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The frequent and clinically benign anomalies of chromosomes 7 and 20 in Shwachman-diamond syndrome may be subject to further clonal variations.
Khan, Abdul Waheed; Kennedy, Alyssa; Furutani, Elissa; Myers, Kasiani; Frattini, Annalisa; Acquati, Francesco; Roccia, Pamela; Micheloni, Giovanni; Minelli, Antonella; Porta, Giovanni; Cipolli, Marco; Cesaro, Simone; Danesino, Cesare; Pasquali, Francesco; Shimamura, Akiko; Valli, Roberto.
Afiliação
  • Khan AW; Genetica Umana e Medica, Dipartimento di Medicina e Chirurgia, Università Dell'Insubria, Via J. H. Dunant, 5, 21100, Varese, Italy.
  • Kennedy A; Dana Farber/Boston Children's Cancer and Blood Disorders Center, Boston, MA, USA.
  • Furutani E; Keros Therapeutics, Lexington, MA, USA.
  • Myers K; Cincinnati Children's Hospital and Medical Center, Cincinnati, OH, USA.
  • Frattini A; Genetica Umana e Medica, Dipartimento di Medicina e Chirurgia, Università Dell'Insubria, Via J. H. Dunant, 5, 21100, Varese, Italy.
  • Acquati F; Istituto di Ricerca Genetica e Biomedica, CNR, Milano, Italy.
  • Roccia P; Dipartimento di Biotecnologie e Scienze della Vita, Università Dell'Insubria, Varese, Italy.
  • Micheloni G; Centro di Medicina Genomica-Università dell'Insubria, Varese, Italy.
  • Minelli A; Genetica Umana e Medica, Dipartimento di Medicina e Chirurgia, Università Dell'Insubria, Via J. H. Dunant, 5, 21100, Varese, Italy.
  • Porta G; Genetica Umana e Medica, Dipartimento di Medicina e Chirurgia, Università Dell'Insubria, Via J. H. Dunant, 5, 21100, Varese, Italy.
  • Cipolli M; Genetica Medica, Fondazione IRCCS Policlinico S. Matteo and Università di Pavia, Pavia, Italy.
  • Cesaro S; Genetica Umana e Medica, Dipartimento di Medicina e Chirurgia, Università Dell'Insubria, Via J. H. Dunant, 5, 21100, Varese, Italy.
  • Danesino C; Centro di Medicina Genomica-Università dell'Insubria, Varese, Italy.
  • Pasquali F; Centro Fibrosi Cistica, Azienda Ospedaliera Universitaria Integrata, Verona, Italy.
  • Shimamura A; Oncoematologia Pediatrica, Azienda Ospedaliera Universitaria Integrata, Verona, Italy.
  • Valli R; Genetica Medica, Fondazione IRCCS Policlinico S. Matteo and Università di Pavia, Pavia, Italy.
Mol Cytogenet ; 14(1): 54, 2021 Nov 24.
Article em En | MEDLINE | ID: mdl-34819134
BACKGROUND: An isochromosome of the long arm of chromosome 7, i(7)(q10), and an interstitial deletion of the long arm of chromosome 20, del(20)(q), are the most frequent anomalies in the bone marrow of patients with Shwachman-Diamond syndrome, which is caused in most cases by mutations of the SBDS gene. These clonal changes imply milder haematological symptoms and lower risk of myelodysplastic syndromes and acute myeloid leukaemia, thanks to already postulated rescue mechanisms. RESULTS: Bone marrow from fourteen patients exhibiting either the i(7)(q10) or the del(20)(q) and coming from two large cohorts of patients, were subjected to chromosome analyses, Fluorescent In Situ Hybridization with informative probes and array-Comparative Genomic Hybridization. One patient with the i(7)(q10) showed a subsequent clonal rearrangement of the normal chromosome 7 across years. Four patients carrying the del(20)(q) evolved further different del(20)(q) independent clones, within a single bone marrow sample, or across sequential samples. One patient with the del(20)(q), developed a parallel different clone with a duplication of chromosome 3 long arm. Eight patients bore the del(20)(q) as the sole chromosomal abnormality. An overall overview of patients with the del(20)(q), also including cases already reported, confirmed that all the deletions were interstitial. The loss of material varied from 1.7 to 26.9 Mb and resulted in the loss of the EIF6 gene in all patients. CONCLUSIONS: Although the i(7)(q) and the del(20)(q) clones are frequent and clinically benign in Shwachman Diamond-syndrome, in the present work we show that they may rearrange, may be lost and then reconstructed de novo, or may evolve with independent clones across years. These findings unravel a striking selective pressure exerted by SBDS deficiency driving to karyotype instability and to specific clonal abnormalities.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article