4.1 Article

Systematic investigation of lycopene effects in LNCaP cells by use of novel large-scale proteomic analysis software

期刊

PROTEOMICS CLINICAL APPLICATIONS
卷 1, 期 5, 页码 513-523

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/prca.200600511

关键词

detoxification enzymes; isotope coded affinity tags; LNCaP; lycopene; teranode

资金

  1. NCI NIH HHS [R01 CA101052-04, R01 CA101052-03, R01 CA101052-05, R01 CA101052, R01 CA101052-02, R01 CA101052-01] Funding Source: Medline
  2. NCRR NIH HHS [S10 RR017262] Funding Source: Medline
  3. NIAID NIH HHS [U54 AI057141] Funding Source: Medline
  4. NIDDK NIH HHS [R21 DK065260] Funding Source: Medline
  5. NIEHS NIH HHS [P30 ES007033] Funding Source: Medline
  6. NIGMS NIH HHS [R33 GM066461] Funding Source: Medline

向作者/读者索取更多资源

Lycopene, the red pigment of tomatoes, is a carotenoid with potent antioxidant properties. Although lycopene may function as a prostate cancer chemoprevention agent, little is known about its effects at the cellular level. To define general changes induced by treatment of cells with lycopene, and to gain insights into the possible chemoprevention properties of lycopene, we investigated changes in protein expression after lycopene treatment in human LNCaP cells. The high throughput proteomics data were then visualized and analyzed by novel biological protein pathway modeling software. Differentially expressed proteins were identified, and the data were analyzed by protein pathway simulation software, without the need for specialized programming, by importing pathway models from a number of sources or by creating our own. One notable outcome was the identification of a group of upregulated proteins involved in detoxification of reactive oxygen species. This finding suggests that a possible mechanism of lycopene chemoprevention is the stimulation of detoxification enzymes associated with the antioxidant response element. Novel biological pathway modeling software enhances analysis of large proteomics data. When applied to the analysis of proteins differentially expressed in prostate cancer cells upon treatment with lycopene, the up-regulation of detoxification enzymes was identified.

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