Long intergenic non-protein coding RNA 324 prevents breast cancer progression by modulating miR-10b-5p

Aging (Albany NY). 2020 Apr 18;12(8):6680-6699. doi: 10.18632/aging.103021. Epub 2020 Apr 18.

Abstract

Mounting evidence suggests that long noncoding RNAs serve as specific biomarkers and potent modulators of multiple cancers. Long intergenic non-protein coding RNA 324 (LINC00324) is ubiquitously expressed in various tissues, including breast cancer. The biological function of LINC00324 in the development and progression of breast cancer remains unknown. Here, we fully elucidate the relation between LINC00324 expression and breast cancer, and suggest a potential mechanism of action. We found that decreased expression of LINC00324 was dramatically correlated with malignancy of breast cancer, both in breast cancer tissues and in cell lines. Overexpression of LINC00324 in MDA-MB-231 cells resulted in a decrease in cell proliferation, invasion, and migration, while increasing cells apoptosis. On the other hand, loss-of-function experiments indicated that deficiency of LINC00324 promoted malignant phenotypes in breast cancer cells. Mechanically, we found that LINC00324 is mainly distributed in the cytoplasm, fostering the expression of E-cadherin by sponging miR-10b-5p. Taken together, these findings suggest that LINC00324 plays a critical role in breast cancer progression by directly interacting with miR-10b-5p. LINC00324 can thus potentially act as an early diagnostic marker and a novel therapeutic agent for breast cancer.

Keywords: E-cadherin; LINC00324; breast cancer; ceRNA; miR-10b-5p.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / genetics
  • Biomarkers
  • Breast Neoplasms / genetics*
  • Breast Neoplasms / pathology*
  • Cadherins / genetics
  • Cadherins / metabolism
  • Cell Line, Tumor
  • Cell Movement / genetics
  • Cell Proliferation / genetics
  • Databases, Genetic
  • Disease Progression*
  • Down-Regulation
  • Epithelial-Mesenchymal Transition / genetics
  • Female
  • Gene Expression
  • Gene Knockdown Techniques
  • Humans
  • Mice
  • MicroRNAs / genetics*
  • Neoplasm Transplantation
  • RNA, Long Noncoding / genetics
  • RNA, Long Noncoding / metabolism*
  • Survival Rate

Substances

  • Biomarkers
  • Cadherins
  • MIRN10 microRNA, human
  • MIRN10 microRNA, mouse
  • MicroRNAs
  • RNA, Long Noncoding