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Correction

Correction: DUSP1 Is a Novel Target for Enhancing Pancreatic Cancer Cell Sensitivity to Gemcitabine

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Due to an error in the preparation of Figure 5B, two of the panels in this figure are incorrect: The "Total JNK" panel for BxPC-3 cells (right) incorrectly duplicates the "Total JNK" panel for AsPC-1 cells (left) The "p-ERK1/2" panel for the BxPC-3 cells (right) incorrectly displays the "p-ERK1/2" panel for AsPC-1 cells (left). The authors apologize for these mistakes and are supplying a corrected Figure 5 and the raw blots for this figure. These errors do not affect the results and conclusions reported in the article.

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Figure 5. Knockdown of MKP2 does not affect JNK/p38 MAPK signaling activity or pancreatic cancer chemosensitivity to gemcitabine.

AsPC-1 and BxPC-3 cells were stably transduced with lentivirus expressing shRNA against scramble control or MKP2. (A) Cells were incubated for 48 h in the absence or presence of varying concentrations of gemcitabine, and MTT assays were performed. (B) AsPC-1 and BxPC-3 cells were incubated for the indicated times with 100 ng/ml and 10 ng/ml gemcitabine, respectively, and immunoblotting was conducted. Data are the means ± SEM of 3 experiments.

https://doi.org/10.1371/journal.pone.0084982.g005

Reference

  1. 1. Liu F, Gore AJ, Wilson JL, Korc M (2014) DUSP1 Is a Novel Target for Enhancing Pancreatic Cancer Cell Sensitivity to Gemcitabine. PLoS ONE 9(1): e84982

Citation: The PLOS ONE Staff (2014) Correction: DUSP1 Is a Novel Target for Enhancing Pancreatic Cancer Cell Sensitivity to Gemcitabine. PLoS ONE 9(9): e108710. https://doi.org/10.1371/journal.pone.0108710

Published: September 15, 2014

Copyright: © 2014 The PLOS ONE Staff. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.