[Identification of Novel Differentially Expressing Long Non- Coding RNAs with Oncogenic Potential]

O I Brovkina1,2,3, I V Pronina1, L A Uroshlev1,4

  • 1Research Institute of General Pathology and Pathophysiology, Moscow, 125315 Russia.

Molekuliarnaia Biologiia
|August 25, 2021
PubMed

Insights

New research identifies long non-coding RNAs (lncRNAs) as key players in ovarian cancer. Lnc-CCL28 and SNHG17 show increased levels in tumors, with LINC00152 and NEAT1 overexpression confirmed, linking them to advanced disease stages and metastasis.

Area of Science:

  • Molecular Biology
  • Genomics
  • Cancer Research

Background:

  • Long non-coding RNAs (lncRNAs) are increasingly recognized for their regulatory roles in gene expression.
  • Dysregulation of lncRNAs is implicated in various human diseases, including cancer.

Purpose of the Study:

  • To identify novel differentially expressed lncRNAs in ovarian tumors using deep machine learning.
  • To investigate the potential of specific lncRNAs as biomarkers for ovarian cancer diagnosis and prognosis.

Main Methods:

  • Deep machine learning was employed to identify differentially expressed lncRNAs in ovarian tumor samples.
  • Reverse transcription quantitative polymerase chain reaction (RT-PCR) was used to validate transcript levels of selected lncRNAs (lnc-CCL28, SNHG17, LINC00152, NEAT1).

Main Results:

  • Four novel lncRNAs (TMEM92-AS1, FAM222A-AS, TXLNB, and lnc-CCL28) were identified as differentially expressed in ovarian tumors.
  • For the first time, increased levels of lnc-CCL28 and SNHG17 were observed in ovarian tumors.
  • Overexpression of LINC00152 and NEAT1 was confirmed, and their levels were significantly associated with advanced stages and metastasis in ovarian cancer.

Conclusions:

  • lnc-CCL28 and SNHG17 represent novel potential biomarkers for ovarian cancer.
  • The overexpression of LINC00152 and lnc-CCL28 is linked to disease progression and metastasis, suggesting their involvement in ovarian carcinogenesis.