The human cell lines VACO-235 and VACO-411 constitute a novel in vitro model of colon adenoma to carcinoma progression. By differential display RT-PCR we identified a transcript that is expressed in the parental nontumorigenic adenoma line (VACO-235E), but is not expressed in the tumorigenic daughter (VACO-235L) or granddaughter (VACO-411) lines. This cDNA represents a previously uncharacterized portion of the 3'UTR of human PIGR. Human PIGR mRNA was found to be highly expressed in normal colon epithelium, but was decreased in 6 of 8 colon tumors and was negligible in 8 of 10 colon tumor cell lines. We sequenced the entire 1.8 kb 3'UTR of human PIGR, and found it to contain multiple repetitive elements as well as elements that could affect the processing and stability of PIGR mRNA. We hypothesize that differential regulation of PIGR mRNA stability may contribute to its downregulation in colon cancer.

Characterization of the human polymeric immunoglobulin receptor (PIGR) 3'UTR and differential expression of PIGR mRNA during colon tumorigenesis / J. L., Traicoff; DE MARCHIS, Laura; B. L., Ginsburg; R. E., Zamora; N. H., Khattar; V. J., Blanch; S., Plummer; S. A., Bargo; D. J., Templeton; G., Casey; C. S., Kaetzel. - In: JOURNAL OF BIOMEDICAL SCIENCE. - ISSN 1021-7770. - 10:(2003), pp. 792-804. [10.1159/000073967]

Characterization of the human polymeric immunoglobulin receptor (PIGR) 3'UTR and differential expression of PIGR mRNA during colon tumorigenesis.

DE MARCHIS, Laura;
2003

Abstract

The human cell lines VACO-235 and VACO-411 constitute a novel in vitro model of colon adenoma to carcinoma progression. By differential display RT-PCR we identified a transcript that is expressed in the parental nontumorigenic adenoma line (VACO-235E), but is not expressed in the tumorigenic daughter (VACO-235L) or granddaughter (VACO-411) lines. This cDNA represents a previously uncharacterized portion of the 3'UTR of human PIGR. Human PIGR mRNA was found to be highly expressed in normal colon epithelium, but was decreased in 6 of 8 colon tumors and was negligible in 8 of 10 colon tumor cell lines. We sequenced the entire 1.8 kb 3'UTR of human PIGR, and found it to contain multiple repetitive elements as well as elements that could affect the processing and stability of PIGR mRNA. We hypothesize that differential regulation of PIGR mRNA stability may contribute to its downregulation in colon cancer.
2003
Adenoma; genetics; Base Sequence; Blotting; Northern; Carcinoma; Cell Line; Tumor; Chromosome Mapping; Colonic Neoplasms; DNA Primers; Gene Expression; physiology; Humans; Molecular Sequence Data; Receptors; Polymeric Immunoglobulin; Reverse Transcriptase Polymerase Chain Reaction; Sequence Alignment; Sequence Analysis; DNA
01 Pubblicazione su rivista::01a Articolo in rivista
Characterization of the human polymeric immunoglobulin receptor (PIGR) 3'UTR and differential expression of PIGR mRNA during colon tumorigenesis / J. L., Traicoff; DE MARCHIS, Laura; B. L., Ginsburg; R. E., Zamora; N. H., Khattar; V. J., Blanch; S., Plummer; S. A., Bargo; D. J., Templeton; G., Casey; C. S., Kaetzel. - In: JOURNAL OF BIOMEDICAL SCIENCE. - ISSN 1021-7770. - 10:(2003), pp. 792-804. [10.1159/000073967]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/387216
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