Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Exp Biol Med (Maywood). 2014 Mar;239(3):253-63. doi: 10.1177/1535370213519213. Epub 2014 Feb 7.
The WW domain-containing oxidoreductase (WWOX) gene, encodes a tumor suppressor located on 16q23.1, spanning FRA16D, one of the most active common fragile sites in the human genome, that is altered in numerous types of cancer. WWOX's alteration in these myriad cancers is due to disparate mechanisms including loss of heterozygosity, homozygous deletion and epigenetic changes. In vitro, WWOX has been found to be reduced or absent in numerous cancer cell lines and WWOX restoration has been found to inhibit tumor cell growth and invasion. Wwox knockout mice developed femoral focal lesions resembling osteosarcomas within one month of their life and aging Wwox heterozygous mice have an increased incidence of spontaneous lung and mammary tumors as well as B-cell lymphomas. We herein review WWOX's role that has been unearthed thus far in different types of malignancies, its clinical significance and future implications.
WW 结构域包含的氧化还原酶(WWOX)基因,编码位于 16q23.1 上的肿瘤抑制因子,跨越了人类基因组中最活跃的常见脆性部位之一 FRA16D,该基因在多种类型的癌症中发生改变。在这些无数的癌症中,WWOX 的改变是由于不同的机制,包括杂合性丢失、纯合性缺失和表观遗传改变。在体外,已经发现许多癌细胞系中 WWOX 的表达减少或缺失,而 WWOX 的恢复被发现可以抑制肿瘤细胞的生长和侵袭。Wwox 敲除小鼠在一个月的生命和衰老时,股骨出现类似于骨肉瘤的局灶性病变,杂合子 Wwox 小鼠自发性肺和乳腺肿瘤以及 B 细胞淋巴瘤的发生率增加。本文综述了 WWOX 在不同类型恶性肿瘤中迄今为止发现的作用、其临床意义和未来意义。