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A computational study of non-coding RNAs on the regulation of activating transcription factor 3 in human breast cancer cells.

Abstract
We previously reported that activating transcription factor 3 (ATF3), an adaptive response gene, plays a dichotomous role in regulating several molecular processes during breast cancer progression. ATF3 promoted the expression of runt-related transcription factor 2 (Runx2, a metastatic gene) and activated matrix metalloproteinase 13 (MMP13, an invasive gene), thereby fostering proliferation and bone-metastasis of the breast cancer cells. Targeting ATF3 may mitigate the metastatic spread of breast cancer and improve the patient's lifespan. Non-coding RNAs (ncRNAs) such as microRNAs (miRNAs), long non-coding RNAs (lncRNAs), and circular RNAs (circRNAs) are the new-era regimens that are currently utilized for diagnosis and treatment of a variety of malignancies including cancer. mir-3674 putatively targets ATF3, but its expression was significantly increased in human breast cancer cells (MDA-MB231), compared to normal human mammary epithelial cells (MCF-10A). Our in silico analysis identified a few lncRNAs and circRNAs showing their putative binding sites for miR-3674. Thus, mir-3674, despite its abundance in the MDA-MB231 cells, could not effectively target ATF3, which could be due to the sponging mechanism of lncRNAs and circRNAs towards mir-3674. More extensive in vitro and in vivo studies are required to validate this and expand the diagnostic and therapeutic perspectives of breast cancer.
AuthorsR L Akshaya, N Akshaya, N Selvamurugan
JournalComputational biology and chemistry (Comput Biol Chem) Vol. 89 Pg. 107386 (Dec 2020) ISSN: 1476-928X [Electronic] England
PMID33068918 (Publication Type: Journal Article)
CopyrightCopyright © 2020 Elsevier Ltd. All rights reserved.
Chemical References
  • ATF3 protein, human
  • Activating Transcription Factor 3
  • MicroRNAs
  • RNA, Circular
  • RNA, Long Noncoding
Topics
  • Activating Transcription Factor 3 (metabolism)
  • Breast Neoplasms (metabolism)
  • Cell Line, Tumor
  • Computational Biology
  • Computer Simulation
  • Disease Progression
  • Gene Expression Regulation, Neoplastic (physiology)
  • Humans
  • MicroRNAs (metabolism)
  • RNA, Circular (metabolism)
  • RNA, Long Noncoding (metabolism)

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