Skip to main content
Top
Published in: BMC Cancer 1/2023

Open Access 01-12-2023 | Esophageal Cancer | Research

Comprehensive analysis of ZNF family genes in prognosis, immunity, and treatment of esophageal cancer

Authors: Kunqiao Hong, Qian Yang, Haisen Yin, Na Wei, Wei Wang, Baoping Yu

Published in: BMC Cancer | Issue 1/2023

Login to get access

Abstract

Background

As a common malignant tumor, esophageal carcinoma (ESCA) has a low early diagnosis rate and poor prognosis. This study aimed to construct the prognostic features composed of ZNF family genes to effectively predict the prognosis of ESCA patients.

Methods

The mRNA expression matrix and clinical data were downloaded from TCGA and GEO database. Using univariate Cox analysis, lasso regression and multivariate Cox analysis, we screened six prognosis-related ZNF family genes to construct the prognostic model. We then used Kaplan-Meier plot, time-dependent receiver operating characteristic (ROC), multivariable Cox regression analysis of clinical information, and nomogram to evaluate the prognostic value within and across sets, separately and combined. We also validated the prognostic value of the six-gene signature using GSE53624 dataset. The different immune status was observed in the single sample Gene Set Enrichment Analysis (ssGSEA). Finally, real-time quantitative PCR was used to detect the expression of six prognostic ZNF genes in twelve pairs of ESCA and adjacent normal tissues.

Results

A six prognosis-related ZNF family genes model consisted of ZNF91, ZNF586, ZNF502, ZNF865, ZNF106 and ZNF225 was identified. Multivariable Cox regression analysis revealed that six prognosis-related ZNF family genes were independent prognostic factors for overall survival of ESCA patients in TCGA and GSE53624. Further, a prognostic nomogram including the riskScore, age, gender, T, stage was constructed, and TCGA/GSE53624-based calibration plots indicated its excellent predictive performance. Drug Sensitivity and ssGSEA analysis showed that the six genes model was closely related to immune cells infiltration and could be used as a potential predictor of chemotherapy sensitivity.

Conclusion

We identified six prognosis-related ZNF family genes model of ESCA, which provide evidence for individualized prevention and treatment.
Appendix
Available only for authorised users
Literature
8.
go back to reference Balogh A, Reiniger L, Hetey S, Kiraly P, Toth E, Karaszi K, Juhasz K, Gelencser Z, Zvara A, Szilagyi A, et al. Decreased expression of ZNF554 in Gliomas is Associated with the activation of Tumor Pathways and shorter patient survival. Int J Mol Sci. 2020;21(16). https://doi.org/10.3390/ijms21165762. Balogh A, Reiniger L, Hetey S, Kiraly P, Toth E, Karaszi K, Juhasz K, Gelencser Z, Zvara A, Szilagyi A, et al. Decreased expression of ZNF554 in Gliomas is Associated with the activation of Tumor Pathways and shorter patient survival. Int J Mol Sci. 2020;21(16). https://​doi.​org/​10.​3390/​ijms21165762.
18.
26.
go back to reference Unoki M, Okutsu J, Nakamura Y. Identification of a novel human gene, ZFP91, involved in acute myelogenous leukemia. Int J Oncol. 2003;22(6):1217–23.PubMed Unoki M, Okutsu J, Nakamura Y. Identification of a novel human gene, ZFP91, involved in acute myelogenous leukemia. Int J Oncol. 2003;22(6):1217–23.PubMed
29.
33.
go back to reference Guo C, Shao T, Jiang X, Wei D, Wang Z, Li M, Bao G. Comprehensive analysis of the functions and prognostic significance of RNA-binding proteins in bladder urothelial carcinoma. Am J Transl Res. 2020;12(11):7160–73.PubMedPubMedCentral Guo C, Shao T, Jiang X, Wei D, Wang Z, Li M, Bao G. Comprehensive analysis of the functions and prognostic significance of RNA-binding proteins in bladder urothelial carcinoma. Am J Transl Res. 2020;12(11):7160–73.PubMedPubMedCentral
39.
go back to reference Gaur P, Sepesi B, Hofstetter WL, Correa AM, Bhutani MS, Vaporciyan AA, Watson TJ, Swisher SG et al. Members of the MDAECG, the University of Rochester School of M. A clinical nomogram predicting pathologic lymph node involvement in esophageal cancer patients. Ann Surg 2010; 252(4):611–617. doi:https://doi.org/10.1097/SLA.0b013e3181f56419 Gaur P, Sepesi B, Hofstetter WL, Correa AM, Bhutani MS, Vaporciyan AA, Watson TJ, Swisher SG et al. Members of the MDAECG, the University of Rochester School of M. A clinical nomogram predicting pathologic lymph node involvement in esophageal cancer patients. Ann Surg 2010; 252(4):611–617. doi:https://​doi.​org/​10.​1097/​SLA.​0b013e3181f56419​
44.
go back to reference Longo M, Raciti GA, Zatterale F, Parrillo L, Desiderio A, Spinelli R, Hammarstedt A, Hedjazifar S, Hoffmann JM, Nigro C, et al. Epigenetic modifications of the Zfp/ZNF423 gene control murine adipogenic commitment and are dysregulated in human hypertrophic obesity. Diabetologia. 2018;61(2):369–80. https://doi.org/10.1007/s00125-017-4471-4.CrossRefPubMed Longo M, Raciti GA, Zatterale F, Parrillo L, Desiderio A, Spinelli R, Hammarstedt A, Hedjazifar S, Hoffmann JM, Nigro C, et al. Epigenetic modifications of the Zfp/ZNF423 gene control murine adipogenic commitment and are dysregulated in human hypertrophic obesity. Diabetologia. 2018;61(2):369–80. https://​doi.​org/​10.​1007/​s00125-017-4471-4.CrossRefPubMed
Metadata
Title
Comprehensive analysis of ZNF family genes in prognosis, immunity, and treatment of esophageal cancer
Authors
Kunqiao Hong
Qian Yang
Haisen Yin
Na Wei
Wei Wang
Baoping Yu
Publication date
01-12-2023
Publisher
BioMed Central
Published in
BMC Cancer / Issue 1/2023
Electronic ISSN: 1471-2407
DOI
https://doi.org/10.1186/s12885-023-10779-5

Other articles of this Issue 1/2023

BMC Cancer 1/2023 Go to the issue
Webinar | 19-02-2024 | 17:30 (CET)

Keynote webinar | Spotlight on antibody–drug conjugates in cancer

Antibody–drug conjugates (ADCs) are novel agents that have shown promise across multiple tumor types. Explore the current landscape of ADCs in breast and lung cancer with our experts, and gain insights into the mechanism of action, key clinical trials data, existing challenges, and future directions.

Dr. Véronique Diéras
Prof. Fabrice Barlesi
Developed by: Springer Medicine