Expression of Cellular and Extracellular TERRA , TERC and TERT in Hepatocellular Carcinoma.
Michele ManganelliIlaria GrossiJessica CorsiVito Giuseppe D'AgostinoKatarína JuríkováEmilio CusanelliSarah MolfinoNazario PortolaniAlessandro SalviGiuseppina De PetroPublished in: International journal of molecular sciences (2022)
Non-coding RNAs are transcribed from telomeres and the telomeric repeat-containing RNAs ( TERRA ) are implicated in telomere homeostasis and in cancer. In this study, we aimed to assess in hepatocellular carcinoma (HCC) the cellular and extracellular expression of TERRA , the telomerase RNA subunit ( TERC ) and the telomerase catalytic subunit ( TERT ). We determined by qPCR the expression level of TERRA 1_2_10_13q, TERRA 15q, TERRA XpYp, TERC and of TERT mRNA in HCC tissues and in the plasma of HCC patients. Further, we profiled the same transcripts in the HCC cell lines, HA22T/VGH and SKHep1C3, and in the extracellular vesicles (EVs) derived from their secretomes. We found that the expression of TERRA and TERT mRNA was significantly deregulated in HCC, being TERRA downregulated and TERT mRNA upregulated in HCC tissues vs. the peritumoral (PT) ones, and the receiver operating characteristic (ROC) curve analyses revealed a significant ability in discriminating HCC from PT tissue. Further, the determinations of circulating TERRA and TERC showed higher amounts of these transcripts in the plasma of HCC patients vs. controls and ROC analyses gave significant results. The expression characterization of the cultured HCC cells showed their ability to produce and secrete TERRA and TERC into the EVs; the ability to produce TERT mRNA that was not detectable in the EVs; and the ability to respond to sorafenib treatment increasing TERRA expression. Our results highlight that: (i) both cellular and extracellular expressions of TERRA and TERC are dysregulated in HCC as well as the cellular expression of TERT mRNA and (ii) the combined detection of TERRA and TERC in plasma may represent a promising approach for non-invasive diagnostic molecular indicators of HCC.
Keyphrases
- poor prognosis
- binding protein
- end stage renal disease
- newly diagnosed
- chronic kidney disease
- ejection fraction
- gene expression
- prognostic factors
- squamous cell carcinoma
- oxidative stress
- dna damage
- single cell
- single molecule
- endoplasmic reticulum stress
- smoking cessation
- lymph node metastasis
- pi k akt
- sensitive detection
- replacement therapy