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Chinese Journal of Colorectal Diseases(Electronic Edition) ›› 2026, Vol. 15 ›› Issue (01): 58-66. doi: 10.3877/cma.j.issn.2095-3224.2026.01.006

• Original Article • Previous Articles    

Expression and clinical significance of STRA6, CYP24A1, and NXPH4 in colorectal cancer liver metastasis

Ziqing Yu1, Duo Li,2(), Huan Wang1, Xueliang Wu3, Jianchun Fan4, Xiao Han5   

  1. 1Graduate School, Hebei North University, Zhangjiakou 075000, China
    2Department of Gastroenterology, the First Affiliated Hospital of Hebei North University, Zhangjiakou 075000, China
    3General Surgery, the First Affiliated Hospital of Hebei North University, Zhangjiakou 075000, China
    4Zhangjiakou Institute of Oncology, the First Affiliated Hospital of Hebei North University, Zhangjiakou 075000, China
    5Department of Anesthesiology, Tongliao People’s Hospital, Tongliao 028000, China
  • Received:2025-11-17 Online:2026-02-25 Published:2026-03-20
  • Contact: Duo Li

Abstract:

Objective

This study aimed to investigate the expression of stimulated by retinoic acid 6(STRA6), cytochrome P450 family 24 subfamily A member 1(CYP24A1), and neurexophilin 4(NXPH4) proteins in colorectal cancer liver metastasis and their correlations with clinicopathological characteristics, prognosis, and diagnostic significance.

Methods

A total of 80 patients with colorectal cancer initially diagnosed and undergoing surgery at the First Affiliated Hospital of Hebei North University between January 2017 and December 2019 were enrolled. Among them, thirty patients developed liver metastasis, while 50 did not. Immunohistochemistry was used to detect the expression levels of STRA6, CYP24A1, and NXPH4. The relationships between these proteins and clinicopathological parameters were analyzed. The Kaplan-Meier method was applied to evaluate the prognostic significance of these proteins in colorectal liver metastasis patients. Univariate and multivariate logistic regression analyses were conducted to identify influencing factors for liver metastasis in colorectal cancer patients. Receiver operating characteristic (ROC) curve analysis was utilized to assess the predictive value of individual and combined detection of these proteins for colorectal liver metastasis.

Results

The expression levels of STRA6, CYP24A1, and NXPH4 were significantly higher in the liver metastasis group compared to the non-metastasis and paracancerous tissue groups (P<0.05). In colorectal liver metastasis patients, high expression of STRA6 and NXPH4 was correlated with lymph node metastasis and depth of invasion, while high expression of CYP24A1 was associated with lymph node metastasis, depth of invasion, and tumor differentiation (P<0.05). Survival analysis showed that colorectal liver metastasis patients with high expression of STRA6, CYP24A1, and NXPH4 had a lower 5-year survival rate (HR=2.690, 4.279, and 2.784, respectively; P<0.05). Liver metastasis in colorectal cancer patients was correlated with lymph node metastasis, depth of invasion, and degree of differentiation, and CEA (P<0.05). Multivariate analysis identified lymph node metastasis, CEA≥5 ng/mL, and elevated levels of STRA6, CYP24A1, and NXPH4 as independent risk factors for liver metastasis (P<0.05). ROC curve analysis demonstrated that the AUC values for predicting colorectal liver metastasis were 0.722 (95%CI: 0.602~0.843) for STRA6, 0.797 (95%CI: 0.696~0.898) for CYP24A1, and 0.696 (95%CI: 0.577~0.814) for NXPH4. The sensitivities and specificities were 46.70% and 94.00% for STRA6, 56.70% and 92.00% for CYP24A1, and 86.70% and 52.00% for NXPH4, respectively. The combined detection of these proteins achieved an AUC of 0.820 (95%CI: 0.719~0.921), with a sensitivity of 66.70% and specificity of 90.00%.

Conclusion

High expression of STRA6, CYP24A1, and NXPH4 indicates an increased risk of liver metastasis and poor prognosis in colorectal cancer patients. These proteins may serve as potential biomarkers for risk stratification and prognosis of colorectal cancer liver metastasis, providing references for early clinical intervention.

Key words: Colorectal cancer, Livermetastases, Clinicopathological features, Prognostic analysis

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