H对人胰腺癌细胞恶性表型的影响。
Oncol Rep. 2016 Nov;36(5):2926-2934. doi: 10.3892/or.2016.5065. Epub 2016 Sep 5.
9
ProNGF siRNA inhibits cell proliferation and invasion of pancreatic cancer cells and promotes anoikis.ProNGF siRNA 抑制胰腺癌细胞的增殖和侵袭,并促进失巢凋亡。
Biomed Pharmacother. 2019 Mar;111:1066-1073. doi: 10.1016/j.biopha.2019.01.002. Epub 2019 Jan 11.
10
Paracrine IL-6 signaling mediates the effects of pancreatic stellate cells on epithelial-mesenchymal transition via Stat3/Nrf2 pathway in pancreatic cancer cells.旁分泌 IL-6 信号通过 Stat3/Nrf2 通路介导胰腺星状细胞对胰腺癌细胞上皮间质转化的影响。
Biochim Biophys Acta Gen Subj. 2017 Feb;1861(2):296-306. doi: 10.1016/j.bbagen.2016.10.006. Epub 2016 Oct 14.

引用本文的文献

1
LINC01354 enhances the metastatic ability of gastric cancer cells by adjusting miR-153-5p/CADM2 expression.LINC01354通过调节miR-153-5p/CADM2的表达增强胃癌细胞的转移能力。
Am J Cancer Res. 2023 Jun 15;13(6):2630-2643. eCollection 2023.
2
Effects of Pgam1-mediated glycolysis pathway in Sertoli cells on Spermatogonial stem cells based on transcriptomics and energy metabolomics.基于转录组学和能量代谢组学研究支持细胞中磷酸甘油酸变位酶1介导的糖酵解途径对精原干细胞的影响
Front Vet Sci. 2022 Sep 23;9:992877. doi: 10.3389/fvets.2022.992877. eCollection 2022.

本文引用的文献

1
Glutaminase isoenzymes in the metabolic therapy of cancer.谷氨酰胺酶同工酶在癌症代谢治疗中的作用。
Biochim Biophys Acta Rev Cancer. 2018 Dec;1870(2):158-164. doi: 10.1016/j.bbcan.2018.07.007. Epub 2018 Jul 24.
2
Pan-Cancer Metabolic Signature Predicts Co-Dependency on Glutaminase and De Novo Glutathione Synthesis Linked to a High-Mesenchymal Cell State.泛癌代谢特征预测谷氨酰胺酶和从头合成谷胱甘肽的共依赖性与高间质细胞状态有关。
Cell Metab. 2018 Sep 4;28(3):383-399.e9. doi: 10.1016/j.cmet.2018.06.003. Epub 2018 Jun 28.
3
Pyruvate Kinase Isozyme M2 Plays a Critical Role in the Interactions Between Pancreatic Stellate Cells and Cancer Cells.
丙酮酸激酶同工酶 M2 在胰腺星状细胞与癌细胞相互作用中发挥关键作用。
Dig Dis Sci. 2018 Jul;63(7):1868-1877. doi: 10.1007/s10620-018-5051-2. Epub 2018 Apr 4.
4
PLEKHN1 promotes apoptosis by enhancing Bax-Bak hetro-oligomerization through interaction with Bid in human colon cancer.在人类结肠癌中,PLEKHN1通过与Bid相互作用增强Bax-Bak异源寡聚化来促进细胞凋亡。
Cell Death Discov. 2018 Feb 8;4:11. doi: 10.1038/s41420-017-0006-5. eCollection 2018 Dec.
5
CADM2, as a new target of miR-10b, promotes tumor metastasis through FAK/AKT pathway in hepatocellular carcinoma.CADM2 作为 miR-10b 的一个新靶点,通过 FAK/AKT 通路促进肝癌的肿瘤转移。
J Exp Clin Cancer Res. 2018 Mar 5;37(1):46. doi: 10.1186/s13046-018-0699-1.
6
MiR-22 suppresses epithelial-mesenchymal transition in bladder cancer by inhibiting Snail and MAPK1/Slug/vimentin feedback loop.miR-22 通过抑制 Snail 和 MAPK1/Slug/vimentin 反馈环抑制膀胱癌中的上皮-间质转化。
Cell Death Dis. 2018 Feb 12;9(2):209. doi: 10.1038/s41419-017-0206-1.
7
Palmatine suppresses glutamine-mediated interaction between pancreatic cancer and stellate cells through simultaneous inhibition of survivin and COL1A1.荷叶碱通过同时抑制生存素和 COL1A1 抑制胰腺癌与星状细胞之间的谷氨酰胺介导的相互作用。
Cancer Lett. 2018 Apr 10;419:103-115. doi: 10.1016/j.canlet.2018.01.057.
8
An image-based small-molecule screen identifies vimentin as a pharmacologically relevant target of simvastatin in cancer cells.基于图像的小分子筛选发现维替泊芬是辛伐他汀在癌细胞中的一个有药效学相关性的靶点。
FASEB J. 2018 May;32(5):2841-2854. doi: 10.1096/fj.201700663R. Epub 2018 Jan 18.
9
Aberrant expression of STYK1 and E-cadherin confer a poor prognosis for pancreatic cancer patients.STYK1和E-钙黏蛋白的异常表达预示着胰腺癌患者的预后不良。
Oncotarget. 2017 Nov 30;8(67):111333-111345. doi: 10.18632/oncotarget.22794. eCollection 2017 Dec 19.
10
Reprogramming pancreatic stellate cells via p53 activation: A putative target for pancreatic cancer therapy.通过激活 p53 重编程胰腺星状细胞:胰腺癌治疗的一个潜在靶点。
PLoS One. 2017 Dec 6;12(12):e0189051. doi: 10.1371/journal.pone.0189051. eCollection 2017.