The TINCR ubiquitin-like microprotein is a tumor suppressor in squamous cell carcinoma.
Lucia Morgado-PalacinJessie A BrownCholsoon JangJuana María García-PedreroFarhad ForouharS Aidan QuinnClara RegleroJoan VaughanYasamin Hajy HeydaryCynthia DonaldsonSandra Rodríguez-PeralesEva AlloncaRocio Granda-DiazAgustin F FernandezMario Fernández FragaArianna L KimJorge Santos-JuanesDavid M OwensJuan P RodrigoAlan SaghatelianAdolfo A FerrandoPublished in: Nature communications (2023)
The TINCR (Terminal differentiation-Induced Non-Coding RNA) gene is selectively expressed in epithelium tissues and is involved in the control of human epidermal differentiation and wound healing. Despite its initial report as a long non-coding RNA, the TINCR locus codes for a highly conserved ubiquitin-like microprotein associated with keratinocyte differentiation. Here we report the identification of TINCR as a tumor suppressor in squamous cell carcinoma (SCC). TINCR is upregulated by UV-induced DNA damage in a TP53-dependent manner in human keratinocytes. Decreased TINCR protein expression is prevalently found in skin and head and neck squamous cell tumors and TINCR expression suppresses the growth of SCC cells in vitro and in vivo. Consistently, Tincr knockout mice show accelerated tumor development following UVB skin carcinogenesis and increased penetrance of invasive SCCs. Finally, genetic analyses identify loss-of-function mutations and deletions encompassing the TINCR gene in SCC clinical samples supporting a tumor suppressor role in human cancer. Altogether, these results demonstrate a role for TINCR as protein coding tumor suppressor gene recurrently lost in squamous cell carcinomas.
Keyphrases
- squamous cell
- wound healing
- squamous cell carcinoma
- long non coding rna
- endothelial cells
- dna damage
- poor prognosis
- genome wide
- copy number
- pluripotent stem cells
- gene expression
- small molecule
- induced pluripotent stem cells
- diabetic rats
- dna methylation
- induced apoptosis
- signaling pathway
- transcription factor
- cell proliferation
- dna repair
- locally advanced