以c-Met為腫瘤治療靶點(diǎn)的受體酪氨酸激酶抑制劑的研究進(jìn)展
發(fā)布時間:2018-08-28 11:12
【摘要】:受體酪氨酸激酶c-Met在細(xì)胞的增殖、代謝以及腫瘤的產(chǎn)生、轉(zhuǎn)移、血管生成中扮演著重要角色,c-Met成為抗腫瘤治療的重要靶點(diǎn)。HGF/c-Met信號通路與VEGFR等其他通路的相互作用(cross-talk)影響了抗腫瘤藥物的作用效果,產(chǎn)生耐藥性,因此,多激酶靶點(diǎn)聯(lián)合用藥成為新的抗腫瘤治療手段。本文介紹了c-Met信號通路與多種膜受體間的相互作用以及由這種相互作用引起的對激酶抑制劑的耐藥性,并綜述了單靶點(diǎn)和多靶點(diǎn)的小分子c-Met抑制劑的研究進(jìn)展。
[Abstract]:Receptor tyrosine kinase c-Met is involved in cell proliferation, metabolism, tumorigenesis and metastasis. Angiogenesis plays an important role in anti-tumor therapy. The interaction between c-Met signaling pathway and other pathways such as VEGFR (cross-talk) affects the effect of anti-tumor drugs and results in drug resistance. The combination of multi-kinase targets has become a new anti-tumor therapy. In this paper, the interaction between c-Met signaling pathway and multiple membrane receptors and the resistance to kinase inhibitors caused by this interaction are reviewed, and the research progress of single-target and multi-target small molecular c-Met inhibitors is reviewed.
【作者單位】: 中國藥科大學(xué)藥物化學(xué)教研室;
【分類號】:R943
本文編號:2209226
[Abstract]:Receptor tyrosine kinase c-Met is involved in cell proliferation, metabolism, tumorigenesis and metastasis. Angiogenesis plays an important role in anti-tumor therapy. The interaction between c-Met signaling pathway and other pathways such as VEGFR (cross-talk) affects the effect of anti-tumor drugs and results in drug resistance. The combination of multi-kinase targets has become a new anti-tumor therapy. In this paper, the interaction between c-Met signaling pathway and multiple membrane receptors and the resistance to kinase inhibitors caused by this interaction are reviewed, and the research progress of single-target and multi-target small molecular c-Met inhibitors is reviewed.
【作者單位】: 中國藥科大學(xué)藥物化學(xué)教研室;
【分類號】:R943
【共引文獻(xiàn)】
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1 張文娟;Streptomyces djakartensis NW35菌株發(fā)酵液的抑菌活性及抑菌成分研究[D];西北農(nóng)林科技大學(xué);2013年
【相似文獻(xiàn)】
相關(guān)碩士學(xué)位論文 前1條
1 孫愛學(xué);以c-Met為靶點(diǎn)的新型抑制劑的設(shè)計與合成研究[D];南京理工大學(xué);2014年
,本文編號:2209226
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