Neoplasma Vol.71, No.2, p. 164–179, 2024
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| Title: Unlocking the paracrine crosstalk: adipocyte-derived factors affect carbonic anhydrase IX expression in colon and breast cancer cells |
| Author: Jana Lapinova, Miroslav Balaz, Lucia Balazova, Lucia Csaderova, Tereza Golias, Miriam Zatovicova, Joerg Heeren, Silvia Pastorekova, Martina Takacova |
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Abstract: Obesity is a major public health concern because it increases the risk of several diseases, including cancer. Crosstalk between obesity and cancer seems to be very complex, and the interaction between adipocytes and cancer cells leads to changes in adipocytes’ function and their paracrine signaling, promoting a microenvironment that supports tumor growth. Carbonic anhydrase IX (CA IX) is a tumor-associated enzyme that not only participates in pH regulation but also facilitates metabolic reprogramming and supports the migration, invasion, and metastasis of cancer cells. In addition, CA IX expression, predominantly regulated via hypoxia-inducible factor (HIF-1), serves as a surrogate marker of hypoxia. In this study, we investigated the impact of adipocytes and adipocyte-derived factors on the expression of CA IX in colon and breast cancer cells. We observed increased expression of CA9 mRNA as well as CA IX protein in the presence of adipocytes and adipocyte-derived conditioned medium. Moreover, we confirmed that adipocytes affect the hypoxia signaling pathway and that the increased CA IX expression results from adipocyte-mediated induction of HIF-1α. Furthermore, we demonstrated that adipocyte-mediated upregulation of CA IX leads to increased migration and decreased adhesion of colon cancer cells. Finally, we brought experimental evidence that adipocytes, and more specifically leptin, upregulate CA IX expression in cancer cells and consequently promote tumor progression.
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| Keywords: carbonic anhydrase IX; hypoxia; adipocytes; co-cultivation; leptin |
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Published online: 20-May-2024
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| Year: 2024, Volume: 71, Issue: 2 |
Page From: 164, Page To: 179 |
doi:10.4149/neo_2024_240321N127
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