Acquati Francesco, Possati Laura, Ferrante Luigi, Campomenosi Paola, Talevi Simona, Bardelli Silvana, Margiotta Chiara, Russo Antonella, Bortoletto Elisabetta, Rocchetti Romina, Calza Roberta, Cinquetti Raffaella, Monti Laura, Salis Silvia, Barbanti-Brodano Giuseppe, Taramelli Roberto
Dipartimento di Biotecnologie e Scienze Molecolari, Università degli Studi dell'Insubria, I-21100 Varese, Italy.
Int J Oncol. 2005 May;26(5):1159-68.
The region 6q27 from human chromosome 6 has been reported to contain one or more tumor suppressor genes on the basis of cytogenetic, molecular and functional studies. We have recently carried out a detailed analysis of a candidate gene from 6q27 to evaluate its putative role as a tumor suppressor gene involved in ovarian cancer pathogenesis. The RNASET2 gene was shown to behave as a class II tumor suppressor and abolish the tumorigenic potential of an ovarian cancer-derived cell line. In this study, we have started the cellular and biochemical characterization of RNASET2 and showed that it is a secreted glycoprotein. Moreover, we have extended our previous studies by evaluating the effect of RNASET2 on the metastatic behavior of the highly-invasive ovarian cancer cell line HEY3MET2. From such analysis, RNASET2 was found to significantly decrease the metastatic potential of this cell line in vivo. Moreover, RNASET2-mediated suppression of tumorigenesis and metastasis was not affected by a double point mutation targeted to the putative ribonuclease catalytic sites, suggesting that tumor suppression by RNASET2 is not mediated by its ribonuclease activity. The potential biological implications of this unexpected finding are discussed in relation to the current evolutionary models.
基于细胞遗传学、分子生物学和功能研究,据报道人类6号染色体的6q27区域含有一个或多个肿瘤抑制基因。我们最近对来自6q27的一个候选基因进行了详细分析,以评估其作为参与卵巢癌发病机制的肿瘤抑制基因的假定作用。RNASET2基因表现为II类肿瘤抑制基因,并消除了卵巢癌衍生细胞系的致瘤潜力。在本研究中,我们开始了对RNASET2的细胞和生化特性分析,并表明它是一种分泌型糖蛋白。此外,我们通过评估RNASET2对高侵袭性卵巢癌细胞系HEY3MET2转移行为的影响,扩展了我们之前的研究。通过这种分析,发现RNASET2在体内显著降低了该细胞系的转移潜力。此外,RNASET2介导的肿瘤发生和转移抑制不受针对假定核糖核酸酶催化位点的双点突变的影响,这表明RNASET2的肿瘤抑制作用不是由其核糖核酸酶活性介导的。结合当前的进化模型讨论了这一意外发现的潜在生物学意义。