摘要
肿瘤细胞侵袭性表达的一个常见特征是酪氨酸激酶受体RTK的异常表达与激活。在RTK,Axl之间,考虑到致癌信号在不同肿瘤类型中促进细胞增殖活化以及迁移和侵袭的过度表达,Tyro3-Axl-Mer族系中的一员表现了潜在的治疗靶向性。 Axl可以通过PI3K/Akt 和/或MAPK/ERK促进不同种类细胞的侵袭性,并且它的表达可以被多因素转录调控。下调 Axl的表达与活化与靶向且传统的抗肿瘤剂相比,具有明显的降低敏感性的特征。作为 Axl抑制剂的几个小分子已经有报道,它们中的一部分正在进行临床调研。在这篇文章中,我们描述面对癌症以及耐药性肿瘤细胞时,Axl的生物作用以及它的表达。抑制剂的发展与酪氨酸激酶受体的特定作用。
关键词: 癌症;酪氨酸激酶受体;Axl;耐药性;侵袭;抑制剂。
Current Medicinal Chemistry
Title:Role of the Receptor Tyrosine Kinase Axl and its Targeting in Cancer Cells
Volume: 23 Issue: 15
Author(s): Cristina Corno, Laura Gatti, Cinzia Lanzi, Nadia Zaffaroni, Diego Colombo, Paola Perego
Affiliation:
关键词: 癌症;酪氨酸激酶受体;Axl;耐药性;侵袭;抑制剂。
摘要: Aberrant expression and activation of receptor tyrosine kinases (RTK) is a frequent feature of tumor cells that may underlie tumor aggressiveness. Among RTK, Axl, a member of the Tyro3-Axl-Mer family, represents a potential therapeutic target in different tumor types given its over-expression which leads to activation of oncogenic signaling promoting cell proliferation and survival, as well as migration and invasion. Axl can promote aggressiveness of various cell types through PI3K/Akt and/or MAPK/ERK, and its expression can be transcriptionally regulated by multiple factors. Deregulated Axl expression and activation have been shown to be implicated in reduced sensitivity of tumor cells to target-specific and conventional antitumor agents, but the precise mechanism underlying these phenomena are still poorly understood. Several small molecules acting as Axl inhibitors have been reported, and some of them are undergoing clinical investigation. In this review, we describe Axl biological functions, its expression in cancer and in drug-resistant tumor cells and the development of inhibitors tailored to this receptor tyrosine kinase.
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Cristina Corno, Laura Gatti, Cinzia Lanzi, Nadia Zaffaroni, Diego Colombo, Paola Perego , Role of the Receptor Tyrosine Kinase Axl and its Targeting in Cancer Cells, Current Medicinal Chemistry 2016; 23 (15) . https://dx.doi.org/10.2174/0929867323666160405112954
DOI https://dx.doi.org/10.2174/0929867323666160405112954 |
Print ISSN 0929-8673 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-533X |
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