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首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Recent advances in hypoxia-inducible factor (HIF)-1 inhibitors.
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Recent advances in hypoxia-inducible factor (HIF)-1 inhibitors.

机译:缺氧诱导因子(HIF)-1抑制剂的最新进展。

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摘要

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.
机译:肿瘤缺氧已被认为是实体瘤的共同特征,也是对癌症患者的治疗和生存反应的不良预后因素。缺氧诱导因子-1(HIF-1)是哺乳动物细胞中对缺氧反应的分子决定因素,这一发现重新激发了人们对利用缺氧肿瘤微环境开发靶向疗法的热情。肿瘤中的HIF-1活性取决于HIF-1α亚基的可用性,该亚基水平在低氧条件下并通过激活癌基因和/或灭活肿瘤抑制基因而增加。 HIF-1的增加与血管生成的增加,侵袭性肿瘤的生长以及患者预后不良相关,从而导致当前对HIF-1作为有希望的抗癌药物靶标的兴趣。尽管HIF-1的假定小分子抑制剂的数量不断增加,但只有少数几种正在通过临床前和早期临床开发而发展。在这篇综述中,我们将讨论发现和开发靶向HIF-1途径作为潜在抗癌药的小分子抑制剂的最新进展。

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