EGA Institute for Women's Health, Gynaecological Cancer Research Laboratories, University College London, London, UK.
Neoplasia. 2010 Jul;12(7):579-89. doi: 10.1593/neo.10340.
We used a functional complementation approach to identify tumor-suppressor genes and putative therapeutic targets for ovarian cancer. Microcell-mediated transfer of chromosome 18 in the ovarian cancer cell line TOV21G induced in vitro and in vivo neoplastic suppression. Gene expression microarray profiling in TOV21G(+18) hybrids identified 14 candidate genes on chromosome 18 that were significantly overexpressed and therefore associated with neoplastic suppression. Further analysis of messenger RNA and protein expression for these genes in additional ovarian cancer cell lines indicated that EPB41L3 (erythrocyte membrane protein band 4.1-like 3, alternative names DAL-1 and 4.1B) was a candidate ovarian cancer-suppressor gene. Immunoblot analysis showed that EPB41L3 was activated in TOV21G(+18) hybrids, expressed in normal ovarian epithelial cell lines, but was absent in 15 (78%) of 19 ovarian cancer cell lines. Using immunohistochemistry, 66% of 794 invasive ovarian tumors showed no EPB41L3 expression compared with only 24% of benign ovarian tumors and 0% of normal ovarian epithelial tissues. EPB41L3 was extensively methylated in ovarian cancer cell lines and primary ovarian tumors compared with normal tissues (P = .00004), suggesting this may be the mechanism of gene inactivation in ovarian cancers. Constitutive reexpression of EPB41L3 in a three-dimensional multicellular spheroid model of ovarian cancer caused significant growth suppression and induced apoptosis. Transmission and scanning electron microscopy demonstrated many similarities between EPB41L3-expressing cells and chromosome 18 donor-recipient hybrids, suggesting that EPB41L3 is the gene responsible for neoplastic suppression after chromosome 18 transfer. Finally, an inducible model of EPB41L3 expression in three-dimensional spheroids confirmed that reexpression of EPB41L3 induces extensive apoptotic cell death in ovarian cancers.
我们采用功能互补方法来鉴定卵巢癌的肿瘤抑制基因和潜在治疗靶点。在卵巢癌细胞系 TOV21G 中,微细胞介导的 18 号染色体转移诱导了体外和体内的肿瘤抑制。在 TOV21G(+18)杂种中进行的基因表达微阵列分析鉴定出 18 号染色体上 14 个候选基因,这些基因显著过表达,因此与肿瘤抑制相关。对这些基因在其他卵巢癌细胞系中的信使 RNA 和蛋白质表达的进一步分析表明,EPB41L3(红细胞膜蛋白带 4.1 样 3,别名 DAL-1 和 4.1B)是候选的卵巢癌抑制基因。免疫印迹分析显示,EPB41L3 在 TOV21G(+18)杂种中被激活,在正常卵巢上皮细胞系中表达,但在 19 个卵巢癌细胞系中的 15 个(78%)中缺失。使用免疫组织化学方法,与良性卵巢肿瘤(24%)和正常卵巢上皮组织(0%)相比,794 例侵袭性卵巢肿瘤中有 66%没有 EPB41L3 表达。与正常组织相比,EPB41L3 在卵巢癌细胞系和原发性卵巢肿瘤中广泛甲基化(P =.00004),提示这可能是卵巢癌中基因失活的机制。在卵巢癌的三维多细胞球体模型中,EPB41L3 的持续表达导致显著的生长抑制和诱导细胞凋亡。透射和扫描电子显微镜显示,表达 EPB41L3 的细胞与 18 号染色体供体-受体杂种之间有许多相似之处,提示 EPB41L3 是 18 号染色体转移后导致肿瘤抑制的基因。最后,在三维球体中的 EPB41L3 表达诱导模型证实,EPB41L3 的重新表达诱导卵巢癌中广泛的凋亡细胞死亡。