Ludes-Meyers J H, Bednarek A K, Popescu N C, Bedford M, Aldaz C M
Department of Carcinogenesis, The University of Texas M.D. Anderson Cancer Center, Science Park-Research Division, Smithville, TX 78957, USA.
Cytogenet Genome Res. 2003;100(1-4):101-10. doi: 10.1159/000072844.
Gross chromosomal rearrangements and aneuploidy are among the most common somatic genomic abnormalities that occur during cancer initiation and progression, in particular in human solid tumor carcinogenesis. The loss of large chromosomal regions as consequence of gross rearrangements (e.g. deletions, monosomies, unbalanced translocations and mitotic recombination) have been traditionally associated with the existence of tumor suppressor genes within the areas affected by the loss of genetic material. The long arm of chromosome 16 was identified as being frequently associated with structural abnormalities in multiple neoplasias, that led us to focus attention on the detailed genetic dissection of this region resulting in the cloning of the putative tumor suppressor gene, WWOX (WW domain containing Oxidoreductase). Interestingly, the WWOX gene resides in the very same region as that of the common chromosomal fragile site 16D (FRA16D). The WWOX gene encodes a protein that contains two WW domains, involved in protein-protein interactions, and a short chain dehydrogenase (SDR) domain, possibly involved in sex-steroid metabolism. We have identified the WWOX WW domain ligand as the PPXY motif confirming the biochemical activity of this domain. WWOX normally resides in the Golgi and we will demonstrate that Golgi localization requires an intact SDR. Inactivation of the WWOX gene during tumorigenesis can occur by homozygous deletions and possibly mutation, however, aberrantly spliced forms of WWOX mRNA have been observed even when one allele is still intact. The aberrantly spliced mRNAs have deletions of the exons that encode the SDR and these WWOX protein isoforms display abnormal intracellular localization to the nucleus possibly functioning as dominant negative inhibitors of full length WWOX. Thus, generation of aberrant transcripts of WWOX may represent a novel mechanism to functionally inactivate WWOX without genomic alteration of the remaining allele. In this article we will review the cloning and identification of WWOX as the target of FRA16D. In addition, we will discuss the possible biochemical functions of WWOX and present evidence that ectopic WWOX expression inhibits tumor growth.
染色体大片段重排和非整倍体是癌症发生和发展过程中最常见的体细胞基因组异常,尤其是在人类实体瘤致癌过程中。由于大片段重排(如缺失、单体、不平衡易位和有丝分裂重组)导致的大染色体区域丢失,传统上与受遗传物质丢失影响区域内肿瘤抑制基因的存在有关。16号染色体长臂被确定经常与多种肿瘤的结构异常相关,这使我们将注意力集中在该区域的详细基因剖析上,从而克隆出了假定的肿瘤抑制基因WWOX(含WW结构域的氧化还原酶)。有趣的是,WWOX基因位于与常见染色体脆性位点16D(FRA16D)相同的区域。WWOX基因编码一种蛋白质,该蛋白质包含两个参与蛋白质-蛋白质相互作用的WW结构域和一个可能参与性甾体代谢的短链脱氢酶(SDR)结构域。我们已确定WWOX WW结构域的配体为PPXY基序,证实了该结构域的生化活性。WWOX通常位于高尔基体中,我们将证明高尔基体定位需要完整的SDR。肿瘤发生过程中WWOX基因的失活可通过纯合缺失以及可能的突变发生,然而,即使一个等位基因仍然完整,也观察到了异常剪接形式的WWOX mRNA。异常剪接的mRNA缺失了编码SDR的外显子,这些WWOX蛋白异构体在细胞核内显示出异常的细胞内定位,可能作为全长WWOX的显性负抑制剂发挥作用。因此,WWOX异常转录本的产生可能代表了一种在不改变其余等位基因基因组的情况下使WWOX功能失活的新机制。在本文中,我们将回顾WWOX作为FRA16D靶点的克隆和鉴定。此外,我们将讨论WWOX可能的生化功能,并提供异位表达WWOX抑制肿瘤生长的证据。