Huang Jiayi, Gao Zixu, Xuan Jiangying, Gao Ningyuan, Wei Chuanyuan, Gu Jianying
Department of Plastic and Reconstructive Surgery, Zhongshan Hospital, Fudan University, Shanghai, 200032, P. R. China.
Cell Oncol (Dordr). 2024 Dec;47(6):2099-2112. doi: 10.1007/s13402-024-01027-4. Epub 2024 Dec 20.
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.
尽管黑色素瘤仅占皮肤癌的一小部分,但它在皮肤癌相关死亡中占显著比例,这些死亡大多由转移性疾病引起,而淋巴转移是主要途径。在本综述中,我们专注于黑色素瘤中肿瘤淋巴结(LN)转移的代谢机制。介绍了黑色素瘤LN转移的两种假说,即前转移生态位(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、自噬和铁死亡的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在肿瘤免疫微环境(TIME)中通过代谢重编程与非肿瘤细胞相互作用来促进LN转移。本综述将加深我们对黑色素瘤淋巴结转移机制的理解。