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Molecular classification and immunologic characteristics of immunoreactive high‐grade serous ovarian cancer.

Authors :
Liu, Zheran
Wu, Haifang
Deng, Jiachen
Wang, Haoqing
Wang, Zixuan
Yang, Ailin
Liang, Bowen
Luo, Ji
Li, Jianyong
Xu, Yanmei
Tang, Xiaoli
Fu, Fen
Deng, Libin
Source :
Journal of Cellular & Molecular Medicine; Jul2020, Vol. 24 Issue 14, p8103-8114, 12p
Publication Year :
2020

Abstract

High‐grade serous ovarian cancer (HGS‐OvCa) is one of the most lethal gynaecological malignancies. Molecular classification identified an immunoreactive subtype of HGS‐OvCa; however, the immunologic characteristics of immunoreactive HGS‐OvcA remain unclear. In this study, 121 immunoreactive HGS‐OvCa samples were identified from a meta‐analysis of 5 large transcriptome profiling data sets using a cross‐platform immunoreactive HGS‐OvCa subgroup‐specific classifier. By comparing the gene expression profiles of immunoreactive HGS‐OvCa samples and normal tissues, 653 differentially expressed genes (DEGs) were identified. KEGG pathway analysis revealed that the leukocyte transendothelial migration pathways were significantly enriched in the immunoreactive HGS‐OvCa. Protein‐protein interaction analysis identified a module that showed strong involvement of the immune‐related chemokine signalling pathway. Moreover, the GSEA enrichment analysis showed a T‐cell subgroup and M1 macrophages were significantly enriched in immunoreactive OvCa compared with normal samples. Macrophage infiltration levels were significantly elevated in immunoreactive HGS‐OvCa compared with other OvCa subtypes. In addition, expression of immune checkpoint molecules VTCN1 and IDO1 was significantly increased in immunoreactive HGS‐OvCa. In summary, our results suggest that the immunoreactive HGS‐OvCa has unique molecular characteristics and a tumour‐associated immune microenvironment featured by increased infiltration of macrophages, rather than lymphocytes. VTCN1 could be potential targets for the treatment of immunoreactive HGS‐OvCa. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
15821838
Volume :
24
Issue :
14
Database :
Complementary Index
Journal :
Journal of Cellular & Molecular Medicine
Publication Type :
Academic Journal
Accession number :
144497478
Full Text :
https://doi.org/10.1111/jcmm.15441