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表达Tie2的单核细胞:肿瘤血管生成的调控及其治疗意义

Tie2-expressing monocytes: regulation of tumor angiogenesis and therapeutic implications.

作者信息

De Palma Michele, Murdoch Craig, Venneri Mary Anna, Naldini Luigi, Lewis Claire E

机构信息

Angiogenesis and Tumor Targeting Research Unit and San Raffaele Telethon Institute for Gene Therapy, San Raffaele Scientific Institute, Via Olgettina, Milan, Italy.

出版信息

Trends Immunol. 2007 Dec;28(12):519-24. doi: 10.1016/j.it.2007.09.004. Epub 2007 Nov 5.

Abstract

Tumor-infiltrating myeloid cells are involved in crucial processes during tumor development. A subset of monocytes that express the angiopoietin receptor Tie2 play an important role in tumor angiogenesis. Selective depletion of these Tie2-expressing monocytes (TEMs) in tumor-bearing mice inhibits tumor angiogenesis and growth, suggesting that they might regulate angiogenic processes in tumors by providing paracrine support to nascent blood vessels. TEMs have also been identified in human blood and tumors. We discuss here the therapeutic opportunities emanating from the discovery of TEMs, which include the identification of new antitumor targets, monitoring TEMs as surrogate markers for clinical responses in cancer patients, and the possible use of TEMs as cellular vehicles for gene delivery to tumors.

摘要

肿瘤浸润性髓样细胞参与肿瘤发展过程中的关键进程。表达血管生成素受体Tie2的单核细胞亚群在肿瘤血管生成中发挥重要作用。在荷瘤小鼠中选择性清除这些表达Tie2的单核细胞(TEMs)可抑制肿瘤血管生成和生长,这表明它们可能通过为新生血管提供旁分泌支持来调节肿瘤中的血管生成过程。在人类血液和肿瘤中也已鉴定出TEMs。我们在此讨论TEMs的发现所带来的治疗机会,其中包括鉴定新的抗肿瘤靶点、将监测TEMs作为癌症患者临床反应的替代标志物,以及可能将TEMs用作将基因递送至肿瘤的细胞载体。

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