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Pregled bibliografske jedinice broj: 817000

IgG Glycome in colorectal Cancer


Vučković, Frano; Theodoratou, Evropi; Thaçi, Kujtim; Timofeeva, Maria; Vojta, Aleksandar; Štambuk, Jerko; Pučić-Baković, Maja; Rudd, Pauline M.; Đerek, Lovorka; Servis, Dražen et al.
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.

Citiraj ovu publikaciju:

Vučković, Frano; Theodoratou, Evropi; Thaçi, Kujtim; Timofeeva, Maria; Vojta, Aleksandar; Štambuk, Jerko; Pučić-Baković, Maja; Rudd, Pauline M.; Đerek, Lovorka; Servis, Dražen et al.
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)
Vučković, F., Theodoratou, E., Thaçi, K., Timofeeva, M., Vojta, A., Štambuk, J., Pučić-Baković, M., Rudd, P., Đerek, L. & Servis, D. (2016) IgG Glycome in colorectal Cancer. Clinical cancer research, 22 (12), 3078-3086 doi:10.1158/1078-0432.CCR-15-1867.
@article{article, author = {Vu\v{c}kovi\'{c}, Frano and Theodoratou, Evropi and Tha\c{c}i, Kujtim and Timofeeva, Maria and Vojta, Aleksandar and \v{S}tambuk, Jerko and Pu\v{c}i\'{c}-Bakovi\'{c}, Maja and Rudd, Pauline M. and \DJerek, Lovorka and Servis, Dra\v{z}en and Wennerstr\"{o}m, Annika and Farrington, Susan M. and Perola, Marcus and Aulchenko, Yurii and Dunlop, Malcolm G. and Campbell, Harry and Lauc, Gordan.}, year = {2016}, pages = {3078-3086}, DOI = {10.1158/1078-0432.CCR-15-1867}, keywords = {colorectal cancer, IgG, glycosylation}, journal = {Clinical cancer research}, doi = {10.1158/1078-0432.CCR-15-1867}, volume = {22}, number = {12}, issn = {1078-0432}, title = {IgG Glycome in colorectal Cancer}, keyword = {colorectal cancer, IgG, glycosylation} }
@article{article, author = {Vu\v{c}kovi\'{c}, Frano and Theodoratou, Evropi and Tha\c{c}i, Kujtim and Timofeeva, Maria and Vojta, Aleksandar and \v{S}tambuk, Jerko and Pu\v{c}i\'{c}-Bakovi\'{c}, Maja and Rudd, Pauline M. and \DJerek, Lovorka and Servis, Dra\v{z}en and Wennerstr\"{o}m, Annika and Farrington, Susan M. and Perola, Marcus and Aulchenko, Yurii and Dunlop, Malcolm G. and Campbell, Harry and Lauc, Gordan.}, year = {2016}, pages = {3078-3086}, DOI = {10.1158/1078-0432.CCR-15-1867}, keywords = {colorectal cancer, IgG, glycosylation}, journal = {Clinical cancer research}, doi = {10.1158/1078-0432.CCR-15-1867}, volume = {22}, number = {12}, issn = {1078-0432}, title = {IgG Glycome in colorectal cancer}, keyword = {colorectal cancer, IgG, glycosylation} }

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


Citati:





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