Chien Wenwen, Kumagai Takashi, Miller Carl W, Desmond Julian C, Frank Jonathan M, Said Jonathan W, Koeffler H Phillip
Department of Hematology/Oncology, Cedars-Sinai Research Institute, UCLA School of Medicine, 110 George Burns Rd., D5065, Los Angeles, CA 90048, USA.
J Biol Chem. 2004 Dec 17;279(51):53087-96. doi: 10.1074/jbc.M410254200. Epub 2004 Oct 7.
Cyr61 (CCN1) is a member of the CCN protein family; these secreted proteins are involved in diverse biological processes such as cell adhesion, angiogenesis, apoptosis, and either growth arrest or growth stimulation depending on the cellular context. We studied the role of Cyr61 in endometrial tumorigenesis. Levels of Cyr61 were decreased in endometrial tumors compared with normal endometrium. Knockdown of Cyr61 expression by RNA interference in a well differentiated endometrial adenocarcinoma cell line (Ishikawa) stimulated its cellular growth. Conversely, overexpression of the protein in the undifferentiated AN3CA endometrial cancer cell line decreased their growth concurrently with increased apoptosis in liquid culture. These same cells had decreased clonogenic capacity and a nearly complete loss of tumorigenicity in vivo. Furthermore, partially purified Cyr61 suppressed growth of endometrial cancer cells. The increased apoptosis in these endometrial cancer cells with forced overexpression of Cyr61 was associated with elevated expression of the pro-apoptotic proteins Bax, Bad, and TRAIL (tumor necrosis factor receptor-associated ligand). Cyr61-induced caspase-3 activation and depolarization of mitochondrial membrane. In summary, endometrial cancer cells have decreased expression of Cyr61 compared with normal endometrium, and this lowered expression may provide the transformed cells a growth advantage over their normal counterpart.
Cyr61(CCN1)是CCN蛋白家族的一员;这些分泌蛋白参与多种生物学过程,如细胞黏附、血管生成、细胞凋亡,以及根据细胞环境而定的生长停滞或生长刺激。我们研究了Cyr61在子宫内膜肿瘤发生中的作用。与正常子宫内膜相比,子宫内膜肿瘤中Cyr61的水平降低。在高分化子宫内膜腺癌细胞系(Ishikawa)中,通过RNA干扰敲低Cyr61表达可刺激其细胞生长。相反,在未分化的AN3CA子宫内膜癌细胞系中过表达该蛋白,会使其在液体培养中生长减少,同时细胞凋亡增加。这些相同的细胞在体内的克隆形成能力降低,致瘤性几乎完全丧失。此外,部分纯化的Cyr61可抑制子宫内膜癌细胞的生长。在这些强制过表达Cyr61的子宫内膜癌细胞中,凋亡增加与促凋亡蛋白Bax、Bad和TRAIL(肿瘤坏死因子受体相关配体)的表达升高有关。Cyr61诱导caspase-3激活和线粒体膜去极化。总之,与正常子宫内膜相比,子宫内膜癌细胞中Cyr61的表达降低,这种降低的表达可能使转化细胞比其正常对应细胞具有生长优势。