Kim Taek-Keun, Park Chang Sik, Jeoung Mee Hyun, Lee Woo Ran, Go Nam Kyung, Choi Jong Rip, Lee Tae Sup, Shim Hyunbo, Lee Sukmook
Laboratory of Molecular Cancer Therapeutics, Scripps Korea Antibody Institute, Chuncheon, South Korea.
Molecular Imaging Research Center, Korea Institute of Radiological and Medical Sciences, Seoul, South Korea.
Biochem Biophys Res Commun. 2015 Dec 25;468(4):774-80. doi: 10.1016/j.bbrc.2015.11.031. Epub 2015 Nov 10.
Tetraspanin 8 (TSPAN8) is a tumor-associated antigen implicated in tumor progression and metastasis. However, the validation of TSPAN8 as a potential therapeutic target in metastatic colorectal cancer (mCRC) has not yet been studied. In this study, through several in vitro methodologies, we identified a large extracellular loop of TSPAN8 (TSPAN8-LEL) as a key domain for regulating mCRC invasion. Using phage display technology, we developed a novel anti-TSPAN8-LEL human antibody with subnanomolar affinity that specifically recognizes amino acids 140-205 of TSPAN8-LEL in a conformation-dependent manner. Finally, we demonstrated that the antibody specifically reduces invasion in the HCT116 and LoVo mCRC cell lines more potently than in the HCT-8 and SW480 non-mCRC cell lines. Our data suggest that TSPAN8-LEL may play an important role in mCRC cell invasion, and that the antibody we have developed could be a useful tool for inhibiting the invasion of TSPAN8-expressing mCRCs.
四跨膜蛋白8(TSPAN8)是一种与肿瘤进展和转移相关的肿瘤相关抗原。然而,TSPAN8作为转移性结直肠癌(mCRC)潜在治疗靶点的验证尚未得到研究。在本研究中,通过多种体外方法,我们确定TSPAN8的一个大的细胞外环(TSPAN8-LEL)是调节mCRC侵袭的关键结构域。利用噬菌体展示技术,我们开发了一种新型的抗TSPAN8-LEL人抗体,其亲和力亚纳摩尔,能以构象依赖的方式特异性识别TSPAN8-LEL的140-205位氨基酸。最后,我们证明该抗体比在HCT-8和SW480非mCRC细胞系中更有效地特异性降低HCT116和LoVo mCRC细胞系中的侵袭。我们的数据表明,TSPAN8-LEL可能在mCRC细胞侵袭中起重要作用,并且我们开发的抗体可能是抑制表达TSPAN8的mCRC侵袭的有用工具。