circRNA-associated ceRNA network construction reveals the circRNAs involved in the progression and prognosis of breast cancer.
Xiaoran MaCun LiuChundi GaoJie LiJing ZhuangLijuan LiuHuayao LiXue WangXiaoming ZhangShixia DongChao ZhouChanggang SunPublished in: Journal of cellular physiology (2019)
Recently, increasing evidences show that circular RNAs (circRNAs) are important regulators of various diseases, especially cancer. However, the regulatory role and the potential mechanism of action of circRNAs in breast cancer remain largely unknown. In this study, weighted gene co-expression network analysis was conducted with the differentially expressed miRNAs and mRNAs in breast cancer from The Cancer Genome Atlas database to identify the key modules associated with the carcinogenesis of breast cancer. In the significant turquoise and brown modules, 22 miRNAs and 1877 mRNAs were identified, respectively. Then, We compared and predicted the target genes and performed survival analysis to identify the miRNAs and mRNAs related to the prognosis of breast cancer. A circRNA-related competitive endogenous RNA network was identified by database co-screening, and deleted in liver cancer 1 (DLC1) was identified as a key gene. Finally, to assess how genes in key modules and key genes contribute to the development of breast cancer, relevant pathway information was obtained through DAVID and Gene Set Enrichment Analysis. These data demonstrated that three circRNAs (hsa-circ-0083373, hsa-circ-0083374, and hsa-circ-0083375) that regulate DLC1 expression via hsa-mir-511 and are involved in the pathogenesis and development of breast cancer.
Keyphrases
- network analysis
- genome wide
- genome wide identification
- poor prognosis
- long non coding rna
- healthcare
- copy number
- transcription factor
- emergency department
- squamous cell carcinoma
- papillary thyroid
- gene expression
- dna methylation
- big data
- climate change
- binding protein
- young adults
- adverse drug
- data analysis
- nucleic acid
- drug induced