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Animal study on stanniocalcin 2 (STC2) and gastric cancer metastasis: discussing possible molecular mechanisms

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Objective: To assess the role of stanniocalcin 2 protein in abdominal invasion and metastasis of gastric cancer, and itsmolecular mechanism.Method: The study was conducted at the Department of General Surgery, Jiangxi Provincial People's Hospital, Nanchang,Jiangxi, China, from January 2020 to March 2022 and comprised female mice that were divided into the experimental groupA and control group B. Satellite glial cells 7901 were inoculated into the stomach wall to induce metastasis. In group A, thecells were genetically modified using short hairpin ribonucleic acid to silence stanniocalcin 2 expression. The silencing effectwas confirmed via Western blot. Tumour metrics, including size, weight and number, were measured, alongside cellmigration and invasion using Transwell assays. Data was analysed using SPSS 21.Results: Of the 36 mice, 18(50%) were in each of the two groups. There was a significant reduction in tumour volume,weight and number in group A compared to group B (p<0.05). Survival time was notably extended in group A than groupB (p<0.001). Western blot analysis revealed significantly lower VEGF-C and interleukin-10 (IL-10) protein levels in group B(approximately a 50% reduction for VEGF-C and a 40% reduction for IL-10, p< 0.01). Transwell assay results suggested thatstanniocalcin 2 (STC2) promotes cell invasion and metastasis, as the invasion rate in the STC2-overexpressing group wassignificantly higher compared to controls (increase of approximately 40%, p< 0.05).Conclusion:The invasion and metastasis potential of gastric pain cells decreased after silencing stanniocalcin 2, suggestingthat it may promote the invasion and metastasis of gastric cancer.Keywords: Stanniocalcin 2, Gastric cancer metastasis, Molecular mechanism, Cancer tumours.
Title: Animal study on stanniocalcin 2 (STC2) and gastric cancer metastasis: discussing possible molecular mechanisms
Description:
Objective: To assess the role of stanniocalcin 2 protein in abdominal invasion and metastasis of gastric cancer, and itsmolecular mechanism.
Method: The study was conducted at the Department of General Surgery, Jiangxi Provincial People's Hospital, Nanchang,Jiangxi, China, from January 2020 to March 2022 and comprised female mice that were divided into the experimental groupA and control group B.
Satellite glial cells 7901 were inoculated into the stomach wall to induce metastasis.
In group A, thecells were genetically modified using short hairpin ribonucleic acid to silence stanniocalcin 2 expression.
The silencing effectwas confirmed via Western blot.
Tumour metrics, including size, weight and number, were measured, alongside cellmigration and invasion using Transwell assays.
Data was analysed using SPSS 21.
Results: Of the 36 mice, 18(50%) were in each of the two groups.
There was a significant reduction in tumour volume,weight and number in group A compared to group B (p<0.
05).
Survival time was notably extended in group A than groupB (p<0.
001).
Western blot analysis revealed significantly lower VEGF-C and interleukin-10 (IL-10) protein levels in group B(approximately a 50% reduction for VEGF-C and a 40% reduction for IL-10, p< 0.
01).
Transwell assay results suggested thatstanniocalcin 2 (STC2) promotes cell invasion and metastasis, as the invasion rate in the STC2-overexpressing group wassignificantly higher compared to controls (increase of approximately 40%, p< 0.
05).
Conclusion:The invasion and metastasis potential of gastric pain cells decreased after silencing stanniocalcin 2, suggestingthat it may promote the invasion and metastasis of gastric cancer.
Keywords: Stanniocalcin 2, Gastric cancer metastasis, Molecular mechanism, Cancer tumours.

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