AI Article Synopsis

  • Head and neck cancers are a major global health concern, with limited predictive biomarkers and unsatisfactory survival rates despite advances in treatment.
  • Telomerase reactivation plays a crucial role in cancer development, and specific mutations in the TERT promoter are frequently observed in head and neck cancers, particularly in aggressive types like HPV-negative tumors.
  • Although several therapies targeting telomerase have been created, only a few have progressed to clinical trials, highlighting the need for more effective treatment options for patients with these mutations.

Article Abstract

Head and neck cancers (HNCs) are among the ten leading malignancies worldwide. Despite significant progress in all therapeutic modalities, predictive biomarkers, and targeted therapies for HNCs are limited and the survival rate is unsatisfactory. The importance of telomere maintenance via telomerase reactivation in carcinogenesis has been demonstrated in recent decades. Several mechanisms could activate telomerase reverse transcriptase (TERT), the most common of which is promoter alternation. Two major hotspot TERT promoter mutations (C228T and C250T) have been reported in different malignancies such as melanoma, genitourinary cancers, CNS tumors, hepatocellular carcinoma, thyroid cancers, sarcomas, and HNCs. The frequencies of TERT promoter mutations vary widely across tumors and is quite high in HNCs (11.9-64.7%). These mutations have been reported to be more enriched in oral cavity SCCs and HPV-negative tumors. The association between TERT promoter mutations and poor survival has also been demonstrated. Till now, several therapeutic strategies targeting telomerase have been developed although only a few drugs have been used in clinical trials. Here, we briefly review and summarize our current understanding and evidence of TERT promoter mutations in HNC patients.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10044978PMC
http://dx.doi.org/10.3390/biomedicines11030691DOI Listing

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