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COPD 和肺癌中的肺部微生物组:探索基于金属药物的潜力。

The Lung Microbiome in COPD and Lung Cancer: Exploring the Potential of Metal-Based Drugs.

机构信息

School of Medicine, Trinity Translational Medicine Institute, Trinity College Dublin, D08 W9RT Dublin, Ireland.

Department of Histopathology and Morbid Anatomy, Trinity Translational Medicine Institute, St. James's Hospital, D08 RX0X Dublin, Ireland.

出版信息

Int J Mol Sci. 2023 Aug 1;24(15):12296. doi: 10.3390/ijms241512296.

Abstract

Chronic obstructive pulmonary disease (COPD) and lung cancer 17 are two of the most prevalent and debilitating respiratory diseases worldwide, both associated with high morbidity and mortality rates. As major global health concerns, they impose a substantial burden on patients, healthcare systems, and society at large. Despite their distinct aetiologies, lung cancer and COPD share common risk factors, clinical features, and pathological pathways, which have spurred increasing research interest in their co-occurrence. One area of particular interest is the role of the lung microbiome in the development and progression of these diseases, including the transition from COPD to lung cancer. Exploring novel therapeutic strategies, such as metal-based drugs, offers a potential avenue for targeting the microbiome in these diseases to improve patient outcomes. This review aims to provide an overview of the current understanding of the lung microbiome, with a particular emphasis on COPD and lung cancer, and to discuss the potential of metal-based drugs as a therapeutic strategy for these conditions, specifically concerning targeting the microbiome.

摘要

慢性阻塞性肺疾病(COPD)和肺癌 17 是全球最常见和最具致残性的呼吸系统疾病之一,两者都与高发病率和死亡率相关。作为主要的全球健康关注点,它们给患者、医疗保健系统和整个社会带来了巨大的负担。尽管它们的病因不同,但肺癌和 COPD 具有共同的风险因素、临床特征和病理途径,这促使人们对它们的同时发生产生了越来越多的研究兴趣。一个特别感兴趣的领域是肺部微生物组在这些疾病的发展和进展中的作用,包括从 COPD 向肺癌的转变。探索新型治疗策略,如金属基药物,为针对这些疾病中的微生物组以改善患者结局提供了一种潜在途径。本综述旨在概述目前对肺部微生物组的理解,特别强调 COPD 和肺癌,并讨论金属基药物作为这些疾病的治疗策略的潜力,特别是针对微生物组的靶向治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0169/10419288/cab5219efea0/ijms-24-12296-g001.jpg

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