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Ovarian Cancer Ascites Proteomic Profile Reflects Metabolic Changes During Disease Progression

Abstract

Ovarian cancer (OC) patients develop ascites, an accumulation of ascitic fluid in the peritoneal cavity anda sign of tumour dissemination within the peritoneal cavity. This body fluid is under-researched, mainly regarding the ascites formed during tumour progression that have no diagnostic value and, therefore, are discarded. We performed a discovery proteomics study to identify new biomarkers in the ascites supernatant of OC patients. In this preliminary study, we analyzed a small amount of OC ascites to highlight the importance of not discarding such biological material during treatment, which could be valuable for OC management. Our findings reveal that OC malignant ascitic fluid (MAF) displays a proliferative environment that promotes the growth of OC cells that shift the metabolic pathway using alternative sources of nutrients, such as the cholesterol pathway. Also, OC ascites drained from patients during treatment showed an immunosuppressive environment, with up-regulation of proteins from the signaling pathways of IL-4 and IL-13 and down-regulation from the MHC-II. This preliminary study pinpointed a new protein (Transmembrane Protein 132A) in the OC context that deserves to be better explored in a more extensive cohort of patients' samples. The proteomic profile of MAF from OC patients provides a unique insight into the metabolic kinetics of cancer cells during disease progression, and this information can be used to develop more effective treatment strategies.

Citing Articles

Metformin Impairs Linsitinib Anti-Tumor Effect on Ovarian Cancer Cell Lines.

Almeida-Nunes D, Silva J, Nunes M, Silva P, Silvestre R, Dinis-Oliveira R Int J Mol Sci. 2024; 25(22).

PMID: 39596005 PMC: 11594113. DOI: 10.3390/ijms252211935.

References
1.
Nakashima H, Terabe M, Berzofsky J, Husain S, Puri R . A novel combination immunotherapy for cancer by IL-13Rα2-targeted DNA vaccine and immunotoxin in murine tumor models. J Immunol. 2011; 187(10):4935-46. PMC: 3730529. DOI: 10.4049/jimmunol.1102095. View

2.
Finkernagel F, Reinartz S, Schuldner M, Malz A, Jansen J, Wagner U . Dual-platform affinity proteomics identifies links between the recurrence of ovarian carcinoma and proteins released into the tumor microenvironment. Theranostics. 2019; 9(22):6601-6617. PMC: 6771240. DOI: 10.7150/thno.37549. View

3.
Wang Y, Zhang Z, Wang J, Zhang X . Association between C-reactive protein level and subsequent risk of ovarian cancer: A meta-analysis of 13 cohorts in 1,852 ovarian cancer patients. Medicine (Baltimore). 2020; 99(5):e18821. PMC: 7004735. DOI: 10.1097/MD.0000000000018821. View

4.
Choi H, Ignacio R, Lee E, Wilson A, Khabele D, Son D . Augmented Serum Amyloid A1/2 Mediated by TNF-induced NF-κB in Human Serous Ovarian Epithelial Tumors. Immune Netw. 2017; 17(2):121-127. PMC: 5407984. DOI: 10.4110/in.2017.17.2.121. View

5.
Shan Y, Yang G, Huang H, Zhou Y, Hu X, Lu Q . Ubiquitin-Like Modifier Activating Enzyme 1 as a Novel Diagnostic and Prognostic Indicator That Correlates With Ferroptosis and the Malignant Phenotypes of Liver Cancer Cells. Front Oncol. 2020; 10:592413. PMC: 7744729. DOI: 10.3389/fonc.2020.592413. View