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The polymorphism in miR-25 attenuated the oncogenic function in gastric cancer
Jianping Zhou1, Jiangang Zhou1, Weimin Wang1
1Department of General Surgery, Yixing People's Hospital Affiliated to Jiangsu University, Yixing, 214200, Jiangsu, China.
Abstract:
miR-25 was identified as an essential oncogene by promoting the growth and metastasis through TOB1 in gastric cancer (GC). The function of the single nucleotide polymorphism (SNP) located in the mature region of miR-25 (rs41274221) has not been investigated. In this study, we aimed to explore the involvement of rs41274221 in miR-25 in gastric cancer. We found that SNP rs41274221 in miR-25 was participated in the occurrence of GC by acting as a tumor protective factor associating with the tumor growth and metastasis. Besides, further investigation found that upregulation of miR-25 with AA genotype could attenuate the proliferation and invasion of tumor cells caused by wild-type miR-25. The dual-luciferase reporter assay also confirmed that miR-25 harbored the A allele which caused an incapacitation of binding at the TOB1. In conclusion, rs41274221 in miR-25 was a subgroup which may protect the patients from further growth and metastasis of gastric cancer and might serve as a novel biomarker for the disease.
Insights
A single nucleotide polymorphism (SNP) in miR-25, rs41274221, acts as a tumor protective factor in gastric cancer (GC). This SNP may offer protection against tumor growth and metastasis, potentially serving as a novel GC biomarker.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- MicroRNA-25 (miR-25) is an established oncogene promoting gastric cancer (GC) growth and metastasis via TOB1.
- The functional impact of single nucleotide polymorphisms (SNPs) within mature microRNAs, specifically rs41274221 in miR-25, remains largely unexplored in GC.
Purpose of the Study:
- To investigate the role of the miR-25 SNP rs41274221 in the development and progression of gastric cancer.
- To determine if rs41274221 influences miR-25's oncogenic functions related to tumor growth and metastasis.
Main Methods:
- Genotyping analysis to assess the association of rs41274221 with GC occurrence.
- Functional assays, including proliferation and invasion assays, to evaluate the impact of different genotypes on tumor cell behavior.
- Dual-luciferase reporter assays to confirm the effect of the A allele on miR-25 binding to its target TOB1.
Main Results:
- The miR-25 SNP rs41274221 was found to be associated with the occurrence of GC, acting as a tumor-protective factor.
- The AA genotype of miR-25 attenuated tumor cell proliferation and invasion, counteracting the effects of wild-type miR-25.
- The A allele of rs41274221 impaired the binding of miR-25 to TOB1, as confirmed by dual-luciferase reporter assays.
Conclusions:
- The rs41274221 polymorphism in miR-25 may confer protection against gastric cancer progression by inhibiting tumor growth and metastasis.
- This specific miR-25 SNP subgroup could serve as a novel diagnostic or prognostic biomarker for gastric cancer patients.
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