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. 2020 Feb 17;13:1413–1419. doi: 10.2147/OTT.S207613

Table 3.

Effects of ABCC2 (G1249A) Polymorphism on the Efflux Activity of Paclitaxel, Docetaxel, Sorafenib, and Doxorubicin in Recombinant LLC-PK1 Monolayers

LLC-PK1 Cells Papp (B→A)/Papp (A→B)
CLT pDNA3.1 1249G 1249A
Paclitaxel 0.87±0.07 0.81±0.06 3.64±0.57** 12.08±0.69**,##
Paclitaxel+MK-571 0.96±0.06 0.89±0.05 1.54±0.07*,† 1.79±0.10*,†
Docetaxel 1.34±0.16 1.47±0.18 5.06±0.34** 4.69±0.41**
Docetaxel+MK-571 1.46±0.19 1.54±0.21 2.12±0.24*,† 1.96±0.26††
Doxorubicin 0.54±0.06 0.67±0.05 4.19±0.14** 13.27±0.24**,##
Doxorubicin+MK-571 0.65±0.05 0.58±0.03 3.64±0.24*,† 3.88±0.29*,†

Notes: Compared with pcDNA3.1 group, *p<0.05, **p<0.01; compared with 1249G group, ##p<0.01; compared with without inhibitor group, p<0.05, ††p<0.01.

Abbreviations: CTL, cells untransfected LLC-PK1 cells; pcDNA3.1, transfected with empty vector; 1249G, transfected with 1249G wild-type allele; 1249A, cells transfected with 1249A variant allele.