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本文引用的文献

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Mutations of the TET2 and CBL genes: novel molecular markers in myeloid malignancies.TET2 和 CBL 基因突变:髓系恶性肿瘤的新型分子标志物。
Ann Hematol. 2010 Jul;89(7):643-52. doi: 10.1007/s00277-010-0920-6. Epub 2010 Mar 2.
2
CBL is frequently altered in lung cancers: its relationship to mutations in MET and EGFR tyrosine kinases.CBL 经常在肺癌中发生改变:其与 MET 和 EGFR 酪氨酸激酶突变的关系。
PLoS One. 2010 Jan 29;5(1):e8972. doi: 10.1371/journal.pone.0008972.
3
The EphB6 receptor cooperates with c-Cbl to regulate the behavior of breast cancer cells.EphB6 受体与 c-Cbl 合作调节乳腺癌细胞的行为。
Cancer Res. 2010 Feb 1;70(3):1141-53. doi: 10.1158/0008-5472.CAN-09-1710. Epub 2010 Jan 19.
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Gain-of-function of mutated C-CBL tumour suppressor in myeloid neoplasms.突变型C-CBL肿瘤抑制因子在髓系肿瘤中的功能获得
Nature. 2009 Aug 13;460(7257):904-8. doi: 10.1038/nature08240. Epub 2009 Jul 20.
5
Dual MET-EGFR combinatorial inhibition against T790M-EGFR-mediated erlotinib-resistant lung cancer.双重MET-EGFR联合抑制对T790M-EGFR介导的厄洛替尼耐药肺癌的作用
Br J Cancer. 2008 Sep 16;99(6):911-22. doi: 10.1038/sj.bjc.6604559.
6
A tale of two Cbls: interplay of c-Cbl and Cbl-b in epidermal growth factor receptor downregulation.两个Cbl的故事:c-Cbl与Cbl-b在表皮生长因子受体下调中的相互作用
Mol Cell Biol. 2008 May;28(9):3020-37. doi: 10.1128/MCB.01809-07. Epub 2008 Mar 3.
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EGFR mutants found in non-small cell lung cancer show different levels of sensitivity to suppression of Src: implications in targeting therapy.在非小细胞肺癌中发现的表皮生长因子受体(EGFR)突变体对Src抑制表现出不同程度的敏感性:对靶向治疗的启示
Oncogene. 2008 Feb 7;27(7):957-65. doi: 10.1038/sj.onc.1210684. Epub 2007 Jul 23.
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Defective ubiquitinylation of EGFR mutants of lung cancer confers prolonged signaling.肺癌表皮生长因子受体(EGFR)突变体的泛素化缺陷导致信号传导延长。
Oncogene. 2007 Oct 25;26(49):6968-78. doi: 10.1038/sj.onc.1210503. Epub 2007 May 7.
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Flt3-dependent transformation by inactivating c-Cbl mutations in AML.急性髓系白血病中通过使c-Cbl突变失活实现的Flt3依赖性转化。
Blood. 2007 Aug 1;110(3):1004-12. doi: 10.1182/blood-2007-01-066076. Epub 2007 Apr 19.
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The Cbl family proteins: ring leaders in regulation of cell signaling.Cbl家族蛋白:细胞信号调节的核心分子
J Cell Physiol. 2006 Oct;209(1):21-43. doi: 10.1002/jcp.20694.

E3 泛素连接酶:c-Cbl:肺癌的一个新的治疗靶点。

An E3 ubiquitin ligase: c-Cbl: a new therapeutic target of lung cancer.

机构信息

Department of Pharmacology, College of Medicine, National Cheng Kung University, Tainan, Taiwan.

出版信息

Cancer. 2011 Dec 1;117(23):5344-50. doi: 10.1002/cncr.26153. Epub 2011 May 23.

DOI:10.1002/cncr.26153
PMID:21607942
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3383858/
Abstract

BACKGROUND

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.

METHODS

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

背景

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。

方法

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。

结果

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。

结论

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。