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早期乳腺癌中的 microRNA 表达谱。

MicroRNA Expression Profile in Early-Stage Breast Cancers.

机构信息

Institute of Bioinformatics, International Technology Park, Bangalore 560066, India.

Amrita School of Biotechnology, Amrita Vishwa Vidyapeetham, Kollam 691001, India.

出版信息

Microrna. 2024;13(1):71-81. doi: 10.2174/0122115366256479231003064842.

Abstract

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.

摘要

背景

乳腺癌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大的希望。导管原位癌被认为是乳腺浸润性导管癌的前驱病变。在这项研究中,我们对 7 例导管原位癌(DCIS)、6 例浸润性导管癌(ⅡA 期)和 5 例未配对的正常乳腺组织样本进行了 microRNA 测序。

方法

我们使用 miRge 进行 microRNA 分析、DESeq 进行差异表达分析以及 Cytoscape 进行竞争内源性 RNA 网络研究。

结果

在此,我们确定了 76 个在 DCIS 和 IDC 中差异表达的 miRNA。此外,我们提供了初步证据表明,miR-365b-3p 和 miR-7-1-3p 在 DCIS 中过表达,而 miR-487b-3p、miR-6507-5p 和 miR-654-3p 在 DCIS 中下调。我们还发现了一个在早期 IDC 中过表达的 miRNA miR-766-3p。在 32 个独立的乳腺癌组织样本中验证了 miR-301a-3p 在 DCIS 和 IDC 中的过表达。

结论

在 TCGA-BRCA 数据集,miR-301a-3p 的高表达与总生存不良相关,表明其可能与 DCIS 进展为 IDC 的高风险相关,值得进一步研究。

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