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http://purl.uniprot.org/citations/37814859http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
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Objective

To investigate the expression of calmodulin-regulated spectrin-associated protein 2 (CAMSAP2) in gastric cancer and its effect on gastric cancer cell invasion and metastasis.

Methods

The association of CAMSAP2 expression levels with progression and prognosis of gastric cancer was analyzed using public cancer data and in 106 patients receiving radical gastrectomy in our hospital from October, 2013 to October, 2017. The biological functions of CAMSAP2 were predicted using bioinformatics analysis. Gastric cancer MGC803 cells with CAMSAP2 overexpression and knockdown were observed for epithelial-mesenchymal transition (EMT), migration and invasion. A nude mouse model bearing orthotopic gastric cancer cell xenografts was established for verifying the results and exploring the underlying molecular mechanism.

Results

Gastric cancer tissues expressed high levels of CAMSAP2, which were positively correlated with CEA and CA19-9 (P<0.001). Cox regression analysis showed that CAMSAP2 expression level was an independent risk factor affecting the 5-year survival rate of gastric cancer patients (HR=2.969, 95% CI: 1.031-8.548). Enrichment analysis suggested that CAMSAP2 was involved in epithelialmesenchymal transition (EMT) and TGF-β signaling. In gastric cancer cells, CAMSAP2 overexpression significantly increased the expressions of vimentin and N-cadherin, inhibited the expression of E-cadherin, and enhanced cell migration and invasion (P<0.05); CAMSAP2 knockdown produced the opposite effects in the cells (P<0.05). In the tumor-bearing mice, xenografts overexpressing CAMSAP2 showed enhanced metastasis (P<0.05), increased vimentin and N-cadherin expressions and lowered E-cadherin expression (P<0.05), and the xenografts with CAMSAP2 knockdown showed the opposite changes (P<0.05). Both the in vivo and in vitro experiments showed that CAMSAP2 overexpression increased and CAMSAP2 knockdown lowered the levels of TGF-β and p-Smad2/3 in the gastric cancer cells (P<0.05).

Conclusion

The high expression of CAMSAP2 contributes to disease progression and poor prognosis of gastric cancer possibly by upregulating TGF-β signaling to promote EMT."xsd:string
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http://purl.uniprot.org/citations/37814859http://purl.uniprot.org/core/author"Li J."xsd:string
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http://purl.uniprot.org/citations/37814859http://purl.uniprot.org/core/author"Wang Y."xsd:string
http://purl.uniprot.org/citations/37814859http://purl.uniprot.org/core/author"Wang L."xsd:string
http://purl.uniprot.org/citations/37814859http://purl.uniprot.org/core/author"Yang Z."xsd:string
http://purl.uniprot.org/citations/37814859http://purl.uniprot.org/core/author"Wang W."xsd:string
http://purl.uniprot.org/citations/37814859http://purl.uniprot.org/core/author"Zuo L."xsd:string
http://purl.uniprot.org/citations/37814859http://purl.uniprot.org/core/author"Geng Z."xsd:string
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http://purl.uniprot.org/citations/37814859http://purl.uniprot.org/core/date"2023"xsd:gYear
http://purl.uniprot.org/citations/37814859http://purl.uniprot.org/core/name"Nan Fang Yi Ke Da Xue Xue Bao"xsd:string
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http://purl.uniprot.org/citations/37814859http://purl.uniprot.org/core/title"[High expression of CAMSAP2 promotes invasion and metastasis of gastric cancer cells by upregulating TGF-beta signaling]."xsd:string
http://purl.uniprot.org/citations/37814859http://purl.uniprot.org/core/volume"43"xsd:string
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