# AMACR and ZFPL1 serum biomarkers enhance precision in predicting postoperative prostate cancer outcomes

**Authors:** Lin Yang, Renguang Lv, Zhao Liu, Gang Chen, Gangli Gu

PMC · DOI: 10.3389/fonc.2026.1625125 · Frontiers in Oncology · 2026-02-17

## TL;DR

This study shows that measuring AMACR and ZFPL1 in blood can improve predictions of prostate cancer recurrence after surgery.

## Contribution

The study introduces AMACR and ZFPL1 as novel serum biomarkers for predicting prostate cancer recurrence and develops a predictive nomogram integrating these markers.

## Key findings

- Elevated AMACR and ZFPL1 levels independently predict recurrence after prostatectomy.
- A nomogram combining these biomarkers with clinicopathological factors shows strong predictive accuracy.
- The model's performance remains stable up to 3 years post-surgery.

## Abstract

Prostate cancer (PCa) remains a major clinical challenge, with postoperative recurrence risk varying substantially among patients. Emerging evidence suggests that serum biomarkers, including α-methylacyl-CoA racemase (AMACR) and zinc finger protein-like 1 (ZFPL1), may provide additional prognostic information beyond conventional clinicopathological factors.

This single-center retrospective study included 115 patients with PCa who underwent radical prostatectomy. Serum AMACR and ZFPL1 levels were analyzed in combination with clinicopathological variables. Univariate and multivariate logistic regression analyses were performed to identify independent predictors of recurrence. A risk nomogram was constructed, and model performance was evaluated using receiver operating characteristic (ROC) curve analysis and Kaplan–Meier survival analysis.

Poor postoperative outcomes were significantly associated with advanced age, lymph node metastasis, higher TNM stage, poor tumor differentiation, and higher Gleason score. Serum AMACR and ZFPL1 levels were significantly elevated in patients who experienced recurrence. Multivariate analysis identified both biomarkers as independent predictors of recurrence. The resulting nomogram demonstrated strong discriminative performance and stable predictive accuracy across multiple postoperative time points.

Elevated serum AMACR and ZFPL1 levels independently predict recurrence following radical prostatectomy in patients with PCa. The proposed nomogram integrates molecular and clinicopathological factors to provide accurate postoperative risk stratification, supporting individualized follow-up and management, with robust performance observed up to 3 years after surgery.

The molecular mechanism by which AMACR and ZFPL1 regulate postoperative recurrence in PCa.Diagram illustrating metabolic reprogramming and Golgi apparatus function in cancer. It shows tumor cells with fatty acid uptake mediated by CD36, AMACR's conversion role, and mitochondrial beta oxidation. It includes PI3K and Akt phosphorylation effects, ZFPL1 secretion, and its complex with EZH2 affecting chromatin modification. Additionally, it highlights Golgi apparatus's role in secreting MMPs and VEGF, leading to tumor suppressor gene silencing. A section illustrates the proximity of a tumor to the bladder and prostate.

The molecular mechanism by which AMACR and ZFPL1 regulate postoperative recurrence in PCa.

## Linked entities

- **Genes:** AMACR (alpha-methylacyl-CoA racemase) [NCBI Gene 23600], ZFPL1 (zinc finger protein like 1) [NCBI Gene 7542], EZH2 (enhancer of zeste 2 polycomb repressive complex 2 subunit) [NCBI Gene 2146], CD36 (CD36 molecule (CD36 blood group)) [NCBI Gene 948]
- **Proteins:** AMACR (alpha-methylacyl-CoA racemase), ZFPL1 (zinc finger protein like 1)
- **Diseases:** prostate cancer (MONDO:0005159)

## Full-text entities

- **Genes:** FUT4 (fucosyltransferase 4) [NCBI Gene 2526] {aka CD15, ELFT, FCT3A, FUC-TIV, FUTIV, LeX}, CDH1 (cadherin 1) [NCBI Gene 999] {aka Arc-1, BCDS1, CD324, CDHE, ECAD, LCAM}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, KLK3 (kallikrein related peptidase 3) [NCBI Gene 354] {aka APS, KLK2A1, PSA, hK3}, FN1 (fibronectin 1) [NCBI Gene 2335] {aka CIG, ED-B, FINC, FN, FNZ, GFND}, MMP9 (matrix metallopeptidase 9) [NCBI Gene 4318] {aka CLG4B, GELB, MANDP2, MMP-9}, MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, TENM1 (teneurin transmembrane protein 1) [NCBI Gene 10178] {aka ODZ1, ODZ3, TEN-M1, TEN1, TNM, TNM1}, ZFPL1 (zinc finger protein like 1) [NCBI Gene 7542] {aka D11S750, MCG4}, PCA3 (prostate cancer associated 3) [NCBI Gene 50652] {aka DD3, NCRNA00019, PCAT3, PRUNE2-AS1}, FOLH1 (folate hydrolase 1) [NCBI Gene 2346] {aka FGCP, FOLH, GCP2, GCPII, NAALAD1, PSM}, AMACR (alpha-methylacyl-CoA racemase) [NCBI Gene 23600] {aka AMACRD, CBAS4, P504S, RACE, RM}, AR (androgen receptor) [NCBI Gene 367] {aka AIS, AR8, DHTR, HPCX3, HUMARA, HYSP1}, SERPINF1 (serpin family F member 1) [NCBI Gene 5176] {aka EPC-1, OI12, OI6, PEDF, PIG35}, IGF1 (insulin like growth factor 1) [NCBI Gene 3479] {aka IGF, IGF-I, IGFI, MGF}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, KLK2 (kallikrein related peptidase 2) [NCBI Gene 3817] {aka KLK2A2, hGK-1, hK2}
- **Diseases:** obstructive urinary tract diseases (MESH:D014570), prostate tumor (MESH:D011472), HPA (MESH:D010661), lymph node metastasis (MESH:D008207), neuroendocrine carcinoma (MESH:D018278), Metastasis (MESH:D009362), death (MESH:D003643), hypertension (MESH:D006973), III (MESH:C537189), strictures (MESH:D003251), gastric neuroendocrine tumors (MESH:D018358), squamous cell carcinoma (MESH:D002294), organ dysfunction (MESH:D009102), tumorigenesis (MESH:D063646), psychiatric disorders (MESH:D001523), Prostate Adenocarcinoma (MESH:D000230), neurogenic bladder (MESH:D001750), Tumor (MESH:D009369), diabetes (MESH:D003920), urinary tract stones (MESH:D014545), inflammatory (MESH:D007249), PCa (MESH:D011471), alcohol abuse (MESH:D000437)
- **Chemicals:** alcohol (MESH:D000438), glucose (MESH:D005947), lipid (MESH:D008055), branched-chain fatty acid (-), cholesterol (MESH:D002784), ethanol (MESH:D000431), prostaglandin E2 (MESH:D015232), triglyceride (MESH:D014280)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** P504S, AUC of 0

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12953113/full.md

## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12953113/full.md

## References

37 references — full list in the complete paper: https://tomesphere.com/paper/PMC12953113/full.md

---
Source: https://tomesphere.com/paper/PMC12953113