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Sökning: WFRF:(Zachariadis Vasilios) > (2015-2019) > Predisposition to c...

Predisposition to childhood acute lymphoblastic leukemia caused by a constitutional translocation disrupting ETV6

Jarviaho, Tekla (författare)
Univ Oulu, PEDEGO Res Unit, Oulu, Finland;Univ Oulu, Med Res Ctr, Oulu, Finland;Oulu Univ Hosp, Oulu, Finland;Univ Oulu, Bioctr Oulu, Oulu, Finland
Bang, Benedicte (författare)
Karolinska Institutet
Zachariadis, Vasilios (författare)
Karolinska Institutet
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Taylan, Fulya (författare)
Karolinska Institutet
Moilanen, Jukka (författare)
Univ Oulu, PEDEGO Res Unit, Oulu, Finland;Univ Oulu, Med Res Ctr, Oulu, Finland;Oulu Univ Hosp, Oulu, Finland;Oulu Univ Hosp, Dept Clin Genet, Oulu, Finland
Mottonen, Merja (författare)
Univ Oulu, PEDEGO Res Unit, Oulu, Finland;Oulu Univ Hosp, Dept Children & Adolescents, Oulu, Finland
Smith, C. I. Edvard (författare)
Karolinska Institutet
Harila-Saari, Arja H. (författare)
Uppsala universitet,Barnneurologi/Barnonkologi
Niinimaki, Riitta (författare)
Univ Oulu, PEDEGO Res Unit, Oulu, Finland;Oulu Univ Hosp, Dept Children & Adolescents, Oulu, Finland
Nordgren, Ann (författare)
Karolinska Institutet
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 (creator_code:org_t)
2019-09-13
2019
Engelska.
Ingår i: Blood Advances. - : American Society of Hematology. - 2473-9529 .- 2473-9537. ; 3:18, s. 2722-2731
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Pathogenic germline variants in ETV6 have been associated with familial predisposition to thrombocytopenia and hematological malignancies, predominantly childhood B-cell precursor acute lymphoblastic leukemia (BCP-ALL). In addition, overrepresentation of a high hyperdiploid subtype and older age at diagnosis have been reported among sporadic BCP-ALL cases with germline variants in ETV6. We studied a family with 2 second-degree relatives who developed childhood high hyperdiploid BCP-ALL at ages 8 and 12 years, respectively. A constitutional balanced reciprocal translocation t(12;14)(p13.2;q23.1) was discovered in both patients by routine karyotyping at diagnosis and, subsequently, in 7 healthy family members who had not experienced hematological malignancies. No carriers had thrombocytopenia. Whole-genome sequencing confirmed the translocation, resulting in 2 actively transcribed but nonfunctional fusion genes, causing heterozygous loss and consequently monoallelic expression of ETV6. Whole-genome sequencing analysis of the affected female subjects' leukemia excluded additional somatic aberrations in ETV6 and RTN1 as well as shared somatic variants in other genes. Expression studies, performed to confirm decreased expression of ETV6, were not conclusive. We suggest that germline aberrations resulting in monoallelic expression of ETV6 contribute to leukemia susceptibility, whereas more severe functional deficiency of ETV6 is required for developing THC5. To our knowledge, this report is the first of a constitutional translocation disrupting ETV6 causing predisposition to childhood ALL.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Hematologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Hematology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Medicinsk genetik (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Medical Genetics (hsv//eng)

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