Two novel monoclonal antibodies against the MUC4 tandem repeat reacting with an antigen overexpressed by lung cancer

被引:8
作者
Botti, C
Seregni, E
Ménard, S
Collini, P
Tagliabue, E
Campiglio, M
Vergani, B
Ghirelli, C
Aiello, P
Pilotti, S
Bombardieri, E
机构
[1] Ist Nazl Studio & Cura Tumori, Div Nucl Med, I-20133 Milan, Italy
[2] Ist Nazl Studio & Cura Tumori, Div Mol Targeting, I-20133 Milan, Italy
[3] Ist Nazl Studio & Cura Tumori, Div Pathol, I-20133 Milan, Italy
关键词
MUC4; mucins; monoclonal antibodies; core peptides; lung cancer;
D O I
10.1177/172460080001500406
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
In this study we investigated the immunochemical and cytochemical reactivity of two monoclonal antibodies against the 16-amino acid tandem repeat of MUC4 to demonstrate a possible variation of the mucin core peptide expression related to lung cancer. The immunocytochemical anti-MUC4 reactivity was analyzed in four lung cancer cell lines (Calu-1, Calu-3, H460, SKMES) and in other tumor cell lines, as well as in frozen materials from 21 lung adenocarcinomas (ACs), including five bronchioloalveolar carcinomas (BACs), and 11 squamous cell lung carcinomas (SqCCs). A weak fluorescence anti-MUC4 positivity (range: 10.3-16.2) was observed only in acetone-fixed lung cancer cell lines Calu-1, Calu-3 and H460. These three lung cancer cell lines also showed a cytoplasmic immunoperoxidase reactivity. The immunostaining in lung cancer tissues showed a granular cytoplasmic reactivity: 15/21 (71%) and 17/21 (80%) ACs were positive with BC-LuC18.2 and 8C-LuCF12, respectively. All BACs were positive. Moderate to strong reactivity was present in well-difterentiated ACs. In the normal lung parenchyma counterparts weak reactivity was found only in bronchiolar cells. All SqCCs were negative. Anti-MUC4 reactivity was also observed in the alveolar mucus. In conclusion, our anti-MUC4 MAbs detect a secretion product present in mucus and this product is elaborated by lung cancer cells and overexpressed in well-differentiated lung ACs.
引用
收藏
页码:312 / 320
页数:9
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