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p16 INK4A gene homozygous deletions in human acute leukaemias with alterations of chromosome 9
Author(s) -
Faienza Maria Felicia,
Ragione Fulviodella,
Basso Guiseppe,
Coppola Brigida,
Miraglia del Giudice Emanuele,
Schettini Francesco,
Iolascon Achille
Publication year - 1996
Publication title -
british journal of haematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.907
H-Index - 186
eISSN - 1365-2141
pISSN - 0007-1048
DOI - 10.1046/j.1365-2141.1996.d01-1674.x
Subject(s) - biology , gene , loss of heterozygosity , genetics , gene dosage , chromosome , microbiology and biotechnology , tumor suppressor gene , chromosomal translocation , cancer research , gene expression , allele , carcinogenesis
Acute leukaemias are characterized by non‐random chromosomal aberrations which are often strictly related to the inactivation of tumour suppressor genes (TSGs). Alterations at the short arm of chromosome 9 have been reported in a remarkable percentage of acute lymphoblastic leukaemias (ALL) and have been suggested to cause the loss of activity of the putative TSG, p16 INK4A (MTS1/CDKN2) gene. In order to evaluate the correlation between this gene inactivation and visible cytogenetic abnormalities, we have investigated p16 INK4A homozygous gene deletions in 10 paediatric acute leukaemias of different cell lineages which demonstrated karyotype aberrations involving chromosome 9. Moreover, the dimension of the genetic alteration was evaluated by studying the loss of heterozygosity of two highly polymorphic markers of chromosome 9p, namely α‐interferon (IFNA) and D9S104, and the deletion of 5′‐methylthioadenosine phosphorylase (MTAPase) gene. Finally, the deletion of a gene belonging to p16 INK4A family, the p18 gene, was analysed in these acute leukaemias. Our results demonstrated that: (i) the biallelic loss of p16 INK4A gene is strictly related to a specific immunophenotype, namely ALL of T‐cell lineage; (ii) no significant correlation exists between alterations at chromosome 9p level and the homozygous deletions of p16 INK4A gene; and (iii) p18 gene was not deleted in the examined cases. These findings suggest a possible correlation between the T‐lymphocyte phenotype and the expression of p16 INK4A gene. Moreover, the absence of MTAPase activity seems to be a valuable marker of p16 INK4A gene inactivation, thus indicating that the deleted chromosomal area on 9p21 very frequently involves the MTAPase gene.