Potter Christian, Harris Adrian L
Molecular Oncology Laboratories, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital Oxford, UK.
Cell Cycle. 2004 Feb;3(2):164-7.
Over 50 genes are inducible by hypoxia, via hypoxia inducible factor 1alpha (HIF-1alpha). Carbonic anhydrase IX (CAIX) is one of the most inducible and most uniformly induced genes and because of its stability and membrane location provides a reliable histochemical marker of hypoxia. Recent studies have shown the importance of pH in cell death under hypoxia, thus mechanisms of pH regulation are likely to be vital pathways for survival. Carbonic anhydrases have a widespread role in normal tissues in regulating pH, with 14 isoforms described, so inhibition may have substantial normal tissue toxicity. Selective nonmembrane permeable inhibitors are available and may synergise with chemotherapy agents more active in acid conditions. CAIX has a major role in regulating hydrogen ion (H+) flux and blockade of CAIX results in increased cell death under hypoxia, indicating that it is one mechanism of hypoxic adaptation. As it is commonly expressed in tumours with the worst prognosis it is a potential target for therapy.
超过50个基因可通过缺氧诱导因子1α(HIF-1α)被缺氧诱导。碳酸酐酶IX(CAIX)是诱导性最强且诱导最一致的基因之一,由于其稳定性和膜定位,它是缺氧的可靠组织化学标志物。最近的研究表明pH在缺氧诱导的细胞死亡中具有重要作用,因此pH调节机制可能是细胞存活的关键途径。碳酸酐酶在正常组织中广泛参与pH调节,已描述的有14种同工型,因此抑制作用可能对正常组织具有显著毒性。选择性非膜通透性抑制剂是可用的,并且可能与在酸性条件下更具活性的化疗药物协同作用。CAIX在调节氢离子(H +)通量方面起主要作用,阻断CAIX会导致缺氧条件下细胞死亡增加,这表明它是缺氧适应的一种机制。由于它在预后最差的肿瘤中普遍表达,它是一个潜在的治疗靶点。