Skip NavigationSkip to Content

P-glycoprotein-overexpressing multidrug-resistant cells are resistant to infection by enveloped viruses that enter via the plasma membrane

  1. Author:
    Raviv, Y.
    Puri, A.
    Blumenthal, R.
  2. Author Address

    Raviv Y NCI, Intramural Res Support Program, SAIC Frederick,Lab Expt & Computat Biol, Frederick Canc Res & Dev Ctr Bldg 469,Room 211 Frederick, MD 21702 USA NCI, Intramural Res Support Program, SAIC Frederick,Lab Expt & Computat Biol, Frederick Canc Res & Dev Ctr Frederick, MD 21702 USA
    1. Year: 2000
  1. Journal: Faseb Journal
    1. 14
    2. 3
    3. Pages: 511-515
  2. Type of Article: Article
  1. Abstract:

    The multidrug resistance gene product P-glycoprotein confers drug resistance to tumor cells by acting as a transporter that blocks: the entry into the cell of a great variety of drugs and hydrophobic pep tides. In this study we find that in drug-resistant cells, the insertion of the influenza virus fusion protein (hemagglutinin-2) into the plasma membrane is blocked and that the fusion of the viral envelope with the plasma membrane of these cells is impaired. Multidrug-resistant cells display significant resistance to infection by envelope viruses that invade cells by fusion with the plasma membrane, but not to infection by pH-dependent viruses that penetrate cells by fusion with endocytic vesicles, These observations suggest that multidrug resistance phenomena may protect cells from infection by a large group of disease-causing viruses that includes human immunodeficiency virus, herpes simplex virus, and some cancer-inducing retroviruses. [References: 24]

    See More

External Sources

  1. No sources found.

Library Notes

  1. No notes added.
NCI at Frederick

You are leaving a government website.

This external link provides additional information that is consistent with the intended purpose of this site. The government cannot attest to the accuracy of a non-federal site.

Linking to a non-federal site does not constitute an endorsement by this institution or any of its employees of the sponsors or the information and products presented on the site. You will be subject to the destination site's privacy policy when you follow the link.

ContinueCancel