1. Coexpression of gastrin and gastrin receptors (CCK-B and delta CCK-B) in gastrointestinal tumour cell lines.
- Author
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McWilliams DF, Watson SA, Crosbee DM, Michaeli D, and Seth R
- Subjects
- Blotting, Southern, Colorectal Neoplasms metabolism, Gastrins metabolism, Humans, Isomerism, Polymerase Chain Reaction, RNA, Messenger metabolism, Receptor, Cholecystokinin B, Receptors, Cholecystokinin metabolism, Stomach Neoplasms metabolism, Tumor Cells, Cultured, Gastrins genetics, Gastrointestinal Neoplasms metabolism, Receptors, Cholecystokinin genetics
- Abstract
Background: The peptide hormone gastrin is a recognised growth factor for gastrointestinal (GI) tumour cells. Carboxyamidated gastrins bind to the cell surface gastrin/cholecystokinin B (CCK-B) receptor which can be expressed as either a normal or a truncated isoform (delta CCK-B)., Aims: To compare gastrin gene expression with delta CCK-B and total CCK-B (both isoforms) gene expression in both GI and non-GI tract derived human tumour cell lines., Methods: Total RNA was extracted and gene expression was assayed by the reverse transcription-polymerase chain reaction followed by Southern blotting and hybridisation with specific oligo probes., Results: Gastrin was expressed by 5/5 gastric and 7/8 colorectal cell lines. Coexpression of gastrin CCK-B isoform was found in 80% of gastric and 75% of colorectal cell lines. Non-GI cell lines, with the exception of a lymphoblastic leukaemia cell line, showed no coexpression. The truncated receptor, delta CCK-B, was shown in 3/5 gastric and 5/8 colorectal cell lines and was always coexpressed with gastrin., Conclusions: The truncated gastrin receptor, delta CCK-B, is coexpressed with gastrin in 8/13 GI tumour cell lines. Gastrin and CCK-B receptor isoforms may be involved in maintaining autocrine/paracrine growth pathways in GI cancer cells.
- Published
- 1998
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