Title : Curcumin-Loaded Solid Lipid Nanoparticles Bypass P-Glycoprotein Mediated Doxorubicin Resistance in Triple Negative Breast Cancer Cells.

Pub. Date : 2020 Jan 24

PMID : 31991669






6 Functional Relationships(s)
Download
Sentence
Compound Name
Protein Name
Organism
1 Curcumin-Loaded Solid Lipid Nanoparticles Bypass P-Glycoprotein Mediated Doxorubicin Resistance in Triple Negative Breast Cancer Cells. Curcumin ATP binding cassette subfamily B member 1 Homo sapiens
2 Curcumin-Loaded Solid Lipid Nanoparticles Bypass P-Glycoprotein Mediated Doxorubicin Resistance in Triple Negative Breast Cancer Cells. Curcumin ATP binding cassette subfamily B member 1 Homo sapiens
3 Curcumin (CURC) is a Pgp inhibitor, but it is poorly soluble and bioavailable. Curcumin ATP binding cassette subfamily B member 1 Homo sapiens
4 Curcumin (CURC) is a Pgp inhibitor, but it is poorly soluble and bioavailable. Curcumin ATP binding cassette subfamily B member 1 Homo sapiens
5 Both CURC-loaded SLNs were 5-10-fold more effective than free CURC in increasing the intracellular retention and toxicity of doxorubicin in Pgp-expressing triple negative breast cancer (TNBC). Curcumin ATP binding cassette subfamily B member 1 Homo sapiens
6 These results suggest that the combination therapy, based on CURC-loaded SLNs and doxorubicin, is an effective and safe approach to overcome the Pgp-mediated chemoresistance in TNBC. Curcumin ATP binding cassette subfamily B member 1 Homo sapiens