Please use this identifier to cite or link to this item:
Scopus Web of Science® Altmetric
Type: Journal article
Title: HPP1: A transmembrane protein-encoding gene commonly methylated in colorectal polyps and cancers
Author: Young, J.
Biden, K.
Simms, L.
Huggard, P.
Karamatic, R.
Eyre, H.
Sutherland, G.
Herath, N.
Barker, M.
Anderson, G.
Fitzpatrick, D.
Ramm, G.
Jass, J.
Leggett, B.
Citation: Proceedings of the National Academy of Sciences of the United States of America, 2001; 98(1):265-270
Publisher: Natl Acad Sciences
Issue Date: 2001
ISSN: 0027-8424
Statement of
Joanne Young, Kelli G. Biden, Lisa A. Simms, Phillip Huggard, Rozemary Karamatic, Helen J. Eyre, Grant R. Sutherland, Nirmitha Herath, Melissa Barker, Gregory J. Anderson, David R. Fitzpatrick, Grant A. Ramm, Jeremy R. Jass, and Barbara A. Leggett
Abstract: Adenomas are the precursors of most colorectal cancers. Hyperplastic polyps have been linked to the subset of colorectal cancers showing DNA microsatellite instability, but little is known of their underlying genetic etiology. Using a strategy that isolates differentially methylated sequences from hyperplastic polyps and normal mucosa, we identified a 370-bp sequence containing the 5' untranslated region and the first exon of a gene that we have called HPP1. Rapid amplification of cDNA ends was used to isolate HPP1 from normal mucosa. Using reverse transcription-PCR, HPP1 was expressed in 28 of 30 (93%) normal colonic samples but in only seven of 30 (23%) colorectal cancers (P < 0.001). The 5' region of HPP1 included a CpG island containing 49 CpG sites, of which 96% were found to be methylated by bisulfite sequencing of DNA from colonic tumor samples. By COBRA analysis, methylation was detected in six of nine (66%) adenomas, 17 of 27 (63%) hyperplastic polyps, and 46 of 55 (84%) colorectal cancers. There was an inverse relationship between methylation level and mRNA expression in cancers (r = -0.67; P < 0.001), and 5-aza-2-deoxycytidine treatment restored HPP1 expression in two colorectal cancer cell lines. In situ hybridization of HPP1 indicated that expression occurs in epithelial and stromal elements in normal mucosa but is silenced in both cell types in early colonic neoplasia. HPP1 is predicted to encode a transmembrane protein containing follistatin and epidermal growth factor-like domains. Silencing of HPP1 by methylation may increase the probability of neoplastic transformation.
Keywords: Chromosomes, Human, Pair 2; Humans; Colorectal Neoplasms; Intestinal Polyps; Hyperplasia; Membrane Proteins; Neoplasm Proteins; RNA, Messenger; Immunohistochemistry; In Situ Hybridization; In Situ Hybridization, Fluorescence; Cloning, Molecular; Sequence Analysis, DNA; DNA Methylation; Gene Expression Regulation, Neoplastic; Amino Acid Sequence; Base Sequence; Microsatellite Repeats; Loss of Heterozygosity; Molecular Sequence Data
Description: Copyright © 2001, The National Academy of Sciences
RMID: 0020010955
DOI: 10.1073/pnas.011415298
Appears in Collections:Paediatrics publications

Files in This Item:
There are no files associated with this item.

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.