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 |
Appears in Collections: | Staff Publications Elements |
Show full item record
Files in This Item:
File | Description | Size | Format | Access Settings | Version | |
---|---|---|---|---|---|---|
path.5769.pdf | 3.71 MB | Adobe PDF | OPEN | Post-print | View/Download |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.