TY - JOUR
T1 - Alteration of the CDKN2/p16 gene is not required for HPV-positive uterine cervical cancer cell lines.
AU - Yoshinouchi, M.
AU - Hongo, A.
AU - Takamoto, N.
AU - Ono, Y.
AU - Nagao, S.
AU - Miyagi, Y.
AU - Kudo, T.
AU - Kodama, J.
PY - 2000/3
Y1 - 2000/3
N2 - To determine whether alterations of the CDKN2/p16 might be involved in HPV-positive cervical cancers, we examined for alterations of this gene and function of the protein p16 to interact with CDK4 in 5 cervical cancer cell lines. No alteration of this gene was detected. Proteins for p16 and CDK4 were normally expressed and function of p16 to interact with CDK4 was not abrogated in these cell lines. These cell lines were human papillomavirus (HPV)-positive and carried wild-type p53. These findings suggest that phosphorylation of pRb by CDK4 is not critical in the carcinogenesis or in the establishment of HPV-positive cervical cancer cell lines, since HPV E6 or E7 viral-transforming proteins inactivate p53 and pRb tumor suppressor protein function, resulting in deregulated progression of the cell cycle.
AB - To determine whether alterations of the CDKN2/p16 might be involved in HPV-positive cervical cancers, we examined for alterations of this gene and function of the protein p16 to interact with CDK4 in 5 cervical cancer cell lines. No alteration of this gene was detected. Proteins for p16 and CDK4 were normally expressed and function of p16 to interact with CDK4 was not abrogated in these cell lines. These cell lines were human papillomavirus (HPV)-positive and carried wild-type p53. These findings suggest that phosphorylation of pRb by CDK4 is not critical in the carcinogenesis or in the establishment of HPV-positive cervical cancer cell lines, since HPV E6 or E7 viral-transforming proteins inactivate p53 and pRb tumor suppressor protein function, resulting in deregulated progression of the cell cycle.
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U2 - 10.3892/ijo.16.3.537
DO - 10.3892/ijo.16.3.537
M3 - Article
C2 - 10675486
AN - SCOPUS:0034146740
SN - 1019-6439
VL - 16
SP - 537
EP - 541
JO - International Journal of Oncology
JF - International Journal of Oncology
IS - 3
ER -