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Germline mutations in Protection of Telomeres 1 in two families with Hodgkin lymphoma.
McMaster, Mary L; Sun, Chongkui; Landi, Maria T; Savage, Sharon A; Rotunno, Melissa; Yang, Xiaohong R; Jones, Kristine; Vogt, Aurélie; Hutchinson, Amy; Zhu, Bin; Wang, Mingyi; Hicks, Belynda; Thirunavukarason, Anand; Stewart, Douglas R; Koutros, Stella; Goldstein, Alisa M; Chanock, Stephen J; Caporaso, Neil E; Tucker, Margaret A; Goldin, Lynn R; Liu, Yie.
Afiliación
  • McMaster ML; Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute; NIH, Bethesda, MD, USA.
  • Sun C; Laboratory of Molecular Gerontology, National Institute on Aging/National Institute of Health, Baltimore, MD, USA.
  • Landi MT; Integrative Tumor Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute; NIH, Bethesda, MD, USA.
  • Savage SA; Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute; NIH, Bethesda, MD, USA.
  • Rotunno M; Epidemiology and Genomics Research Program, Division of Cancer Control and Population Sciences, National Cancer Institute, NIH, Bethesda, MD, USA.
  • Yang XR; Integrative Tumor Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute; NIH, Bethesda, MD, USA.
  • Jones K; Cancer Genomics Research Laboratory, Division of Cancer Epidemiology and Genetics, National Cancer Institute; NIH, Bethesda, MD, USA.
  • Vogt A; Cancer Genomics Research Laboratory, Division of Cancer Epidemiology and Genetics, National Cancer Institute; NIH, Bethesda, MD, USA.
  • Hutchinson A; Cancer Genomics Research Laboratory, Division of Cancer Epidemiology and Genetics, National Cancer Institute; NIH, Bethesda, MD, USA.
  • Zhu B; Cancer Genomics Research Laboratory, Division of Cancer Epidemiology and Genetics, National Cancer Institute; NIH, Bethesda, MD, USA.
  • Wang M; Cancer Genomics Research Laboratory, Division of Cancer Epidemiology and Genetics, National Cancer Institute; NIH, Bethesda, MD, USA.
  • Hicks B; Cancer Genomics Research Laboratory, Division of Cancer Epidemiology and Genetics, National Cancer Institute; NIH, Bethesda, MD, USA.
  • Thirunavukarason A; Laboratory of Molecular Gerontology, National Institute on Aging/National Institute of Health, Baltimore, MD, USA.
  • Stewart DR; Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute; NIH, Bethesda, MD, USA.
  • Koutros S; Occupational and Environmental Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute; NIH, Bethesda, MD, USA.
  • Goldstein AM; Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute; NIH, Bethesda, MD, USA.
  • Chanock SJ; Division of Cancer Epidemiology and Genetics, National Cancer Institute; NIH, Bethesda, MD, USA.
  • Caporaso NE; Occupational and Environmental Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute; NIH, Bethesda, MD, USA.
  • Tucker MA; Human Genetics Program, Division of Cancer Epidemiology and Genetics, National Cancer Institute; NIH, Bethesda, MD, USA.
  • Goldin LR; Integrative Tumor Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute; NIH, Bethesda, MD, USA.
  • Liu Y; Laboratory of Molecular Gerontology, National Institute on Aging/National Institute of Health, Baltimore, MD, USA.
Br J Haematol ; 181(3): 372-377, 2018 05.
Article en En | MEDLINE | ID: mdl-29693246
ABSTRACT
In a previous whole exome sequencing of patients from 41 families with Hodgkin lymphoma, we identified two families with distinct heterozygous rare coding variants in POT1 (D224N and Y36H), both in a highly conserved region of the gene. POT1 D224N mutant did not bind to a single-stranded telomere oligonucleotide in vitro suggesting the mutation perturbs POT1's ability to bind to the telomeric G-rich overhang. Human HT1080 cells expressing POT1 D224N and lymphoblastoid cells carrying Y36H both showed increased telomere length and fragility in comparison to wild type cells. This strongly suggests that mutant POT1 causes chromosome instability and may play a role in lymphomagenesis in these families.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedad de Hodgkin / Familia / Mutación de Línea Germinal / Mutación Missense / Proteínas de Unión a Telómeros / Inestabilidad Cromosómica Tipo de estudio: Prognostic_studies Límite: Female / Humans / Male Idioma: En Revista: Br J Haematol Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedad de Hodgkin / Familia / Mutación de Línea Germinal / Mutación Missense / Proteínas de Unión a Telómeros / Inestabilidad Cromosómica Tipo de estudio: Prognostic_studies Límite: Female / Humans / Male Idioma: En Revista: Br J Haematol Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos
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