Rothberg P G, Erisman M D, Diehl R E, Rovigatti U G, Astrin S M
Mol Cell Biol. 1984 Jun;4(6):1096-103. doi: 10.1128/mcb.4.6.1096-1103.1984.
c-myc is the cellular gene homologous to the transforming sequence of MC29, an acute avian retrovirus. The human c-myc gene was cloned and used to study the structure and expression of c-myc in a variety of human hematopoietic malignancies. In a careful study of 106 patients, c-myc RNA was found to be expressed at elevated levels in tumor cells of 17 leukemia patients and five lymphoma patients. The c-myc gene was found to be rearranged in two lymphomas, an African Burkitt's lymphoma and a non-Hodgkins lymphoma in leukemic phase. The Burkitt's rearrangement involved the insertion of new DNA sequences upstream from the c-myc 5' coding region, presumably replacing the normal c-myc transcriptional promoter. None of the other 104 patients, including 20 with elevated myc expression, exhibited any evidence of a genetic rearrangement involving the c-myc gene. Our results show that there is a subset of hematopoietic malignancies characterized by elevated expression of c-myc. This elevated expression in most cases is not due to obvious genetic changes (rearrangement, amplification) at the c-myc locus nor to chromosomal translocations in the vicinity of this gene.
c-myc是与急性禽逆转录病毒MC29的转化序列同源的细胞基因。人类c-myc基因被克隆出来,用于研究c-myc在多种人类造血系统恶性肿瘤中的结构和表达。在一项对106名患者的仔细研究中,发现17名白血病患者和5名淋巴瘤患者的肿瘤细胞中c-myc RNA表达水平升高。在两例淋巴瘤中发现c-myc基因发生重排,一例非洲伯基特淋巴瘤和一例处于白血病期的非霍奇金淋巴瘤。伯基特重排涉及在c-myc 5'编码区上游插入新的DNA序列,推测取代了正常的c-myc转录启动子。其他104名患者,包括20名myc表达升高的患者,均未表现出任何涉及c-myc基因的基因重排证据。我们的结果表明,存在一部分以c-myc表达升高为特征的造血系统恶性肿瘤。在大多数情况下,这种表达升高并非由于c-myc基因座处明显的基因变化(重排、扩增),也不是由于该基因附近的染色体易位。