PTRF/Cavin-1 is Essential for Multidrug Resistance in Cancer Cells
- Authors
- Yi, Jae-Sung; Mun, Dong-Gi; Lee, Hyun; Park, Jun-sub; Lee, Jung-Woo; Lee, Jae-Seon; Kim, Su-Jin; Cho, Bong-Rae; Lee, Sang-Won; Ko, Young-Gyu
- Issue Date
- 2월-2013
- Publisher
- AMER CHEMICAL SOC
- Keywords
- lipid rafts; label-free quantitative proteomics; PTRF; cavin-1; multidrug resistance
- Citation
- JOURNAL OF PROTEOME RESEARCH, v.12, no.2, pp.605 - 614
- Indexed
- SCIE
SCOPUS
- Journal Title
- JOURNAL OF PROTEOME RESEARCH
- Volume
- 12
- Number
- 2
- Start Page
- 605
- End Page
- 614
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/104019
- DOI
- 10.1021/pr300651m
- ISSN
- 1535-3893
- Abstract
- Since detergent-resistant lipid rafts play important roles in multidrug resistance (MDR), their comprehensive proteomics could provide new insights to understand the underlying molecular mechanism of MDR in cancer cells. In the present work, lipid rafts were isolated from MCF-7 and adriamycin-resistant MCF-7/ADR cells and their proteomes were analyzed by label-free quantitative proteomics. Polymerase I and transcript release factor (PTRF)/cavin-1 was measured to be upregulated along with multidrug-resistant P-glycoprotein, caveolin-1, and serum deprivation protein response/cavin-2 in the lipid rafts of MCF-7/ADR cells. PTRF knockdown led to reduction in the amount of lipid rafts on the surface of MCF7/ADR cells as determined by cellular staining with lipid raft-specific dyes such as S-laurdan2 and FITC-conjugated cholera toxin B. PTRF knockdown also reduced MDR in MCF-7/ADR cells. These data indicate that PTRF is necessary for MDR in cancer cells via the fortification of lipid rafts.
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Collections - College of Science > Department of Chemistry > 1. Journal Articles
- Graduate School > Department of Life Sciences > 1. Journal Articles
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