Department of Medical Microbiology, Immunology, and Cell Biology, Southern Illinois University School of Medicine, PO Box 19629, Springfield, IL 62794, USA.
Front Biosci (Landmark Ed). 2010 Jan 1;15(1):213-25. doi: 10.2741/3616.
By a multiplicity of mechanisms, hypoxia and acidosis create a nurturing environment for tumor progression and the evolution of metastatic, drug-resistant cells. Acidosis drives mutagenesis and promotes the subversion of checkpoints and apoptotic mechanisms. Hypoxic tissues secrete cytokines that undermine normal anti-tumor surveillance by macrophages, turning them into accomplices and facilitators of invasion and angiogenesis. Invasiveness is also abetted by acidosis, the result of shifting to an anaerobic glycolytic metabolism. These factors explain the generally poor prognosis indicated by tumors expressing hypoxia-inducible factor-1 (HIF-1). However, these insights into the physiology of hypoxic tumors have inspired the development of new chemotherapeutic approaches directed at these tissues, including bioreductive drugs and gene therapies, some of which are in clinical trials. The ability to target the hypoxic compartment should allow longer progression-free survival and overall survival of patients bearing solid tumor malignancies.
缺氧和酸中毒通过多种机制为肿瘤的进展和转移性、耐药细胞的进化创造了有利的环境。酸中毒会导致突变,并促进检查点和细胞凋亡机制的颠覆。缺氧组织分泌细胞因子,削弱了巨噬细胞对正常抗肿瘤的监测,使它们成为肿瘤侵袭和血管生成的帮凶和促进者。酸中毒也会促进侵袭,这是转向无氧糖酵解代谢的结果。这些因素解释了表达缺氧诱导因子-1 (HIF-1) 的肿瘤通常预后不良的原因。然而,这些对缺氧肿瘤生理学的认识激发了针对这些组织的新化疗方法的发展,包括生物还原药物和基因治疗,其中一些正在临床试验中。靶向缺氧区的能力应该可以延长患有实体瘤恶性肿瘤的患者的无进展生存期和总生存期。