Fabbri Muller, Iliopoulos Dimitrios, Trapasso Francesco, Aqeilan Rami I, Cimmino Amelia, Zanesi Nicola, Yendamuri Sai, Han Shuang-Yin, Amadori Dino, Huebner Kay, Croce Carlo M
Department of Molecular Virology, Immunology, and Medical Genetics, Comprehensive Cancer Center, Ohio State University, 410 West 12th Avenue, Columbus, OH 43201, USA.
Proc Natl Acad Sci U S A. 2005 Oct 25;102(43):15611-6. doi: 10.1073/pnas.0505485102. Epub 2005 Oct 13.
The WWOX (WW domain containing oxidoreductase) gene at the common fragile site, FRA16D, is altered in many types of cancer, including lung cancer. We have examined the tumor suppressor function of WWOX in preclinical lung cancer models. The WWOX gene was expressed in lung cancer cell lines through recombinant adenovirus (Ad) infection (Ad-WWOX), and through a drug [ponasterone A, (ponA)]-inducible system. After WWOX restoration in vitro, endogenous Wwox protein-negative cell lines (A549, H460, and H1299) underwent apoptosis through activation of the intrinsic apoptotic caspase cascade in A549 and H460 cells. Ectopic expression of Wwox caused dramatic suppression of tumorigenicity of A549, H460, and H1299 cells in nude mice after Ad-WWOX infection and after ponA induction of Wwox expression in H1299 lung cancer cells. Tumorigenicity and in vitro growth of U2020 (Wwox-positive) lung cancer cells was unaffected by Wwox overexpression. This study confirms that WWOX is a tumor suppressor gene and is highly effective in preventing growth of lung cancer xenografts, whether introduced through viral infection or by induction of a silent WWOX transgene.
位于常见脆性位点FRA16D的WWOX(含WW结构域的氧化还原酶)基因在包括肺癌在内的多种癌症中发生改变。我们已经在临床前肺癌模型中研究了WWOX的肿瘤抑制功能。通过重组腺病毒(Ad)感染(Ad-WWOX)以及药物[ponasterone A,(ponA)]诱导系统,WWOX基因在肺癌细胞系中得以表达。在体外恢复WWOX表达后,内源性Wwox蛋白阴性的细胞系(A549、H460和H1299)通过激活A549和H460细胞中的内源性凋亡半胱天冬酶级联反应而发生凋亡。在Ad-WWOX感染后以及在ponA诱导H1299肺癌细胞中Wwox表达后,Wwox的异位表达导致A549、H460和H1299细胞在裸鼠中的致瘤性显著受到抑制。U2020(Wwox阳性)肺癌细胞的致瘤性和体外生长不受Wwox过表达的影响。本研究证实,WWOX是一种肿瘤抑制基因,无论通过病毒感染还是诱导沉默的WWOX转基因导入,它在预防肺癌异种移植瘤生长方面都非常有效。