POFUT1 as a Promising Novel Biomarker of Colorectal Cancer

While protein -fucosyltransferase 1 ( ) overexpression has been recently proposed as a potential biomarker for different cancer types, no study was carried out on POFUT1 implication in colorectal cancer (CRC). Data from 626 tumors and 51 non-tumor adjacent tissues available in FireBrowse had been us...

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Published inCancers Vol. 10; no. 11; p. 411
Main Authors Chabanais, Julien, Labrousse, François, Chaunavel, Alain, Germot, Agnès, Maftah, Abderrahman
Format Journal Article
LanguageEnglish
Published Switzerland MDPI 30.10.2018
MDPI AG
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Summary:While protein -fucosyltransferase 1 ( ) overexpression has been recently proposed as a potential biomarker for different cancer types, no study was carried out on POFUT1 implication in colorectal cancer (CRC). Data from 626 tumors and 51 non-tumor adjacent tissues available in FireBrowse had been used in this study. Statistical analyses on expression and gene copy number, receptors (main targets of POFUT1 enzymatic activity) expression and association of and expressions with clinical parameters were investigated. Data were completed by POFUT1 histological labeling on six tumor tissues from patients with CRC. We found that is overexpressed from the stage I ( < 0.001) and 76.02% of tumors have a 20q11.21 amplification, associated in 90.13% of cases with a overexpression, compared to non-tumor adjacent tissues. The copy number in tumors is mainly between 2 and 3. is positively correlated with (r = 0.34, < 0.001), (r = 0.087, = 0.0297), and (r = 0.097, = 0.0148) expressions, while negatively correlated with expression (r = -0.098, = 0.0142). overexpression is markedly associated with rectal location, non-mucinous adenocarcinoma and cancer stages IV and M1. overexpression is only associated with rectal location and non-mucinous adenocarcinoma. We conclude that is overexpressed in CRC from stage I, and its high expression is associated with metastatic process, probably through NOTCH pathway activation. Then, POFUT1 could represent a potential novel biomarker for CRC diagnosis.
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Abderrahman Maftah and Agnès Germot are considered co-last authors and contributed equally to this work.
ISSN:2072-6694
2072-6694
DOI:10.3390/cancers10110411