Suppr超能文献

DNA高甲基化导致BRMS1表达下调及其与三阴性乳腺癌转移进展的关系

Down-regulation of BRMS1 by DNA hypermethylation and its association with metastatic progression in triple-negative breast cancer.

作者信息

Kong Bin, Lv Zhi-Dong, Wang Yu, Jin Li-Ying, Ding Lei, Yang Zhao-Chuan

机构信息

Department of Breast Surgery, The Affiliated Hospital of Qingdao University Qingdao 266003, P. R. China.

Department of Cerebrovascular Disease Research Institute, The Affiliated Hospital of Qingdao University Qingdao 266003, P. R. China.

出版信息

Int J Clin Exp Pathol. 2015 Sep 1;8(9):11076-83. eCollection 2015.

Abstract

Breast cancer metastasis suppressor 1 (BRMS1) is a metastasis suppressor gene in several solid tumors. However, the expression and function of BRMS1 in triple-negative breast cancer (TNBC) have not been reported. In this study, we found that BRMS1 was down-regulation in breast cancer cell lines and primary TNBC, while decreased expression of BRMS1 mRNA was significantly associated with lymph node metastasis. And this down-regulation was found to be in accordance with aberrant methylation of the gene. Hypermethylation of the gene was observed in 53.4% (62/116) of the TNBC primary breast carcinomas, while it was found in only 24.1% (28/116) of the corresponding nonmalignant tissues. In addition, BRMS1 expression was restored in MDA-MB-231 after treatment with the demethylating agent, 5-aza-2-deoxycytidine (5-Aza-dC), and demethylation of the highly metastatic cells MDA-MB-231 induced invasion suppression of the cells. Furthermore, the suppression of BRMS1 by siRNA transfection enhanced cancer cells invasion. Collectively, our results suggest that the aberrant methylation of BRMS1 frequently occurs in the down-regulation of BRMS1 in TNBC and that it may play a role in the metastasis of breast cancer.

摘要

乳腺癌转移抑制因子1(BRMS1)是多种实体瘤中的一种转移抑制基因。然而,BRMS1在三阴性乳腺癌(TNBC)中的表达及功能尚未见报道。在本研究中,我们发现BRMS1在乳腺癌细胞系及原发性TNBC中表达下调,而BRMS1 mRNA表达降低与淋巴结转移显著相关。并且这种下调与该基因的异常甲基化有关。在53.4%(62/116)的TNBC原发性乳腺癌中观察到该基因的高甲基化,而在相应的非恶性组织中仅24.1%(28/116)发现高甲基化。此外,用去甲基化剂5-氮杂-2'-脱氧胞苷(5-Aza-dC)处理后,MDA-MB-231细胞中BRMS1表达得以恢复,且高转移性细胞MDA-MB-231的去甲基化诱导了细胞侵袭抑制。此外,通过小干扰RNA转染抑制BRMS1可增强癌细胞侵袭。总之,我们的结果表明,BRMS1的异常甲基化在TNBC中BRMS1下调时频繁发生,并且它可能在乳腺癌转移中起作用。

相似文献

2
[DNA methylation modification of BRMS1 in triple-negative breast cancer and its correlation with tumor metastasis].
Zhonghua Yi Xue Za Zhi. 2017 Nov 28;97(44):3483-3487. doi: 10.3760/cma.j.issn.0376-2491.2017.44.010.
3
Down-regulation of CXCL12 by DNA hypermethylation and its involvement in gastric cancer metastatic progression.
Dig Dis Sci. 2012 Mar;57(3):650-9. doi: 10.1007/s10620-011-1922-5. Epub 2011 Sep 29.
4
Suppression of human ovarian carcinoma metastasis by the metastasis-suppressor gene, BRMS1.
Int J Gynecol Cancer. 2006 Mar-Apr;16(2):522-31. doi: 10.1111/j.1525-1438.2006.00547.x.
5
Correlation of deregulated like-acetylglucosaminyl transferase and aberrant α-dystroglycan expression with human tongue cancer metastasis.
J Oral Maxillofac Surg. 2014 Jun;72(6):1106-18. doi: 10.1016/j.joms.2013.12.031. Epub 2014 Jan 15.
6
Epigenetic silencing of triple negative breast cancer hallmarks by Withaferin A.
Oncotarget. 2017 Jun 20;8(25):40434-40453. doi: 10.18632/oncotarget.17107.
7
XAF1 is frequently methylated in human esophageal cancer.
World J Gastroenterol. 2012 Jun 14;18(22):2844-9. doi: 10.3748/wjg.v18.i22.2844.
10
Aberrant methylation of WD-repeat protein 41 contributes to tumour progression in triple-negative breast cancer.
J Cell Mol Med. 2020 Jun;24(12):6869-6882. doi: 10.1111/jcmm.15344. Epub 2020 May 12.

引用本文的文献

2
Molecular interaction of metastasis suppressor genes and tumor microenvironment in breast cancer.
Explor Target Antitumor Ther. 2023;4(5):912-932. doi: 10.37349/etat.2023.00173. Epub 2023 Oct 11.
3
Metastasis suppressor genes in clinical practice: are they druggable?
Cancer Metastasis Rev. 2023 Dec;42(4):1169-1188. doi: 10.1007/s10555-023-10135-w. Epub 2023 Sep 25.
4
Cancer metastasis under the magnifying glass of epigenetics and epitranscriptomics.
Cancer Metastasis Rev. 2023 Dec;42(4):1071-1112. doi: 10.1007/s10555-023-10120-3. Epub 2023 Jun 28.
7
Epigenetic Alterations in Triple-Negative Breast Cancer-The Critical Role of Extracellular Matrix.
Cancers (Basel). 2021 Feb 9;13(4):713. doi: 10.3390/cancers13040713.
8
Small Ones to Fight a Big Problem-Intervention of Cancer Metastasis by Small Molecules.
Cancers (Basel). 2020 Jun 3;12(6):1454. doi: 10.3390/cancers12061454.
9
BRMS1: a multifunctional signaling molecule in metastasis.
Cancer Metastasis Rev. 2020 Sep;39(3):755-768. doi: 10.1007/s10555-020-09871-0.
10

本文引用的文献

1
Review of the development of DNA methylation as a marker of response to neoadjuvant therapy and outcomes in rectal cancer.
Clin Epigenetics. 2015 Jul 22;7(1):70. doi: 10.1186/s13148-015-0111-3. eCollection 2015.
2
Role of DNA methylation in renal cell carcinoma.
J Hematol Oncol. 2015 Jul 22;8:88. doi: 10.1186/s13045-015-0180-y.
5
Current approaches in treatment of triple-negative breast cancer.
Cancer Biol Med. 2015 Jun;12(2):106-16. doi: 10.7497/j.issn.2095-3941.2015.0030.
6
CIB1 depletion impairs cell survival and tumor growth in triple-negative breast cancer.
Breast Cancer Res Treat. 2015 Jul;152(2):337-46. doi: 10.1007/s10549-015-3458-4. Epub 2015 Jun 24.
7
Predictors for contralateral prophylactic mastectomy in breast cancer patients.
Int J Clin Exp Pathol. 2015 Apr 1;8(4):3748-64. eCollection 2015.
8
Differences in breast cancer characteristics and outcomes between Caucasian and Chinese women in the US.
Oncotarget. 2015 May 20;6(14):12774-82. doi: 10.18632/oncotarget.3666.
9
Novel role of PELP1 in regulating chemotherapy response in mutant p53-expressing triple negative breast cancer cells.
Breast Cancer Res Treat. 2015 Apr;150(3):487-99. doi: 10.1007/s10549-015-3339-x. Epub 2015 Mar 19.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验