A comprehensive analysis of coding and non-coding transcriptomic changes in cutaneous squamous cell carcinoma.
Kunal Das MahapatraLorenzo PasqualiJonas Nørskov SøndergaardJan LapinsIstván Balazs NemethEszter BaltásLajos KemenyBernhard HomeyLiviu-Ionut MoldovanJørgen KjemsClaudia KutterEnikö SonkolyLasse Sommer KristensenAndor PivarcsiPublished in: Scientific reports (2020)
Cutaneous Squamous Cell Carcinoma (cSCC) is the most common and fastest-increasing cancer with metastatic potential. Long non-coding RNAs (lncRNAs) and circular RNAs (circRNAs) are novel regulators of gene expression. To identify mRNAs, lncRNAs and circRNAs, which can be involved in cSCC, RNA-seq was performed on nine cSCCs and seven healthy skin samples. Representative transcripts were validated by NanoString nCounter assays using an extended cohort, which also included samples from pre-cancerous skin lesions (actinic keratosis). 5,352 protein-coding genes, 908 lncRNAs and 55 circular RNAs were identified to be differentially expressed in cSCC. Targets of 519 transcription factors were enriched among differentially expressed genes, 105 of which displayed altered level in cSCCs, including fundamental regulators of skin development (MYC, RELA, ETS1, TP63). Pathways related to cell cycle, apoptosis, inflammation and epidermal differentiation were enriched. In addition to known oncogenic lncRNAs (PVT1, LUCAT1, CASC9), a set of skin-specific lncRNAs were were identified to be dysregulated. A global downregulation of circRNAs was observed in cSCC, and novel skin-enriched circRNAs, circ_IFFO2 and circ_POF1B, were identified and validated. In conclusion, a reference set of coding and non-coding transcripts were identified in cSCC, which may become potential therapeutic targets or biomarkers.
Keyphrases
- transcription factor
- genome wide identification
- squamous cell carcinoma
- rna seq
- genome wide analysis
- cell cycle
- wound healing
- soft tissue
- gene expression
- long non coding rna
- single cell
- oxidative stress
- network analysis
- cell proliferation
- genome wide
- small cell lung cancer
- poor prognosis
- dna methylation
- high throughput
- dna binding
- lymph node metastasis
- endoplasmic reticulum stress
- small molecule
- human health
- radiation therapy
- amino acid