# Development and validation of a combined diagnostic model for prostate cancer integrating MRI parameters with p504s, CK5/6, and Ki-67 expression

**Authors:** Qingchang Ren, Jialong Gu, Nankang Lu

PMC · DOI: 10.1515/biol-2025-1244 · Open Life Sciences · 2026-01-23

## TL;DR

This study creates a diagnostic model for prostate cancer by combining MRI data with biomarker expression to improve accuracy and reduce unnecessary biopsies.

## Contribution

A novel diagnostic nomogram integrating MRI parameters and biomarker expression for prostate cancer detection is developed and validated.

## Key findings

- The combined model achieved high accuracy with an AUC of 0.971 in training and 0.977 in validation.
- Seven variables were identified as independent predictors of prostate cancer.
- The model outperformed clinical indicators alone in diagnostic performance.

## Abstract

This study aimed to develop and validate a diagnostic model for prostate cancer (PCa) by integrating magnetic resonance imaging (MRI) parameters with the immunohistochemical expression of p504s, CK5/6, and Ki-67. A total of 448 patients undergoing prostate needle biopsy were included and randomly allocated into training (70 %) and validation (30 %) cohorts. Clinical data, MRI findings, and biomarker expression levels were analyzed. Multivariate logistic regression identified independent predictors, which were used to construct a diagnostic nomogram. Compared to controls, PCa patients had significantly higher PSA levels, lower f-PSA/t-PSA ratios, a greater frequency of palpable nodules, higher CC/C ratios, lower ADC values, increased p504s and Ki-67 positivity, and reduced CK5/6 expression. Seven variables were ultimately identified as independent predictors for the model. The resulting nomogram demonstrated excellent discrimination, with an area under the curve (AUC) of 0.971 in the training set and 0.977 in the validation set. It significantly outperformed a model using clinical indicators alone. This combined MRI-biomarker model shows high diagnostic accuracy for PCa and could potentially aid clinical decision-making and reduce unnecessary biopsies. External validation is required prior to clinical application.

## Linked entities

- **Proteins:** AMACR (alpha-methylacyl-CoA racemase), ck56 (hypothetical protein), Mki67 (antigen identified by monoclonal antibody Ki 67)
- **Diseases:** prostate cancer (MONDO:0005159)

## Full-text entities

- **Genes:** KLK3 (kallikrein related peptidase 3) [NCBI Gene 354] {aka APS, KLK2A1, PSA, hK3}, NPEPPS (aminopeptidase puromycin sensitive) [NCBI Gene 9520] {aka AAP-S, MP100, PSA}, PIN4 (peptidylprolyl cis/trans isomerase, NIMA-interacting 4) [NCBI Gene 5303] {aka EPVH, PAR14, PAR17, hEPVH, hPar14, hPar17}, ERG (ETS transcription factor ERG) [NCBI Gene 2078] {aka LMPHM14, erg-3, p55}, PTEN (phosphatase and tensin homolog) [NCBI Gene 5728] {aka 10q23del, BZS, CWS1, DEC, GLM2, MHAM}, AMACR (alpha-methylacyl-CoA racemase) [NCBI Gene 23600] {aka AMACRD, CBAS4, P504S, RACE, RM}
- **Diseases:** androgen (MESH:D014770), benign lesions (MESH:D001932), invasive carcinoma (MESH:D009361), prostate carcinogenesis (MESH:D011472), benign hyperplasia (MESH:D006965), hypertension (MESH:D006973), carcinogenesis (MESH:D063646), prostatic intraepithelial neoplasia (MESH:D019048), PCa (MESH:D011471), edema (MESH:D004487), diabetes mellitus (MESH:D003920), cancer (MESH:D009369)
- **Chemicals:** lipid (MESH:D008055), Cit (MESH:D019343), ROS (MESH:D017382), alcohol (MESH:D000438), 1H (-), Cr (MESH:D003401), fatty acid (MESH:D005227), acetyl-CoA (MESH:D000105), water (MESH:D014867), C (MESH:D002244), Cho (MESH:D002794)
- **Species:** Homo sapiens (human, species) [taxon 9606], Nicotiana tabacum (American tobacco, species) [taxon 4097], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12919719/full.md

## References

22 references — full list in the complete paper: https://tomesphere.com/paper/PMC12919719/full.md

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Source: https://tomesphere.com/paper/PMC12919719