Please use this identifier to cite or link to this item: https://doi.org/10.1002/path.5769
Title: A multi‐ethnic analysis of immune‐related gene expression signatures in patients with ovarian clear cell carcinoma
Authors: Heong, Valerie
Tan Tuan Zea 
Miwa, Maiko
Ye, Jieru
Lim, Diana
Herrington, C Simon
Iida, Yasushi
Yano, Mitsutake
Yasuda, Masanori
Ngoi, Natalie YL
Wong, SB Justin
Okamoto, Aikou
Gourley, Charlie
Hasegawa, Kosei
Tan, David SP
Huang, Ruby YJ
Keywords: Ovarian cancer
clear cell cancer
Gene expression signaturesimmune microenvironment
microsatellite instability
mismatch repair protein
immune subtypes
RNA expression and ethnicity
Issue Date: 28-Jul-2021
Publisher: Wiley
Citation: Heong, Valerie, Tan Tuan Zea, Miwa, Maiko, Ye, Jieru, Lim, Diana, Herrington, C Simon, Iida, Yasushi, Yano, Mitsutake, Yasuda, Masanori, Ngoi, Natalie YL, Wong, SB Justin, Okamoto, Aikou, Gourley, Charlie, Hasegawa, Kosei, Tan, David SP, Huang, Ruby YJ (2021-07-28). A multi‐ethnic analysis of immune‐related gene expression signatures in patients with ovarian clear cell carcinoma. The Journal of Pathology. ScholarBank@NUS Repository. https://doi.org/10.1002/path.5769
Abstract: Little is known about the immune environment of ovarian clear cell carcinoma (OCCC) and its impact on various ethnic backgrounds. The aim of this OCCC immune-related gene expression signatures (irGES) study was to address the interaction between tumour and immune environment of ethnically-diverse Asian and Caucasian populations and to identify relevant molecular subsets of biological and clinical importance. Our study included 264 women from three different countries (Singapore, Japan, and UK) and identified four novel immune subtypes (PD1-high, CTLA4-high, antigen-presentation and pro-angiogenic subtype) with differentially expressed pathways, and gene ontologies using the NanoString nCounter PanCancer Immune Profiling Panel. The PD1-high and CTLA4-high subtypes demonstrated significantly higher PD1, PDL1 and CTLA4 expression and were associated with poorer clinical outcomes. Mismatch repair (MMR) protein expression, assessed by immunohistochemistry, revealed that about 5% of OCCC had deficient MMR expression. The prevalence was similar across the three countries and appeared to cluster in the CTLA4-high subtype. Our results suggest OCCC from women of Asian and Caucasian descent share significant clinical and molecular similarities. To our knowledge, our study is the first study to include both Asian and Caucasian women with OCCC and helps shine light on the impact of ethnic differences on the immune microenvironment of OCCC.
Source Title: The Journal of Pathology
URI: https://scholarbank.nus.edu.sg/handle/10635/195449
ISSN: 0022-3417
1096-9896
DOI: 10.1002/path.5769
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