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Antimicrobial Agents and Chemotherapy logoLink to Antimicrobial Agents and Chemotherapy
. 2017 Sep 22;61(10):e01753-17. doi: 10.1128/AAC.01753-17

Correction for Tun-Yhong et al., “Tenofovir Disoproxil Fumarate Is a New Substrate of ATP-Binding Cassette Subfamily C Member 11”

Wisith Tun-Yhong a, Chatchai Chinpaisal b, Perayot Pamonsinlapatham c, Sindchai Kaewkitichai a
PMCID: PMC5610500  PMID: 28939584

AUTHOR CORRECTION

Volume 61, no. 4, e01725-16, 2017, https://doi.org/10.1128/AAC.01725-16. Page 5, Figure 4: the order of magnitude of TDF in Fig. 4C should read 1.75 × 104 instead of 1.75 × 103 and that of MTX in Fig. 4D should read 1.6 × 104 instead of 1.6 × 103. The correct figure is shown below.

FIG 4.

FIG 4

Cell viability assays with TDF and methotrexate in the presence and absence of the specific inhibitor MK-571. (A) Specific inhibitor MK-571 at various concentrations did not reduce MRP8-overexpressing and parental cell viability. (B) Cytotoxic effects of TDF on MRP8-overexpressing and parental cells. (C) MK-571 further reduced viability of the MRP8-overexpressing cells, but not parental cells, treated with TDF. (D) MK-571 also enhanced cytotoxicity of methotrexate only in MRP8-overexpressing cells. (E and F) Cytotoxicity assays showing methotrexate and TDF concentrations that reduced cell viability by 50% (CC50) in MRP8-overexpressing LLC-PK1 or parental cells with or without the specific inhibitor MK-571. Statistical significance was analyzed by a two-way ANOVA multiple comparison assuming equal variance (*, P < 0.01; **, P < 0.001; ***, P < 0.0001). All values are the means ± standard deviations from five independent experiments.


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