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用血管内皮生长因子抑制剂抑制或促进转移:重新审视抗血管生成

Silencing or fueling metastasis with VEGF inhibitors: antiangiogenesis revisited.

作者信息

Loges Sonja, Mazzone Massimiliano, Hohensinner Philipp, Carmeliet Peter

机构信息

Vesalius Research Center, VIB, B-3000 Leuven, Belgium.

出版信息

Cancer Cell. 2009 Mar 3;15(3):167-70. doi: 10.1016/j.ccr.2009.02.007.

Abstract

Clinical practice reveals that therapy with angiogenesis inhibitors often does not prolong survival of cancer patients for more than months, because tumors elicit evasive resistance. In this issue of Cancer Cell, two papers report that VEGF inhibitors reduce primary tumor growth but promote tumor invasiveness and metastasis. These perplexing findings help to explain resistance to these drugs but raise pertinent questions of how to best treat cancer patients with antiangiogenic medicine in the future. We discuss here how VEGF inhibitors can induce such divergent effects on primary tumor growth and metastasis.

摘要

临床实践表明,使用血管生成抑制剂进行治疗往往无法使癌症患者的生存期延长数月以上,因为肿瘤会产生逃避性耐药。在本期《癌细胞》杂志中,两篇论文报道血管内皮生长因子(VEGF)抑制剂可减少原发性肿瘤的生长,但会促进肿瘤的侵袭和转移。这些令人困惑的发现有助于解释对这些药物的耐药性,但也引发了关于未来如何最好地使用抗血管生成药物治疗癌症患者的相关问题。我们在此讨论VEGF抑制剂如何能对原发性肿瘤生长和转移产生如此不同的影响。

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