Skip to content Skip to navigation
University of Warwick
  • Study
  • |
  • Research
  • |
  • Business
  • |
  • Alumni
  • |
  • News
  • |
  • About

University of Warwick
Publications service & WRAP

Highlight your research

  • WRAP
    • Home
    • Search WRAP
    • Browse by Warwick Author
    • Browse WRAP by Year
    • Browse WRAP by Subject
    • Browse WRAP by Department
    • Browse WRAP by Funder
    • Browse Theses by Department
  • Publications Service
    • Home
    • Search Publications Service
    • Browse by Warwick Author
    • Browse Publications service by Year
    • Browse Publications service by Subject
    • Browse Publications service by Department
    • Browse Publications service by Funder
  • Help & Advice
University of Warwick

The Library

  • Login
  • Admin

Antimetastatic action of Pentoxifylline, a methyl xanthine derivative, through its effect on PKC Mediated integrin transport in B16F10 melanoma cells

Tools
- Tools
+ Tools

Ratheesh, Aparna, Meenakashi, Jain and Gudea, Rajiv P. (2010) Antimetastatic action of Pentoxifylline, a methyl xanthine derivative, through its effect on PKC Mediated integrin transport in B16F10 melanoma cells. World Journal of Oncology, 1 (5). pp. 194-203. doi:10.4021/wjon252e

Research output not available from this repository, contact author.
Official URL: http://dx.doi.org/10.4021/wjon252e

Request Changes to record.

Abstract

Integrins are adhesion molecules known to regulate cellular processes like adhesion, migration and proliferation. At the same time role of integrin in progress of cancer metastasis is well established, increased integrin expression is reported to be linked to high metastasis potential of cells. Pentoxifylline a methyl xanthine derivative is a potent antimetastatic agent. Studies on the mechanism of inhibition of lung homing of B16F10 melanoma cells by PTX shows that it can inhibit cell- Extracellular Matrix adhesion, cell surface integrin expression as well as Protein kinase C activity. Previous study from our laboratory have shown PTX treatment can selectively inhibit the cell surface expression of α5 integrin in B16F10 cells without affecting its total cellular protein levels. Numerous studies have documented that differences in surface expression and distribution of integrins affects metastasis. The purpose of present study is to observe the effect of PTX on cellular distribution/ redistribution of integrins and to study the underlying molecular mechanism of PTX action.

Item Type: Journal Article
Divisions: Faculty of Medicine > Warwick Medical School > Biomedical Sciences > Cell & Developmental Biology
Faculty of Medicine > Warwick Medical School > Biomedical Sciences
Faculty of Medicine > Warwick Medical School
Journal or Publication Title: World Journal of Oncology
Publisher: Elmer Press Inc.
ISSN: 1920-4531
Official Date: 2010
Dates:
DateEvent
2010Published
27 October 2010Accepted
Volume: 1
Number: 5
Page Range: pp. 194-203
DOI: 10.4021/wjon252e
Status: Peer Reviewed
Publication Status: Published
Access rights to Published version: Open Access

Request changes or add full text files to a record

Repository staff actions (login required)

View Item View Item
twitter

Email us: wrap@warwick.ac.uk
Contact Details
About Us