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[Cancer Research 40, 4640-4647, December 1, 1980]
© 1980 American Association for Cancer Research

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Reaction Patterns of Herpes Simplex Virus Type 1 and Type 2 Proteins with Sera of Patients with Uterine Cervical Carcinoma and Matched Controls1

Steven C. Gilman2, John J. Docherty3, Aileen Clarke and William E. Rawls

Department of Microbiology, Cell Biology, Biochemistry, and Biophysics, The Pennsylvania State University, University Park, Pennsylvania 16802 [S. C. G., J. J. D.]; Department of Preventive Medicine and Biostatistics, University of Toronto, Toronto, Ontario M5S 1A8 Canada [A. C.]; and Department of Pathology, McMaster University, Hamilton, Ontario L8N 3Z5 Canada [W. E. R.]

Serum from 105 individuals with diagnosed uterine cervical cancer and 231 matched controls were examined for their ability to react with a large number of herpes simplex virus type 1 or type 2 (HSV-1, HSV-2) proteins. Radiolabeled HSV-1 or HSV-2 proteins were mixed with test serum and immune complexes were isolated with staphylococcal protein A. Viral proteins in the immune complexes were resolved by polyacrylamide gel electrophoresis and visualized by fluorography. When the frequency of precipitation for cancer and control serum was calculated for each HSV-1 and HSV-2 protein, the results demonstrated that four HSV-1 and 11 HSV-2 proteins were precipitated more frequently by cases than by controls (p ≤ 0.05). However, since these results could be influenced by the presence or absence of HSV-2-specific antibodies as well as social, economic, and sexual history, the data were grouped and analyzed according to these parameters. This enabled all significant differences between case and control sera in the precipitation of HSV-1 or HSV-2 proteins to be abolished except for two HSV-2 proteins with molecular weights of 38,000 and 118,000. These two proteins appear to be tumor associated and not merely covariables of past infection or risk factors alone.

1 This work was supported by Contract N01-CB-74171 from The Division of Cancer Biology and Diagnosis of The National Cancer Institute, NIH, and grants from The National Cancer Institute of Canada and The Ontario Treatment and Research Foundation.

2 Present address: Scripps Clinic and Research Foundation, 10666 North Torrey Pines Road, La Jolla, Calif. 92037.

3 To whom requests for reprints should be addressed, at Department of Microbiology, Cell Biology, Biochemistry and Biophysics, 101 South Frear Building, The Pennsylvania State University, University Park, Pa. 16802.

Received 6/18/80. Accepted 9/ 8/80.







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
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1980 by the American Association for Cancer Research.