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Discovery of a biomarker candidate for surgical stratification in high-grade serous ovarian cancer
File | Description | Size | Format | |
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Final accepted version ALG5 manuscript.pdf | Accepted version | 1.31 MB | Adobe PDF | View/Open |
Title: | Discovery of a biomarker candidate for surgical stratification in high-grade serous ovarian cancer |
Authors: | Lu, H Cunnea, P Nixon, K Rinne, N Aboagye, EO Fotopoulou, C |
Item Type: | Journal Article |
Abstract: | Background: Maximal effort cytoreductive surgery is associated with improved outcomes in advanced high-grade serous ovarian cancer (HGSOC). However, despite complete gross resection (CGR), there is a percentage of patients who will relapse and die early. The aim of this study is to identify potential candidate biomarkers to help personalise surgical radicality. Methods: 136 advanced HGSOC cases who underwent CGR were identified from three public transcriptomic datasets. Candidate prognostic biomarkers were discovered in this cohort by Cox regression analysis, and further validated by targeted RNA-sequencing in HGSOC cases from Imperial College Healthcare NHS Trust (n = 59), and a public dataset. Gene set enrichment analysis was performed to understand the biological significance of the candidate biomarker. Results: We identified ALG5 as a prognostic biomarker for early tumour progression in advanced HGSOC despite CGR (HR = 2.42, 95% CI (1.57–3.75), p < 0.0001). The prognostic value of this new candidate biomarker was additionally confirmed in two independent datasets (HR = 1.60, 95% CI (1.03–2.49), p = 0.0368; HR = 3.08, 95% CI (1.07–8.81), p = 0.0365). Mechanistically, the oxidative phosphorylation was demonstrated as a potential biological pathway of ALG5-high expression in patients with early relapse (p < 0.001). Conclusion: ALG5 has been identified as an independent prognostic biomarker for poor prognosis in advanced HGSOC patients despite CGR. This sets a promising platform for biomarker combinations and further validations towards future personalised surgical care. |
Issue Date: | 30-Mar-2021 |
Date of Acceptance: | 17-Dec-2020 |
URI: | http://hdl.handle.net/10044/1/86329 |
DOI: | 10.1038/s41416-020-01252-2 |
ISSN: | 0007-0920 |
Publisher: | Springer Nature [academic journals on nature.com] |
Start Page: | 1286 |
End Page: | 1293 |
Journal / Book Title: | British Journal of Cancer |
Volume: | 124 |
Issue: | 7 |
Copyright Statement: | ©The Author(s), under exclusive licence to Cancer Research UK 2021. The final publication is available at Springer via https://doi.org/10.1038/s41416-020-01252-2. This work is published under the standard license to publish agreement. After 12 months the work will become freely available and the license terms will switch to a Creative Commons Attribution 4.0 International (CC BY 4.0). |
Sponsor/Funder: | Myrovlytis Trust Limited Imperial College Healthcare NHS Trust- BRC Funding Imperial College Healthcare NHS Trust- BRC Funding Imperial College Healthcare NHS Trust- BRC Funding Medical Research Council |
Funder's Grant Number: | n/a RDC04 79560 RDC04 79560 RDC04 |
Keywords: | Science & Technology Life Sciences & Biomedicine Oncology CELLS RECOMMENDATIONS METABOLISM PLATINUM SOCIETY Oncology & Carcinogenesis 1112 Oncology and Carcinogenesis 1117 Public Health and Health Services |
Publication Status: | Published |
Online Publication Date: | 2021-01-21 |
Appears in Collections: | Department of Surgery and Cancer Faculty of Medicine |