2020
DOI: 10.1007/s12288-020-01295-8
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Recent Advances in Molecular Diagnosis and Prognosis of Childhood B Cell Lineage Acute Lymphoblastic Leukemia (B-ALL)

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Cited by 6 publications
(5 citation statements)
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“…Most patients present a common immunophenotype and belong to the intermediate risk group. The frequency of genetic alterations is also within common ranges reported in European countries 19 . After preprocessing and filtering (see 'Methods' and Figure S1), 188 patients were retained for analysis.…”
Section: Patient Cohort Is Representative Of Childhood Bcp-all Popula...supporting
confidence: 75%
“…Most patients present a common immunophenotype and belong to the intermediate risk group. The frequency of genetic alterations is also within common ranges reported in European countries 19 . After preprocessing and filtering (see 'Methods' and Figure S1), 188 patients were retained for analysis.…”
Section: Patient Cohort Is Representative Of Childhood Bcp-all Popula...supporting
confidence: 75%
“…Deletions of the IKZF1 gene which result in haploinsufficiency constitute up to 55% of B-ALL with IKZF1 deletions. Focal exons 4-7 deletions affecting the DNA-binding domain compose of 33% of IKZF1 deletions, and exert a dominantnegative effect over the unaffected allele, resulting in loss of the tumor suppressor function attributed to wildtype IKZF1 (60). Exons 4-7 deletions lead to more severe phenotype than haploinsufficiency in B-ALL patients.…”
Section: Other Significant Gene Alterationsmentioning
confidence: 99%
“…Other genes, which have been reported to be deleted in B-ALL, include ABL1, CASP8AP2, CD200/BTLA, MLLT3, IKZF2, NF1, PHF6, PTEN, PTPN2, TBL1XR1, TP53, and VPREB1. Deletions in VPREB1, RB1, IKZF2, and TBL1XR1 can be biallelic (60).…”
Section: Other Significant Gene Alterationsmentioning
confidence: 99%
“…Las leucemias en los niños provienen a partir de las primitivas células B y T. que sufren cambios moleculares, aun en estado inmaduro. En los últimos años hubo importantes avances en el diagnóstico y tratamiento, basado en estudios ( 4) moleculares . Los cambios en las líneas, moleculares pueden ser secundarios a eventos prenatales o postnatales relacionados con factores genéticos y epigenéticos, con traslocaciones y mutaciones genéticas⁽⁵⁾.…”
Section: Introductionunclassified