Pregled bibliografske jedinice broj: 817000
IgG Glycome in colorectal Cancer
IgG Glycome in colorectal Cancer // Clinical cancer research, 22 (2016), 12; 3078-3086 doi:10.1158/1078-0432.CCR-15-1867 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 817000 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
IgG Glycome in colorectal Cancer
(IgG Glycome in colorectal cancer)
Autori
Vučković, Frano ; Theodoratou, Evropi ; Thaçi, Kujtim ; Timofeeva, Maria ; Vojta, Aleksandar ; Štambuk, Jerko ; Pučić-Baković, Maja ; Rudd, Pauline M. ; Đerek, Lovorka ; Servis, Dražen ; Wennerström, Annika ; Farrington, Susan M. ; Perola, Marcus ; Aulchenko, Yurii ; Dunlop, Malcolm G. ; Campbell, Harry ; Lauc, Gordan.
Izvornik
Clinical cancer research (1078-0432) 22
(2016), 12;
3078-3086
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
colorectal cancer ; IgG ; glycosylation
Sažetak
Alternative glycosylation has significant structural and functional consequences on IgG and consequently also on cancer immunosurveillance. Because of technological limitations, the effects of highly heritable individual variations and the differences in the dynamics of changes in IgG glycosylation on colorectal cancer were never investigated before. Using recently developed high-throughput UPLC technology for IgG glycosylation analysis, we analyzed IgG glycome composition in 760 patients with colorectal cancer and 538 matching controls. Effects of surgery were evaluated in 28 patients sampled before and three times after surgery. A predictive model was built using regularized logistic regression and evaluated using a 10-cross validation procedure. Furthermore, IgG glycome composition was analyzed in 39 plasma samples collected before initial diagnosis of colorectal cancer. We have found that colorectal cancer associates with decrease in IgG galactosylation, IgG sialylation and increase in core-fucosylation of neutral glycans with concurrent decrease of core-fucosylation of sialylated glycans. Although a model based on age and sex did not show discriminative power (AUC = 0.499), the addition of glycan variables into the model considerably increased the discriminative power of the model (AUC = 0.755). However, none of these differences were significant in the small set of samples collected before the initial diagnosis. Considering the functional relevance of IgG glycosylation for both tumor immunosurveillance and clinical efficacy of therapy with mAbs, individual variation in IgG glycosylation may turn out to be important for prediction of disease course or the choice of therapy, thus warranting further, more detailed studies of IgG glycosylation in colorectal cancer.
Izvorni jezik
Engleski
Znanstvena područja
Biologija, Temeljne medicinske znanosti
POVEZANOST RADA
Ustanove:
Farmaceutsko-biokemijski fakultet, Zagreb,
Klinička bolnica "Merkur",
Prirodoslovno-matematički fakultet, Zagreb,
GENOS d.o.o.
Profili:
JERKO ŠTAMBUK
(autor)
Gordan Lauc
(autor)
Dražen Servis
(autor)
Lovorka Đerek
(autor)
Aleksandar Vojta
(autor)
Maja Pučić Baković
(autor)
Poveznice na cjeloviti tekst rada:
doi clincancerres.aacrjournals.org clincancerres.aacrjournals.orgCitiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE