A novel, nuclear pore-associated, widely distributed molecule overexpressed in oncogenesis and development

被引:45
作者
Gould, VE
Martinez, N
Orucevic, A
Schneider, J
Alonso, A
机构
[1] Rush Med Coll, Dept Pathol, Chicago, IL 60612 USA
[2] German Canc Res Ctr, D-6900 Heidelberg, Germany
[3] Univ Basque Country, Dept Especialidades Medicoquirurg, E-48080 Bilbao, Spain
关键词
D O I
10.1016/S0002-9440(10)64798-0
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Nuclear pore complexes are large, elaborate macromolecular structures that mediate the bidirectional nucleocytoplasmic traffic. In vertebrates, nuclear pore complexes comprise 50 to 100 proteins termed nucleoporins (Nup). An 88-kd nucleoporin (Nup88) has been recently cloned and characterized, and found to be associated in a dynamic subcomplex with the oncogenic nucleoporin CAN/Nup 214. We have produced a polyclonal antiserum to Nup88, and found that it immunoreacts convincingly in conventional tissue sections of 214 samples of malignant tumors of many types. All carcinomas were stained irrespective of site or line of differentiation; the majority of cases reacted strongly and extensively, In situ carcinomas and highly dysplastic epithelia were similarly reactive. Samples of malignant mesotheliomas, gliomas, sarcomas, and lymphoreticular tumors were also stained. Substantial reactions were also found in certain fetal tissues, Focal reactions were noted in some reactive-proliferative processes. Most benign epithelial and mesenchymal tumors and hyperplasias, and normal adult tissues reacted weakly and sporadically or not at all. Immunoblot analysis of selected samples strongly corroborated those findings. If further substantiated, our findings indicate that Nup88 could be regarded as a selective yet broadly based proliferation marker of potential significance in the histological evaluation and diagnosis of malignant transformation. Its ready applicability on conventional paraffin sections acid on cytological preparations may broaden its clinical and investigative significance.
引用
收藏
页码:1605 / 1613
页数:9
相关论文
共 37 条
[1]  
Allen TD, 2000, J CELL SCI, V113, P1651
[2]   IMMUNOLOCALIZATION OF TENASCIN AND CELLULAR FIBRONECTINS IN DIVERSE GLOMERULOPATHIES [J].
ASSAD, L ;
SCHWARTZ, MM ;
VIRTANEN, I ;
GOULD, VE .
VIRCHOWS ARCHIV B-CELL PATHOLOGY INCLUDING MOLECULAR PATHOLOGY, 1993, 63 (05) :307-316
[3]   Proteomics for the pore [J].
Blobel, G ;
Wozniak, RW .
NATURE, 2000, 403 (6772) :835-836
[4]   The nucleoporin CAN/Nup214 binds to both the cytoplasmic and the nucleoplasmic sides of the nuclear pore complex in overexpressing cells [J].
Boer, JM ;
vanDeursen, JMA ;
Croes, HJ ;
Fransen, JAM ;
Grosveld, GC .
EXPERIMENTAL CELL RESEARCH, 1997, 232 (01) :182-185
[5]   The nuclear localization sequences of the BRCA1 protein interact with the importin-alpha subunit of the nuclear transport signal receptor [J].
Chen, CF ;
Li, S ;
Chen, YM ;
Chen, PL ;
Sharp, ZD ;
Lee, WH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (51) :32863-32868
[6]  
CORDES VC, 1995, EUR J CELL BIOL, V68, P240
[7]  
Ewald A, 1996, J CELL SCI, V109, P1813
[8]  
FELDHERR CM, 1995, MEM PROT TR, V2, P237
[9]   A conserved biogenesis pathway for nucleoporins: Proteolytic processing of a 186-kilodalton precursor generates Nup98 and the novel nucleoporin, Nup96 [J].
Fontoura, BMA ;
Blobel, G ;
Matunis, MJ .
JOURNAL OF CELL BIOLOGY, 1999, 144 (06) :1097-1112
[10]  
Fornerod M, 1996, ONCOGENE, V13, P1801