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L1细胞黏附分子作为肿瘤细胞侵袭的调节因子。

L1 cell adhesion molecules as regulators of tumor cell invasiveness.

作者信息

Siesser Priscila F, Maness Patricia F

机构信息

Department of Biochemistry and Biophysics, University of North Carolina, Chapel Hill, NC 27599-7260, USA.

出版信息

Cell Adh Migr. 2009 Jul-Sep;3(3):275-7. doi: 10.4161/cam.3.3.8689. Epub 2009 Jul 7.

DOI:10.4161/cam.3.3.8689
PMID:19483471
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2712809/
Abstract

Fast growing malignant cancers represent a major therapeutic challenge. Basic cancer research has concentrated efforts to determine the mechanisms underlying cancer initiation and progression and reveal candidate targets for future therapeutic treatment of cancer patients. With known roles in fundamental processes required for proper development and function of the nervous system, L1-CAMs have been recently identified as key players in cancer biology. In particular L1 has been implicated in cancer invasiveness and metastasis, and has been pursued as a powerful prognostic factor, indicating poor outcome for patients. Interestingly, L1 has been shown to be important for the survival of cancer stem cells, which are thought to be the source of cancer recurrence. The newly recognized roles for L1CAMs in cancer prompt a search for alternative therapeutic approaches. Despite the promising advances in cancer basic research, a better understanding of the molecular mechanisms dictating L1-mediated signaling is needed for the development of effective therapeutic treatment for cancer patients.

摘要

快速生长的恶性肿瘤是一个重大的治疗挑战。基础癌症研究集中力量确定癌症发生和发展的潜在机制,并揭示未来癌症患者治疗的候选靶点。由于在神经系统正常发育和功能所需的基本过程中发挥已知作用,L1细胞粘附分子(L1-CAMs)最近被确定为癌症生物学中的关键因素。特别是L1与癌症侵袭和转移有关,并已被视为一个强大的预后因素,表明患者预后不良。有趣的是,L1已被证明对癌症干细胞的存活很重要,而癌症干细胞被认为是癌症复发的根源。L1细胞粘附分子在癌症中的新认识作用促使人们寻找替代治疗方法。尽管癌症基础研究取得了有前景的进展,但为了开发有效的癌症患者治疗方法,仍需要更好地理解决定L1介导信号传导的分子机制。

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本文引用的文献

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L1 and NCAM adhesion molecules as signaling coreceptors in neuronal migration and process outgrowth.L1和神经细胞黏附分子作为神经元迁移和轴突生长中的信号共受体。
Curr Opin Neurobiol. 2008 Jun;18(3):245-50. doi: 10.1016/j.conb.2008.07.015.
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Targeting cancer stem cells through L1CAM suppresses glioma growth.通过L1CAM靶向癌症干细胞可抑制胶质瘤生长。
Cancer Res. 2008 Aug 1;68(15):6043-8. doi: 10.1158/0008-5472.CAN-08-1079.
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Invincible, but not invisible: imaging approaches toward in vivo detection of cancer stem cells.无敌却并非无形:用于体内检测癌症干细胞的成像方法
J Clin Oncol. 2008 Jun 10;26(17):2901-10. doi: 10.1200/JCO.2008.16.9573.
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The differential role of L1 in ovarian carcinoma and normal ovarian surface epithelium.L1在卵巢癌和正常卵巢表面上皮中的差异作用。
Cancer Res. 2008 Feb 15;68(4):1110-8. doi: 10.1158/0008-5472.CAN-07-2897.
5
The cytoplasmic part of L1-CAM controls growth and gene expression in human tumors that is reversed by therapeutic antibodies.L1细胞粘附分子的胞质部分控制人类肿瘤中的生长和基因表达,而治疗性抗体可逆转这种情况。
Oncogene. 2008 Feb 21;27(9):1281-9. doi: 10.1038/sj.onc.1210747. Epub 2007 Oct 22.
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L1 is associated with micrometastatic spread and poor outcome in colorectal cancer.L1与结直肠癌的微转移扩散及不良预后相关。
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Int J Cancer. 2007 Dec 1;121(11):2421-33. doi: 10.1002/ijc.22949.
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