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Pharmacological Inhibition of CA-IX Impairs Tumor Cell Proliferation, Migration and Invasiveness.

Abstract
Carbonic anhydrase IX (CA-IX) plays a pivotal role in regulation of pH in tumor milieu catalyzing carbonic acid formation by hydrating CO2. An acidification of tumor microenvironment contributes to tumor progression via multiple processes, including reduced cell-cell adhesion, increased migration and matrix invasion. We aimed to assess whether the pharmacological inhibition of CA-IX could impair tumor cell proliferation and invasion. Tumor epithelial cells from breast (MDA-MB-231) and lung (A549) cancer were used to evaluate the cytotoxic effect of sulfonamide CA-IX inhibitors. Two CA-IX enzyme blockers were tested, SLC-0111 (at present in phase Ib clinical trial) and AA-06-05. In these cells, the drugs inhibited cell proliferation, migration and invasion through shifting of the mesenchymal phenotype toward an epithelial one and by impairing matrix metalloprotease-2 (MMP-2) activity. The antitumor activity was elicited via apoptosis pathway activation. An upregulation of p53 was observed, which in turn regulated the activation of caspase-3. Inhibition of proteolytic activity was accompanied by upregulation of the endogenous tissue inhibitor TIMP-2. Collectively, these data confirm the potential use of CA-IX inhibitors, and in particular SLC-0111 and AA-06-05, as agents to be further developed, alone or in combination with other conventional anticancer drugs.
AuthorsValerio Ciccone, Arianna Filippelli, Andrea Angeli, Claudiu T Supuran, Lucia Morbidelli
JournalInternational journal of molecular sciences (Int J Mol Sci) Vol. 21 Issue 8 (Apr 23 2020) ISSN: 1422-0067 [Electronic] Switzerland
PMID32340282 (Publication Type: Journal Article)
Chemical References
  • Antineoplastic Agents
  • Carbonic Anhydrase Inhibitors
  • Isoenzymes
  • Matrix Metalloproteinase 2
  • Carbonic Anhydrase IX
Topics
  • Antineoplastic Agents (pharmacology)
  • Apoptosis (drug effects)
  • Carbonic Anhydrase IX (antagonists & inhibitors, genetics, metabolism)
  • Carbonic Anhydrase Inhibitors (pharmacology)
  • Cell Line, Tumor
  • Cell Movement (drug effects)
  • Cell Proliferation (drug effects)
  • Dose-Response Relationship, Drug
  • Gene Expression
  • Humans
  • Isoenzymes
  • Matrix Metalloproteinase 2

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