PXD022203 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | Proteomics analysis on COE inhibiting vasculogenic mimicry in hepatocellular carcinoma |
Description | New strategies and drugs are urgently needed to improve the treatment of hepatocellular carcinoma (HCC). Vasculogenic mimicry (VM) has been elucidated being associated with the progression of HCC and anti-VM could be a promising strategy. Celastrus orbiculatus extract (COE), a mixture of 11 terpenoids isolated from the Chinese Herb Celastrus Orbiculatus Vine, has been elucidated to be able to disrupt VM formation in HCC. This study aims to dissect and identify the potential targets of COE on anti-VM formation both in vitro and in vivo that are distinct from our previous study. Proteomics analysis was used to identify differential proteins in HCC cells treated with or without COE. Cells invasion was examined using Transwell. Matrigel was used to establish a 3-D culture condition for VM formation in vitro. RT-PCR and Western Blot were used to examine changes of mRNA and protein respectively. Clinical resected samples were applied to confirm association between VM formation and identified targets. Subcutaneous xenograft tumor model was established to observe tumor growth and VM formation in vivo. PAS-CD34 dual staining was used to detect VM in vivo. A total of 194 proteins were identified to be differentially expressed in HCC cells treated with or without COE. In the 93 down-regulated proteins EphA2 stood out to be regulated on both RNA and protein level. Disruption EphA2 using COE or NVP inhibited VM formation and decreased VM associated biomarkers. In xenograft mouse model, COE inhibited tumor growth and VM formation via down-regulating EphA2. Taken together, our results indicate that COE could be used in HCC treatment because of its promising anti-VM effect. |
HostingRepository | PRIDE |
AnnounceDate | 2021-05-03 |
AnnouncementXML | Submission_2021-05-02_23:25:33.120.xml |
DigitalObjectIdentifier | |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Unsupported dataset by repository |
PrimarySubmitter | CHEN JUE |
SpeciesList | scientific name: Celastrus; NCBI TaxID: 85180; |
ModificationList | No PTMs are included in the dataset |
Instrument | Q Exactive |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2020-10-27 02:26:17 | ID requested | |
⏵ 1 | 2021-05-02 23:25:33 | announced | |
Publication List
Chu Z, Shi X, Chen G, He X, Qian Y, Wang H, Tao L, Liu Y, Jiang W, Chen J, COE Inhibits Vasculogenic Mimicry by Targeting EphA2 in Hepatocellular Carcinoma, a Research Based on Proteomics Analysis. Front Pharmacol, 12():619732(2021) [pubmed] |
Keyword List
submitter keyword: EphA2 |
hepatocellular carcinoma |
proteomics |
vasculogenic mimicry |
cancer treatment |
Contact List
Jue Chen |
contact affiliation | Institution of Integrated Traditional Chinese and Western Medicine, Medical College, Yangzhou University, Yangzhou, Jiangsu, China |
contact email | 1019924551@qq.com |
lab head | |
CHEN JUE |
contact affiliation | Yangzhou University |
contact email | 1019924551@qq.com |
dataset submitter | |
Full Dataset Link List
Dataset FTP location
NOTE: Most web browsers have now discontinued native support for FTP access within the browser window. But you can usually install another FTP app (we recommend FileZilla) and configure your browser to launch the external application when you click on this FTP link. Or otherwise, launch an app that supports FTP (like FileZilla) and use this address: ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2021/05/PXD022203 |
PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD022203
- Label: PRIDE project
- Name: Proteomics analysis on COE inhibiting vasculogenic mimicry in hepatocellular carcinoma