Clinical implication of p53 mutation in lung cancer

被引:50
作者
Campling, BG [1 ]
El-Deiry, WS [1 ]
机构
[1] Univ Penn, Sch Med, Philadelphia, PA 19104 USA
关键词
p53; tobacco; carcinogen; mutation; gene therapy; apoptosis; SCLC; NSCLC; SSCP; BPDE; antibodies; lung cancer;
D O I
10.1385/MB:24:2:141
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Lung cancer development involves multiple genetic abnormalities leading to malignant transformation of the bronchial epithelial cells, followed by invasion and metastasis. One of the most common changes is mutation of the p53 tumor suppressor gene. The frequency of p53 alterations in lung cancer is highest in small cell and squamous cell carcinomas. A genetic "signature" of the type of p53 mutations has been associated with carcinogens in cigarette smoke. The majority of clinical studies suggest that lung cancers with p53 alterations carry a worse prognosis, and may be relatively more resistant to chemotherapy and radiation. An understanding of the role of p53 in human lung cancer may lead to more rational targeted approaches for treating this disease. P53 gene replacement is currently under clinical investigation but clearly more effective means of gene deliver to the tumor cells are required. Novel approaches to lung cancer therapy are needed to improve the observed poor patient survival despite current therapies.
引用
收藏
页码:141 / 156
页数:16
相关论文
共 134 条
[91]   Cell suicide for beginners [J].
Raff, M .
NATURE, 1998, 396 (6707) :119-122
[92]  
Righetti SC, 1996, CANCER RES, V56, P689
[93]   Serum anti-p53 antibodies and prognosis of patients with small-cell lung cancer [J].
Rosenfeld, MR ;
Malats, N ;
Schramm, L ;
Graus, F ;
Cardenal, F ;
Vinolas, N ;
Rosell, R ;
Tora, M ;
Real, FX ;
Posner, JB ;
Dalmau, J .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1997, 89 (05) :381-385
[94]   Retrovirus-mediated wild-type p53 gene transfer to tumors of patients with lung cancer [J].
Roth, JA ;
Nguyen, D ;
Lawrence, DD ;
Kemp, BL ;
Carrasco, CH ;
Ferson, DZ ;
Hong, WK ;
Komaki, R ;
Lee, JJ ;
Nesbitt, JC ;
Pisters, KMW ;
Putnam, JB ;
Schea, R ;
Shin, DM ;
Walsh, GL ;
Dolormente, MM ;
Han, CI ;
Martin, FD ;
Yen, N ;
Xu, K ;
Stephens, LC ;
McDonnell, TJ ;
Mukhopadhyay, T ;
Cai, D .
NATURE MEDICINE, 1996, 2 (09) :985-991
[95]   ATM: A mediator of multiple responses to genotoxic stress [J].
Rotman, G ;
Shiloh, Y .
ONCOGENE, 1999, 18 (45) :6135-6144
[96]  
RUSCH V, 1995, CANCER RES, V55, P5038
[97]  
SAMESHIMA Y, 1992, ONCOGENE, V7, P451
[98]   THE E6 ONCOPROTEIN ENCODED BY HUMAN PAPILLOMAVIRUS TYPE-16 AND TYPE-18 PROMOTES THE DEGRADATION OF P53 [J].
SCHEFFNER, M ;
WERNESS, BA ;
HUIBREGTSE, JM ;
LEVINE, AJ ;
HOWLEY, PM .
CELL, 1990, 63 (06) :1129-1136
[99]   ANALYSES OF P53 ANTIBODIES IN SERA OF PATIENTS WITH LUNG-CARCINOMA DEFINE IMMUNODOMINANT REGIONS IN THE P53 PROTEIN [J].
SCHLICHTHOLZ, B ;
TREDANIEL, J ;
LUBIN, R ;
ZALCMAN, G ;
HIRSCH, A ;
SOUSSI, T .
BRITISH JOURNAL OF CANCER, 1994, 69 (05) :809-816
[100]   Measurement and evaluation of serum anti-p53 antibody levels in patients with lung cancer at its initial presentation: a prospective study [J].
Segawa, Y ;
Kageyama, M ;
Suzuki, S ;
Jinno, K ;
Takigawa, N ;
Fujimoto, N ;
Hotta, K ;
Eguchi, K .
BRITISH JOURNAL OF CANCER, 1998, 78 (05) :667-672