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白血病和淋巴瘤中c-myb基因座与6号染色体异常之间的关系。

Relationship between the c-myb locus and the 6q-chromosomal aberration in leukemias and lymphomas.

作者信息

Barletta C, Pelicci P G, Kenyon L C, Smith S D, Dalla-Favera R

出版信息

Science. 1987 Feb 27;235(4792):1064-7. doi: 10.1126/science.3469751.

Abstract

Deletions of the long arm of chromosome 6 (6q-) are frequently found in hematopoietic neoplasms, including acute lymphoblastic leukemias, non-Hodgkin lymphomas and (less frequently) myeloid leukemias. The c-myb proto-oncogene has been mapped to region 6q21-24, which suggests that it could be involved in the 6q- aberrations. By means of in situ chromosomal hybridization on cells from six hematopoietic malignancies, it was demonstrated that the c-myb locus is not deleted, but is retained on band q22, which is consistently bordered by the chromosomal breakpoints in both interstitial and terminal 6q- deletions. The deletion breakpoints were located at some distance from the myb locus since no rearrangement of c-myb sequences was found. In one case, however, amplification of the entire c-myb locus was detectable. Furthermore, in all cases tested that carry 6q- deletions, myb messenger RNA levels were significantly higher than in normal cells or in malignant cells matched for lineage and stage of differentiation but lacking the 6q- marker. These results indicate that 6q- deletions are accompanied by structural and functional alterations of the c-myb locus and that these alterations may be involved in the pathogenesis of leukemias and lymphomas.

摘要

6号染色体长臂缺失(6q-)在造血系统肿瘤中很常见,包括急性淋巴细胞白血病、非霍奇金淋巴瘤以及(较少见的)髓系白血病。c-myb原癌基因已定位于6q21-24区域,这表明它可能与6q-异常有关。通过对六种造血系统恶性肿瘤细胞进行原位染色体杂交,结果表明c-myb基因座未缺失,而是保留在q22带,在间质性和末端6q-缺失中,该带始终以染色体断点为边界。由于未发现c-myb序列重排,缺失断点位于距myb基因座一定距离处。然而,在一个病例中,可检测到整个c-myb基因座的扩增。此外,在所有检测的携带6q-缺失的病例中,myb信使RNA水平显著高于正常细胞或与缺失6q-标记的恶性细胞在谱系和分化阶段相匹配的恶性细胞。这些结果表明,6q-缺失伴随着c-myb基因座的结构和功能改变,并且这些改变可能参与白血病和淋巴瘤的发病机制。

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