EBioMedicine (Oct 2018)

Long non-coding RNA LINC-01572:28 inhibits granulosa cell growth via a decrease in p27 (Kip1) degradation in patients with polycystic ovary syndromeResearch in context

  • Jun Zhao,
  • Jieying Xu,
  • Wangshen Wang,
  • Han Zhao,
  • Hongbin Liu,
  • Xiaojing Liu,
  • Jiansheng Liu,
  • Yun Sun,
  • Andrea Dunaif,
  • Yanzhi Du,
  • Zi-Jiang Chen

Journal volume & issue
Vol. 36
pp. 526 – 538

Abstract

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Background: Disordered folliculogenesis is a key feature of polycystic ovary syndrome (PCOS), but the underlying molecular mechanism remains unclear. Methods: Long non-coding RNA (lncRNA) expression in luteinized granulosa cells (hLGCs) derived from women with and without PCOS were analyzed using microarray and qRT-PCR. Immortalized human granulosa cell lines were cultured for proliferation assays after transfection with the LINC-01572:28 over-expression vector in the presence or absence of p27 siRNA. Protein expression analysis, rescue assays, and RNA immunoprecipitation (RIP) were used to confirm the LINC-01572:28 substrate. Findings: LINC-01572:28 and p27 protein were elevated whereas proliferating cell nuclear antigen protein was decreased in the hLGCs of women with PCOS. LINC-01572:28 expression was positively correlated with basal testosterone levels. Over-expression of LINC-01572:28 inhibited cell proliferation and impeded G1/S transition, which were partially reversed by siRNA-mediated p27 knockdown. Interpretation: Our findings, therefore, suggest that LINC-01572:28 suppresses cell proliferation and cell cycle progression by reducing the degradation of p27 protein via SKP2 binding. Keywords: Polycystic ovary syndrome, lncRNA, Granulosa cells, Proliferation