Emami Nejad Asieh, Najafgholian Simin, Rostami Alireza, Sistani Alireza, Shojaeifar Samaneh, Esparvarinha Mojgan, Nedaeinia Reza, Haghjooy Javanmard Shaghayegh, Taherian Marjan, Ahmadlou Mojtaba, Salehi Rasoul, Sadeghi Bahman, Manian Mostafa
Department of Biology, Payame Noor University (PNU), P.O.Box 19395-3697, Tehran, Iran.
Department of Emergency Medicine, School of Medicine , Arak University of Medical Sciences, Arak, Iran.
Cancer Cell Int. 2021 Jan 20;21(1):62. doi: 10.1186/s12935-020-01719-5.
Hypoxia is a common feature of solid tumors, and develops because of the rapid growth of the tumor that outstrips the oxygen supply, and impaired blood flow due to the formation of abnormal blood vessels supplying the tumor. It has been reported that tumor hypoxia can: activate angiogenesis, thereby enhancing invasiveness and risk of metastasis; increase survival of tumor, as well as suppress anti-tumor immunity and hamper the therapeutic response. Hypoxia mediates these effects by several potential mechanisms: altering gene expression, the activation of oncogenes, inactivation of suppressor genes, reducing genomic stability and clonal selection. We have reviewed the effects of hypoxia on tumor biology and the possible strategiesto manage the hypoxic tumor microenvironment (TME), highlighting the potential use of cancer stem cells in tumor treatment.
缺氧是实体瘤的一个常见特征,其产生是由于肿瘤生长迅速,超过了氧气供应,以及为肿瘤供血的异常血管形成导致血流受损。据报道,肿瘤缺氧可:激活血管生成,从而增强侵袭性和转移风险;提高肿瘤存活率,同时抑制抗肿瘤免疫并阻碍治疗反应。缺氧通过几种潜在机制介导这些效应:改变基因表达、激活癌基因、使抑癌基因失活、降低基因组稳定性和进行克隆选择。我们综述了缺氧对肿瘤生物学的影响以及管理缺氧肿瘤微环境(TME)的可能策略,重点介绍了癌症干细胞在肿瘤治疗中的潜在用途。