Serum Lipidome Profiling Reveals a Distinct Signature of Ovarian Cancer in Korean Women

Author:

Sah Samyukta12ORCID,Bifarin Olatomiwa O.1ORCID,Moore Samuel G.2ORCID,Gaul David A.12ORCID,Chung Hyewon3ORCID,Kwon Sun Young4ORCID,Cho Hanbyoul5ORCID,Cho Chi-Heum3ORCID,Kim Jae-Hoon6ORCID,Kim Jaeyeon7ORCID,Fernández Facundo M.12ORCID

Affiliation:

1. 1School of Chemistry and Biochemistry, Georgia Institute of Technology, Atlanta, Georgia.

2. 2Petit Institute of Bioengineering and Bioscience, Georgia Institute of Technology, Atlanta, Georgia.

3. 3Department of Obstetrics and Gynecology, School of Medicine, Keimyung University, Daegu Republic of Korea.

4. 4Department of Pathology, School of Medicine, Keimyung University, Daegu, Republic of Korea.

5. 5Department of Obstetrics and Gynecology, Institute of Women's Life Medical Science, Yonsei University College of Medicine, Seoul, Republic of Korea.

6. 6Department of Obstetrics and Gynecology, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.

7. 7Department of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indianapolis, Indiana.

Abstract

Abstract Background: Distinguishing ovarian cancer from other gynecological malignancies is crucial for patient survival yet hindered by non-specific symptoms and limited understanding of ovarian cancer pathogenesis. Accumulating evidence suggests a link between ovarian cancer and deregulated lipid metabolism. Most studies have small sample sizes, especially for early-stage cases, and lack racial/ethnic diversity, necessitating more inclusive research for improved ovarian cancer diagnosis and prevention. Methods: Here, we profiled the serum lipidome of 208 ovarian cancer, including 93 early-stage patients with ovarian cancer and 117 nonovarian cancer (other gynecological malignancies) patients of Korean descent. Serum samples were analyzed with a high-coverage liquid chromatography high-resolution mass spectrometry platform, and lipidome alterations were investigated via statistical and machine learning (ML) approaches. Results: We found that lipidome alterations unique to ovarian cancer were present in Korean women as early as when the cancer is localized, and those changes increase in magnitude as the diseases progresses. Analysis of relative lipid abundances revealed specific patterns for various lipid classes, with most classes showing decreased abundance in ovarian cancer in comparison with other gynecological diseases. ML methods selected a panel of 17 lipids that discriminated ovarian cancer from nonovarian cancer cases with an AUC value of 0.85 for an independent test set. Conclusions: This study provides a systemic analysis of lipidome alterations in human ovarian cancer, specifically in Korean women. Impact: Here, we show the potential of circulating lipids in distinguishing ovarian cancer from nonovarian cancer conditions.

Funder

National Institutes of Health

U.S. Army

National Science Foundation

Publisher

American Association for Cancer Research (AACR)

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