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癌症患者传统和免疫治疗协议中的氧疗:当前现实与未来前景

英文原题:Oxygen therapy in traditional and immunotherapeutic treatment protocols of cancer patients: current reality and future prospects.

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Oxygen therapy in traditional and immunotherapeutic treatment protocols of cancer patients: current reality and future prospects.

PubMed 2022/04/29(内容时间) Expert Rev Anticancer Ther Q3 · IF 3(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

研究概要

由于 ROS 对先天性和适应性免疫均有深远影响,氧疗与免疫治疗干预(如免疫检查点抑制、药物诱导的免疫刺激、过继性细胞治疗、热疗等)同时或序贯联合应用,可被视为一种新型高效的癌症临床生物学治疗方法。

研究思路结论见上方概要

已知缺血和缺氧肿瘤中的代谢环境有助于癌症进展。重要的是,恶性细胞中发生的特殊代谢变化(糖酵解增强和Krebs循环受阻)可能导致缺血和缺氧肿瘤中抗氧化依赖性防御能力下降。涵盖领域:在临床上,肿瘤的氧饱和度通常通过应用水溶性臭氧和高压氧治疗来实现。在动物实验和临床环境中,已证明肿瘤氧合可抑制肿瘤生长并增强放化疗的抗肿瘤效果。肿瘤氧合可增强通过肿瘤血管闭塞或血管抑制治疗所达到的抗肿瘤效果。

展开英文摘要原文

INTRODUCTION: The metabolic environment in ischemic and hypoxic tumors is known to contribute to cancer progression.

Importantly, peculiar metabolic changes occurring in malignant cells (the increased glycolysis and the hampered Krebs cycle) may contribute to decreased antioxidant-dependent defense in ischemic and hypoxic tumors. AREAS COVERED: In the clinic, oxygen saturation of tumors is usually achieved by the application of water-soluble ozone and hyperbaric oxygen therapy. Tumor oxygenation has been shown to inhibit tumor growth and potentiate anti-tumor effects of chemoradiotherapy in animal experiments and the clinical setting.

Tumor oxygenation could enhance anti-tumor effects achieved by tumor blood vessel occlusion or angiostatic therapy. EXPERT OPINION: Owing to a profound influence of ROS on both the innate and adaptive immunity, oxygen therapy, when combined simultaneously or sequentially with immunotherapeutic interventions (such as immune checkpoint inhibition, drug-induced immunostimulation, adoptive cell therapy, hyperthermia, etc.) , could be considered as a novel highly-effective clinical biological approach to cancer treatment.

论文信息

作者
Seledtsov VI、von Delwig AA
单位
Department of Immunology, Innovita Research Company, Vilnius, Lithuania.Lithuania
期刊
Expert review of anticancer therapy2022 Jun
原文标识
PubMed 35468308 · DOI 10.1080/14737140.2022.2070153