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Expression of BCL6 in paediatric B-cell acute lymphoblastic leukaemia and association with prognosis

Tutkimustuotos: ArtikkeliTieteellinenvertaisarvioitu

3 Sitaatiot (Scopus)
15 Lataukset (Pure)

Abstrakti

B-cell lineage acute lymphoblastic leukaemia (B-ALL) is the most common paediatric malignancy. Transcription factor B-cell lymphoma 6 (BCL6) is essential to germinal centre formation and antibody affinity maturation and plays a major role in mature B-cell malignancies. More recently, it was shown to act as a critical downstream regulator in pre-BCR+ B-ALL. We investigated the expression of the BCL6 protein in a population-based cohort of paediatric B-ALL cases and detected moderate to strong positivity through immunohistochemistry in 7% of cases (8/117); however, only two of eight BCL6 cases (25%) co-expressed the ZAP70 protein. In light of these data, the subtype with active pre-BCR signalling constitutes a rare entity in paediatric B-ALL. In three independent larger cohorts with gene expression data, high BCL6 mRNA levels were associated with the TCF3-PBX1, Ph-like, NUTM1, MEF2D and PAX5-alt subgroups and the ‘metagene’ signature for pre-BCR-associated genes. However, higher-than-median BCL6 mRNA level alone was associated with favourable event free survival in the Nordic paediatric cohort, indicating that using BCL6 as a diagnostic marker requires careful design, and evaluation of protein level is needed alongside the genetic or transcriptomic data.

AlkuperäiskieliEnglanti
JulkaisuPathology
Vuosikerta53
Numero7
DOI - pysyväislinkit
TilaJulkaistu - 2021
OKM-julkaisutyyppiA1 Alkuperäisartikkeli tieteellisessä aikakauslehdessä

Rahoitus

The work was supported by Competitive State Research Financing of the Expert Responsibility at Tampere University Hospital (9X027) and grants from the Academy of Finland (no. 277816 and 310106, OL), Sigrid Jus?lius Foundation (MH and OL), the Cancer Society of Finland (MH, OL), the Jane and Aatos Erkko Foundation (OL, MH) and the V?re Foundation for paediatric Cancer Research (AM). The authors declare no competing interests. The work was supported by Competitive State Research Financing of the Expert Responsibility at Tampere University Hospital ( 9X027 ) and grants from the Academy of Finland (no. 277816 and 310106 , OL), Sigrid Jusélius Foundation (MH and OL), the Cancer Society of Finland (MH, OL), the Jane and Aatos Erkko Foundation (OL, MH) and the Väre Foundation for paediatric Cancer Research (AM). The authors declare no competing interests.

Julkaisufoorumi-taso

  • Jufo-taso 1

!!ASJC Scopus subject areas

  • Pathology and Forensic Medicine

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