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Updated: Jul 8, 2026

Multiomics Analysis of TMEM200A as a Pan-Cancer Biomarker
Published on: September 15, 2023
Expression of 15-PGDH is downregulated by COX-2 in gastric cancer
Zhenxiong Liu1, Xin Wang, Yuanyuan Lu
1State key Laboratory of Cancer Biology and Institute of Digestive Diseases, Xijing Hospital, Fourth Military Medical University, 15 Changle West Road, Shaanxi Province, Xi'an 710032, China.
Abstract:
To explore the proteins regulated by cyclooxygenase-2 (COX-2) in gastric cancer, the expression plasmid of COX-2siRNA was constructed and transfected into gastric cancer cell line SGC7901. Then, two-dimensional electrophoresis and the PDQuest software analysis were applied to discover the differentially expressed proteins. The differential protein spots were analyzed by matrix-assisted laser desorption/ionization time of flight mass spectrometry. Fourteen differentially expressed proteins between the two cell lines were identified. 15-Hydroxyprostaglandin dehydrogenase [NAD(+)] (15-PGDH), a key enzyme in prostaglandin degradation, was identified as an upregulated protein in SGC7901 cells transfected with the COX-2siRNA plasmid. To further explore whether the 15-PGDH is regulated by COX-2, western blotting and immunocytochemical assay were performed to detect the expression of 15-PGDH in different cell lines with different expression level of COX-2. The results showed that the expression of 15-PGDH was upregulated (128.57%) as COX-2 was suppressed by small interfering RNA and downregulated (51.72%) as COX-2 was enhanced by COX-2 cDNA transfection in gastric cancer cells. In tissue specimens with gastric cancer, there was a decreased expression of 15-PGDH and an increased expression of COX-2 simultaneously. A significantly negative correlation of 15-PGDH expression was found to COX-2 level, tumor differentiation, tumor, lymph node, metastasis (TNM) staging and lymph node metastasis of gastric cancer. All the results suggest that 15-PGDH is downregulated by COX-2 in human gastric cancer and may contribute to the carcinogenesis and development of human gastric cancer in combination with COX-2.
Insights
Cyclooxygenase-2 (COX-2) downregulates 15-Hydroxyprostaglandin dehydrogenase [NAD(+)] (15-PGDH) in gastric cancer. This interaction may promote cancer development and progression.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Cyclooxygenase-2 (COX-2) is implicated in gastric cancer development.
- Understanding proteins regulated by COX-2 is crucial for identifying therapeutic targets.
Purpose of the Study:
- To identify proteins regulated by COX-2 in gastric cancer cells.
- To investigate the regulatory relationship between COX-2 and 15-Hydroxyprostaglandin dehydrogenase [NAD(+)] (15-PGDH).
Main Methods:
- Differential protein expression analysis using two-dimensional electrophoresis and mass spectrometry.
- Validation of protein expression changes via western blotting and immunocytochemistry.
- Correlation analysis of protein expression with clinical parameters in gastric cancer tissues.
Main Results:
- Fourteen differentially expressed proteins were identified upon COX-2 knockdown.
- 15-Hydroxyprostaglandin dehydrogenase [NAD(+)] (15-PGDH) expression was inversely correlated with COX-2 levels.
- Decreased 15-PGDH and increased COX-2 expression were observed in gastric cancer tissues, correlating with advanced tumor stage and poor differentiation.
Conclusions:
- COX-2 downregulates 15-PGDH expression in gastric cancer.
- The interplay between COX-2 and 15-PGDH may contribute to gastric carcinogenesis and progression.
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