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Telomere sequence content can be used to determine ALT activity in tumours.
Lee, Michael; Teber, Erdahl T; Holmes, Oliver; Nones, Katia; Patch, Ann-Marie; Dagg, Rebecca A; Lau, Loretta M S; Lee, Joyce H; Napier, Christine E; Arthur, Jonathan W; Grimmond, Sean M; Hayward, Nicholas K; Johansson, Peter A; Mann, Graham J; Scolyer, Richard A; Wilmott, James S; Reddel, Roger R; Pearson, John V; Waddell, Nicola; Pickett, Hilda A.
Afiliación
  • Lee M; Telomere Length Regulation Unit, Children's Medical Research Institute, University of Sydney, Westmead, New South Wales, Australia.
  • Teber ET; Bioinformatics Unit, Children's Medical Research Institute, University of Sydney, Westmead, New South Wales, Australia.
  • Holmes O; Genome Informatics Group, QIMR Berghofer Medical Research Institute, Herston, Queensland, Australia.
  • Nones K; Medical Genomics Group, QIMR Berghofer Medical Research Institute, Herston, Queensland, Australia.
  • Patch AM; Medical Genomics Group, QIMR Berghofer Medical Research Institute, Herston, Queensland, Australia.
  • Dagg RA; Cancer Research Unit, Children's Medical Research Institute, University of Sydney, Westmead, New South Wales, Australia.
  • Lau LMS; Cancer Research Unit, Children's Medical Research Institute, University of Sydney, Westmead, New South Wales, Australia.
  • Lee JH; Cancer Research Unit, Children's Medical Research Institute, University of Sydney, Westmead, New South Wales, Australia.
  • Napier CE; Cancer Research Unit, Children's Medical Research Institute, University of Sydney, Westmead, New South Wales, Australia.
  • Arthur JW; Bioinformatics Unit, Children's Medical Research Institute, University of Sydney, Westmead, New South Wales, Australia.
  • Grimmond SM; University of Melbourne Centre for Cancer Research, University of Melbourne, Melbourne, Victoria, Australia.
  • Hayward NK; Melanoma Institute Australia, University of Sydney, North Sydney, New South Wales, Australia.
  • Johansson PA; Oncogenomics Group, QIMR Berghofer Medical Research Institute, Herston, Queensland, Australia.
  • Mann GJ; Oncogenomics Group, QIMR Berghofer Medical Research Institute, Herston, Queensland, Australia.
  • Scolyer RA; Melanoma Institute Australia, University of Sydney, North Sydney, New South Wales, Australia.
  • Wilmott JS; Centre for Cancer Research, Westmead Institute for Medical Research, University of Sydney, Westmead, New South Wales, Australia.
  • Reddel RR; Melanoma Institute Australia, University of Sydney, North Sydney, New South Wales, Australia.
  • Pearson JV; Discipline of Pathology, Sydney Medical School, University of Sydney, Sydney, New South Wales, Australia.
  • Waddell N; Tissue Pathology and Diagnostic Oncology, Royal Prince Alfred Hospital, New South Wales, Australia.
  • Pickett HA; Melanoma Institute Australia, University of Sydney, North Sydney, New South Wales, Australia.
Nucleic Acids Res ; 46(10): 4903-4918, 2018 06 01.
Article en En | MEDLINE | ID: mdl-29718321
ABSTRACT
The replicative immortality of human cancer cells is achieved by activation of a telomere maintenance mechanism (TMM). To achieve this, cancer cells utilise either the enzyme telomerase, or the Alternative Lengthening of Telomeres (ALT) pathway. These distinct molecular pathways are incompletely understood with respect to activation and propagation, as well as their associations with clinical outcomes. We have identified significant differences in the telomere repeat composition of tumours that use ALT compared to tumours that do not. We then employed a machine learning approach to stratify tumours according to telomere repeat content with an accuracy of 91.6%. Importantly, this classification approach is applicable across all tumour types. Analysis of pathway mutations that were under-represented in ALT tumours, across 1,075 tumour samples, revealed that the autophagy, cell cycle control of chromosomal replication, and transcriptional regulatory network in embryonic stem cells pathways are involved in the survival of ALT tumours. Overall, our approach demonstrates that telomere sequence content can be used to stratify ALT activity in cancers, and begin to define the molecular pathways involved in ALT activation.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Telómero / Biología Computacional / Homeostasis del Telómero / Neoplasias Límite: Female / Humans Idioma: En Revista: Nucleic Acids Res Año: 2018 Tipo del documento: Article País de afiliación: Australia

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Telómero / Biología Computacional / Homeostasis del Telómero / Neoplasias Límite: Female / Humans Idioma: En Revista: Nucleic Acids Res Año: 2018 Tipo del documento: Article País de afiliación: Australia