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首页> 外文期刊>Frontiers in Cell and Developmental Biology >Overcoming Hypoxia-Mediated Tumor Progression: Combinatorial Approaches Targeting pH Regulation, Angiogenesis and Immune Dysfunction
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Overcoming Hypoxia-Mediated Tumor Progression: Combinatorial Approaches Targeting pH Regulation, Angiogenesis and Immune Dysfunction

机译:克服缺氧介导的肿瘤进展:针对pH调节,血管生成和免疫功能障碍的组合方法。

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Hypoxia is an important contributor to the heterogeneity of the microenvironment of solid tumors and is a significant environmental stressor that drives adaptations which are essential for the survival and metastatic capabilities of tumor cells. Critical adaptive mechanisms include altered metabolism, pH regulation, epithelial-mesenchymal transition, angiogenesis, migration/invasion, diminished response to immune cells and resistance to chemotherapy and radiation therapy. In particular, pH regulation by hypoxic tumor cells, through the modulation of cell surface molecules such as extracellular carbonic anhydrases (CAIX and CAXII) and monocarboxylate transporters (MCT-1 and MCT-4) functions to increase cancer cell survival and enhance cell invasion while also contributing to immune evasion. Indeed, CAIX is a vital regulator of hypoxia mediated tumor progression, and targeted inhibition of its function results in reduced tumor growth, metastasis, and cancer stem cell function. However, the integrated contributions of the repertoire of hypoxia-induced effectors of pH regulation for tumor survival and invasion remain to be fully explored and exploited as therapeutic avenues. For example, the clinical use of anti-angiogenic agents has identified a conundrum whereby this treatment increases hypoxia and cancer stem cell components of tumors, and accelerates metastasis. Furthermore, hypoxia results in the infiltration of myeloid-derived suppressor cells (MDSCs), regulatory T cells (Treg) and Tumor Associated Macrophages (TAMs), and also stimulates the expression of PD-L1 on tumor cells, which collectively suppress T-cell mediated tumor cell killing. Therefore, combinatorial targeting of angiogenesis, the immune system and pH regulation in the context of hypoxia may lead to more effective strategies for curbing tumor progression and therapeutic resistance, thereby increasing therapeutic efficacy and leading to more effective strategies for the treatment of patients with aggressive cancer.
机译:缺氧是导致实体瘤微环境异质性的重要因素,并且是驱动适应环境的重要环境压力,而适应环境对于肿瘤细胞的存活和转移能力至关重要。关键的适应性机制包括代谢改变,pH调节,上皮-间充质转化,血管生成,迁移/侵袭,对免疫细胞的应答减弱以及对化学疗法和放射疗法的抵抗力。尤其是低氧肿瘤细胞通过调节细胞表面分子(例如细胞外碳酸酐酶(CAIX和CAXII)和单羧酸盐转运蛋白(MCT-1和MCT-4))来调节pH的作用是增加癌细胞的存活率并增强细胞侵袭性,也有助于逃避免疫。确实,CAIX是缺氧介导的肿瘤进展的重要调节剂,其功能的靶向抑制导致肿瘤生长,转移和癌症干细胞功能降低。然而,缺氧诱导的pH调节效应子库对于肿瘤存活和侵袭的综合贡献尚待充分探索和开发作为治疗途径。例如,抗血管生成剂的临床使用已经确定了一个难题,由此这种治疗增加了肿瘤的缺氧和癌症干细胞成分,并加速了转移。此外,低氧导致髓样来源的抑制细胞(MDSC),调节性T细胞(Treg)和肿瘤相关巨噬细胞(TAM)的浸润,并且还刺激PD-L1在肿瘤细胞上的表达,从而共同抑制T细胞。介导的肿瘤细胞杀伤。因此,在缺氧的情况下血管生成,免疫系统和pH调节的组合靶向可导致更有效的策略来抑制肿瘤的进展和治疗抗性,从而提高治疗效果并导致更有效的策略来治疗侵袭性癌症患者。

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