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Updated: Apr 27, 2026

Author Spotlight: Unveiling Transmembrane Protein Family-Related Markers in Gastric Cancer and Implications for Targeted Therapies
Published on: September 15, 2023
miR-129-1-3p inhibits cell migration by targeting BDKRB2 in gastric cancer
Danping Wang1, Lin Luo, Junming Guo
1Zhejiang Provincial Key Laboratory of Pathophysiology, Department of Biochemistry and Molecular Biology, Ningbo University School of Medicine, 818 Fenghua Road, Ningbo, 315211, China.
Abstract:
MicroRNAs (miRNAs) are a class of small noncoding RNAs, which regulate gene expression in the posttranscriptional level. They are involved in cancer occurrence and development. Different members of the same miRNA family may have different roles. Since the fact that metastasis is the main cause of cancer-related death and miR-129 has three members, in this study, we focused on the migration inhibitory role of miR-129-1-3p in gastric cancer and explored the possible mechanisms. We first compared the expression of three miR-129 family members, miR-129-5p, miR-129-1-3p, and miR-129-2-3p, between gastric carcinoma tissues and surgical margin non-cancer samples by quantitative real-time reverse transcription-polymerase chain reaction (QRT-PCR). Then, we selected miR-129-1-3p for further analysis and transfected its mimic and inhibitor into gastric cancer BGC-823 cells, respectively. Then, we compared the BGC-823 cells' migration capacity by transwell assay. Finally, we predicted the possible targets of miR-129-1-3p and selected one target for further analysis by QRT-PCR and luciferase reporter assay. The results showed that the expression of miR-129-1-3p in gastric carcinoma was significantly lower than that in surgical margin samples. And miR-129-1-3p could inhibit the migration of BGC-823 cells. From the candidates, we selected bradykinin receptor B2 (BDKRB2), which was reported relating to metastasis, as a target for further analysis. QRT-PCR showed that the expression of BDKRB2 was negatively related to miR-129-1-3p. Luciferase reporter assay showed that BDKRB2 was the target of the miR-129-1-3p. In summary, miR-129-1-3p inhibits the BGC-823 cell migration by targeting BDKRB2.
Insights
MicroRNA-129-1-3p (miR-129-1-3p) is downregulated in gastric cancer and inhibits cell migration. It targets bradykinin receptor B2 (BDKRB2), suggesting a role in preventing cancer metastasis.
Area of Science:
- Molecular Biology
- Oncology
- Gene Regulation
Background:
- MicroRNAs (miRNAs) are small noncoding RNAs regulating gene expression posttranscriptionally.
- miRNAs play crucial roles in cancer development and progression.
- Metastasis is a primary cause of cancer mortality, necessitating research into migration inhibitory factors.
Purpose of the Study:
- To investigate the migration inhibitory role of miR-129-1-3p in gastric cancer.
- To explore the underlying molecular mechanisms, including target identification.
- To compare the expression of miR-129 family members in gastric cancer tissues.
Main Methods:
- Quantitative real-time reverse transcription-polymerase chain reaction (QRT-PCR) to compare miRNA expression.
- Cell transfection with miR-129-1-3p mimic and inhibitor in BGC-823 gastric cancer cells.
- Transwell migration assays to assess cell motility.
- Bioinformatic target prediction, followed by QRT-PCR and luciferase reporter assays for target validation.
Main Results:
- miR-129-1-3p expression was significantly lower in gastric carcinoma tissues compared to surgical margins.
- Overexpression of miR-129-1-3p inhibited the migration capacity of BGC-823 cells.
- Bradykinin receptor B2 (BDKRB2) was identified as a direct target of miR-129-1-3p, with its expression negatively correlated with miR-129-1-3p levels.
Conclusions:
- miR-129-1-3p functions as a tumor suppressor in gastric cancer by inhibiting cell migration.
- The inhibitory effect is mediated through the direct targeting of BDKRB2.
- Restoring miR-129-1-3p levels may represent a potential therapeutic strategy against gastric cancer metastasis.
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