Combined Phosphoproteomics and Bioinformatics Strategy in Deciphering Drug Resistant Related Pathways in Triple Negative Breast Cancer. (12th November 2014)
- Record Type:
- Journal Article
- Title:
- Combined Phosphoproteomics and Bioinformatics Strategy in Deciphering Drug Resistant Related Pathways in Triple Negative Breast Cancer. (12th November 2014)
- Main Title:
- Combined Phosphoproteomics and Bioinformatics Strategy in Deciphering Drug Resistant Related Pathways in Triple Negative Breast Cancer
- Authors:
- Deng, Xinyu
Kohanfars, Morris
Hsu, Huan Ming
Souda, Puneet
Capri, Joe
Whitelegge, Julian P.
Chang, Helena R. - Other Names:
- Chiu Jen-Fu Academic Editor.
- Abstract:
- Abstract : Because of the absence of a clear therapeutic target for triple negative breast cancer (TNBC), conventional chemotherapy is the only available systemic treatment option for these patients. Despite chemotherapy treatment, TNBC patients still have worse prognosis when compared with other breast cancer patients. The study is to investigate unique phosphorylated proteins expressed in chemoresistant TNBC cell lines. In the current study, twelve TNBC cell lines were subjected to drug sensitivity assays against chemotherapy drugs docetaxel, doxorubicin, gemcitabine, and cisplatin. Based on their half maximal inhibitory concentrations, four resistant and two sensitive cell lines were selected for further analysis. The phosphopeptides from these cells were enriched with TiO2 beads and fractionated using strong cation exchange. 1, 645 phosphoprotein groups and 9, 585 unique phosphopeptides were identified by a high throughput LC-MS/MS system LTQ-Orbitrap. The phosphopeptides were further filtered with Ascore system and 1, 340 phosphoprotein groups, 2, 760 unique phosphopeptides, and 4, 549 unique phosphosites were identified. Our study suggested that differentially phosphorylated Cdk5, PML, AP-1, and HSF-1 might work together to promote vimentin induced epithelial to mesenchymal transition (EMT) in the drug resistant cells. EGFR and HGF were also shown to be involved in this process.
- Is Part Of:
- International journal of proteomics. Volume 2014(2014)
- Journal:
- International journal of proteomics
- Issue:
- Volume 2014(2014)
- Issue Display:
- Volume 2014, Issue 2014 (2014)
- Year:
- 2014
- Volume:
- 2014
- Issue:
- 2014
- Issue Sort Value:
- 2014-2014-2014-0000
- Page Start:
- Page End:
- Publication Date:
- 2014-11-12
- Subjects:
- Proteomics -- Periodicals
Proteomics
Proteomics
Electronic journals
Periodical
Fulltext
Internet Resources
Periodicals
Periodicals
572.6 - Journal URLs:
- http://bibpurl.oclc.org/web/44802 ↗
https://www.hindawi.com/journals/ijpro/ ↗
http://bibpurl.oclc.org/web/44803 ↗
http://www.ncbi.nlm.nih.gov/pmc/journals/1629/ ↗ - DOI:
- 10.1155/2014/390781 ↗
- Languages:
- English
- ISSNs:
- 2090-2166
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library HMNTS - ELD Digital store
- Ingest File:
- 10555.xml