Suppr超能文献

仅使用一种手段可能并不够:癌症抗血管生成治疗的局限性与未来

Playing only one instrument may be not enough: limitations and future of the antiangiogenic treatment of cancer.

作者信息

Quesada Ana R, Medina Miguel Angel, Alba Emilio

机构信息

Department of Molecular Biology and Biochemistry, Faculty of Science, University of Málaga, Spain.

出版信息

Bioessays. 2007 Nov;29(11):1159-68. doi: 10.1002/bies.20655.

Abstract

Angiogenesis plays an essential role in tumor growth, invasion and metastasis. After initial pessimism about the usefulness of the antiangiogenic therapeutic approach for cancer, interest has increased in the development of antiangiogenic compounds after the first clinical approval of an antiangiogenic therapy. The anti-vascular endothelial growth factor (VEGF) antibody bevacizumab has recently been approved for use in combination with chemotherapy for the treatment of metastatic colorectal and non-small cell lung cancer patients. However, no survival benefit has been demonstrated in anti-VEGF monotherapy trials, probably due to the high complexity of tumor angiogenesis regulation. Experimental and clinical data, including the approval of the multitargeted drugs sunitinib and sorafenib, indicate that exciting results, including tumor regression, can be expected from the combined targeting of different pathways in the tumor angiogenesis scenario. Several obstacles, including the high cost of new molecular targeted drugs make this therapeutic approach difficult.

摘要

血管生成在肿瘤生长、侵袭和转移过程中起着至关重要的作用。在最初对癌症抗血管生成治疗方法的有效性持悲观态度之后,随着抗血管生成疗法首次获得临床批准,对抗血管生成化合物的研发兴趣有所增加。抗血管内皮生长因子(VEGF)抗体贝伐单抗最近已被批准与化疗联合用于治疗转移性结直肠癌和非小细胞肺癌患者。然而,在抗VEGF单药治疗试验中尚未证明有生存获益,这可能是由于肿瘤血管生成调节的高度复杂性所致。包括多靶点药物舒尼替尼和索拉非尼获批在内的实验和临床数据表明,在肿瘤血管生成情况下联合靶向不同途径有望取得令人振奋的结果,包括肿瘤消退。包括新型分子靶向药物成本高昂在内的几个障碍使得这种治疗方法颇具难度。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验