Department of Pharmacology, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Cancer. 2011 Dec 1;117(23):5344-50. doi: 10.1002/cncr.26153. Epub 2011 May 23.
Casitas B-lineage lymphoma (Cbl) is an E3 ubiquitin ligase of many tyrosine kinase receptors. The authors previously detected c-Cbl mutation and low protein expression in non-small cell lung cancer (NSCLC). Therefore, it was hypothesized that overexpression of wild-type c-Cbl (c-Cbl WT) exhibits tumor growth inhibition.
Wound healing and transwell assays were conducted to examine cell motility after c-Cbl WT transfection in NSCLC cell lines. The cell cycle was investigated by flow cytometry. A549 and H1299-Luc c-Cbl WT-transfected xenografts and experimental metastasis models were performed to investigate tumor growth and metastasis inhibition in vivo.
Wound healing and transwell assays demonstrated inhibition of migration in the A549 and H226br cells 4 to 24 hours after transfection. Ectopic c-Cbl WT expression was found to reduce cell proliferation at 48 hours in A549 cells. It is important to note that A549 and H1299-Luc cells with ectopic c-Cbl WT expression demonstrated inhibition of tumor growth in vivo. A549 cells overexpressing c-Cbl WT inhibited tumor metastasis in animal models.
To the best of the authors' knowledge, the current study is the first to demonstrate that c-Cbl WT protein overexpression inhibits tumor metastasis and tumor growth in lung cancer xenograft models. These results provide evidence that ectopic expression of c-Cbl WT protein can be potentially applied as targeted therapy for the treatment of lung cancer.
Casitas B 细胞淋巴瘤(Cbl)是许多酪氨酸激酶受体的 E3 泛素连接酶。作者先前在非小细胞肺癌(NSCLC)中检测到 c-Cbl 突变和低蛋白表达。因此,假设野生型 c-Cbl(c-Cbl WT)的过表达会抑制肿瘤生长。
在 NSCLC 细胞系中转染 c-Cbl WT 后,通过划痕愈合和 Transwell 测定来检测细胞迁移。通过流式细胞术研究细胞周期。进行 A549 和 H1299-Luc c-Cbl WT 转染的异种移植和实验性转移模型,以研究体内肿瘤生长和转移抑制。
划痕愈合和 Transwell 测定显示,转染后 4 至 24 小时,A549 和 H226br 细胞的迁移受到抑制。在 A549 细胞中,异位 c-Cbl WT 表达在 48 小时时发现可降低细胞增殖。重要的是要注意,具有异位 c-Cbl WT 表达的 A549 和 H1299-Luc 细胞在体内显示出肿瘤生长抑制。过表达 c-Cbl WT 的 A549 细胞抑制了动物模型中的肿瘤转移。
据作者所知,目前的研究首次表明 c-Cbl WT 蛋白过表达可抑制肺癌异种移植模型中的肿瘤转移和肿瘤生长。这些结果提供了证据,表明异位表达 c-Cbl WT 蛋白可作为治疗肺癌的潜在靶向治疗。