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ZNF326 as a potential prognostic and predictive biomarker in stage II colorectal cancer.
Pu, Hongjiang; Zhang, Shuai; Yan, Shan; Li, Chunxia; Fu, Jiangping; You, Dingyun; Zhang, Tao; Li, Zhenhui.
Affiliation
  • Pu H; Department of Oncology, Dazhou Central Hospital, Dazhou, China.
  • Zhang S; Department of Biostatistics, School of Public Health, Cheeloo College of Medicine, Shandong University, Jinan, China.
  • Yan S; Institute for Medical Dataology, Cheeloo College of Medicine, Shandong University, Jinan, China.
  • Li C; Yunnan Key Laboratory of Stem Cell and Regenerative Medicine, School of Biomedical Engineering Research, Kunming Medical University, Kunming, China.
  • Fu J; Department of Biostatistics, School of Public Health, Cheeloo College of Medicine, Shandong University, Jinan, China.
  • You D; Institute for Medical Dataology, Cheeloo College of Medicine, Shandong University, Jinan, China.
  • Zhang T; Department of Oncology, Dazhou Central Hospital, Dazhou, China.
  • Li Z; Yunnan Key Laboratory of Stem Cell and Regenerative Medicine, School of Biomedical Engineering Research, Kunming Medical University, Kunming, China.
J Gastrointest Oncol ; 15(1): 179-189, 2024 Feb 29.
Article de En | MEDLINE | ID: mdl-38482244
ABSTRACT

Background:

Adjuvant chemotherapy is considered for stage II colorectal cancer (CRC) patients with poor prognostic risk factors. However, current stratification algorithms are still insufficient to identify high-risk patients.

Methods:

We conducted a screening strategy to define ZNF326 based on quantitative proteomics in 11 paired CRC patients selected by a nested case-control design, and tested the association between ZNF326 expression level with the prognosis of stage II CRC patients and the benefit from adjuvant chemotherapy in public datasets; further investigation was conducted through subgroup analyses.

Results:

We found that low ZNF326 expression was significantly associated with a lower 5-year overall survival (OS) rate among stage II patients in both the discovery [P=0.008; hazard ratio (HR) 3.13, 95% confidence interval (CI) 1.29-7.58] and validation (P=0.025; HR 1.98, 95% CI 1.08-3.65) cohorts. In the Cox multivariable analysis, low ZNF326 expression was both associated with shorter OS after adjustment for age, sex, and adjuvant chemotherapy in the discovery and validation data sets. Subgroup analyses yielded largely similar results. In a pooled database, the rate of 5-year OS was higher among stage II ZNF326-high tumors who were treated with adjuvant chemotherapy than it was among those who were not treated with adjuvant chemotherapy (P=0.011; HR 0.28, 95% CI 0.10-0.80).

Conclusions:

ZNF326 has the potential to be used in clinical practice for risk classification. ZNF326-low expression level identified a subgroup of patients with high-risk stage II CRC who appeared to less benefit from adjuvant chemotherapy.
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: J Gastrointest Oncol Année: 2024 Type de document: Article Pays d'affiliation: Chine

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: J Gastrointest Oncol Année: 2024 Type de document: Article Pays d'affiliation: Chine
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