Entering the TiME machine: How age-related changes in the tumor immune microenvironment impact melanoma progression and therapy response

被引:0
|
作者
Carey, Alexis E. [1 ,2 ]
Weeraratna, Ashani T. [1 ,2 ]
机构
[1] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Biochem & Mol Biol, Baltimore, MD USA
[2] Johns Hopkins Sch Med, Sidney Kimmel Canc Ctr, Dept Oncol, Baltimore, MD USA
关键词
Aging; Cancer; Immunotherapy; Immunology; Melanoma; BONE-MARROW ADIPOCYTES; CD8(+) T-CELLS; METASTATIC MELANOMA; IMMUNOLOGICAL SYNAPSE; ANTI-PD-1; THERAPY; MUTATIONAL BURDEN; DENDRITIC CELLS; BRAF MUTATIONS; SURVIVAL; IMMUNOTHERAPY;
D O I
10.1016/j.pharmthera.2024.108698
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Melanoma is the deadliest form of skin cancer in the United States, with its incidence rates rising in older populations. As the immune system undergoes age-related changes, these alterations can significantly influence tumor progression and the effectiveness of cancer treatments. Recent advancements in understanding immune checkpoint molecules have paved the way for the development of innovative immunotherapies targeting solid tumors. However, the aging tumor microenvironment can play a crucial role in modulating the response to these immunotherapeutic approaches. This review seeks to examine the intricate relationship between agerelated changes in the immune system and their impact on the efficacy of immunotherapies, particularly in the context of melanoma. By exploring this complex interplay, we hope to elucidate potential strategies to optimize treatment outcomes for older patients with melanoma, and draw parallels to other cancers. (c) 2024 Published by Elsevier Inc.
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页数:10
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