P-glycoprotein expression in brain tumors

JW Henson, C Cordon-Cardo, JB Posner - Journal of neuro-oncology, 1992 - Springer
JW Henson, C Cordon-Cardo, JB Posner
Journal of neuro-oncology, 1992Springer
Overexpression of P-glycoprotein (P-gp) in cancer cells can result in resistance to several
chemotherapy agents (multidrug resistance) including doxorubicin and vincristine. The
drugs to which resistance develops also penetrate the blood brain barrier poorly. P-gp
expression in brain capillary endothelial cells suggests that P-gp may restrict drug entry into
brain tumors and thus be another mechanism of drug resistance. To seek evidence for either
of these roles in the drug resistance of brain tumors, we examined the location of expression …
Summary
Overexpression of P-glycoprotein (P-gp) in cancer cells can result in resistance to several chemotherapy agents (multidrug resistance) including doxorubicin and vincristine. The drugs to which resistance develops also penetrate the blood brain barrier poorly. P-gp expression in brain capillary endothelial cells suggests that P-gp may restrict drug entry into brain tumors and thus be another mechanism of drug resistance. To seek evidence for either of these roles in the drug resistance of brain tumors, we examined the location of expression of P-gp in 49 brain tumors, using an anti-P-gp mouse monoclonal antibody and immunohistochemistry. P-gp expression was observed in tumor cells of two glioblastomas and a meningeal sarcoma but not in low-grade primary or metastatic tumors. In low-grade primary tumors, P-gp was present in all vascular endothelial cells. In the vascular endothelial cells of anaplastic primary brain tumors and brain metastases, P-gp expression was heterogeneous or absent. These findings are consistent with a role for P-gp in the resistance of some brain tumors to chemotherapy agents.
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