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胰岛素受体通过降低细胞迁移能力与三阴性乳腺癌相关。

Insulin receptor is implicated in triple-negative breast cancer by decreasing cell mobility.

作者信息

Yang Ying, Chen Xiang, Ma Changyan

机构信息

Department of Medical Genetics, School of Basic Medical Sciences, Nanjing Medical University, Nanjing, Jiangsu 211166, China.

Department of General Surgery, the Affiliated Yixing Hospital of Jiangsu University, Yixing, Jiangsu 214200, China.

出版信息

J Biomed Res. 2020 Aug 28;35(3):189-196. doi: 10.7555/JBR.34.20200082.

DOI:10.7555/JBR.34.20200082
PMID:33911052
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8193710/
Abstract

Triple-negative breast cancer (TNBC) has a poor prognosis and typically earlier onset of metastasis in comparison with other breast cancer subtypes. It has been reported that insulin receptor (INSR) is downregulated in TNBC, however, its clinical significance and functions in TNBC remain to be elucidated. In this study, we found that INSR expression was significantly downregulated in TNBC, and overexpression of INSR suppressed cell migration and invasion in TNBC. In addition, the survival rate of breast cancer patients with low INSR expression was lower than that of patients with high INSR expression. INSR expression was significantly correlated with lymph node metastasis, clinical tumor stages, ER status, PR status, and the proliferation index Ki-67 expression. In summary, our study suggests that INSR may serve as a biomarker for breast cancer prognosis and it may be a potential target for TNBC treatment.

摘要

三阴性乳腺癌(TNBC)预后较差,与其他乳腺癌亚型相比,通常转移发生得更早。据报道,胰岛素受体(INSR)在TNBC中表达下调,然而,其在TNBC中的临床意义和功能仍有待阐明。在本研究中,我们发现INSR表达在TNBC中显著下调,并且INSR的过表达抑制了TNBC中的细胞迁移和侵袭。此外,INSR低表达的乳腺癌患者的生存率低于INSR高表达的患者。INSR表达与淋巴结转移、临床肿瘤分期、雌激素受体(ER)状态、孕激素受体(PR)状态以及增殖指数Ki-67表达显著相关。总之,我们的研究表明,INSR可能作为乳腺癌预后的生物标志物,并且它可能是TNBC治疗的潜在靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01a6/8193710/5da746648af5/jbr-35-3-189-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01a6/8193710/44b29af977b7/jbr-35-3-189-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01a6/8193710/77849f207b11/jbr-35-3-189-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01a6/8193710/5da746648af5/jbr-35-3-189-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01a6/8193710/44b29af977b7/jbr-35-3-189-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01a6/8193710/77849f207b11/jbr-35-3-189-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01a6/8193710/5da746648af5/jbr-35-3-189-3.jpg

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Targeting DNA methylation for treating triple-negative breast cancer.针对 DNA 甲基化治疗三阴性乳腺癌。
Pharmacogenomics. 2019 Nov;20(16):1151-1157. doi: 10.2217/pgs-2019-0078.
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Patterns of Mutation Enrichment in Metastatic Triple-Negative Breast Cancer.转移性三阴性乳腺癌中的突变富集模式
Clin Med Insights Oncol. 2019 Aug 9;13:1179554919868482. doi: 10.1177/1179554919868482. eCollection 2019.
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STAT3 as a potential therapeutic target in triple negative breast cancer: a systematic review.STAT3 作为三阴性乳腺癌潜在治疗靶点的系统评价。
J Exp Clin Cancer Res. 2019 May 14;38(1):195. doi: 10.1186/s13046-019-1206-z.
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New Insights into the Implication of Epigenetic Alterations in the EMT of Triple Negative Breast Cancer.三阴性乳腺癌上皮-间质转化中表观遗传改变影响的新见解
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