Among other things, we have identified one mechanism of multi-drug resistance (MDR) involving P - glycoprotein (Pgp) which functions as
a drug efflux pump of broad specificity.
Heterogeneity in a bacterial population that arises through a mechanism of biased partitioning of
drug efflux pumps, as we identified in our study, could be a stepping - stone on the path of bacterial populations towards antibiotic resistance.»
Not exact matches
To address this challenge, our research group is using nanoparticles not only to deliver more chemotherapy
drugs to the target site within cancer cells, but also to compromise the function of the
efflux pumps and thereby significantly improve safety and efficacy of cancer therapy.»
Studies have revealed that the
drug also inhibits bacterial
efflux pumps that permit bacteria to survive within cells.
If a pathogenic strain of bacteria acquires a gene encoding one of these
efflux pumps, then it will suddenly become resistant to multiple antibacterial
drugs.
«There are
efflux pumps that can export multiple
drugs that have different structures and mechanisms of action.
New supercomputer simulations have revealed the role of transport proteins called
efflux pumps in creating
drug - resistance in bacteria, research that could lead to improving the
drugs» effectiveness against life - threatening diseases and restoring the efficacy of defunct antibiotics.
Since an
efflux pump could compromise the potency of even a newly developed antibacterial
drug, we need to think about ways to circumvent these
efflux pumps.»
The TB bacteria use
efflux pumps as a strategy to remove
drugs and other threats from the cell before they can work against the bacteria.
Efflux pumps are surface proteins that prevent antimicrobial
drugs from getting a foothold in a bacterial cell by identifying and
pumping them out of the cell.
: This study evaluated the effects of an antagonistic analog of growth hormone - releasing hormone, MIA - 602, on tumor growth, response to doxorubicin, expression of
drug resistance genes, and
efflux pump function in human triple negative breast cancers.
Introduction: This study evaluated the effects of an antagonistic analog of growth hormone - releasing hormone, MIA - 602, on tumor growth, response to doxorubicin, expression of
drug resistance genes, and
efflux pump function in human triple negative breast cancers.
We examined the effects of treatment on tumor growth,
drug resistance, GHRH - R levels, expression of MDR1 and Nanog, and
efflux pump activity.
decreases
drug resistance in Lyme by blocking
efflux pumps that remove antibiotics from germs,