Bossolasco M, Veillette F, Bertrand R, Mes-Masson A-M
Centre de recherche du Centre Hospitalier de l'Université de Montréal (CR-CHUM) and Institut du cancer de Montréal, Montreal, Quebec, Canada.
Oncogene. 2006 Aug 3;25(33):4549-58. doi: 10.1038/sj.onc.1209488. Epub 2006 Mar 20.
We have previously described hTDE1, the human homologue of the recently described TDE1/TMS family of proteins whose members have been identified in several species. Although a defined biochemical activity has yet to be assigned to TDE1/TMS family members, previous results point to the overexpression of family members in tumor cell lines or tissues. To define whether hTDE1 may directly impact on neoplastic transformation, we derived and characterized stable Rat-1 transfectants that constitutively express hTDE1 at the plasma membrane. Expression of hTDE1 in Rat-1 transfectants had a significant effect on cell contact inhibition in vitro as judged by a focus formation assay. In addition, by monitoring caspase-3 activity and Hoechst staining, we determined that hTDE1 overexpression partially protects cells from serum starvation- and etoposide-induced apoptosis. Finally, hTDE1 Rat-1-expressing clones accelerated the formation of tumors in a nude mouse assay. Our results suggest that hTDE1 contributes directly to oncogenesis in vivo that may in part be explained by its effect on apoptosis in vitro.
我们之前描述过hTDE1,它是最近描述的TDE1/TMS蛋白家族的人类同源物,该家族成员已在多个物种中被鉴定出来。尽管尚未确定TDE1/TMS家族成员的特定生化活性,但先前的结果表明该家族成员在肿瘤细胞系或组织中过表达。为了确定hTDE1是否可能直接影响肿瘤转化,我们构建并鉴定了在质膜上组成性表达hTDE1的稳定Rat-1转染细胞系。通过集落形成试验判断,hTDE1在Rat-1转染细胞系中的表达对体外细胞接触抑制有显著影响。此外,通过监测caspase-3活性和Hoechst染色,我们确定hTDE1的过表达部分保护细胞免受血清饥饿和依托泊苷诱导的凋亡。最后,在裸鼠试验中,表达hTDE1的Rat-1克隆加速了肿瘤的形成。我们的结果表明,hTDE1直接促进体内肿瘤发生,这部分可能是由其对体外凋亡的影响所解释的。