Bagchi Anindya, Mills Alea A
Cold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724, USA.
Cancer Res. 2008 Apr 15;68(8):2551-6. doi: 10.1158/0008-5472.CAN-07-2095.
Genomic analyses of late-stage human cancers have uncovered deletions encompassing 1p36, thereby providing an extensive body of literature supporting the idea that a potent tumor suppressor resides in this interval. Although several genes have been proposed as 1p36 candidate tumor suppressors, convincing evidence that their encoded products protect from cancer has been scanty. A recent functional study identified chromodomain helicase DNA-binding protein 5 (CHD5) as a novel tumor suppressor mapping to 1p36. Here, we discuss evidence supporting the tumor-suppressive role of CHD5. Together, these findings suggest that strategies designed to enhance CHD5 activity could provide novel approaches for treating a broad range of human malignancies.
对晚期人类癌症的基因组分析发现了包含1p36区域的缺失,从而产生了大量文献支持这样一种观点,即一个有效的肿瘤抑制基因位于这个区间。尽管已有几个基因被提议作为1p36候选肿瘤抑制基因,但关于它们编码的产物具有抗癌作用的确凿证据却很少。最近一项功能研究将染色质结构域解旋酶DNA结合蛋白5(CHD5)鉴定为定位于1p36的一种新型肿瘤抑制基因。在此,我们讨论支持CHD5肿瘤抑制作用的证据。这些发现共同表明,旨在增强CHD5活性的策略可为治疗多种人类恶性肿瘤提供新方法。