| Literature DB >> 32209117 |
Shaoquan Zheng1,2, Lu Yang1,2, Yutian Zou1,2, Jie-Ying Liang3,2, Peng Liu1,2, Guanfeng Gao1,2, Anli Yang1,2, Hailin Tang4,5, Xiaoming Xie6,7.
Abstract
The original article [1] contains an error in Fig. 5b whereby two panels have been mistakenly duplicated. The correct version of Fig. 5b can be viewed ahead alongside the rest of Fig. 5.Entities:
Year: 2020 PMID: 32209117 PMCID: PMC7093945 DOI: 10.1186/s13045-020-00861-x
Source DB: PubMed Journal: J Hematol Oncol ISSN: 1756-8722 Impact factor: 17.388
Fig. 5HUMT exerted its function by regulating the FOXK1 expression and downstream signaling. a Western blot analysis of the corresponding signaling in HUMT-KO- and FOXK1-overexpressed MDA-MB-231 cells. b–d Representative graphs and quantification of wound healing assay, Transwell migration, and invasion assay in the MDA-MB-231 and BT549 cells cotransfected with HUMT overexpression vector or empty vector together with si-FOXK1 or scrambled control. e Representative pictures of tube formation assay in HLECs cultured in medium supernatant of the abovementioned cells. f Quantitative analysis of the branch number and total tube length in tube formation assay. g Representative graphs and quantification of Transwell migration assay in HLECs cultured in medium supernatant of the abovementioned cells. h Western blot analysis of the corresponding signaling in MDA-MB-231 and BT549 cotransfected with HUMT overexpression vector or empty vector together with si-FOXK1 or scrambled control. Data were shown as mean ± SD; *P < 0.05; **P < 0.01