Abstract
A full length cDNA for the human mucin gene, MUC1, under the control of human β actin promoter, was transfected into a carcinogen induced hamster pancreatic ductal tumor cell line, HP-1. Transfectants were selected by resistance to geneticin. Integration of the foreign human MUC1 cDNA occurred at multiple sites in the genome of HP-1. Northern blot analysis showed MUC1 expression in cells transfected with MUC1 cDNA placed in the correct orientation, but not in control cells (HP-1 cells transfected with vector alone, or with the MUC1 cDNA placed in the antisense orientation). Western blot analysis using monoclonal antibody HMFG-2, which is reactive with the MUC1 protein, showed results consistent with the Northern blot data. Positive immunoperoxidase staining using HMFG-2 was seen in HP-1 cells transfected with MUC1 cDNA but not with untransfected or HP-1 control cells. The integration of human MUC1 mucin gene in HP-1 cells caused no significant change in the growth rate of HP-1 cells in vitro, but resulted in an enhanced growth rate for xenografts of MUC1 transfected HP-1 cells grown in nude mice.
Original language | English (US) |
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Pages (from-to) | 271-283 |
Number of pages | 13 |
Journal | International Journal of Pancreatology |
Volume | 12 |
Issue number | 3 |
DOIs | |
State | Published - Dec 1992 |
Keywords
- MUC1 expression
- Pancreatic cancer
- mucin
ASJC Scopus subject areas
- Oncology
- Endocrinology
- Gastroenterology