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Analysis of anti-cancer factor and transformation of human hybrid cells between salivary gland cells and oral cancer cells

Research Project

Project/Area Number 62570902
Research Category

Grant-in-Aid for General Scientific Research (C)

Allocation TypeSingle-year Grants
Research Field 外科・放射線系歯学
Research InstitutionTokushima University

Principal Investigator

HIRAIWA Kiyotaka  Tokushima University, 歯学部附病院, 講師 (30173214)

Co-Investigator(Kenkyū-buntansha) KINJOH Seiichiro  Tokushima University, 歯学部附属病院, 助手 (90205055)
NAGAYAMA Masaru  Tokushima University, 歯学部, 教授 (30022867)
金城 清一郎  徳島大学, 歯学部・附属病院, 医員 (20180565)
Project Period (FY) 1987 – 1988
Project Status Completed (Fiscal Year 1988)
Budget Amount *help
¥500,000 (Direct Cost: ¥500,000)
Fiscal Year 1988: ¥500,000 (Direct Cost: ¥500,000)
Keywordscancer cells / sublingual gland cells / human / hybrid cells / fusion / anti-cancer factors / コラーゲンゲル / 薬剤耐性株 / クローニング
Research Abstract

Salivary gland tumors are characteristic in frequency and histologic type when compared with other oral tissue tumors. Of major salivary glands, it has been reported that there occures rate tumors in the sublingual gland. We investigated anti-cancer factors in the sublingual gland by examining hybrid cells resulting from the cell fusion. The mutant cells, ZK-1 E2・HGPRT^-OUA^R cells, were isolated from ZK-1 cells that has established from a well-differentiated squamous cell carcinoma of the tongue. The isolated mutant cells showed almost same morphological feature, growth rate and serum-dependency as the parent ZK-1 cells. Sublingual gland cells were isolated in outgrowth from the sublingual gland tissues embedded in collagen gel, and cultures in sweum-free medium containing cholera toxin and MITO^+ serum expander. The sublingual gland cells were cultured by monolayer after primary culture. Two type of cell, epithelial cell and fibroblast-like cell, was observed in monolayer culture of the cells, and these cells had different resistancy to trypsin treatment, so that the cells could be separeted by trypsin treatment. When embedded in collagen gel, epithelial cells formed duct-like or massive colonies and fibroblast-like cells spread sparsely. ZK-1 E2・HGPRT^-OUA^R cells were fused with either these fractionated sublingual gland cells. The hybrid cells had round, ovoid, polygonal or spindle shape in culture. By chromosomal analysis, the hybrid cell had 70-80 chromosome and considered to be derived from cell fusion. Each clone also had different adhesiveness to culture dishes. The protein in the hybrid cells were analyzed and different pattern was observed between ZK-1 E2・HGPRT^-OUA^R cells and hybrid cells. Analysis of thses hybrid cells would be an important approach to the cloning of anti-cancer gene.

Report

(3 results)
  • 1988 Annual Research Report   Final Research Report Summary
  • 1987 Annual Research Report

URL: 

Published: 1988-04-01   Modified: 2016-04-21  

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