• 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

亚致死热疗促进乳腺癌转移及其定量蛋白质组学分析揭示的分子机制。

Sublethal heat treatment promotes breast cancer metastasis and its molecular mechanism revealed by quantitative proteomic analysis.

机构信息

Department of Ultrasound, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

Department of Ultrasound, Ruijin Hospital Luwan Branch, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.

出版信息

Aging (Albany NY). 2022 Feb 12;14(3):1389-1406. doi: 10.18632/aging.203884.

DOI:10.18632/aging.203884
PMID:35150481
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8876919/
Abstract

Radiofrequency ablation (RFA) is a frequently used thermal ablation technique for breast tumors. The study aimed to identify the effect of sublethal heat treatment on biological function of breast cancer cells and reveal its potential molecular mechanism. The expression profile of dysregulated proteins in sublethal heat treated breast cancer cells was analyzed by quantitative proteomic analysis. The differentially expressed proteins in the sublethal heat treated breast cancer were identified. The potential biological functions of these proteins were evaluated. The proliferation and invasion ability of breast cancer cells were enhanced after sublethal heat treatment. The expression profile of proteins in sublethal heat treated breast cancer cells was abundant, and most of which were newly discovered. A total of 206 differentially expressed proteins were identified. Among them, 101 proteins were downregulated while 105 proteins were upregulated. GO and KEGG analysis indicated that various systems were involved in the process of sublethal heat treatment including cancer, immune system, et al. Immunohistochemistry staining showed that the expression of Heat shock protein 1B, NOB1 and CRIP1 was highly expressed while the expression of BCLAF1 was lower in sublethal heat treated group. The proliferation and invasion ability of breast cancer cells were enhanced after sublethal heat treatment. Sublethal heat treatment caused gene alterations in cancer and immune system. Heat shock protein 1B, NOB1 and CRIP1 were upregulated while BCLAF1 was downregulated in breast cancer after sublethal heat treatment.

摘要

射频消融(RFA)是一种常用于治疗乳腺肿瘤的热消融技术。本研究旨在确定亚致死热疗对乳腺癌细胞生物学功能的影响,并揭示其潜在的分子机制。通过定量蛋白质组学分析,分析了亚致死热处理的乳腺癌细胞中失调蛋白的表达谱。鉴定了亚致死热处理的乳腺癌中差异表达的蛋白质。评估了这些蛋白质的潜在生物学功能。亚致死热处理后,乳腺癌细胞的增殖和侵袭能力增强。亚致死热处理的乳腺癌细胞的蛋白质表达谱丰富,其中大多数是新发现的。共鉴定出 206 个差异表达蛋白。其中,101 个蛋白下调,105 个蛋白上调。GO 和 KEGG 分析表明,各种系统参与了亚致死热处理过程,包括癌症、免疫系统等。免疫组织化学染色显示,亚致死热处理组中热休克蛋白 1B、NOB1 和 CRIP1 的表达高度上调,而 BCLAF1 的表达下调。亚致死热处理后,乳腺癌细胞的增殖和侵袭能力增强。亚致死热处理导致癌症和免疫系统的基因改变。亚致死热处理后,乳腺癌中热休克蛋白 1B、NOB1 和 CRIP1 上调,而 BCLAF1 下调。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d3a/8876919/b2c6d4eaf90e/aging-14-203884-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d3a/8876919/a359e2090223/aging-14-203884-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d3a/8876919/0a01797b4698/aging-14-203884-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d3a/8876919/700d39dac5ef/aging-14-203884-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d3a/8876919/8ed7ca6a708b/aging-14-203884-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d3a/8876919/0293b45d95cd/aging-14-203884-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d3a/8876919/b2c6d4eaf90e/aging-14-203884-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d3a/8876919/a359e2090223/aging-14-203884-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d3a/8876919/0a01797b4698/aging-14-203884-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d3a/8876919/700d39dac5ef/aging-14-203884-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d3a/8876919/8ed7ca6a708b/aging-14-203884-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d3a/8876919/0293b45d95cd/aging-14-203884-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d3a/8876919/b2c6d4eaf90e/aging-14-203884-g006.jpg

相似文献

1
Sublethal heat treatment promotes breast cancer metastasis and its molecular mechanism revealed by quantitative proteomic analysis.亚致死热疗促进乳腺癌转移及其定量蛋白质组学分析揭示的分子机制。
Aging (Albany NY). 2022 Feb 12;14(3):1389-1406. doi: 10.18632/aging.203884.
2
Stress-induced phosphoprotein 1 mediates hepatocellular carcinoma metastasis after insufficient radiofrequency ablation.应激诱导磷蛋白 1 介导线粒体功能障碍在射频消融术后肝癌转移中的作用
Oncogene. 2018 Jun;37(26):3514-3527. doi: 10.1038/s41388-018-0169-4. Epub 2018 Mar 21.
3
Insufficient Radiofrequency Ablation Promotes Hepatocellular Carcinoma Metastasis Through N6-Methyladenosine mRNA Methylation-Dependent Mechanism.射频消融不足通过N6-甲基腺苷mRNA甲基化依赖性机制促进肝细胞癌转移
Hepatology. 2021 Sep;74(3):1339-1356. doi: 10.1002/hep.31766.
4
Sublethal heat treatment promotes epithelial-mesenchymal transition and enhances the malignant potential of hepatocellular carcinoma.亚致死热疗促进上皮-间充质转化,增强肝癌的恶性潜能。
Hepatology. 2013 Nov;58(5):1667-80. doi: 10.1002/hep.26526. Epub 2013 Sep 19.
5
Proteomic study reveals that proteins involved in metabolic and detoxification pathways are highly expressed in HER-2/neu-positive breast cancer.蛋白质组学研究表明,参与代谢和解毒途径的蛋白质在HER-2/neu阳性乳腺癌中高度表达。
Mol Cell Proteomics. 2005 Nov;4(11):1686-96. doi: 10.1074/mcp.M400221-MCP200. Epub 2005 Jul 26.
6
Regulation of heat shock protein 72 kDa and 90 kDa in human breast cancer MDA-MB-231 cells.人乳腺癌MDA-MB-231细胞中72 kDa和90 kDa热休克蛋白的调控
Mol Cell Biochem. 2000 Jan;204(1-2):169-78. doi: 10.1023/a:1007016822939.
7
Heat shock protein 70 is induced in mouse human colon tumor xenografts after sublethal radiofrequency ablation.亚致死性射频消融后,小鼠人结肠肿瘤异种移植瘤中诱导产生热休克蛋白70。
Ann Surg Oncol. 2004 Apr;11(4):399-406. doi: 10.1245/ASO.2004.08.013.
8
Biochemical requirements for the expression of heat shock protein 72 kda in human breast cancer MCF-7 cells.人乳腺癌MCF-7细胞中72 kDa热休克蛋白表达的生化需求。
Mol Cell Biochem. 1999 Sep;199(1-2):179-88. doi: 10.1023/a:1006946329581.
9
Heat Shock Protein 27 Enhances SUMOylation of Heat Shock Protein B8 to Accelerate the Progression of Breast Cancer.热休克蛋白 27 增强热休克蛋白 B8 的 SUMOylation 以加速乳腺癌的进展。
Am J Pathol. 2020 Dec;190(12):2464-2477. doi: 10.1016/j.ajpath.2020.04.012.
10
17beta-hydroxysteroid dehydrogenase type 5 is negatively correlated to apoptosis inhibitor GRP78 and tumor-secreted protein PGK1, and modulates breast cancer cell viability and proliferation.17β-羟类固醇脱氢酶5型与凋亡抑制因子GRP78和肿瘤分泌蛋白PGK1呈负相关,并调节乳腺癌细胞的活力和增殖。
J Steroid Biochem Mol Biol. 2017 Jul;171:270-280. doi: 10.1016/j.jsbmb.2017.04.009. Epub 2017 Apr 27.

引用本文的文献

1
Incomplete ablation of thyroid cancer: Achilles' Heel?甲状腺癌消融不完全:阿喀琉斯之踵?
BMC Endocr Disord. 2024 Aug 9;24(1):146. doi: 10.1186/s12902-024-01659-5.
2
CRIP1 involves the pathogenesis of multiple myeloma via dual-regulation of proteasome and autophagy.CRIP1 通过双重调节蛋白酶体和自噬参与多发性骨髓瘤的发病机制。
EBioMedicine. 2024 Feb;100:104961. doi: 10.1016/j.ebiom.2023.104961. Epub 2024 Jan 9.

本文引用的文献

1
A novel tonicity-responsive microRNA miR-23a-5p modulates renal cell survival under osmotic stress through targeting heat shock protein 70 HSPA1B.一种新型的渗透压响应 microRNA miR-23a-5p 通过靶向热休克蛋白 70 HSPA1B 调节渗透压应激下的肾细胞存活。
Am J Physiol Cell Physiol. 2021 Feb 1;320(2):C225-C239. doi: 10.1152/ajpcell.00441.2020. Epub 2020 Nov 18.
2
MicroRNA-363-3p downregulation in papillary thyroid cancer inhibits tumor progression by targeting NOB1.微小 RNA-363-3p 在甲状腺乳头状癌中的下调通过靶向 NOB1 抑制肿瘤进展。
J Investig Med. 2021 Jan;69(1):66-74. doi: 10.1136/jim-2020-001562. Epub 2020 Oct 19.
3
BCLAF1 induces cisplatin resistance in lung cancer cells.
BCLAF1诱导肺癌细胞产生顺铂耐药性。
Oncol Lett. 2020 Nov;20(5):227. doi: 10.3892/ol.2020.12090. Epub 2020 Sep 11.
4
MiR-363 suppresses cell migration, invasion, and epithelial-mesenchymal transition of osteosarcoma by binding to NOB1.miR-363 通过与 NOB1 结合抑制骨肉瘤细胞迁移、侵袭和上皮-间充质转化。
World J Surg Oncol. 2020 May 1;18(1):83. doi: 10.1186/s12957-020-01859-y.
5
Bclaf1 is a direct target of HIF-1 and critically regulates the stability of HIF-1α under hypoxia.Bclaf1 是 HIF-1 的直接靶标,并在低氧条件下对 HIF-1α 的稳定性进行关键调控。
Oncogene. 2020 Mar;39(13):2807-2818. doi: 10.1038/s41388-020-1185-8. Epub 2020 Feb 6.
6
The Interplay Between the DNA Damage Response, RNA Processing and Extracellular Vesicles.DNA损伤反应、RNA加工与细胞外囊泡之间的相互作用
Front Oncol. 2020 Jan 17;9:1538. doi: 10.3389/fonc.2019.01538. eCollection 2019.
7
MicroRNA-612 inhibits cervical cancer progression by targeting NOB1.microRNA-612 通过靶向 NOB1 抑制宫颈癌进展。
J Cell Mol Med. 2020 Mar;24(5):3149-3156. doi: 10.1111/jcmm.14985. Epub 2020 Jan 22.
8
Silencing NOB1 Can Affect Cell Proliferation and Apoptosis Via the C-Jun N-Terminal Kinase Pathway in Colorectal Cancer.沉默NOB1可通过c-Jun氨基末端激酶途径影响结直肠癌细胞的增殖和凋亡。
J Invest Surg. 2021 Aug;34(8):819-825. doi: 10.1080/08941939.2019.1697401. Epub 2020 Jan 6.
9
BCLAF1 promotes cell proliferation, invasion and drug-resistance though targeting lncRNA NEAT1 in hepatocellular carcinoma.BCLAF1 通过靶向长链非编码 RNA NEAT1 促进肝癌细胞增殖、侵袭和耐药性。
Life Sci. 2020 Feb 1;242:117177. doi: 10.1016/j.lfs.2019.117177. Epub 2019 Dec 20.
10
Membrane-anchored heat-shock protein 70 (Hsp70) in cancer.膜结合热休克蛋白 70(Hsp70)与癌症。
Cancer Lett. 2020 Jan 28;469:134-141. doi: 10.1016/j.canlet.2019.10.037. Epub 2019 Oct 25.