早期乳腺癌中微小RNA的表达谱。

Krishna Patel, Deva Magendhra Rao, Shirley Sundersingh, Sridevi Velusami, Thangarajan Rajkumar, Bipin Nair, Akhilesh Pandey, Aditi Chatterjee, Samson Mani, Harsha Gowda
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引用次数: 0

摘要

背景:癌症是女性癌症死亡的主要原因之一。早期诊断为治愈提供了最好的希望。原位导管癌被认为是乳腺浸润性导管癌的前兆。在本研究中,我们对7例导管原位癌(DCIS)、6例浸润性导管癌(IDC IIA期)的配对正常和5例未配对正常乳腺组织样本进行了微小RNA测序。我们鉴定了76种在DCIS和IDC中差异表达的miRNA。我们还鉴定了一种在早期IDC中过表达的miRNA miR-766-3p。在32个独立的癌症组织样本中证实了miR-301a-3p在DCIS和IDC中的过度表达。结果:在Can-cer基因组图谱乳腺癌症(TCGA-BRCA)数据集中,miR-301a-3p的高表达与总体生存率低有关,这表明它可能与DCIS有关,进展为IDC的风险很高,需要进行更深入的研究。结论:我们还分析了与差异表达miRNA相关的竞争性内源性网络,并确定LRRC75A-AS1和MAGI2-AS3是可能在早期乳腺癌中发挥重要作用的lncRNA。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
MicroRNA Expression Profile in Early-Stage Breast Cancers.

Background: Breast cancer is one of the leading causes of cancer deaths in women. Early diagnosis offers the best hope for a cure. Ductal carcinoma in situ is considered a precursor of invasive ductal carcinoma of the breast. In this study, we carried out microRNA sequencing from 7 ductal carcinoma in situ (DCIS), 6 infiltrating ductal carcinomas (IDC Stage IIA) with paired normal, and 5 unpaired normal breast tissue samples.

Methods: We have deployed miRge for microRNA analysis, DESeq for differential expression analysis, and Cytoscape for competing endogenous RNA network investigation.

Results: Here, we identified 76 miRNAs that were differentially expressed in DCIS and IDC. Additionally, we provide preliminary evidence of miR-365b-3p and miR-7-1-3p being overexpressed, and miR-6507-5p, miR-487b-3p, and miR-654-3p being downregulated in DCIS relative to normal breast tissue. We also identified a miRNA miR-766-3p that was overexpressed in earlystage IDCs. The overexpression of miR-301a-3p in DCIS and IDC was confirmed in 32 independent breast cancer tissue samples.

Conclusion: Higher expression of miR-301a-3p is associated with poor overall survival in The Cancer Genome Atlas Breast Cancer (TCGA-BRCA) dataset, indicating that it may be associated with DCIS at high risk of progressing to IDC and warrants deeper investigation.

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