Deguchi Atsuko, Maru Yoshiro
Institute of Advanced Biomedical Engineering and Science, Tokyo Women's Medical University, Tokyo, Japan.
Department of Pharmacology, Tokyo Women's Medical University, Tokyo, Japan.
Cancer Sci. 2025 Feb;116(2):322-328. doi: 10.1111/cas.16407. Epub 2024 Nov 24.
Metastasis is a major cause of cancer-related deaths. Similar to the tumor microenvironment formation, the premetastatic niche develops in distant organs before the arrival of tumor cells. Elucidating the mechanism(s) underlying premetastatic niche formation could contribute to the establishment of effective therapeutic targets for metastasis. Our research indicates that primary tumors hijack Toll-like receptor 4 (TLR4) signaling to establish a premetastatic niche in the lungs by utilizing an endogenous ligand S100A8. S100A8 is expressed not only in immune cells but also in various types of tumor cells. By focusing on S100A8 as a therapeutic target, we identified at least three multivalent S100A8 inhibitory peptides. Here, we review the tumor-promoting role of S100A8-mediated TLR4 signaling and propose S100A8 as a potential therapeutic target for aggressive cancer.
转移是癌症相关死亡的主要原因。与肿瘤微环境的形成类似,在肿瘤细胞到达之前,远处器官中会形成前转移生态位。阐明前转移生态位形成的潜在机制有助于确立有效的转移治疗靶点。我们的研究表明,原发性肿瘤通过利用内源性配体S100A8劫持Toll样受体4(TLR4)信号通路,在肺部建立前转移生态位。S100A8不仅在免疫细胞中表达,也在各种类型的肿瘤细胞中表达。通过将S100A8作为治疗靶点,我们鉴定出至少三种多价S100A8抑制肽。在此,我们综述S100A8介导的TLR4信号通路在肿瘤促进中的作用,并提出S100A8作为侵袭性癌症的潜在治疗靶点。