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Mutational signatures and mutagenic impacts associated with betel quid chewing in oral squamous cell carcinoma.
Su, Shih-Chi; Chang, Lun-Ching; Lin, Chiao-Wen; Chen, Mu-Kuan; Yu, Chun-Ping; Chung, Wen-Hung; Yang, Shun-Fa.
Afiliação
  • Su SC; Whole-Genome Research Core Laboratory of Human Diseases, Chang Gung Memorial Hospital, Keelung, Taiwan.
  • Chang LC; Department of Dermatology, Drug Hypersensitivity Clinical and Research Center, Chang Gung Memorial Hospital, Linkou, Taiwan.
  • Lin CW; Department of Mathematical Sciences, Florida Atlantic University, Boca Raton, FL, USA.
  • Chen MK; Institute of Oral Sciences, Chung Shan Medical University, Taichung, Taiwan.
  • Yu CP; Department of Dentistry, Chung Shan Medical University Hospital, Taichung, Taiwan.
  • Chung WH; Department of Otorhinolaryngology-Head and Neck Surgery, Changhua Christian Hospital, Changhua, Taiwan.
  • Yang SF; Biodiversity Research Center, Academia Sinica, Taipei, Taiwan.
Hum Genet ; 138(11-12): 1379-1389, 2019 Dec.
Article em En | MEDLINE | ID: mdl-31679052
ABSTRACT
Betel quid (BQ) chewing is a prevailing risk for oral squamous cell carcinoma (OSCC) in Southeast Asia. Yet, the detailed mechanisms by which BQ chewing damages the genome are still not fully understood. Through exome sequencing of tumor-normal pairs from 196 male patients with OSCC, including 95 habitual BQ chewers and 101 non-BQ users, we conducted a quantitative survey of mutational signatures and genomic aberrations and explored their association with BQ chewing. We found that BQ-associated elevation in mutation rate was seen in cancers of the tongue, but not in overall OSCC. Additionally, we identified a mutational signature that is enriched in tumors from BQ users. Moreover, the numbers of small insertions and deletions (INDELs) and breakpoints derived from structural variations (SV) were increased, whereas the extent of loss of heterozygosity was decreased in BQ-related OSCC genomes. However, neither the number of base substitutions and microsatellite instability events nor the extent of copy-number alterations differed between BQ-related and -unrelated OSCC. In conclusion, consistent with the proposition that BQ chewing increases OSCC risk as a mutagen, our results unveil a BQ-associated mutational signature and indicate mutagenic impacts of BQ chewing on preferentially eliciting INDELs and SV-related breakpoints in OSCC genomes.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Areca / Neoplasias Bucais / Carcinoma de Células Escamosas / Biomarcadores Tumorais / Regulação Neoplásica da Expressão Gênica / Mastigação / Mutação Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Hum Genet Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Taiwan

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Areca / Neoplasias Bucais / Carcinoma de Células Escamosas / Biomarcadores Tumorais / Regulação Neoplásica da Expressão Gênica / Mastigação / Mutação Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Hum Genet Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Taiwan