Cancer Research Infection and Cancer: Biology, Therapeutics, and Prevention  AACR Conference on Molecular Diagnostics - 2008
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[Cancer Research 35, 1854-1857, July 1, 1975]
© 1975 American Association for Cancer Research

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Alteration of the Syncytium-forming Property of XC Cells by Productive Moloney Leukemia Virus Infection1

James C. Chan, Nora Vera, Patton T. Allen, James L. East, John E. Knesek, James M. Bowen and Leon Dmochowski

Department of Virology, The University of Texas System Cancer Center, M. D. Anderson Hospital and Tumor Institute, Texas Medical Center, Houston, Texas 77025

The effect of productive murine leukemia virus (MuLV) infection on the syncytium-forming property of XC cells was studied. MuLV-Moloney-infected XC cells, designated XC(M), initially went through a period of spontaneous syncytium formation. The syncytia then disappeared, and XC(M) cells continued to propagate and produce both infectious MuLV and MuLV group-specific antigens. However, XC(M) cells became refractory to syncytium formation that was induced by Kirsten, Friend, Rauscher, and Moloney strains of murine oncornaviruses. These data suggest that XC(M) cells lost their syncytium-forming ability as a result of productive MuLV infection.

1 This study was supported in part by Contract NO1-CP-33304 within the Virus Cancer Program of the National Cancer Institute; by Grants CA-05831 and RR-05511 from the National Cancer Institute, NIH, USPHS; and by Grant ACS IN-43N from the American Cancer Society, Inc.

Received 2/20/75. Accepted 4/ 7/75.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
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Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1975 by the American Association for Cancer Research.