The SLITRK4-CNPY3 axis promotes liver metastasis of gastric cancer by enhancing the endocytosis and recycling of TrkB in tumour cells

• Published in: Cellular oncology (Dordrecht) Vol. 46; no. 4; pp. 1049 - 1067
• Main Authors: Zhou, Yao-Qi, Bao, Tian-Shang, Xie, Jia-Xuan, Yao, Lin-Li, Yu, Si-Te, Li, Qing, Huang, Pei-Qi, Zhou, Wan-Zhen, Wang, Yang-Yang, Chen, Su-Yuan, Wang, Xiao-Qi, Zhang, Xue-Li, Jiang, Shu-Heng, Yi, Shuang-Qin, Zhang, Zhi-Gang, Ma, Ming-Ze, Hu, Li-Peng, Xu, Jia, Li, Jun
• Format: Journal Article
• Language: English
• Published: Dordrecht Springer Netherlands 01.08.2023; Springer Nature B.V
• Subjects: Animals; Bioinformatics; Biomedical and Life Sciences; Biomedicine; Cancer Research; Cell Line, Tumor; Cell Proliferation - genetics; Endocytosis; Gastric cancer; Immunohistochemistry; Kinases; Liver; Liver cancer; Liver Neoplasms - pathology; Metastases; Metastasis; Mice; Nervous system; Oncology; Pathology; Prognosis; Protein turnover; Protein-tyrosine kinase receptors; Signal Transduction; Stomach Neoplasms - genetics; Synaptogenesis; Therapeutic targets; Transcriptomes; TrkB receptors; Tumors; Tyrosine Kinase receptor B (TrkB); SLIT- and NTRK-like family member 4 (SLITRK4); Endocytosis and recycling; Gastric cancer; Liver metastasis; Canopy FGF Signalling Regulator 3 (CNPY3)
• ISSN: 2211-3428; 2211-3436; 2211-3436
• DOI: 10.1007/s13402-023-00795-9

Purpose Gastric cancer (GC) is a malignant tumour with high mortality, and liver metastasis is one of the main causes of poor prognosis. SLIT- and NTRK-like family member 4 (SLITRK4) plays an important role in the nervous system, such as synapse formation. Our study aimed to explore the functional role of SLITRK4 in GC and liver metastasis. Methods The mRNA level of SLITRK4 was evaluated using publicly available transcriptome GEO datasets and Renji cohort. The protein level of SLITRK4 in the tissue microarray of GC was observed using immunohistochemistry. Cell Counting Kit-8, colony formation, transwell migration assays in vitro and mouse model of liver metastasis in vivo was performed to investigate the functional roles of SLITRK4 in GC. Bioinformatics predictions and Co-IP experiments were applied to screen and identify SLITRK4-binding proteins. Western blot was performed to detect Tyrosine Kinase receptor B (TrkB)-related signaling molecules. Results By comparing primary and liver metastases from GC, SLITRK4 was found to be upregulated in tissues of GC with liver metastasis and to be closely related to poor clinical prognosis. SLITRK4 knockdown significantly abrogated the growth, invasion, and metastasis of GC in vitro and in vivo . Further study revealed that SLITRK4 could interact with Canopy FGF Signalling Regulator 3 (CNPY3), thus enhancing TrkB- related signaling by promoting the endocytosis and recycling of the TrkB receptor. Conclusion In conclusion, the CNPY3-SLITRK4 axis contributes to liver metastasis of GC according to the TrkB-related signaling pathway. which may be a therapeutic target for the treatment of GC with liver metastasis.