MicroRNA Expression Profile in Early-Stage Breast Cancers

被引:0
|
作者
Patel, Krishna [1 ,2 ]
Rao, Deva Magendhra [3 ]
Sundersingh, Shirley [4 ]
Velusami, Sridevi [5 ]
Rajkumar, Thangarajan [3 ]
Nair, Bipin [2 ]
Pandey, Akhilesh [1 ,6 ,7 ,8 ,9 ]
Chatterjee, Aditi [1 ,8 ]
Mani, Samson [3 ]
Gowda, Harsha [1 ,2 ,8 ]
机构
[1] Int Technol Pk, Inst Bioinformat, Bangalore 560066, India
[2] Amrita Vishwa Vidyapeetham, Amrita Sch Biotechnol, Kollam 691001, India
[3] Canc Inst WIA, Dept Mol Oncol, Chennai 600036, India
[4] Canc Inst WIA, Dept Oncopathol, Chennai, India
[5] Canc Inst WIA, Dept Surg Oncol, Chennai, India
[6] Mayo Clin, Dept Lab Med & Pathol, Rochester, MN 55905 USA
[7] Mayo Clin, Ctr Individualized Med, Rochester, MN 55905 USA
[8] Manipal Acad Higher Educ MAHE, Manipal 576104, Karnataka, India
[9] Natl Inst Mental Hlth & Neurosci NIMHANS, Ctr Mol Med, Hosur Rd, Bangalore 560029, India
关键词
Next Generation sequencing; small RNAs; benign tumor; breast cancer; ceRNA; DCIS; CARCINOMA IN-SITU; RNA EXPRESSION; PROGRESSION; BIOMARKERS; SIGNATURE; ALIGNMENT; DATABASE; MIRNAS; MARKER; GENES;
D O I
10.2174/0122115366256479231003064842
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 early-stage 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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页码:71 / 81
页数:11
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