Gene expression profiles for a prognostic immunoscore in gastric cancer

Author:

Zeng D1,Zhou R1,Yu Y2,Luo Y1,Zhang J1,Sun H1,Bin J3,Liao Y3,Rao J4,Zhang Y5,Liao W1

Affiliation:

1. Department of Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China

2. Guangdong Provincial Key Laboratory of Malignant Tumour Epigenetics and Gene Regulation, Breast Tumour Centre, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, Guangdong, China

3. Department of Cardiology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China

4. Key Laboratory of New Drug Screening of Guangdong Province, School of Pharmaceutical Sciences, Southern Medical University, Guangzhou, Guangdong, China

5. Key Laboratory of Zebrafish Modelling and Drug Screening for Human Diseases of Guangdong Higher Education Institutes, Department of Developmental Biology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, Guangdong, China

Abstract

Abstract Background Increasing evidence has indicated an association between immune infiltration in gastric cancer and clinical outcome. However, reliable prognostic signatures, based on systematic assessments of the immune landscape inferred from bulk tumour transcriptomes, have not been established. The aim was to develop an immune signature, based on the cellular composition of the immune infiltrate inferred from bulk tumour transcriptomes, to improve the prognostic predictions of gastric cancer. Methods Twenty-two types of immune cell fraction were estimated based on large public gastric cancer cohorts from the Gene Expression Omnibus using CIBERSORT. An immunoscore based on the fraction of immune cell types was then constructed using a least absolute shrinkage and selection operator (LASSO) Cox regression model. Results Using the LASSO model, an immunoscore was established consisting of 11 types of immune cell fraction. In the training cohort (490 patients), significant differences were found between high- and low-immunoscore groups in overall survival across and within subpopulations with an identical TNM stage. Multivariable analysis revealed that the immunoscore was an independent prognostic factor (hazard ratio 1·92, 95 per cent c.i. 1·54 to 2·40). The prognostic value of the immunoscore was also confirmed in the validation (210) and entire (700) cohorts. Conclusion The proposed immunoscore represents a promising signature for estimating overall survival in patients with gastric cancer.

Funder

National Natural Science Foundation of China

Publisher

Oxford University Press (OUP)

Subject

Surgery

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