Functional Analysis of Membrane-Associated Scaffolding Tight Junction (TJ) Proteins in Tumorigenic Characteristics of B16-F10 Mouse Melanoma Cells

• Published in: International journal of molecular sciences 2024-01, Vol.25 (2), p.833
• Main Authors: Ko, Eun-Ji, Kim, Do-Ye, Kim, Min-Hye, An, Hyojin, Kim, Jeongtae, Jeong, Jee-Yeong, Song, Kyoung Seob, Cha, Hee-Jae
• Format: Article
• Language: English
• Subjects: Analysis; Animals; Cancer; Carcinogenesis - genetics; Cell adhesion & migration; Cell Adhesion Molecules, Neuronal; Cell cycle; Cell growth; Cell Proliferation; Chromatin; Cloning; CRISPR; Diabetes; Genes; Inflammation; Lung diseases; Melanoma; Melanoma, Experimental - genetics; Membrane proteins; Metastasis; Mice; Nerve Growth Factors; Permeability; Protein binding; Proteins; Signal transduction; Tight Junction Proteins - genetics; Tight Junctions; Tumors
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms25020833

Tight junction (TJ) proteins (Tjps), Tjp1 and Tjp2, are tight junction-associated scaffold proteins that bind to the transmembrane proteins of tight junctions and the underlying cytoskeleton. In this study, we first analyzed the tumorigenic characteristics of B16-F10 melanoma cells, including cell proliferation, migration, invasion, metastatic potential, and the expression patterns of related proteins, after the CRISPR-Cas9-mediated knockout (KO) of genes. The proliferation of and KO cells significantly increased in vitro. Other tumorigenic characteristics, including migration and invasion, were significantly enhanced in and KO cells. Zonula occludens (ZO)-associated protein Claudin-1 (CLDN-1), which is a major component of tight junctions and functions in controlling cell-to-cell adhesion, was decreased in KO cells. Additionally, KO significantly stimulated tumor growth and metastasis in an in vivo mouse model. We performed a transcriptome analysis using next-generation sequencing (NGS) to elucidate the key genes involved in the mechanisms of action of and . Among the various genes affected by KO-, cell cycle-, cell migration-, angiogenesis-, and cell-cell adhesion-related genes were significantly altered. In particular, we found that the ( ) and ( ) genes, which are known to play fundamental roles in Tjps, were significantly downregulated in KO cells. In summary, tumorigenic characteristics, including cell proliferation, migration, invasion, tumor growth, and metastatic potential, were significantly increased in and KO cells, and the knockout of genes significantly affected the expression of related proteins.