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缺氧诱导因子 (HIF)-1 抑制剂的最新进展。

Recent advances in hypoxia-inducible factor (HIF)-1 inhibitors.

机构信息

College of Pharmacy, Dongguk University-Seoul, Seoul, Republic of Korea.

出版信息

Eur J Med Chem. 2012 Mar;49:24-40. doi: 10.1016/j.ejmech.2012.01.033. Epub 2012 Jan 24.

Abstract

Tumor hypoxia has been recognized as a common feature of solid tumors and a negative prognostic factor for response to treatment and survival of cancer patients. The discovery of hypoxia-inducible factor-1 (HIF-1), a molecular determinant of responses to hypoxia in mammalian cells, has renewed enthusiasm for discovery and development of targeted therapies exploiting the hypoxic tumor microenvironment. HIF-1 activity in tumors depends on availability of the HIF-1α subunit, the levels of which increase under hypoxic conditions and through activation of oncogenes and/or inactivation of tumor suppressor genes. Increased HIF-1 has been correlated with increased angiogenesis, aggressive tumor growth, and poor patient prognosis, leading to current interest in HIF-1 as promising anticancer drug target. In spite of an ever increasing number of putative small molecule inhibitors of HIF-1, only a few are progressing through preclinical and early clinical development. In this review, we will discuss recent advances in discovery and development of small molecule inhibitors that target the HIF-1 pathway as potential anticancer agents.

摘要

肿瘤缺氧已被认为是实体瘤的常见特征,也是对治疗反应和癌症患者生存的负面预后因素。缺氧诱导因子-1(HIF-1)的发现,作为哺乳动物细胞对缺氧反应的分子决定因素,重新激发了利用缺氧肿瘤微环境开发靶向治疗的发现和开发的热情。肿瘤中的 HIF-1 活性取决于 HIF-1α 亚基的可用性,在缺氧条件下和通过激活癌基因和/或失活肿瘤抑制基因,HIF-1α 水平增加。HIF-1 的增加与血管生成增加、侵袭性肿瘤生长和患者预后不良相关,这导致当前对 HIF-1 作为有前途的抗癌药物靶点的兴趣。尽管有越来越多的 HIF-1 的假定小分子抑制剂,但只有少数正在进行临床前和早期临床开发。在这篇综述中,我们将讨论发现和开发靶向 HIF-1 途径的小分子抑制剂作为潜在抗癌药物的最新进展。

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