Carbonic anhydrase ix promotes tumor growth and necrosis in vivo and inhibition enhances anti-VEGF therapy
Clinical Cancer Research, 05/11/2012
McIntyre A et al. – This work provides evidence that inhibition of the hypoxic adaptation to antiangiogenic therapy enhances bevacizumab treatment and highlights the value of developing small molecules or antibodies which inhibit CAIX for combination therapy.
We knocked down CAIX expression by short hairpin RNA in a colon cancer (HT29) and a glioblastoma (U87) cell line which have high hypoxic induction of CAIX and overexpressed CAIX in HCT116 cells which has low CAIX.
We investigated the effect on growth rate in three-dimensional (3D) culture and in vivo, and examined the effect of CAIX knockdown in combination with bevacizumab.
CAIX expression was associated with increased growth rate in spheroids and in vivo.
Surprisingly, CAIX expression was associated with increased necrosis and apoptosis in vivo and in vitro.
We found that acidity inhibits CAIX activity over the pH range found in tumors (pK = 6.84), and this may be the mechanism whereby excess acid self-limits the build-up of extracellular acid.
Expression of another hypoxia inducible CA isoform, CAXII, was upregulated in 3D but not two-dimensional culture in response to CAIX knockdown.
CAIX knockdown enhanced the effect of bevacizumab treatment, reducing tumor growth rate in vivo.
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