期刊
CURRENT PHARMACEUTICAL DESIGN
卷 28, 期 42, 页码 3446-3455出版社
BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/1381612829666221117124048
关键词
RBJ; NSCLC; epithelial-mesenchymal transition (EMT); MEK; ERK; GTPase; Ras superfamily
The study found that the levels of RBJ protein were increased in tumor tissue of non-small cell lung cancer (NSCLC) and correlated positively with clinical stage. Silencing RBJ inhibited the growth, invasion, and migration of NSCLC cells, while overexpression of RBJ accelerated tumor formation. The results suggest that RBJ promotes the progression of NSCLC by activating the epithelial-mesenchymal transition (EMT) signaling pathway.
Background Although the majority of members belonging to the small GTPase Ras superfamily have been studied in several malignancies, the function of RBJ has remained unclear, particularly in non-small cell lung cancer (NSCLC). Objective The research aims to determine the function of RBJ in NSCLC. Methods The levels of RBJ protein in tumor tissue and para-carcinoma normal tissue were ascertained via immunohistochemistry (IHC). The growth, migration, and invasion of NSCLC cells were assessed by 5-ethynyl-2-deoxyuridine (EdU) assay, colony formation, cell counting kit-8 (CCK8), transwell and wound healing assays. Furthermore, a nude mouse xenograft model was established to study the function of RBJ in tumorigenesis in vivo. Results The IHC analysis revealed that the protein levels of RBJ were notably increased in tumor tissue and positively associated with the clinical stage. In addition, the knockdown of RBJ restrained the growth, invasion, and migration of NSCLC cell lines by inhibiting the epithelial-mesenchymal transition (EMT) through the MEK/ERK signaling pathway. Accordingly, opposite results were observed when RBJ was overexpressed. In addition, the overexpression of RBJ accelerated tumor formation by A549 cells in nude mice. Conclusion RBJ promoted cancer progression in NSCLC by activating EMT via the MEK/ERK signaling. Thus, RBJ could be used as a potential therapeutic against NSCLC.
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