Metabolic insights into tumor lymph node metastasis in melanoma.

IF 4.9 2区 医学 Q2 CELL BIOLOGY
Cellular Oncology Pub Date : 2024-12-01 Epub Date: 2024-12-20 DOI:10.1007/s13402-024-01027-4
Jiayi Huang, Zixu Gao, Jiangying Xuan, Ningyuan Gao, Chuanyuan Wei, Jianying Gu
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引用次数: 0

Abstract

Although accounting for only a small amount of skin cancers, melanoma contributes prominently to skin cancer-related deaths, which are mostly caused by metastatic diseases, and lymphatic metastasis constitutes the main route. In this review, we concentrate on the metabolic mechanisms of tumor lymph node (LN) metastasis in melanoma. Two hypotheses of melanoma LN metastasis are introduced, which are the premetastatic niche (PMN) and parallel progression model. Dysregulation of oxidative stress, lactic acid concentration, fatty acid synthesis, amino acid metabolism, autophagy, and ferroptosis construct the metabolic mechanisms in LN metastasis of melanoma. Moreover, melanoma cells also promote LN metastasis by interacting with non-tumor cells through metabolic reprogramming in TIME. This review will deepen our understanding of the mechanism of lymph node metastasis in melanoma.

黑色素瘤中肿瘤淋巴结转移的代谢见解。
虽然黑色素瘤只占皮肤癌的一小部分,但它是皮肤癌相关死亡的重要原因,皮肤癌相关死亡主要由转移性疾病引起,而淋巴转移是主要途径。本文就黑色素瘤淋巴结转移的代谢机制作一综述。介绍了黑色素瘤淋巴结转移的两种假设,即转移前生态位(PMN)和平行进展模型。氧化应激、乳酸浓度、脂肪酸合成、氨基酸代谢、自噬、铁下垂等失调构成了黑色素瘤LN转移的代谢机制。此外,黑色素瘤细胞还通过TIME中的代谢重编程与非肿瘤细胞相互作用,促进淋巴结转移。本文综述将加深我们对黑色素瘤淋巴结转移机制的认识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cellular Oncology
Cellular Oncology ONCOLOGY-CELL BIOLOGY
CiteScore
10.30
自引率
1.50%
发文量
86
审稿时长
12 months
期刊介绍: The Official Journal of the International Society for Cellular Oncology Focuses on translational research Addresses the conversion of cell biology to clinical applications Cellular Oncology publishes scientific contributions from various biomedical and clinical disciplines involved in basic and translational cancer research on the cell and tissue level, technical and bioinformatics developments in this area, and clinical applications. This includes a variety of fields like genome technology, micro-arrays and other high-throughput techniques, genomic instability, SNP, DNA methylation, signaling pathways, DNA organization, (sub)microscopic imaging, proteomics, bioinformatics, functional effects of genomics, drug design and development, molecular diagnostics and targeted cancer therapies, genotype-phenotype interactions. A major goal is to translate the latest developments in these fields from the research laboratory into routine patient management. To this end Cellular Oncology forms a platform of scientific information exchange between molecular biologists and geneticists, technical developers, pathologists, (medical) oncologists and other clinicians involved in the management of cancer patients. In vitro studies are preferentially supported by validations in tumor tissue with clinicopathological associations.
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