Association of CYP7B1 expression with the prognosis of endometrial cancer: a retrospective study.


Journal

World journal of surgical oncology
ISSN: 1477-7819
Titre abrégé: World J Surg Oncol
Pays: England
ID NLM: 101170544

Informations de publication

Date de publication:
17 Sep 2024
Historique:
received: 09 02 2024
accepted: 13 08 2024
medline: 18 9 2024
pubmed: 18 9 2024
entrez: 17 9 2024
Statut: epublish

Résumé

Endometrial cancer (EC) tissues express CYP7B1, but its association with prognosis needs to be investigated. Immunohistochemistry and image analysis software were used to assess CYP7B1 protein expression in paraffin-embedded endometrial tumor sections. Associations between CYP7B1 and clinical factors were tested with the Wilcoxon rank-sum test. Kaplan-Meier curves were employed to describe survival, and differences were assessed using the log-rank test. Cox regression analysis was used to assess the association between CYP7B1 expression and the prognosis of patients with EC. A total of 307 patients were enrolled with an average age of 52.6 ± 8.0 years at diagnosis. During the period of follow-up, 46 patients (15.0%) died, and 29 (9.4%) suffered recurrence. The expression of CYP7B1 protein is significantly higher in the cytoplasm than in the nucleus (P < 0.001). Patients aged < 55 years (P = 0.040), ER-positive patients (P = 0.028) and PR-positive patients (P < 0.001) report higher levels of CYP7B1 protein. Both univariate (HR = 0.41, 95% CI: 0.18-0.90, P = 0.025) and multivariate (HR = 0.35, 95%CI:0.16-0.79, P = 0.011) Cox regression analyses demonstrate that high CYP7B1 protein expression predicts longer overall survival (OS). When considering only ER-positive patients (n = 265), CYP7B1 protein expression is more strongly associated with OS (HR = 0.20,95%CI:0.08-0.52, P = 0.001). The 3-year OS and 5-year OS in the low-CYP7B1 subgroup are 81.6% and 76.8%, respectively; while in the high-CYP7B1 subgroup are 93.0% and 92.0%, respectively (P = 0.021). High CYP7B1 protein expression predicted longer OS, suggesting that it may serve as an important molecular marker for EC prognosis.

Sections du résumé

BACKGROUND BACKGROUND
Endometrial cancer (EC) tissues express CYP7B1, but its association with prognosis needs to be investigated.
METHODS METHODS
Immunohistochemistry and image analysis software were used to assess CYP7B1 protein expression in paraffin-embedded endometrial tumor sections. Associations between CYP7B1 and clinical factors were tested with the Wilcoxon rank-sum test. Kaplan-Meier curves were employed to describe survival, and differences were assessed using the log-rank test. Cox regression analysis was used to assess the association between CYP7B1 expression and the prognosis of patients with EC.
RESULTS RESULTS
A total of 307 patients were enrolled with an average age of 52.6 ± 8.0 years at diagnosis. During the period of follow-up, 46 patients (15.0%) died, and 29 (9.4%) suffered recurrence. The expression of CYP7B1 protein is significantly higher in the cytoplasm than in the nucleus (P < 0.001). Patients aged < 55 years (P = 0.040), ER-positive patients (P = 0.028) and PR-positive patients (P < 0.001) report higher levels of CYP7B1 protein. Both univariate (HR = 0.41, 95% CI: 0.18-0.90, P = 0.025) and multivariate (HR = 0.35, 95%CI:0.16-0.79, P = 0.011) Cox regression analyses demonstrate that high CYP7B1 protein expression predicts longer overall survival (OS). When considering only ER-positive patients (n = 265), CYP7B1 protein expression is more strongly associated with OS (HR = 0.20,95%CI:0.08-0.52, P = 0.001). The 3-year OS and 5-year OS in the low-CYP7B1 subgroup are 81.6% and 76.8%, respectively; while in the high-CYP7B1 subgroup are 93.0% and 92.0%, respectively (P = 0.021).
CONCLUSIONS CONCLUSIONS
High CYP7B1 protein expression predicted longer OS, suggesting that it may serve as an important molecular marker for EC prognosis.

Identifiants

pubmed: 39289693
doi: 10.1186/s12957-024-03504-4
pii: 10.1186/s12957-024-03504-4
doi:

Substances chimiques

Biomarkers, Tumor 0
CYP7B1 protein, human EC 1.14.14.29
Cytochrome P450 Family 7 EC 1.14.14.23
Receptors, Estrogen 0
Receptors, Progesterone 0
Steroid Hydroxylases EC 1.14.-

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

251

Subventions

Organisme : National Natural Science Foundation of China
ID : 82003522

Informations de copyright

© 2024. The Author(s).

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Auteurs

Xiao-Fang Lu (XF)

Department of Epidemiology, School of Medicine, Jinan University, No. 601, Huangpu Avenue West, Tianhe District, Guangzhou, 510632, China.

Tao Huang (T)

Department of Gynecology, Wuzhou Red Cross Hospital, No. 3-1, Xinxing 1st Road, Wanxiu District, Wuzhou, 543002, China.

Chang Chen (C)

Department of Pathology, Wuzhou Red Cross Hospital, Wuzhou, China.

Jing Zhang (J)

Department of Epidemiology, School of Medicine, Jinan University, No. 601, Huangpu Avenue West, Tianhe District, Guangzhou, 510632, China.

Xu-Yong Fu (XY)

Department of Epidemiology, School of Medicine, Jinan University, No. 601, Huangpu Avenue West, Tianhe District, Guangzhou, 510632, China.

Bo Cheng (B)

Department of Pathology, Chinese People's Liberation Army Rocket Force Characteristic Medical Center, Beijing, China.

Ya-Yan Zhou (YY)

Department of Radiation Oncology, Shenzhen People's Hospital (The Second Clinical Medical College, Jinan University; The First Affiliated Hospital, Southern University of Science and Technology), Shenzhen, China.

Jia Lei (J)

Department of Gynecology, Wuzhou Red Cross Hospital, No. 3-1, Xinxing 1st Road, Wanxiu District, Wuzhou, 543002, China. leijia33333@sina.com.

Da-Lin Lu (DL)

Department of Epidemiology, School of Medicine, Jinan University, No. 601, Huangpu Avenue West, Tianhe District, Guangzhou, 510632, China. dalinlu@jnu.edu.cn.

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