Evidence map›Paper›PMID 41980898›Full record

ArticleCancer reports (Hoboken, N.J.)2026

PRKD3 Overexpression May Improve Survival and Suppresses Proliferation in Colorectal Cancer.

Bin Zhang, Chen Chang, Jingli Chen, Yue Cao, Yu Chang, Lele Liu, Wensheng Li, Guorong Wang

Abstract read
In one paragraph

Article in Cancer reports (Hoboken, N.J.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Bin ZhangFirst Department of General Surgery, Shaanxi Provincial People's Hospital, Xi'an, China.ORCID 0009-0005-0517-627X
Chen ChangThe Third Affiliated Hospital of The School of Medicine, Xi'an Jiaotong University, Xi'an, China.ORCID 0009-0009-6043-0209
Jingli ChenXi'an Medical University, Xi'an, China.ORCID 0009-0000-0727-8740
Yue CaoXi'an Medical University, Xi'an, China.ORCID 0009-0009-6005-9921
Yu ChangThe Third Affiliated Hospital of The School of Medicine, Xi'an Jiaotong University, Xi'an, China.ORCID 0009-0000-5533-1702
Lele LiuThe Third Affiliated Hospital of The School of Medicine, Xi'an Jiaotong University, Xi'an, China.
Wensheng LiThe Third Affiliated Hospital of The School of Medicine, Xi'an Jiaotong University, Xi'an, China.ORCID 0009-0007-6092-6680
Guorong WangFirst Department of General Surgery, Shaanxi Provincial People's Hospital, Xi'an, China.ORCID 0000-0001-7746-6085

Funding

Shaanxi Province Science and Technology Innovation Team 2020TD-048the Natural Science Foundation of Shaanxi Province 2023-JC-QN-0851the Scientific and Technological Personnel Support Program of Shaanxi Provincial People's Hospital 2021LJ-08
6 · The paper itself

Abstract

objectiveThe study aimed to explore PRKD3 protein expression in colorectal cancer and its clinical implications.

methodsPRKD3 expression was assessed in 189 paired colorectal cancer tissues and their corresponding adjacent non-cancerous counterparts using tissue microarray-based immunohistochemistry. The associations of PRKD3 expression with clinicopathological parameters and patient prognosis were analyzed. PRKD3 mRNA levels were quantified by quantitative real-time polymerase chain reaction (qPCR), and its protein expression in colorectal cancer cell lines was detected by Western blot analysis. To investigate the functional role of PRKD3 in cell proliferation, its expression was knocked down using siRNA transfection, followed by proliferation assays.

resultsImmunohistochemical analysis revealed that PRKD3 protein was predominantly localized in the cytoplasm of both colorectal cancer and adjacent normal epithelial cells (sampled from > 5 cm beyond the tumor margin). The positive expression rate was 51.8% (72/139) in adjacent normal tissues and 68.7% (114/166) in colorectal cancer tissues, showing a statistically significant increase in cancer tissues (p < 0.05). PRKD3 expression was significantly associated with the clinical diagnosis (colon vs. rectal cancer) (p < 0.05). Kaplan-Meier survival analysis demonstrated that patients with high PRKD3 expression had a significantly longer postoperative survival than those with low expression (p < 0.05). Furthermore, cell proliferation assays showed that knockdown of PRKD3 significantly enhanced proliferation ability compared with the control group.

conclusionTaken together, the positive expression of PRKD3 may be associated with better prognosis. These findings suggest that PRKD3 may be involved in the development and progression of colorectal cancer and could represent a potential prognostic biomarker and therapeutic target for this disease.

Indexed as

Biomarkers, TumorColorectal NeoplasmsAgedCell Line, TumorCell ProliferationFemaleGene Expression Regulation, NeoplasticHumansKaplan-Meier EstimateMaleMiddle AgedPrognosisBiomarkers, Tumordiagnosismolecular markersPRKD3prognosiscolorectal cancer

Identifiers

PMID41980898
PMCPMC13079073

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.