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Potential in a Single Cancer Cell to Produce Heterogeneous Morphology, Radiosensitivity and Gene Expression
Author(s) -
Sadayuki Ban,
Kenichi L. Ishikawa,
S Kawai,
Kumiko Koyama-Saegusa,
Atsuko Ishikawa,
Yutaka Shimada,
Johji Inazawa,
Takashi Imai
Publication year - 2005
Publication title -
journal of radiation research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.643
H-Index - 60
eISSN - 1349-9157
pISSN - 0449-3060
DOI - 10.1269/jrr.46.43
Subject(s) - clone (java method) , radiosensitivity , biology , gene , microbiology and biotechnology , cell , cell culture , gene expression , cancer cell , cancer research , genetics , cancer , irradiation , physics , nuclear physics
Morphologically heterogeneous colonies were formed from a cultured cell line (KYSE70) established from one human esophageal carcinoma tissue. Two subclones were separated from a single clone (clone13) of KYSE70 cells. One subclone (clone13-3G) formed mainly mounding colonies and the other (clone 13-6G) formed flat, diffusive colonies. X-irradiation stimulated the cells to dedifferentiate from the mounding state to the flat, diffusive state. Clone 13-6G cells were more radiosensitive than the other 3 cell lines. Clustering analysis for gene expression level by oligonucleotide microarray demonstrated that in the radiosensitive clone13-6G cells, expression of genes involved in cell adhesion was upregulated, but genes involved in the response to DNA damage stimulus were downregulated. The data demonstrated that a single cancer cell had the potential to produce progeny heterogeneous in terms of morphology, radiation sensitivity and gene expression, and irradiation enhanced the dedifferentiation of cancer cells.

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