TY - JOUR
T1 - Epigenetic Control of Tumor Cell Morphology
AU - Horio, Keizo
AU - Yoshikura, Hiroshi
AU - Kawabata, Masahiro
AU - Odawara, Takashi
AU - Sudo, Katsuko
AU - Fujitani, Yohei
AU - Lee, Ganghong
AU - Iwamoto, Aikichi
PY - 1991/6
Y1 - 1991/6
N2 - XC cell line derived from a single rat cell transformed by the Prague strain of Rons sarcoma virus produced morphologically different colonies. Among them, two distinct cell types consisting of thick, fusiform cells (L‐type), and of flat, polygonal cells (R‐type) were apparent. By repeated subclonings, pure cultures, L1 and R1, respectively, were obtained. These clones underwent morphological conversion during prolonged culture; L‐type colonies appeared in the R‐type clone and vice versa. The kinetic curve suggested that the conversion was multi‐stepped. When inoculated into nude mice, L‐type cells produced much larger tumors at a higher frequency than R‐type cells, and the tumors induced by these two clones were histologically different. The expression of v‐src gene was higher in L‐type than in R‐type cells at both mRNA and protein levels.
AB - XC cell line derived from a single rat cell transformed by the Prague strain of Rons sarcoma virus produced morphologically different colonies. Among them, two distinct cell types consisting of thick, fusiform cells (L‐type), and of flat, polygonal cells (R‐type) were apparent. By repeated subclonings, pure cultures, L1 and R1, respectively, were obtained. These clones underwent morphological conversion during prolonged culture; L‐type colonies appeared in the R‐type clone and vice versa. The kinetic curve suggested that the conversion was multi‐stepped. When inoculated into nude mice, L‐type cells produced much larger tumors at a higher frequency than R‐type cells, and the tumors induced by these two clones were histologically different. The expression of v‐src gene was higher in L‐type than in R‐type cells at both mRNA and protein levels.
KW - Morphological conversion
KW - XC cells
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UR - http://www.scopus.com/inward/citedby.url?scp=0025821999&partnerID=8YFLogxK
U2 - 10.1111/j.1349-7006.1991.tb01903.x
DO - 10.1111/j.1349-7006.1991.tb01903.x
M3 - Article
C2 - 1649811
AN - SCOPUS:0025821999
SN - 1347-9032
VL - 82
SP - 676
EP - 685
JO - Cancer Science
JF - Cancer Science
IS - 6
ER -