Proteomic identification of proteins differentially expressed following overexpression of hTERT (human telomerase reverse transcriptase) in cancer cells

PLoS One. 2017 Jul 13;12(7):e0181027. doi: 10.1371/journal.pone.0181027. eCollection 2017.

Abstract

Reverse transcriptase activity of telomerase adds telomeric repeat sequences at extreme ends of the newly replicated chromosome in actively dividing cells. Telomerase expression is not detected in terminally differentiated cells but is noticeable in 90% of the cancer cells. hTERT (human telomerase reverse transcriptase) expression seems to promote invasiveness of cancer cells. We here present proteomic profiles of cells overexpressing or knocked down for hTERT. This study also attempts to find out the potential interacting partners of hTERT in cancer cell lines. Two-dimensional gel electrophoresis (2-DE) of two different cell lines U2OS (a naturally hTERT negative cell line) and HeLa revealed differential expression of proteins in hTERT over-expressing cells. In U2OS cell line 28 spots were picked among which 23 spots represented upregulated and 5 represented down regulated proteins. In HeLa cells 21 were upregulated and 2 were down regulated out of 23 selected spots under otherwise identical experimental conditions. Some heat shock proteins viz. Hsp60 and Hsp70 and GAPDH, which is a housekeeping gene, were found similarly upregulated in both the cell lines. The upregulation of these proteins were further confirmed at RNA and protein level by real-time PCR and western blotting respectively.

MeSH terms

  • Cell Line, Tumor
  • Gene Expression Regulation, Neoplastic
  • HeLa Cells
  • Humans
  • Neoplasms / genetics
  • Neoplasms / metabolism*
  • Proteome / genetics
  • Proteome / metabolism*
  • Proteomics / methods
  • Telomerase / genetics*

Substances

  • Proteome
  • TERT protein, human
  • Telomerase

Grants and funding

The authors received no specific funding for this work.