Abnormalities of the retinoblastoma gene in the pathogenesis of acute leukemia

• Published in: Blood Vol. 78; no. 12; pp. 3259 - 3268
• Main Authors: AHUJA, H. G, JAT, P. S, FOTI, A, BAR-ELI, M, CLINE, M. J
• Format: Journal Article
• Language: English
• Published: Washington, DC The Americain Society of Hematology 15.12.1991
• Subjects: Acute Disease; Adolescent; Adult; Antibodies, Monoclonal; Biological and medical sciences; Blast Crisis - genetics; Blotting, Southern; Child; DNA, Neoplasm - chemistry; DNA, Neoplasm - genetics; Gene Expression; Genes, Retinoblastoma - genetics; Hematologic and hematopoietic diseases; Humans; Immunoblotting; Leukemia - genetics; Leukemia, Myelogenous, Chronic, BCR-ABL Positive - genetics; Leukemia, Myelogenous, Chronic, BCR-ABL Positive - pathology; Leukemia, Myeloid, Acute - genetics; Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis; Lymphoma - genetics; Medical sciences; Myelodysplastic Syndromes - genetics; Philadelphia Chromosome; Polymorphism, Restriction Fragment Length; Precursor Cell Lymphoblastic Leukemia-Lymphoma - genetics; Human; Cell line; Pathogenesis; Acute; Leukemia; Exploration; Malignant hemopathy; Molecular biology; Southern blotting; Retinoblastoma; Tumor cell
• ISSN: 0006-4971; 1528-0020
• DOI: 10.1182/blood.V78.12.3259.3259

The retinoblastoma-susceptibility (Rb) gene is an antioncogene that is frequently altered in retinoblastomas, sarcomas, and some epithelial tumors. We examined the structure of the Rb gene by Southern blotting in 215 cases of leukemias and lymphomas of diverse phenotype and in 15 leukemic cell lines. In selected cases Rb protein expression was examined with specific monoclonal antibodies. Structural abnormalities of the Rb gene with absent protein expression were frequent in all types of human acute leukemia, but were particularly common (27% incidence) in M4 and M5 myeloid leukemia with monocytic differentiation and in Philadelphia chromosome (Ph1)-positive leukemia of lymphoid phenotype (11% to 29% incidence). Changes in Rb were observed early in the transition to acute leukemia in cases of myelodysplastic syndrome and in the accelerated phase of chronic myelocytic leukemia in transition to blast crisis. In one case, molecular changes in Rb could be correlated with leukemia remission and relapse. We conclude that the Rb antioncogene is commonly involved in the evolution of human acute leukemias, particularly in those of a monocytic phenotype and in lymphoid leukemia in which there is an antecedent alteration of the Ph1 chromosome.