p63 expression in lung carcinoma - A tissue microarray study of 408 cases

被引:126
作者
Au, NHC
Gown, AM
Cheang, M
Huntsman, D
Yorida, E
Elliott, WM
Flint, J
English, J
Gilks, CB
Grimes, HL
机构
[1] Vancouver Gen Hosp, Dept Pathol, Genet Pathol Evaluat Ctr, Vancouver, BC V5Z 1MT, Canada
[2] Vancouver Gen Hosp, Prostate Res Ctr, Vancouver, BC V5Z 1MT, Canada
[3] British Columbia Canc Agcy, Vancouver, BC V5Z 4E6, Canada
[4] Univ British Columbia, Dept Pathol, Vancouver, BC V5Z 1M9, Canada
[5] PhenoPath Labs, Seattle, WA USA
[6] St Pauls Hosp, James Hogg iCapture Ctr, Vancouver, BC V6Z 1Y6, Canada
[7] Univ Louisville, Inst Cellular Therapeut, Louisville, KY 40292 USA
[8] Univ Louisville, Dept Surg, Louisville, KY 40292 USA
关键词
p63; immunohistochemistry; lung cancer; neuroendocrine tumors;
D O I
10.1097/00129039-200409000-00010
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
p63 is a recently discovered member of the p53 family that has been shown to be important in the development of epithelial tissues. p63 may also play a role in squamous cell carcinomas of the lung, head and neck, and cervix, and its expression is increased in these tumors. The purpose of this study was to investigate the expression of p63 in a broad spectrum of histologic types of lung tumors. A total of 441 cases of primary lung tumors with follow-up data were identified, and the paraffin-embedded tissue blocks were used to construct a duplicate core tissue microarray. After review of the tissue cores, 408 cases, consisting of 123 squamous cell carcinomas, 93 adenocarcinomas, 68 large cell carcinomas, 68 classic carcinoids, 31 atypical carcinoids, I I large cell neuroendocrine carcinomas, and 14 small cell carcinomas, were adequate for analysis. Immunohistochemistry was performed at 2 different laboratories using monoclonal antibody 4A4 to detect the expression of p63, using different staining protocols. p53 expression was also studied with immunohistochemistry using monoclonal antibody DO-7. Kaplan-Meier curves were plotted to compare the survival of p63 -expressing versus nonexpressing tumors. A large proportion of squamous cell carcinomas expressed p63 (96.9%), most showing strong positive nuclear immunoreactivity. Expression in other nonsmall cell lung cancers was also present. Thirty percent of adenocarcinomas and 37% of large cell carcinomas showed p63 expression. In the neuroendocrine tumors, an increasing proportion of tumors stained for p63 as tumor grade increased; 1.9% of classic carcinoids, 30.8% of atypical carcinoids, 50% of large cell neuroendocrine carcinomas, and 76.9% of small cell carcinomas were positive. Approximately half of the positively staining neuroendocrine cases showed strong staining. Expression of p63 was of prognostic significance in neuroendocrine tumors (P < 0.0001), with higher-grade tumors more likely to express p63. Correlation between p63 and p53 expression was not observed (P = 0.18) in nonsmall cell lung cancer; however, a significant correlation between the 2 markers was found in neuroendocrine tumors (P < 0.0001). p63 staining was repeated with a different staining protocol, yielding similar results overall but a lower percentage of positive cases (34.2% vs. 48.4% of tumors positive). In conclusion, p63 expression is consistently expressed in squamous cell carcinoma in the lung, but is also expressed in a subset of adenocarcinomas and large cell carcinomas. Pulmonary neuroendocrine tumors also show p63 staining in some instances, particularly in higher-grade tumors, and the majority of small cell carcinomas are p63-positive. These results suggest that p63 may be involved in oncogenesis in a broader range of tumors than was previously thought.
引用
收藏
页码:240 / 247
页数:8
相关论文
共 43 条
[1]   p63 is expressed in basal and myoepithelial cells of human normal and tumor salivary gland tissues [J].
Bilal, H ;
Handra-Luca, A ;
Bertrand, JC ;
Fouret, PJ .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 2003, 51 (02) :133-139
[2]   P63 gene mutations and human developmental syndromes [J].
Brunner, HG ;
Hamel, BCJ ;
van Bokhoven, H .
AMERICAN JOURNAL OF MEDICAL GENETICS, 2002, 112 (03) :284-290
[3]   Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome [J].
Celli, J ;
Duijf, P ;
Hamel, BCJ ;
Bamshad, M ;
Kramer, B ;
Smits, APT ;
Newbury-Ecob, R ;
Hennekam, RCM ;
Van Buggenhout, G ;
van Haeringen, B ;
Woods, CG ;
van Essen, AJ ;
de Waal, R ;
Vriend, G ;
Haber, DA ;
Yang, A ;
McKeon, F ;
Brunner, HG ;
van Bokhoven, H .
CELL, 1999, 99 (02) :143-153
[4]   Differential expression of p53 gene family members p63 and p73 in head and neck squamous tumorigenesis [J].
Choi, HR ;
Batsakis, JG ;
Zhan, F ;
Sturgis, E ;
Luna, MA ;
El-Naggar, AK .
HUMAN PATHOLOGY, 2002, 33 (02) :158-164
[5]  
Di Como CJ, 2002, CLIN CANCER RES, V8, P494
[6]   Differential protein expression, DNA binding and interaction with SV40 large tumour antigen implicate the p63-family of proteins in replicative senescence [J].
Djelloul, S ;
Tarunina, M ;
Barnouin, K ;
Mackay, A ;
Jat, PS .
ONCOGENE, 2002, 21 (07) :981-989
[7]   p63 and p73 are required for p53-dependent apoptosis in response to DNA damage [J].
Flores, ER ;
Tsai, KY ;
Crowley, D ;
Sengupta, S ;
Yang, A ;
McKeon, F ;
Jacks, T .
NATURE, 2002, 416 (6880) :560-564
[8]   p63α mutations lead to aberrant splicing of keratinocyte growth factor receptor in the Hay-Wells syndrome [J].
Fomenkov, A ;
Huang, YP ;
Topaloglu, O ;
Brechman, A ;
Osada, M ;
Fomenkova, T ;
Yuriditsky, E ;
Trink, B ;
Sidransky, D ;
Ratovitski, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (26) :23906-23914
[9]   Complex transcriptional effects of p63 isoforms: Identification of novel activation and repression domains [J].
Ghioni, P ;
Bolognese, F ;
Duijf, PHG ;
van Bokhoven, H ;
Mantovani, R ;
Guerrini, L .
MOLECULAR AND CELLULAR BIOLOGY, 2002, 22 (24) :8659-8668
[10]   Expression of p53-related protein p63 in the gastrointestinal tract and in esophageal metaplastic and neoplastic disorders [J].
Glickman, JN ;
Yang, A ;
Shahsafaei, A ;
McKeon, F ;
Odze, RD .
HUMAN PATHOLOGY, 2001, 32 (11) :1157-1165