Frequent loss of KAI1 expression in squamous and lymphoid neoplasms - An immunohistochemical study of archival tissues

被引:39
作者
Geradts, J
Maynard, R
Birrer, MJ
Hendricks, D
Abbondanzo, SL
Fong, KM
Barrett, JC
Lombardi, DP
机构
[1] Univ Oxford, Nuffield Dept Pathol & Bacteriol, Oxford, England
[2] Univ N Carolina Hosp, Dept Hosp Labs, Chapel Hill, NC 27514 USA
[3] NCI, Biomarkers & Prevent Res Branch, Rockville, MD USA
[4] Armed Forces Inst Pathol, Dept Hematol & Lymphat Pathol, Washington, DC 20306 USA
[5] Prince Charles Hosp, Dept Thorac Med, Chermside, Qld, Australia
[6] Natl Inst Environm Hlth Sci, Res Triangle Pk, NC 27709 USA
[7] Univ N Carolina, Dept Med, Chapel Hill, NC 27514 USA
关键词
D O I
10.1016/S0002-9440(10)65422-3
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The metastasis suppressor gene KAI1 was identified by its ability to inhibit the formation of pulmonary metastases in experimental models for prostatic carcinoma. Down-regulation of this gene may be correlated with the invasive phenotype in melanomas and colon and bladder carcinomas and with the metastatic phenotype in carcinomas of the lung, breast, prostate, and pancreas. The goal of our study was to establish an immunohistochemical method to detect KAI1 expression in archival tissues. Using cell lines with known KAI1 levels and paraffin-embedded KAI1 positive tissues as controls,we observed strong membrane staining in lymphoid follicular centers and squamous epithelia. We then demonstrated the utility of our assay by studying KAI1 expression in 34 lymphoid and 57 squamous lesions. All eight reactive lymph nodes were KAI1 positive. In contrast, three of 13 follicular small cleaved and five of 13 diffuse large cell lymphomas were KAI1 negative. Seventy-nine percent (37 of 47) of invasive squamous cell carcinomas from the lung (n = 15), head and neck (n = 18), and cervix (n = 14) showed extensive KAI1 down-regulation. Loss of KAI1 expression was also found in a subset of 10 high-grade cervical dysplasias. Our data show that (i) immunohistochemistry is a suitable technique for evaluating KAI1 expression in archival tissues; (ii) KAI1 was not expressed in a subset of both low-grade and high-grade lymphomas; and (iii) there was extensive down-regulation of KAI1 in squamous cell carcinomas, suggestive of an important role of the gene in the suppression of invasion in these malignancies.
引用
收藏
页码:1665 / 1671
页数:7
相关论文
共 33 条
[1]  
Adachi M, 1996, CANCER RES, V56, P1751
[2]   Novel staging protocol for non-small-cell lung cancers according to MRP-1/CD9 and KAI1/CD82 gene expression [J].
Adachi, M ;
Taki, T ;
Konishi, T ;
Huang, CI ;
Higashiyama, M ;
Miyake, M .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (04) :1397-1406
[3]  
Asada M, 1997, CANCER RES, V57, P1073
[4]  
Dong JT, 1996, WORLD J UROL, V14, P182
[5]   KAI1, A METASTASIS SUPPRESSOR GENE FOR PROSTATE-CANCER ON HUMAN-CHROMOSOME 11P11.2 [J].
DONG, JT ;
LAMB, PW ;
RINKERSCHAEFFER, CW ;
VUKANOVIC, J ;
ICHIKAWA, T ;
ISAACS, JT ;
BARRETT, JC .
SCIENCE, 1995, 268 (5212) :884-886
[6]   Genomic organization of the human KAl1 metastasis-suppressor gene [J].
Dong, JT ;
Isaacs, WB ;
Barrett, JC ;
Isaacs, JT .
GENOMICS, 1997, 41 (01) :25-32
[7]  
Dong JT, 1996, CANCER RES, V56, P4387
[8]  
Friess H, 1998, INT J CANCER, V79, P349, DOI 10.1002/(SICI)1097-0215(19980821)79:4<349::AID-IJC7>3.0.CO
[9]  
2-V
[10]   IDENTIFICATION OF MEMBRANE ANTIGEN C33 RECOGNIZED BY MONOCLONAL-ANTIBODIES INHIBITORY TO HUMAN T-CELL LEUKEMIA-VIRUS TYPE-1 (HTLV-1)-INDUCED SYNCYTIUM FORMATION - ALTERED GLYCOSYLATION OF C33 ANTIGEN IN HTLV-1-POSITIVE T-CELLS [J].
FUKUDOME, K ;
FURUSE, M ;
IMAI, T ;
NISHIMURA, M ;
TAKAGI, S ;
HINUMA, Y ;
YOSHIE, O .
JOURNAL OF VIROLOGY, 1992, 66 (03) :1394-1401