Ovarian cancer remains the gynecological cancer with the highest mortality rate. In our study, we compare a number of proteins from different effector pathways to assess their usefulness in the diagnosis of ovarian cancer. The tissue expression of the tested proteins was assessed by two methods: qRT-PCR and an immunohistochemical analysis. A significantly higher level of mRNA expression was found in the ovarian cancer group for and ( = 0.004 and = 0.003, respectively). There was no statistical significance in the expression of mRNA for , and there was borderline statistical significance for between the groups of ovarian cancer patients and other subgroups of patients with simple cysts and healthy ovarian tissue ( = 0.726 and = 0.046, respectively). Significantly higher levels of transferrin receptor (), , and gene expression were found in the ovarian cancer group compared to the control group for , and TEAD4 showed strong nuclear and cytoplasmic staining in ovarian carcinoma and weak staining in non-carcinoma ovarian samples, ADH1A1 showed strong staining in the cytoplasm of carcinoma sections and a weak positive reaction in the non-carcinoma section, H2A.X showed strong positive nuclear staining in carcinoma sections and moderate positive staining in non-carcinoma samples, and CD71 showed moderate positive staining in carcinoma and non-carcinoma samples. YAP, TEAD4, and ADH1A proteins appear to be promising biomarkers in the diagnosis of ovarian cancer.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8227487PMC
http://dx.doi.org/10.3390/diagnostics11061026DOI Listing

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