Chang Nan-Shan, Hsu Li-Jin, Lin Yee-Shin, Lai Feng-Jie, Sheu Hamm-Ming
Institute of Molecular Medicine, National Cheng Kung University Medical College, Tainan, Taiwan 70101, Republic of China.
Trends Mol Med. 2007 Jan;13(1):12-22. doi: 10.1016/j.molmed.2006.11.006. Epub 2006 Dec 4.
Common fragile site gene WWOX encodes a candidate tumor suppressor WW domain-containing oxidoreductase. Alteration of this gene, along with dramatic downregulation of WWOX protein, is shown in the majority of invasive cancer cells. Ectopic WWOX exhibits proapoptotic and tumor inhibitory functions in vitro and in vivo, probably interacting with growth regulatory proteins p53, p73 and others. Hyaluronidases regulate WWOX expression, increase cancer invasiveness and seem to be involved in the development of hormone-independent growth of invasive cancer cells. Estrogen and androgen stimulate phosphorylation and nuclear translocation of WWOX, although binding of WWOX to these sex hormones is unknown. We propose that suppression of WWOX expression by overexpressed hyaluronidases might contribute in part to the development of hormone independence in invasive cancer.
常见脆性位点基因WWOX编码一种候选肿瘤抑制因子——含WW结构域的氧化还原酶。在大多数侵袭性癌细胞中,该基因发生改变,同时WWOX蛋白显著下调。异位表达的WWOX在体外和体内均表现出促凋亡和肿瘤抑制功能,可能与生长调节蛋白p53、p73等相互作用。透明质酸酶调节WWOX表达,增加癌症侵袭性,似乎参与侵袭性癌细胞激素非依赖性生长的发展。雌激素和雄激素刺激WWOX的磷酸化和核转位,尽管WWOX与这些性激素的结合情况尚不清楚。我们认为,过表达的透明质酸酶对WWOX表达的抑制可能在一定程度上促成了侵袭性癌症中激素非依赖性的发展。