Jozkowicz Alicja, Was Halina, Dulak Jozef
Department of Medical Biotechnology, Faculty of Biochemistry, Biophysics, and Biotechnology, Jagiellonian University, Krakow, Poland.
Antioxid Redox Signal. 2007 Dec;9(12):2099-117. doi: 10.1089/ars.2007.1659.
Heme oxygenase-1 (HO-1) catalyzes the oxidation of heme to biologically active products: carbon monoxide (CO), biliverdin, and ferrous iron. It participates in maintaining cellular homeostasis and plays an important protective role in the tissues by reducing oxidative injury, attenuating the inflammatory response, inhibiting cell apoptosis, and regulating cell proliferation. HO-1 is also an important proangiogenic mediator. Most studies have focused on the role of HO-1 in cardiovascular diseases, in which its significant, beneficial activity is well recognized. A growing body of evidence indicates, however, that HO-1 activation may play a role in carcinogenesis and can potently influence the growth and metastasis of tumors. HO-1 is very often upregulated in tumor tissues, and its expression is further increased in response to therapies. Although the exact effect can be tissue specific, HO-1 can be regarded as an enzyme facilitating tumor progression. Accordingly, inhibition of HO-1 can be suggested as a potential therapeutic approach sensitizing tumors to radiation, chemotherapy, or photodynamic therapy.
血红素加氧酶-1(HO-1)催化血红素氧化生成具有生物活性的产物:一氧化碳(CO)、胆绿素和亚铁离子。它参与维持细胞稳态,并通过减少氧化损伤、减轻炎症反应、抑制细胞凋亡和调节细胞增殖,在组织中发挥重要的保护作用。HO-1也是一种重要的促血管生成介质。大多数研究集中于HO-1在心血管疾病中的作用,其显著的有益活性已得到充分认可。然而,越来越多的证据表明,HO-1激活可能在致癌过程中发挥作用,并能有力地影响肿瘤的生长和转移。HO-1在肿瘤组织中常常上调,并且其表达在治疗后会进一步增加。尽管确切的作用可能具有组织特异性,但HO-1可被视为一种促进肿瘤进展的酶。因此,抑制HO-1可被认为是一种使肿瘤对放疗、化疗或光动力治疗敏感的潜在治疗方法。