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Systematic analysis of telomere length and somatic alterations in 31 cancer types.
Barthel, Floris P; Wei, Wei; Tang, Ming; Martinez-Ledesma, Emmanuel; Hu, Xin; Amin, Samirkumar B; Akdemir, Kadir C; Seth, Sahil; Song, Xingzhi; Wang, Qianghu; Lichtenberg, Tara; Hu, Jian; Zhang, Jianhua; Zheng, Siyuan; Verhaak, Roel G W.
Afiliação
  • Barthel FP; The Jackson Laboratory for Genomic Medicine, Farmington, Connecticut, USA.
  • Wei W; Oncology Graduate School Amsterdam, VU University Medical Center, Amsterdam, the Netherlands.
  • Tang M; Department of Genomic Medicine, the University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Martinez-Ledesma E; Department of Biostatistics, the University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Hu X; Department of Genomic Medicine, the University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Amin SB; Department of Genomic Medicine, the University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Akdemir KC; Department of Neuro-Oncology, the University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Seth S; Department of Genomic Medicine, the University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Song X; Program in Biostatistics, Bioinformatics, and Systems Biology, the University of Texas Graduate School of Biomedical Sciences at Houston, Houston, Texas, USA.
  • Wang Q; Department of Genomic Medicine, the University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Lichtenberg T; Graduate Program in Structural and Computational Biology and Molecular Biophysics, Baylor College of Medicine, Houston, Texas, USA.
  • Hu J; Department of Genomic Medicine, the University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Zhang J; Institute for Applied Cancer Science, the University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Zheng S; Institute for Applied Cancer Science, the University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Verhaak RG; Department of Genomic Medicine, the University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Nat Genet ; 49(3): 349-357, 2017 Mar.
Article em En | MEDLINE | ID: mdl-28135248
Cancer cells survive cellular crisis through telomere maintenance mechanisms. We report telomere lengths in 18,430 samples, including tumors and non-neoplastic samples, across 31 cancer types. Telomeres were shorter in tumors than in normal tissues and longer in sarcomas and gliomas than in other cancers. Among 6,835 cancers, 73% expressed telomerase reverse transcriptase (TERT), which was associated with TERT point mutations, rearrangements, DNA amplifications and transcript fusions and predictive of telomerase activity. TERT promoter methylation provided an additional deregulatory TERT expression mechanism. Five percent of cases, characterized by undetectable TERT expression and alterations in ATRX or DAXX, demonstrated elongated telomeres and increased telomeric repeat-containing RNA (TERRA). The remaining 22% of tumors neither expressed TERT nor harbored alterations in ATRX or DAXX. In this group, telomere length positively correlated with TP53 and RB1 mutations. Our analysis integrates TERT abnormalities, telomerase activity and genomic alterations with telomere length in cancer.
Assuntos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Telômero / Mutação Puntual / Neoplasias Limite: Humans Idioma: En Revista: Nat Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Telômero / Mutação Puntual / Neoplasias Limite: Humans Idioma: En Revista: Nat Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos