Cancer Research Infection and Cancer: Biology, Therapeutics, and Prevention
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[Cancer Research 40, 4204-4208, November 1, 1980]
© 1980 American Association for Cancer Research

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Immunogenic Properties of Soluble Cytosol Fractions of Meth A Sarcoma Cells

Garrett C. DuBois, Ettore Appella, Lloyd W. Law1, Albert B. DeLeo and Lloyd J. Old

Laboratory of Cell Biology, National Cancer Institute, Bethesda, Maryland 20205 [G. C. D., E. A., L. W. L.], and The Memorial Sloan-Kettering Cancer Center, New York, New York 10021 [A. B. D., L. J. O.]

Tumor-associated transplantation antigen (TATA) was found to be present in fractions derived from the cytosol of the Meth A cell. Meth A ascites cells were disrupted, nuclei and membranes were removed by low- and high-speed centrifugation, and the soluble protein was fractionated by ammonium sulfate precipitation and gel filtration chromatography. The TATA of the soluble cytosol fractions appears to be identical with the TATA solubilized from plasma membranes. The TATA of the cytosol fractions was found to be associated with proteins of an approximate apparent molecular weight of 60,000, specific for the Meth A tumor, and as immunogenic as the membranederived TATA. In addition, the most enriched TATA cytosol fraction shows inhibition of an antiserum capable of detecting a tumor-specific surface antigen of Meth A. These results suggest that Meth A TATA is not an integral membrane protein and may be related to the tumor-specific surface antigen detected serologically.

1 To whom requests for reprints should be addressed.

Received 4/21/80. Accepted 8/ 4/80.




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[Abstract]




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.