TY - JOUR
T1 - Heterogeneous induction of apoptosis in colon cancer cells by wild-type p53 gene transfection
AU - Namoto, Masaaki
AU - Yonemitsu, Yoshikazu
AU - Nakagawa, Kazunori
AU - Hashimoto, Shuichi
AU - Kaneda, Yasufumi
AU - Nawata, Hajime
AU - Sueishi, Katsuo
PY - 1998/4
Y1 - 1998/4
N2 - To examine the effects of wild-type (wt)-p53 gene transfer on cancer cell growth and apoptosis induction, we transduced human wt-p53 cDNA into three colon cancer cell lines either with or without a mutation of the p53 gene using the HVJ-cationic liposome method. Wt-p53 gene transfer, thus, induced an apparent growth arrest in all cell lines, but itsenhancement of the apoptotic rate varied (from about 4 to 70 times). The simultaneous doxorubicin treatment was able to enhance growth arrest and the apoptosis induction rate. These findings suggest that wt-p53 gene transfer using HVJ- cationic liposomes seems to be a potentially effective therapeutic strategy, however wt-p53 gene transfer still appears to be more effective in combination with other cytotoxic treatments.
AB - To examine the effects of wild-type (wt)-p53 gene transfer on cancer cell growth and apoptosis induction, we transduced human wt-p53 cDNA into three colon cancer cell lines either with or without a mutation of the p53 gene using the HVJ-cationic liposome method. Wt-p53 gene transfer, thus, induced an apparent growth arrest in all cell lines, but itsenhancement of the apoptotic rate varied (from about 4 to 70 times). The simultaneous doxorubicin treatment was able to enhance growth arrest and the apoptosis induction rate. These findings suggest that wt-p53 gene transfer using HVJ- cationic liposomes seems to be a potentially effective therapeutic strategy, however wt-p53 gene transfer still appears to be more effective in combination with other cytotoxic treatments.
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U2 - 10.3892/ijo.12.4.777
DO - 10.3892/ijo.12.4.777
M3 - Article
C2 - 9499436
AN - SCOPUS:0031916809
SN - 1019-6439
VL - 12
SP - 777
EP - 784
JO - International journal of oncology
JF - International journal of oncology
IS - 4
ER -