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  Vol. 109 No. 11, November 1983 TABLE OF CONTENTS
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  AMERICAN SOCIETY FOR HEAD AND NECK SURGERY MEETING
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Colony-Forming Assay of Human Salivary Gland Tumors

Applications for Chemosensitivity and Histogenetic Studies

Michael E. Johns, MD; Stacey E. Mills, MD; Kim K. Thompson

Arch Otolaryngol. 1983;109(11):709-714.


Abstract

• Eight malignant and nine benign salivary gland neoplasms were cultured using a soft agar technique. Eleven of these tumors were successfully grown, two were contaminated, and only four demonstrated no growth. Cloning efficiency varied from 0.004% to 0.225%. These efficiencies and the 65% successful growth rate are much higher than those reported for head and neck squamous cell carcinomas. Single cell disaggregation with resultant clonal growth can be accomplished with salivary gland neoplasms. Ultrastructural study of colonies from three mixed tumors did not demonstrate distinct epithelial and mesenchymal populations of cells, the expected finding if mixed tumors were composed of two independent cell lines. Rather, mixed tumors invariably consisted of a monoclonal population of cells with evidence of ambivalent, mesenchymal, and epithelial differentiation. Myoepithelial cells were not present.

(Arch Otolaryngol 1983;109:709-714)



Author Affiliations

From the Division of Head and Neck Oncology, Departments of Otolaryngology (Dr Johns and Ms Thompson) and Pathology (Dr Mills), University of Virginia Medical Center, Charlottesville.


Footnotes

Accepted for publication May 23, 1983.

Read before the American Society for Head and Neck Surgery, Palm Springs, Calif, March 10, 1983.

Reprint requests to Division of Head and Neck Oncology, Department of Otolaryngology, University of Virginia Medical Center, Box 430, Charlottesville, VA 22908 (Dr Johns).



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