The microenvironment of secondary lymphedema. The key to finding effective treatments?

IF 4.2 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Biochimica et biophysica acta. Molecular basis of disease Pub Date : 2025-01-17 DOI:10.1016/j.bbadis.2025.167677
Lazina Hossain, Karina P. Gomes, Samaneh Safarpour, Spencer B. Gibson
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Abstract

Lymphedema is characterized by the swelling of extremities due to the accumulation of interstitial fluids. It is a painful and devastating disease that increases the risk of infections and destroys patients' quality of life. Secondary lymphedema is caused by damage to the lymphatic system due to infections, obesity, surgery, and cancer treatments. This damage fails to be repaired and leads to fluid accumulation, tissue remodeling, inflammation, and ultimately fibrosis. The lymphedema microenvironment is altered by stress, immune dysfunction, and changes in metabolism. Stress in the microenvironment includes increased hypoxia and oxidative stress but how this contributes to lymphedema progression is unclear. The immune system plays a critical role in lymphedema through T cell helper type 2 (Th2) immune responses and the infiltration of macrophages into lymphedematous tissue. The inflammatory cytokines released by immune cells lead to tissue remodeling and fibrosis. There are also changes in metabolism in the lymphedema microenvironment with altered lipid oxidation, ketone body oxidation, and glycolysis. How these changes affect lymphedema and treatment interventions has been the focus of clinical trials. Lymphedema is also associated with cancer and obesity through damage to the lymphatic system. This review will illustrate microenvironmental changes in lymphedema and how this relates to cancer and obesity. In addition, we will discuss new therapeutic strategies to treat lymphedema. Finally, we will address the prospects of lymphedema research in the context of the microenvironment.
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继发性淋巴水肿的微环境。找到有效治疗方法的关键是什么?
淋巴水肿的特征是由于组织间液的积聚而导致四肢肿胀。这是一种痛苦和毁灭性的疾病,增加了感染的风险,破坏了患者的生活质量。继发性淋巴水肿是由感染、肥胖、手术和癌症治疗引起的淋巴系统损伤引起的。这种损伤无法修复,导致液体积聚、组织重塑、炎症,最终导致纤维化。淋巴水肿微环境可因应激、免疫功能障碍和代谢变化而改变。微环境中的应激包括缺氧和氧化应激的增加,但这如何导致淋巴水肿进展尚不清楚。免疫系统通过T细胞辅助2型(Th2)免疫反应和巨噬细胞浸润到淋巴水肿组织中,在淋巴水肿中起关键作用。免疫细胞释放的炎性细胞因子导致组织重塑和纤维化。淋巴水肿微环境中的代谢也发生变化,脂质氧化、酮体氧化和糖酵解发生改变。这些变化如何影响淋巴水肿和治疗干预一直是临床试验的重点。淋巴水肿也与癌症和肥胖有关,因为它会损害淋巴系统。这篇综述将阐述淋巴水肿的微环境变化及其与癌症和肥胖的关系。此外,我们将讨论治疗淋巴水肿的新治疗策略。最后,我们将讨论在微环境背景下淋巴水肿研究的前景。
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来源期刊
CiteScore
12.30
自引率
0.00%
发文量
218
审稿时长
32 days
期刊介绍: BBA Molecular Basis of Disease addresses the biochemistry and molecular genetics of disease processes and models of human disease. This journal covers aspects of aging, cancer, metabolic-, neurological-, and immunological-based disease. Manuscripts focused on using animal models to elucidate biochemical and mechanistic insight in each of these conditions, are particularly encouraged. Manuscripts should emphasize the underlying mechanisms of disease pathways and provide novel contributions to the understanding and/or treatment of these disorders. Highly descriptive and method development submissions may be declined without full review. The submission of uninvited reviews to BBA - Molecular Basis of Disease is strongly discouraged, and any such uninvited review should be accompanied by a coverletter outlining the compelling reasons why the review should be considered.
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