Tissue-based long non-coding RNAs "PVT1, TUG1 and MEG3" signature predicts Cisplatin resistance in ovarian Cancer

Genomics. 2020 Nov;112(6):4640-4646. doi: 10.1016/j.ygeno.2020.08.005. Epub 2020 Aug 8.

Abstract

Objectives: The current study aimed to investigate the potentiality of three lncRNAs "Plasmacytoma variant translocation 1(lnc-PVT1), Taurine upregulated gene type 1(lnc-TUG1) and Maternally expressed gene 3 (lnc-MEG-3)", to predict Cisplatin resistance in ovarian cancer (OC), in addition, to access their prognostic significance.

Methods: The expression level of lncRNAs were measured in 100 formalin-fixed paraffin-embedded tissue (FFET) samples of OC patients who were treated by Cisplatin-based chemotherapy using qPCR.

Results: The results showed that lnc_PVT1 was significantly upregulated by 2.3 folds in Cisplatin resistant tissues, while, lnc-TUG1 and lnc-MEG3 were downregulated by 1.2 and 3 folds, respectively. In addition, the three lncRNAs exhibited high sensitivity and specificity in predicting chemo-resistance and they were negatively associated with OS and progression-free survival (p < 0.001).

Conclusion: The lnc-PVT1, lnc-TUG1, and lnc-MEG3 transcriptome signatures could be used for predicting resistance to Cisplatin in OC patients.

Keywords: Cisplatin resistance; Lnc-MEG3; Lnc-PVT1; Lnc-TUG1; Long non-coding RNA; Ovarian cancer.

MeSH terms

  • Adult
  • Antineoplastic Agents / therapeutic use*
  • Cisplatin / therapeutic use*
  • Drug Resistance, Neoplasm / genetics
  • Female
  • Humans
  • Middle Aged
  • Ovarian Neoplasms / drug therapy*
  • Ovarian Neoplasms / genetics*
  • Ovarian Neoplasms / metabolism
  • Ovarian Neoplasms / mortality
  • RNA, Long Noncoding / metabolism*
  • Retrospective Studies

Substances

  • Antineoplastic Agents
  • MEG3 non-coding RNA, human
  • PVT1 long-non-coding RNA, human
  • RNA, Long Noncoding
  • TUG1 long noncoding RNA, human
  • Cisplatin