Paclitaxel has been widely used as an anti-mitotic agent in chemotherapy for a variety of cancers and adds substantial efficacy as the first-line chemotherapeutic regimen for ovarian cancers. However, the frequent occurrence of paclitaxel resistance limits its function in long-term management. Despite abundant clinical and cellular demonstration of paclitaxel resistant tumors, the molecular mechanisms leading to paclitaxel resistance are poorly understood. Using genomic approaches, we have previously identified an association between a BTB/POZ gene, NAC1, and paclitaxel resistance in ovarian cancer. The experiments presented here have applied multiple quantitative proteomic methods to identify protein changes associated with paclitaxel resistance and NAC1 function. The SKOV-3 ovarian serous carcinoma cell line, which has inducible expression of dominant-negative NAC1, was used to determine the paclitaxel treatment associated changes in the presence and absence of functional NAC1. Quantitative proteomic analyses were performed using iTRAQ labeling and MS. Two label-free quantitative proteomic methods: LC-MS and spectral count were used to increase confidence of proteomic quantification. Candidate proteins related to paclitaxel and NAC1 function were identified in this study. Gene ontology analysis of the protein changes identified upon paclitaxel resistance revealed that cell component enrichment related to mitochondria. Moreover, tubulin and mitochondrial proteins were the major cellular components with changes associated with paclitaxel treatment. This suggests that mitochondria may play a role in paclitaxel resistance.
|Number of pages||8|
|Journal||Proteomics - Clinical Applications|
|Publication status||Published - 2009 Dec|
- Ovarian cancer
ASJC Scopus subject areas
- Clinical Biochemistry