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Updated: Apr 26, 2026

Detection of a Circulating MicroRNA Custom Panel in Patients with Metastatic Colorectal Cancer
Published on: March 14, 2019
Association between miR-27a genetic variants and susceptibility to colorectal cancer
Zaiqiu Wang, Xiaoli Sun, Yeli Wang
1Department of General Surgery, Qilu Hospital of Shandong University, Jinan, Shandong 250012, China. prhusanyuan@163.com.
Background:
MicroRNAs (miRNAs) are short, non-coding RNAs that negatively regulate target genes. A single nucleotide polymorphism (SNP) in a miRNA sequence may alter miRNA expression and/or maturation, which was proposed to associate with the development and progression of cancer. The rs895819 polymorphism, located in the terminal loop of pre-miR-27a, has been reported to have relevance to several cancers. In this study, we investigated the possibility of association between polymorphism in rs895819 and susceptibility to colorectal cancer (CRC).
Methods:
We identified a single SNP, rs895819 in pre-miR-27a, for further investigation, were determined in 205 CRC patients and 455 healthy controls.
Results:
When taking the AA genotype as a reference, we found that AG genotype was not statistically significantly associated with the risk of CRC (AG vs. AA, OR 1.245, 95% CI: 0.806 - 1.923). However, the GG genotype was significantly associated with risk of CRC (GG vs. AA, OR 1.599, 95% CI: 1.052 - 2.430). In the AG + GG vs GG group, no significant difference was detected (OR 1.424, 95% CI, 0.974 - 1.801). GG genotype and G allele was associated with an increased risk of metastasis in this study (P < 0.001 and P = 0.003, respectively).
Conclusions:
This study found significant association between rs895819 polymorphism in pre-miR-27a and CRC risk. Population-based studies with large number of subjects and long-term follow-up are needed to verify the association of miR-27a polymorphism with CRC susceptibility and severity.
Virtual Slides:
The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/2061490734125077.
Insights
The rs895819 polymorphism in microRNA-27a (miR-27a) is linked to increased colorectal cancer (CRC) risk, particularly the GG genotype. This genetic variation may also correlate with a higher likelihood of CRC metastasis.
Area of Science:
- Genetics
- Molecular Biology
- Oncology
Background:
- MicroRNAs (miRNAs) are key regulators of gene expression.
- Single nucleotide polymorphisms (SNPs) in miRNAs can affect their function and are implicated in cancer.
- The pre-miR-27a rs895819 polymorphism has been previously associated with various cancers.
Purpose of the Study:
- To investigate the association between the rs895819 polymorphism in pre-microRNA-27a (pre-miR-27a) and susceptibility to colorectal cancer (CRC).
- To evaluate the potential impact of this polymorphism on CRC risk and metastasis.
Main Methods:
- A case-control study was conducted involving 205 CRC patients and 455 healthy controls.
- Genotyping for the rs895819 single nucleotide polymorphism (SNP) in pre-miR-27a was performed.
Main Results:
- The GG genotype of rs895819 was significantly associated with an increased risk of CRC compared to the AA genotype (OR 1.599, 95% CI: 1.052 - 2.430).
- No significant association was found between the AG genotype and CRC risk.
- Both the GG genotype and the G allele were significantly associated with an increased risk of metastasis in CRC patients (P < 0.001 and P = 0.003, respectively).
Conclusions:
- The rs895819 polymorphism in pre-miR-27a is significantly associated with colorectal cancer risk.
- Further large-scale, population-based studies are warranted to confirm these findings and explore the role of miR-27a polymorphism in CRC susceptibility and severity.
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