Longo L, Pandolfi P P, Biondi A, Rambaldi A, Mencarelli A, Lo Coco F, Diverio D, Pegoraro L, Avanzi G, Tabilio A
Istituto di Clinica Medica I, University of Perugia, Policlinico Monteluce, Italy.
J Exp Med. 1990 Dec 1;172(6):1571-5. doi: 10.1084/jem.172.6.1571.
Although acute promyelocytic leukemias (APLs) are consistently associated with a reciprocal chromosome 15;17 translocation, the gene(s) directly affected by the breakpoints have never been isolated. The chromosome 17 breakpoint maps to near the retinoic acid receptor alpha (RAR alpha) locus. Investigation of 20 APLs and a large series of other neoplastic patients and normal controls revealed RAR alpha gene rearrangements and aberrant transcripts only in the APL cases. These findings suggest that the RAR alpha gene is involved in the APL chromosome 17 breakpoint, is implicated in leukemogenesis, and could be used as a marker for identifying leukemic promyelocytes.
尽管急性早幼粒细胞白血病(APL)始终与15号和17号染色体的相互易位有关,但受断点直接影响的基因从未被分离出来。17号染色体断点定位于维甲酸受体α(RARα)基因座附近。对20例APL患者以及大量其他肿瘤患者和正常对照的研究发现,仅在APL病例中存在RARα基因重排和异常转录本。这些发现表明,RARα基因与APL的17号染色体断点有关,参与白血病的发生,并且可作为识别白血病早幼粒细胞的标志物。