TY - JOUR
T1 - Corrigendum to High Keratin 8/18 Ratio Predicts Aggressive Hepatocellular Cancer Phenotype12 (Translational Oncology (2019) 12(2) (256–268), (S193652331830439X), (10.1016/j.tranon.2018.10.010))
AU - Golob-Schwarzl, N.
AU - Bettermann, K.
AU - Mehta, A. K.
AU - Kessler, S. M.
AU - Unterluggauer, J.
AU - Krassnig, S.
AU - Kojima, K.
AU - Chen, X.
AU - Hoshida, Y.
AU - Bardeesy, N. M.
AU - Müller, H.
AU - Svendova, V.
AU - Schimek, M. G.
AU - Diwoky, C.
AU - Lipfert, A.
AU - Mahajan, V.
AU - Stumptner, C.
AU - Thüringer, A.
AU - Fröhlich, L. F.
AU - Stojakovic, T.
AU - Nilsson, K. P.R.
AU - Kolbe, T.
AU - Rülicke, T.
AU - Magin, T. M.
AU - Strnad, P.
AU - Kiemer, A. K.
AU - Moriggl, R.
AU - Haybaeck, Johannes
N1 - Publisher Copyright:
© 2019 The Authors
PY - 2020/2
Y1 - 2020/2
N2 - The authors regret . The authors would like to apologize for any inconvenience caused. The authors regret that an error in Figure S1 of the manuscript has been identified. Some images in Figure 1 were duplicated within Figure S1; hence, this corrigendum addresses this error. Following changes were made to improve the quality of the results section: To further address the contribution of KRT8 and KRT18 with respect to liver pathology in livers of wild-type (wt), Krt8+/−, Krt8−/−, Krt18+/ −, and Krt18−/− mice aged 3 and 17-20 months, we performed, in addition to light microscopy, double immunofluorescence microscopy (DIF) using antibodies against K8/18 and p62. Moreover, heptameric oligothiophene, h-HTAA (Mahajan et al., 2011), was used to confirm ß-sheet conformation (Figure 1). In livers of 6-month-old Krt18+/− and Krt18−/− mice, total FA amounts were significantly increased compared to wt mice (Figure 2, Figure S1, and Table S1). The following NAFLD-related mRNAs remained largely unchanged: Malonyl-CoA decarboxylase (Mlycd), Microsomal triglyceride transfer protein (Mttp), ATP-binding cassette, sub-family C, member 2 (Cftr/Mrp) (Figure S2A), Insulin receptor substrate 1 (Isr1), Glutamate-cysteine ligase, modifier subunit (Gclm), Fatty acid synthase (Fasn) (Figure S2B), Diacylglycerol O-acyltransferase 2 (Dgat2), Angiotensin II receptor 1a (Agtr1α), Adiponectin receptor 2 (Adipor2) (Figure S2C) and Peroxisome proliferator activated receptor alpha (Pparα) (Figure S2D). In addition, the following changes have been made in the discussion section qRT-PCR analyses revealed a significant increase of Srebpb1 mRNA level in Krt18−/− mice aged 3 and 6 months, whereas no increased mRNA expression of Pparα was identified (Figure 3; Figure S2).
AB - The authors regret . The authors would like to apologize for any inconvenience caused. The authors regret that an error in Figure S1 of the manuscript has been identified. Some images in Figure 1 were duplicated within Figure S1; hence, this corrigendum addresses this error. Following changes were made to improve the quality of the results section: To further address the contribution of KRT8 and KRT18 with respect to liver pathology in livers of wild-type (wt), Krt8+/−, Krt8−/−, Krt18+/ −, and Krt18−/− mice aged 3 and 17-20 months, we performed, in addition to light microscopy, double immunofluorescence microscopy (DIF) using antibodies against K8/18 and p62. Moreover, heptameric oligothiophene, h-HTAA (Mahajan et al., 2011), was used to confirm ß-sheet conformation (Figure 1). In livers of 6-month-old Krt18+/− and Krt18−/− mice, total FA amounts were significantly increased compared to wt mice (Figure 2, Figure S1, and Table S1). The following NAFLD-related mRNAs remained largely unchanged: Malonyl-CoA decarboxylase (Mlycd), Microsomal triglyceride transfer protein (Mttp), ATP-binding cassette, sub-family C, member 2 (Cftr/Mrp) (Figure S2A), Insulin receptor substrate 1 (Isr1), Glutamate-cysteine ligase, modifier subunit (Gclm), Fatty acid synthase (Fasn) (Figure S2B), Diacylglycerol O-acyltransferase 2 (Dgat2), Angiotensin II receptor 1a (Agtr1α), Adiponectin receptor 2 (Adipor2) (Figure S2C) and Peroxisome proliferator activated receptor alpha (Pparα) (Figure S2D). In addition, the following changes have been made in the discussion section qRT-PCR analyses revealed a significant increase of Srebpb1 mRNA level in Krt18−/− mice aged 3 and 6 months, whereas no increased mRNA expression of Pparα was identified (Figure 3; Figure S2).
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UR - http://www.scopus.com/inward/citedby.url?scp=85071090615&partnerID=8YFLogxK
U2 - 10.1016/j.tranon.2019.08.001
DO - 10.1016/j.tranon.2019.08.001
M3 - Comment/debate
C2 - 32081369
AN - SCOPUS:85071090615
SN - 1936-5233
VL - 13
SP - 490
EP - 492
JO - Translational Oncology
JF - Translational Oncology
IS - 2
ER -