| Literature DB >> 30917786 |
Ping Zhao1, Jun Wu1, Feiteng Lu1, Xuan Peng1, Chenlin Liu1, Nanjin Zhou2, Muying Ying3,4.
Abstract
Following publication of the original article [1], it was noticed that Fig. 3c was omitted from the final published article.Entities:
Year: 2019 PMID: 30917786 PMCID: PMC6436228 DOI: 10.1186/s12885-019-5478-7
Source DB: PubMed Journal: BMC Cancer ISSN: 1471-2407 Impact factor: 4.430
Fig. 3Co-culture with lung cancer cells improved hepatocyte complement synthesis and secretion. Co-culture of QSG-7701 hepatocytes with lung cancer cells (A549, LTEP-α-2 or NCI-H1703) improved complement synthesis at both the mRNA (a) and protein levels (b). c Complement protein synthesis (in QSG-7701 hepatocytes co-cultured with A549 cells) and secretion (in supernatants from co-cultures of QSG-7701 and A549 cells) were significantly increased compared to co-cultures of QSG-7701 hepatocytes and HBE cells. Q-Q, Q-A, Q-L, Q-H1, Q-H, A-A and H-H indicate paired co-cultures of both QSG-7701 hepatocytes, QSG-7701 hepatocytes and A549 cells, QSG-7701 hepatocytes and LTEP-α-2 cells, QSG-7701 hepatocytes and NCI-H1703 cells, QSG-7701 hepatocytes and HBE cells, both A549 cells or both HBE cells, respectively. α-Tubulin was used as the loading control for co-cultured QSG-7701 hepatocytes. Loading controls for co-cultured supernatants were quantitated by performing Coomassie blue staining due to the lack of proper secreted protein as control in co-cultured supernatants. For loading controls of co-cultured supernatants, please refer to Additional file 4: Fig. S4