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1
Combination mTOR and IGF-1R inhibition: phase I trial of everolimus and figitumumab in patients with advanced sarcomas and other solid tumors.mTOR 和 IGF-1R 联合抑制:依维莫司和菲特鲁单抗治疗晚期肉瘤和其他实体瘤患者的 I 期试验。
Clin Cancer Res. 2011 Feb 15;17(4):871-9. doi: 10.1158/1078-0432.CCR-10-2621. Epub 2010 Dec 22.
2
Type 1 insulin-like growth factor receptor translocates to the nucleus of human tumor cells.1 型胰岛素样生长因子受体易位至人肿瘤细胞的核内。
Cancer Res. 2010 Aug 15;70(16):6412-9. doi: 10.1158/0008-5472.CAN-10-0052.
3
Molecular analysis of non-small cell lung cancer identifies subsets with different sensitivity to insulin-like growth factor I receptor inhibition.非小细胞肺癌的分子分析确定了对胰岛素样生长因子 I 受体抑制具有不同敏感性的亚组。
Clin Cancer Res. 2010 Sep 15;16(18):4654-65. doi: 10.1158/1078-0432.CCR-10-0089. Epub 2010 Jul 29.
4
Reprogramming the posttranslational code of SRC-3 confers a switch in mammalian systems biology.重新编程 SRC-3 的翻译后密码赋予了哺乳动物系统生物学中的一种转变。
Proc Natl Acad Sci U S A. 2010 Jun 15;107(24):11122-7. doi: 10.1073/pnas.1005262107. Epub 2010 Jun 1.
5
IGF2 over-expression in solitary fibrous tumours is independent of anatomical location and is related to loss of imprinting.孤立性纤维性肿瘤中 IGF2 的过度表达与解剖位置无关,而是与印迹丢失有关。
J Pathol. 2010 Jul;221(3):300-7. doi: 10.1002/path.2715.
6
Sunitinib malate and figitumumab in solitary fibrous tumor: patterns and molecular bases of tumor response.马来酸舒尼替尼和菲特图单抗治疗孤立性纤维瘤:肿瘤反应的模式和分子基础。
Mol Cancer Ther. 2010 May;9(5):1286-97. doi: 10.1158/1535-7163.MCT-09-1205.
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A chromatin-mediated reversible drug-tolerant state in cancer cell subpopulations.肿瘤细胞亚群中染色质介导的可逆药物耐受状态。
Cell. 2010 Apr 2;141(1):69-80. doi: 10.1016/j.cell.2010.02.027.
8
SUMOylation mediates the nuclear translocation and signaling of the IGF-1 receptor.SUMOylation 介导 IGF-1 受体的核转位和信号转导。
Sci Signal. 2010 Feb 9;3(108):ra10. doi: 10.1126/scisignal.2000628.
9
IGF1 and its binding proteins 3 and 1 are differentially associated with metabolic syndrome in older men.胰岛素样生长因子 1 及其结合蛋白 3 和 1 与老年男性代谢综合征的相关性存在差异。
Eur J Endocrinol. 2010 Feb;162(2):249-57. doi: 10.1530/EJE-09-0852. Epub 2009 Nov 16.
10
Impaired insulin secretion and uptake in patients with diffuse idiopathic skeletal hyperostosis.弥漫性特发性骨肥厚患者胰岛素分泌及摄取受损。
Endocr Regul. 2009 Oct;43(4):149-55.

小即是美:胰岛素样生长因子及其在生长、发育和癌症中的作用。

Small is beautiful: insulin-like growth factors and their role in growth, development, and cancer.

机构信息

Memorial Sloan-Kettering Cancer Center, New York, NY 10065-6007, USA.

出版信息

J Clin Oncol. 2010 Nov 20;28(33):4985-95. doi: 10.1200/JCO.2009.27.5040. Epub 2010 Oct 25.

DOI:10.1200/JCO.2009.27.5040
PMID:20975071
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3039924/
Abstract

Insulin-like growth factors were discovered more than 50 years ago as mediators of growth hormone that effect growth and differentiation of bone and skeletal muscle. Interest of the role of insulin-like growth factors in cancer reached a peak in the 1990s, and then waned until the availability in the past 5 years of monoclonal antibodies and small molecules that block the insulin-like growth factor 1 receptor. In this article, we review the history of insulin-like growth factors and their role in growth, development, organism survival, and in cancer, both epithelial cancers and sarcomas. Recent developments regarding phase I to II clinical trials of such agents are discussed, as well as potential studies to consider in the future, given the lack of efficacy of one such monoclonal antibody in combination with cytotoxic chemotherapy in a first-line study in metastatic non-small-cell lung adenocarcinoma. Greater success with these agents clinically is expected when combining the agents with inhibitors of other cell signaling pathways in which cross-resistance has been observed.

摘要

胰岛素样生长因子是 50 多年前作为生长激素的介质被发现的,它影响骨骼和骨骼肌的生长和分化。20 世纪 90 年代,人们对胰岛素样生长因子在癌症中的作用产生了浓厚的兴趣,然后这种兴趣逐渐减弱,直到过去 5 年出现了能够阻断胰岛素样生长因子 1 受体的单克隆抗体和小分子药物。本文回顾了胰岛素样生长因子的历史及其在生长、发育、机体生存以及上皮癌和肉瘤等癌症中的作用。讨论了此类药物的 I 期至 II 期临床试验的最新进展,以及鉴于在转移性非小细胞肺腺癌一线研究中,一种此类单克隆抗体联合细胞毒化疗无效,未来可能需要考虑的潜在研究。当将这些药物与其他已观察到交叉耐药性的细胞信号通路抑制剂联合使用时,预计这些药物在临床上会取得更大的成功。