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Updated: May 21, 2026

Analysis of Combinatorial miRNA Treatments to Regulate Cell Cycle and Angiogenesis
Published on: March 30, 2019
Identifying microRNA-mRNA regulatory network in colorectal cancer by a combination of expression profile and
Jihong Fu1, Wentao Tang, Peng Du
1Colorectal Surgery Department, Xinhua Hospital, School of Medicine, Shanghai Jiaotong University, Kongjiang Road 1665, Shanghai 200092, China.
Background:
MicroRNAs (miRNAs) are involved in carcinogenesis and tumor progression by regulating post-transcriptional gene expression. However, the miRNA-mRNA regulatory network is far from being fully understood. The objective of this study is to identify the colorectal cancer (CRC) specific miRNAs and their target mRNAs using a multi-step approach.
Results:
A multi-step approach combining microarray miRNA and mRNA expression profile and bioinformatics analysis was adopted to identify the CRC specific miRNA-mRNA regulatory network. First, 32 differentially expressed miRNAs and 2916 mRNAs from CRC samples and their corresponding normal epithelial tissues were identified by miRNA and mRNA microarray, respectively. Secondly, 22 dysregulated miRNAs and their 58 target mRNAs (72 miRNA-mRNA pairs) were identified by a combination of Pearson's correlation analysis and prediction by databases TargetScan and miRanda. Bioinformatics analysis revealed that these miRNA-mRNAs pairs were involved in Wnt signaling pathway. Additionally, 6 up-regulated miRNAs (mir-21, mir-223, mir-224, mir-29a, mir-29b, and mir-27a) and 4 down-regulated predicted target mRNAs (SFRP1, SFRP2, RNF138, and KLF4) were selected to validate the expression level and their anti-correlationship in an extended cohort of CRC patients by qRT-PCR. Except for mir-27a, the differential expression and their anti-correlationship were proven. Finally, a transfection assay was performed to validate a regulatory relationship between mir-29a and KLF4 at both RNA and protein levels.
Conclusions:
Seventy-two miRNA-mRNA pairs combined by 22 dysregulated miRNAs and their 58 target mRNAs identified by the multi-step approach appear to be involved in CRC tumorigenesis. The results in our study were worthwhile to further investigation via a functional study to fully understand the underlying regulatory mechanisms of miRNA in CRC.
Insights
This study identifies key microRNA (miRNA)-messenger RNA (mRNA) interactions in colorectal cancer (CRC). Researchers found 72 specific miRNA-mRNA pairs involved in CRC development, offering new targets for cancer research.
Area of Science:
- Molecular Biology
- Genomics
- Cancer Research
Background:
- MicroRNAs (miRNAs) regulate gene expression and are implicated in cancer.
- The specific miRNA-mRNA regulatory network in colorectal cancer (CRC) remains incompletely understood.
- Identifying these networks is crucial for understanding CRC pathogenesis.
Purpose of the Study:
- To identify colorectal cancer (CRC)-specific microRNAs (miRNAs) and their target messenger RNAs (mRNAs).
- To elucidate the miRNA-mRNA regulatory network involved in CRC tumorigenesis.
- To provide a foundation for further functional studies in CRC.
Main Methods:
- Combined microarray analysis of miRNA and mRNA expression profiles from CRC and normal tissues.
- Bioinformatics analysis, including Pearson's correlation and prediction databases (TargetScan, miRanda).
- Quantitative real-time PCR (qRT-PCR) for validation and transfection assays for regulatory confirmation.
Main Results:
- Identified 32 differentially expressed miRNAs and 2916 mRNAs, leading to 72 miRNA-mRNA pairs involving 22 dysregulated miRNAs and 58 target mRNAs.
- Bioinformatics analysis linked these pairs to the Wnt signaling pathway.
- Validated differential expression and anti-correlation for most identified miRNA-mRNA pairs, including mir-29a and KLF4.
Conclusions:
- The identified 72 miRNA-mRNA pairs are significantly involved in colorectal cancer (CRC) tumorigenesis.
- These findings highlight the critical role of miRNA regulation in CRC.
- Further functional investigation is warranted to fully understand the regulatory mechanisms of miRNAs in CRC.
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