Nickerson J A
Department of Cell Biology, University of Massachusetts Medical School, Worcester 01655, USA.
J Cell Biochem. 1998 Aug 1;70(2):172-80.
Cancer is diagnosed by examining the architectural alterations to cells and tissues. Changes in nuclear structure are among the most universal of these and include increases in nuclear size, deformities in nuclear shape, and changes in the internal organization of the nucleus. These may all reflect changes in the nuclear matrix, a non-chromatin nuclear scaffolding determining nuclear form, higher order chromatin folding, and the spatial organization of nucleic acid metabolism. Malignancy-induced changes in this structure may have profound effects on chromatin folding, on the fidelity of genome replication, and on gene expression. Elucidating the mechanisms and the biological consequences of nuclear changes will require the identification of the major structural molecules of the internal nuclear matrix and an understanding of their assembly into structural elements. If biochemical correlates to malignant alterations in nuclear structure can be identified then nuclear matrix proteins and, perhaps nuclear matrix-associated structural RNAs, may be an attractive set of diagnostic markers and therapeutic targets.
癌症是通过检查细胞和组织的结构改变来诊断的。核结构的变化是其中最普遍的,包括核大小增加、核形状畸形以及核内部组织的变化。这些都可能反映核基质的变化,核基质是一种非染色质核支架,决定核形态、高阶染色质折叠以及核酸代谢的空间组织。这种结构中由恶性肿瘤引起的变化可能对染色质折叠、基因组复制的保真度以及基因表达产生深远影响。阐明核变化的机制和生物学后果将需要鉴定核内基质的主要结构分子,并了解它们组装成结构元件的过程。如果能够确定与核结构恶性改变相关的生化指标,那么核基质蛋白以及可能的核基质相关结构RNA,可能是一组有吸引力的诊断标志物和治疗靶点。