Abstract |
Targeting the tumor-associated carbonic anhydrase XII (CA XII) is considered a promising strategy to improve cancer treatment. As such progress is highly demanded for ovarian carcinomas, the present study aimed to provide deeper information about their CA XII expression profile. A large collection of tissue specimens was stained immunohistochemically with a specific anti-CA XII antibody to evaluate the expression in neoplastic and non-neoplastic epithelial ovarian cells. In addition, flow cytometry was used to measure CA XII expression on tumor cells from malignant ascites fluid. Binding of the antibody revealed a significant CA XII expression in most ovarian carcinoma tissue samples and ascites-derived ovarian carcinoma cells. Moreover, CA XII was expressed at higher levels in ovarian carcinomas as compared to borderline ovarian tumors and non-neoplastic ovarian epithelia. Within the carcinoma tissues, high expression of CA XII was associated with higher tumor grading and a trend towards shorter overall survival. Our results indicate that CA XII plays a crucial role for the malignancy of ovarian carcinoma cells and emphasize the potential of CA XII as a diagnostic marker and therapeutic target in the management of ovarian carcinomas.
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Authors | Lisa Hiepp, Doris Mayr, Kathrin Gärtner, Elisa Schmoeckel, Frederick Klauschen, Alexander Burges, Sven Mahner, Reinhard Zeidler, Bastian Czogalla |
Journal | PloS one
(PLoS One)
Vol. 17
Issue 7
Pg. e0271630
( 2022)
ISSN: 1932-6203 [Electronic] United States |
PMID | 35901081
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antigens, Neoplasm
- Biomarkers
- Carbonic Anhydrase Inhibitors
- Intracellular Signaling Peptides and Proteins
- Isoenzymes
- CA8 protein, human
- Carbonic Anhydrase IX
- Carbonic Anhydrases
- carbonic anhydrase XII
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Topics |
- Antigens, Neoplasm
(metabolism)
- Ascites
- Biomarkers
- Carbonic Anhydrase IX
- Carbonic Anhydrase Inhibitors
- Carbonic Anhydrases
(metabolism)
- Carcinoma
- Female
- Humans
- Intracellular Signaling Peptides and Proteins
(metabolism)
- Isoenzymes
(metabolism)
- Ovarian Neoplasms
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