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Hypoxia-induced dedifferentiation of tumor cells - A mechanism behind heterogeneity and aggressiveness of solid tumors

机译:低氧诱导的肿瘤细胞去分化-实体瘤异质性和侵袭性的机制

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Histopathological examination of solid tumors frequently reveals pronounced tumor cell heterogeneity with regards to cell organization, cell morphology, cell size, nuclei morphology, etc. Analyses of gene expression patterns by immunohistochemistry or in situ hybridization techniques further strengthen the actual presence of phenotypic heterogeneity, often demonstrating substantial diversity within a given tumor. The molecular mechanisms underlying the phenotypic heterogeneity are very complex with genetic, epigenetic and environmental components. Hypoxia, shortage in oxygen, greatly influences cellular phenotypes by altering the expression of specific genes, and is an important contributor to intra- and inter-tumor cell diversity as revealed by the pronounced but non-uniform expression of hypoxia driven genes in solid tumors (reviewed in [Semenza GL. Targeting HIF-1 for cancer therapy. Nat Rev Cancer 2003;3:721-32; Harris AL. Hypoxia - a key regulatory factor in tumour growth. Nat Rev Cancer 2002;2:38-47.]). The oxygen pressure in solid tumors is generally lower than in the surrounding non-malignant tissues, and tumors exhibiting extensive hypoxia have been shown to be more aggressive than corresponding tumors that are better oxygenized [Vaupel P. Oxygen transport in tumors: characteristics and clinical implications. Adv Exp Med Biol 1996;388:341-51; Vaupel P, Thews 0, Hoeckel M. Treatment resistance of solid tumors: role of hypoxia and anemia. Med Oncol 2001; 18:243-59.]. We recently observed that hypoxic neuroblastoma cells and breast cancer cells loose their differentiated gene expression patterns and develop stem cell-like phenotypes [Jogi A, Ora I, Nilsson H, Lindeheim A, Makino Y, Poellinger L, et a]. Hypoxia alters gene expression in human neuroblastoma cells toward an immature and neural crest-like phenotype. Proc Natl Acad Sci USA 2002;99:7021-6; Helczynska K, Kronblad A, Jogi A, Nilsson E, Beckman S, Landberg G, et al. Hypoxia promotes a dedifferentiated phenotype in ductal breast carcinoma in situ. Cancer Res 2003;63:1441-4.]. As low stage of differentiation in neuroblastoma and in breast cancer is linked to poor prognosis, hypoxia-induced dedifferentiation will not only contribute to tumor heterogeneity but could also be one mechanism behind increased aggressiveness of hypoxic tumors. The effect(s) of hypoxia on tumor cell differentiation status is the focus of this review. (c) 2005 Elsevier Ltd. All rights reserved.
机译:实体瘤的组织病理学检查通常显示出明显的肿瘤细胞在细胞组织,细胞形态,细胞大小,细胞核形态等方面的异质性。通过免疫组织化学或原位杂交技术对基因表达模式的分析进一步加强了表型异质性的实际存在,通常表明给定肿瘤内的实质性多样性。表型异质性的潜在分子机制与遗传,表观遗传和环境成分非常复杂。缺氧,缺氧会通过改变特定基因的表达极大地影响细胞表型,并且是肿瘤内和肿瘤间细胞多样性的重要因素,这由实体肿瘤中缺氧驱动基因的明显但不均匀的表达所揭示( [Semenza GL。HIF-1靶向用于癌症治疗的综述。Nat Rev Cancer 2003; 3:721-32; Harris AL。Hypoxia-肿瘤生长的关键调控因素。Nat Rev Cancer 2002; 2:38-47。]中综述)。实体瘤中的氧气压力通常低于周围的非恶性组织,并且已显示出广泛缺氧的肿瘤比相应的具有更好氧合的肿瘤更具侵略性[Vaupel P.肿瘤中的氧气转运:特征和临床意义。 Adv Exp Med Biol 1996; 388:341-51; Vaupel P,Thews 0,HoeckelM。实体瘤的治疗抗性:缺氧和贫血的作用。 Med Oncol 2001; 18:243-59。]。我们最近观察到缺氧神经母细胞瘤细胞和乳腺癌细胞失去了它们分化的基因表达模式,并发展出干细胞样表型[Jogi A,Ora I,Nilsson H,Lindeheim A,Makino Y,Poellinger L等。缺氧会改变人类神经母细胞瘤细胞的基因表达,使其趋向于未成熟和神经c样表型。美国国家科学院院刊2002; 99:7021-6; Helczynska K,Kronblad A,Jogi A,Nilsson E,Beckman S,Landberg G等。低氧促进乳腺导管原位癌的去分化表型。癌症研究2003; 63:1441-4。]。由于神经母细胞瘤和乳腺癌的低分化阶段与不良预后有关,低氧诱导的去分化不仅会导致肿瘤异质性,而且可能是缺氧肿瘤侵袭性增强的一种机制。缺氧对肿瘤细胞分化状态的影响是本综述的重点。 (c)2005 Elsevier Ltd.保留所有权利。

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