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新型多价 S100A8 抑制肽通过抑制 TLR4 依赖性途径来减弱肿瘤的进展和转移。

Novel multivalent S100A8 inhibitory peptides attenuate tumor progression and metastasis by inhibiting the TLR4-dependent pathway.

机构信息

Department of Pharmacology, Tokyo Women's Medical University, 8-1 Kawada-cho, Shinjuku-ku, Tokyo, 162-8666, Japan.

Faculty of Life and Medical Sciences, Doshisha University, 1-3 Miyakotani, Tatara, Kyotanabe, Kyoto, 610-0321, Japan.

出版信息

Cancer Gene Ther. 2023 Jul;30(7):973-984. doi: 10.1038/s41417-023-00604-3. Epub 2023 Mar 17.

Abstract

The tumor-elicited inflammation is closely related to tumor microenvironment during tumor progression. S100A8, an endogenous ligand of Toll-like receptor 4 (TLR4), is known as a key molecule in the tumor microenvironment and premetastatic niche formation. We firstly generated a novel multivalent S100A8 competitive inhibitory peptide (divalent peptide3A5) against TLR4/MD-2, using the alanine scanning. Divalent peptide3A5 suppressed S100A8-mediated interleukin-8 and vascular endothelial growth factor production in human colorectal tumor SW480 cells. Using SW480-transplanted xenograft models, divalent peptide3A5 suppressed tumor progression in a dose-dependent manner. We demonstrated that combination therapy with divalent peptide3A5 and bevacizumab synergistically suppressed tumor growth in SW480 xenograft models. Using syngeneic mouse models, we found that divalent peptide3A5 improved the efficacy of anti-programmed death (PD)1 antibody, and lung metastasis. In addition, by using multivalent peptide library screening based on peptide3A5, we then isolated two more candidates; divalent ILVIK, and tetravalent ILVIK. Of note, multivalent ILVIK, but not monovalent ILVIK showed competitive inhibitory activity against TLR4/MD-2 complex, and anti-tumoral activity in SW480 xenograft models. As most tumor cells including SW480 cells also express TLR4, S100A8 inhibitory peptides would target both the tumor microenvironment and tumor cells. Thus, multivalent S100A8 inhibitory peptides would provide new pharmaceutical options for aggressive cancers.

摘要

肿瘤诱导的炎症与肿瘤进展过程中的肿瘤微环境密切相关。S100A8 是 Toll 样受体 4(TLR4)的内源性配体,是肿瘤微环境和前转移龛形成的关键分子。我们首先使用丙氨酸扫描生成了一种针对 TLR4/MD-2 的新型多价 S100A8 竞争抑制肽(二价肽 3A5)。二价肽 3A5 抑制人结直肠肿瘤 SW480 细胞中 S100A8 介导的白细胞介素-8 和血管内皮生长因子的产生。在 SW480 移植异种移植模型中,二价肽 3A5 以剂量依赖性方式抑制肿瘤进展。我们证明,二价肽 3A5 与贝伐单抗联合治疗可协同抑制 SW480 异种移植模型中的肿瘤生长。使用同基因小鼠模型,我们发现二价肽 3A5 可提高抗程序性死亡(PD)1 抗体的疗效,并减少肺部转移。此外,通过基于肽 3A5 的多价肽文库筛选,我们随后分离出另外两个候选物;二价 ILVIK 和四价 ILVIK。值得注意的是,多价 ILVIK 而非单价 ILVIK 对 TLR4/MD-2 复合物具有竞争抑制活性,并在 SW480 异种移植模型中具有抗肿瘤活性。由于包括 SW480 细胞在内的大多数肿瘤细胞也表达 TLR4,因此 S100A8 抑制肽将靶向肿瘤微环境和肿瘤细胞。因此,多价 S100A8 抑制肽将为侵袭性癌症提供新的药物选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bfd/10353929/eb824b4ea06e/41417_2023_604_Fig1_HTML.jpg

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