CELL-SURFACE EXPRESSION OF PARANEOPLASTIC ENCEPHALOMYELITIS SENSORY NEURONOPATHY-ASSOCIATED HU ANTIGENS IN SMALL-CELL LUNG CANCERS AND NEUROBLASTOMAS/

Citation
M. Tora et al., CELL-SURFACE EXPRESSION OF PARANEOPLASTIC ENCEPHALOMYELITIS SENSORY NEURONOPATHY-ASSOCIATED HU ANTIGENS IN SMALL-CELL LUNG CANCERS AND NEUROBLASTOMAS/, Neurology, 48(3), 1997, pp. 735-741
Citations number
41
Categorie Soggetti
Clinical Neurology
Journal title
ISSN journal
00283878
Volume
48
Issue
3
Year of publication
1997
Pages
735 - 741
Database
ISI
SICI code
0028-3878(1997)48:3<735:CEOPES>2.0.ZU;2-A
Abstract
Background: Serum from patients with small-cell lung cancer-associated paraneoplastic encephalomyelitis/sensory neuronopathy contains autoan tibodies recognizing 35- to 40-kDa nuclear antigens present in neurons , small-cell lung cancers, and some neuroblastomas (anti-Hu). Aim: Bec ause the mechanisms by which Hu autoantibodies may contribute to the p araneoplastic syndrome are largely unknown, we sought to examine if Hu antigens are expressed at the plasma membrane of cultured cells from Hu-expressing tumors. Methods and results: Hu-related molecules of 35 to 41 kDa were detected in the membrane of small-cell lung cancers and neuroblastomas using: (1) immunofluorescence, (2) absorption assays, (3) Western blotting on membrane fractions, and (4) surface biotinylat ion. The antibodies recognizing these membrane components were specifi cally absorbed by recombinant HuD protein. There was a perfect correla tion between nuclear and membrane Hu expression. To determine the puri ty of the subcellular fractions, their reactivity with antibodies reco gnizing the A2 nuclear ribonucleoprotein and the cytoplasmic mitogen-a ctivated protein kinase was examined. None of them was detected in the membrane fractions reactive with sera containing Hu antibodies. Concl usions: Hu-related antigens can be detected both in the nucleus and th e membrane of small-cell lung cancer and neuroblastomas. Implications: These results provide an experimental basis for surface binding-media ted pathogenic mechanisms in paraneoplastic encephalomyelitis/sensory neuronopathy and in Hu-expressing tumors.