Evidence map›Paper›PMID 41142323›Full record

ArticleGlobal medical genetics2025

Hierarchical clustering defines hypermethylated RSPO2 as early-stage potential biomarker in colorectal cancer.

Ankit Srivastava, Gaurav Kant, Manish Pratap Singh, Sameer Srivastava

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Article in Global medical genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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1 citing paper in PubMed.

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5 · Who and what money

Authors and funding

4 authors.

Ankit SrivastavaDepartment of Biotechnology, Motilal Nehru National Institute of Technology Allahabad, Prayagraj 211004, India.
Gaurav KantDepartment of Biotechnology, Motilal Nehru National Institute of Technology Allahabad, Prayagraj 211004, India.
Manish Pratap SinghDepartment of Zoology, Deen Dayal Upadhyay Gorakhpur University, Gorakhpur, Uttar Pradesh 273009, India.
Sameer SrivastavaDepartment of Biotechnology, Motilal Nehru National Institute of Technology Allahabad, Prayagraj 211004, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Early-stage diagnosis, absence of specific reliable biomarkers, and better clinical management of colorectal cancer (CRC) remain major challenges. The Rspondin2 (RSPO2) gene is one of the most potent enablers of Wnt signaling, having contrasting aspects in tumor development and progression. Aim: We aimed to identify the role of RSPO2 as a molecular biomarker by evaluating its methylation and expression profiles in CRC tissue samples to identify biomarker potential. Methodology: Combined bisulfite restriction analysis Results: RSPO2 was hypermethylated (33/52; 63.46 %) and significantly associated with early-stage (I+II, p = 0.04) CRC tissue and exhibited low RSPO2 expression (42/52; 80.76 %). Hierarchical clustering stratified the samples into two distinct clusters that share some significant clinical and molecular factors specific for cluster 1 such as LN status (p < 0.0001) and lymphovascular invasion (p = 0.0013) while staging (p < 0.0001) and RSPO2 methylation (p = 0.0402) in cluster 2, which are valuable for personalized medicine. K-M plot analysis showed that patients with low RSPO2 expression have poor disease-free survival but could not be a risk factor. Conclusion: RSPO2 may be a potential biomarker for early-stage detection and provide valuable insight into the diagnosis of patients with CRC.

Indexed as

BiomarkerColorectal cancerExpressionMethylationPrognosticRSPO2

Identifiers

PMID41142323
PMCPMC12547467

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