Differential expression and function of CAIX and CAXII in breast cancer: A comparison between tumorgraft models and cells.

Autor: Chen Z; The Department of Biochemistry and Molecular Biology, University of Florida, Gainesville, FL, United States of America., Ai L; The Department of Medicine, University of Florida, Gainesville, FL, United States of America., Mboge MY; The Department of Biochemistry and Molecular Biology, University of Florida, Gainesville, FL, United States of America., Tu C; The Department of Biochemistry and Molecular Biology, University of Florida, Gainesville, FL, United States of America., McKenna R; The Department of Biochemistry and Molecular Biology, University of Florida, Gainesville, FL, United States of America., Brown KD; The Department of Biochemistry and Molecular Biology, University of Florida, Gainesville, FL, United States of America., Heldermon CD; The Department of Medicine, University of Florida, Gainesville, FL, United States of America., Frost SC; The Department of Biochemistry and Molecular Biology, University of Florida, Gainesville, FL, United States of America.
Jazyk: angličtina
Zdroj: PloS one [PLoS One] 2018 Jul 02; Vol. 13 (7), pp. e0199476. Date of Electronic Publication: 2018 Jul 02 (Print Publication: 2018).
DOI: 10.1371/journal.pone.0199476
Abstrakt: Carbonic anhydrase IX (CAIX) and XII (CAXII) are transmembrane proteins that are associated with cancer progression. We have previously described the catalytic properties of CAIX in MDA-MB-231 breast cancer cells, a line of cells that were derived from a patient with triple negative breast cancer. We chose this line because CAIX expression in breast cancer is a marker of hypoxia and a prognosticator for reduced survival. However, CAXII expression is associated with better survival statistics than those patients with low CAXII expression. Yet CAIX and CAXII have similar catalytic activities. Here we compare the potential roles of CAIX and CAXII in the context of TNBC and estrogen receptor (ER)-positive breast cancer. In tumor graft models, we show that CAIX and CAXII exhibit distinct expression patterns and non-overlapping. We find the same pattern across a panel of TNBC and luminal breast cancer cell lines. This affords an opportunity to compare directly CAIX and CAXII function. Our data suggest that CAIX expression is associated with growth potentiation in the tumor graft model and in a TNBC line using knockdown strategies and blocking activity with an impermeant sulfonamide inhibitor, N-3500. CAXII was not associated with growth potentiation. The catalytic activities of both CAIX and CAXII were sensitive to inhibition by N-3500 and activated at low pH. However, pH titration of activity in membrane ghosts revealed significant differences in the catalytic efficiency and pKa values. These features provide evidence that CAIX is a more efficient enzyme than CAXII at low pH and that CAIX shifts the equilibrium between CO2 and bicarbonate in favor of CO2 production by consuming protons. This suggests that in the acidic microenvironment of tumors, CAIX plays a role in stabilizing pH at a value that favors cancer cell survival.
Competing Interests: The authors have declared that no competing interests exist.
Databáze: MEDLINE
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