TY - JOUR
T1 - The expression of p73 is increased in lung cancer, independent of p53 gene alteration
AU - Tokuchi, Y.
AU - Hashimoto, T.
AU - Kobayashi, Y.
AU - Hayashi, M.
AU - Nishida, K.
AU - Hayashi, S.
AU - Imai, K.
AU - Nakachi, K.
AU - Ishikawa, Y.
AU - Nakagawa, K.
AU - Kawakami, Y.
AU - Tsuchiya, E.
N1 - Funding Information:
We thank Drs H Sugano (Cancer Institute) and T Kozu (Saitama Cancer Center) for their helpful advice. We also thank Drs S Tsuchiya and S Okumura at Cancer Institute Hospital, for kindly providing lung cancer samples. The technical assistance of T Yoshikawa and Y Yamaoka is gratefully acknowledged. This work is supported by Grant-in-Aid for Science Research from Ministry of Education, Science, Sports and Culture of Japan; Ministry of Health and Welfare of Japan; Selectively Applied and Developed Research from Saitama Prefecture and the Smoking Research Foundation.
PY - 1999
Y1 - 1999
N2 - p73 gene, a new p53 homologue, has been identified: it supposedly acts as tumour suppressor gene in neuroblastoma. To clarify whether p73 might be involved in lung carcinogenesis, we examined p73 expression in resected lung cancer and paired normal lung in 60 cases using semi-quantitative reverse transcription-polymerase chain reaction (RT-PCR). We also examined p73 gene status in three representative cases using Southern blot, and p53 gene alteration in 49 cases using PCR-single-strand conformation polymorphism (PCR-SSCP) and direct sequence. In 87% of the cases (52/60) p73 expression in tumour was more than twice as high as that in paired normal lung tissues, and the difference between p73 expression in tumour and normal lung tissue was significant (P < 0.0001). However, Southern blot analysis revealed that none of the cases showed p73 gene amplification. Compared with clinicopathological characteristics, p73 expression correlates significantly with histological differences and age of patient, independently (P < 0.05). Concerning p53 gene status, 43% (21/49) showed p53 gene alteration, but there was no correlation between p73 overexpression and p53 gene alteration. Our results suggest that need for further functional analysis of the role of p73 in lung carcinogenesis.
AB - p73 gene, a new p53 homologue, has been identified: it supposedly acts as tumour suppressor gene in neuroblastoma. To clarify whether p73 might be involved in lung carcinogenesis, we examined p73 expression in resected lung cancer and paired normal lung in 60 cases using semi-quantitative reverse transcription-polymerase chain reaction (RT-PCR). We also examined p73 gene status in three representative cases using Southern blot, and p53 gene alteration in 49 cases using PCR-single-strand conformation polymorphism (PCR-SSCP) and direct sequence. In 87% of the cases (52/60) p73 expression in tumour was more than twice as high as that in paired normal lung tissues, and the difference between p73 expression in tumour and normal lung tissue was significant (P < 0.0001). However, Southern blot analysis revealed that none of the cases showed p73 gene amplification. Compared with clinicopathological characteristics, p73 expression correlates significantly with histological differences and age of patient, independently (P < 0.05). Concerning p53 gene status, 43% (21/49) showed p53 gene alteration, but there was no correlation between p73 overexpression and p53 gene alteration. Our results suggest that need for further functional analysis of the role of p73 in lung carcinogenesis.
KW - 1p36
KW - Lung cancer
KW - Tumour suppressor gene
KW - p53
KW - p73
UR - http://www.scopus.com/inward/record.url?scp=0032988708&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0032988708&partnerID=8YFLogxK
U2 - 10.1038/sj.bjc.6690572
DO - 10.1038/sj.bjc.6690572
M3 - Article
C2 - 10408409
AN - SCOPUS:0032988708
SN - 0007-0920
VL - 80
SP - 1623
EP - 1629
JO - British Journal of Cancer
JF - British Journal of Cancer
IS - 10
ER -