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Updated: Oct 15, 2025

Genome-Wide Analysis of DNA Methylation in Gastrointestinal Cancer
Published on: September 18, 2020
Epigenetic DNA Modifications Upregulate SPRY2 in Human Colorectal Cancers
Alexei J Stuckel1, Shuai Zeng2,3, Zhen Lyu2,3
1Department of Medicine, Division of Gastroenterology and Hepatology, University of Missouri, Columbia, MO 65212, USA.
Abstract:
Conventional wisdom is that Sprouty2 (SPRY2), a suppressor of Receptor Tyrosine Kinase (RTK) signaling, functions as a tumor suppressor and is downregulated in many solid tumors. We reported, for the first time, that increased expression of SPRY2 augments cancer phenotype and Epithelial-Mesenchymal-Transition (EMT) in colorectal cancer (CRC). In this report, we assessed epigenetic DNA modifications that regulate SPRY2 expression in CRC. A total of 4 loci within SPRY2 were evaluated for 5mC using Combined Bisulfite Restriction Analysis (COBRA). Previously sequenced 5hmC nano-hmC seal data within SPRY2 promoter and gene body were evaluated in CRC. Combined bioinformatics analyses of SPRY2 CRC transcripts by RNA-seq/microarray and 450K methyl-array data archived in The Cancer Genome Atlas (TCGA) and GEO database were performed. SPRY2 protein in CRC tumors and cells was measured by Western blotting. Increased SPRY2 mRNA was observed across several CRC datasets and increased protein expression was observed among CRC patient samples. For the first time, SPRY2 hypomethylation was identified in adenocarcinomas in the promoter and gene body. We also revealed, for the first time, increases of 5hmC deposition in the promoter region of SPRY2 in CRC. SPRY2 promoter hypomethylation and increased 5hmC may play an influential role in upregulating SPRY2 in CRC.
Insights
Sprouty2 (SPRY2) is upregulated in colorectal cancer (CRC), contrary to its known tumor suppressor role. Epigenetic changes, including hypomethylation and increased 5hmC in the SPRY2 gene, drive this increased expression in CRC.
Area of Science:
- Oncology
- Epigenetics
- Molecular Biology
Background:
- Sprouty2 (SPRY2) traditionally suppresses Receptor Tyrosine Kinase (RTK) signaling and is considered a tumor suppressor.
- Contrary to established roles, SPRY2 upregulation has been linked to augmented cancer phenotypes and Epithelial-Mesenchymal-Transition (EMT) in colorectal cancer (CRC).
Purpose of the Study:
- To investigate the epigenetic mechanisms regulating SPRY2 expression in colorectal cancer.
- To determine the role of DNA methylation (5mC) and hydroxymethylation (5hmC) in SPRY2 dysregulation in CRC.
Main Methods:
- Analysis of 5mC at four loci within the SPRY2 gene using Combined Bisulfite Restriction Analysis (COBRA).
- Evaluation of 5hmC data in the SPRY2 promoter and gene body.
- Bioinformatic analysis of SPRY2 transcriptomic and methylation data from TCGA and GEO databases.
- Western blotting to measure SPRY2 protein levels in CRC tumors and cells.
Main Results:
- Increased SPRY2 mRNA and protein expression were observed in CRC datasets and patient samples.
- Novel identification of SPRY2 promoter and gene body hypomethylation in colorectal adenocarcinomas.
- First-time observation of increased 5hmC deposition in the SPRY2 promoter region in CRC.
Conclusions:
- SPRY2 hypomethylation and increased promoter 5hmC are identified as potential drivers of SPRY2 upregulation in colorectal cancer.
- These epigenetic modifications may contribute to the pro-cancer effects of SPRY2 in CRC, challenging its traditional tumor suppressor function.
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