| Literature DB >> 29179762 |
Yue Pang1,2, Changzhi Li1,2, Shiyue Wang1,2, Wei Ba1,2, Tao Yu1,2, Guangying Pei1,2, Dan Bi1,2, Hongfang Liang1,2, Xiong Pan1,2, Ting Zhu1,2, Meng Gou1,2, Yinglun Han1,2, Qingwei Li3,4.
Abstract
CORRECTION: Unfortunately, following publication of this article [1], it was noticed that the key in Figure 5c incorrectly showed '0 h', '5 h' and '10 h'. The corrected version, showing '0 h', '12 h' and '24 h', can be seen below and the original article has been updated to reflect this.Entities:
Year: 2017 PMID: 29179762 PMCID: PMC5702966 DOI: 10.1186/s12964-017-0202-1
Source DB: PubMed Journal: Cell Commun Signal ISSN: 1478-811X Impact factor: 5.712
Fig. 5LIP can significantly increase the expression of inflammatory molecules in MCF-7 cells. a Heat map representation of candidate genes involved in the pathways induced by LIP. Blue and red colors represent low-to-high expression levels, and the color scales correspond to the expression values of the microarray. b Q-PCR analysis of inflammatory molecule (TNF-α, IL-1β) expression in MCF-7 and K562 cells incubated with LIP for different times. Total RNA was quantified by qRT-PCR and normalized to gapdh expression. c Western blot analysis of inflammatory factor expression in MCF-7 and K562 cells. Western blot analysis for the expression of TNF-α & IL-1β in MCF-7 and K562 cells incubated with LIP for different times. β-actin served as a loading control(left pane). Histogram showing statistics of the above results (right pane). Means ± SDs are shown (n = 3 per group). **P < 0.01