HMGI(Y) and HMGI-C dysregulation: A common occurrence in human tumors

被引:110
作者
Tallini, G
Dal Cin, P
机构
[1] Yale Univ, Sch Med, Dept Pathol, New Haven, CT 06250 USA
[2] Harvard Univ, Brigham & Womens Hosp, Sch Med, Dept Pathol, Boston, MA 02115 USA
关键词
high mobility group proteins; HMGI(Y); HMGI-C; molecular genetics; mesenchymal tumor genetics; uterine leiomyoma; lipoma;
D O I
10.1097/00125480-199909000-00001
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
HMGI(Y) and HMGI-C are members of a distinct family of "high mobility group" (HMG) proteins that are nonhistone chromatin-associated proteins initially characterized by high electrophoretic mobility in polyacrylamide gels (hence the acronym HMG). Recent studies have shown that HMGI(Y) and HMGI-C are important elements with a role in the regulation of chromatin structure and function. Like other HMG proteins they are responsible for the correct three-dimensional configuration of protein-DNA complexes and therefore play a key role in important cellular processes such as DNA transcription. Aberrant HMGI(Y) and HMGI-C expression generally correlates with a malignant tumor phenotype. However, HMGI(Y) and HMGI-C dysregulation, as a result of specific chromosomal rearrangements, is also being identified in a variety of common benign mesenchymal tumors such as lipomas and uterine leiomyomas making HMGI(Y) and HMGI-C genes probably the most commonly rearranged genes in human neoplasms. While a precise definition of the HMGI(Y) and HMGI-C role in tumor initiation and progression is still missing, it is likely that future investigations will contribute valuable insights to the understanding of human neoplasia.
引用
收藏
页码:237 / 246
页数:10
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