Detailed Information on Publication Record
2021
N-Glycome changes reflecting resistance to platinum-based chemotherapy in ovarian cancer
ZAHRADNÍKOVÁ, Martina, Ivana IHNATOVÁ, Erika LATTOVÁ, Lukáš UHRÍK, Eliška STUCHLÍKOVÁ et. al.Basic information
Original name
N-Glycome changes reflecting resistance to platinum-based chemotherapy in ovarian cancer
Authors
ZAHRADNÍKOVÁ, Martina (203 Czech Republic), Ivana IHNATOVÁ (703 Slovakia, belonging to the institution), Erika LATTOVÁ (703 Slovakia, guarantor, belonging to the institution), Lukáš UHRÍK (703 Slovakia), Eliška STUCHLÍKOVÁ (203 Czech Republic), Rudolf NENUTIL (203 Czech Republic), Dalibor VALÍK (203 Czech Republic), Monika NÁLEŽINSKÁ (203 Czech Republic), Josef CHOVANEC (203 Czech Republic), Zbyněk ZDRÁHAL (203 Czech Republic, belonging to the institution), Bořivoj VOJTĚŠEK (203 Czech Republic), Lenka HERNYCHOVÁ (203 Czech Republic) and Miloš NOVOTNÝ (840 United States of America)
Edition
JOURNAL OF PROTEOMICS, Elsevier, 2021, 1874-3919
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10608 Biochemistry and molecular biology
Country of publisher
Netherlands
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 3.855
RIV identification code
RIV/00216224:14740/21:00121165
Organization unit
Central European Institute of Technology
UT WoS
000597303500009
Keywords in English
Ovarian cancer; N-Glycans; MALDI-TOF-MS
Tags
International impact, Reviewed
Změněno: 10/10/2024 14:15, Ing. Martina Blahová
Abstract
V originále
A number of studies have reported aberrant glycosylation in connection with malignancy. Our investigation further expands on this topic through the examination of N-glycans, which could be associated with the resistance of advanced stage, high-grade non-mucinous ovarian cancer to platinum/taxane based chemotherapy. We used tissue samples of 83 ovarian cancer patients, randomly divided into two independent cohorts (basic and validation). Both groups involved either cases with/without postoperative tumor residue or the cases determined either resistant or sensitive to this chemotherapy. In the validation cohort, preoperative serum samples were also available. N-glycans released from tumors and sera were permethylated and analyzed by matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS). The MS analysis yielded a consecutive detection of 68 (tissue) and 63 (serum) N-glycan spectral signals. Eight of these were found to be differentially abundant in tissues of both independent cohorts including the cases with a postoperative cancer residue. One of these glycans was detected as differentially abundant in sera of the validation cohort. No statistically significant differences in intensities due to the same N-glycans were found in the cases without postoperative macroscopic residues in either the basic or validation cohort. From the biochemical point of view, the statistically significant N-glycans correspond to the structures carrying bisecting (terminal) GlcNAc residue and tetra-antennary structures with sialic acid and/or fucose residues. Among them, six tissue N-glycans could be considered potential markers connected with a resistance to chemotherapy in ovarian cancer patients. The prediction of primary resistance to standard chemotherapy may identify the group of patients suitable for alternative treatment strategies. Significance: Drug resistance has become a major impediment to a successful treatment of patients with advanced ovarian cancer. The glycomic measurements related to cancer are becoming increasingly popular in identification of the key molecules as potential diagnostic and prognostic indicators. Our report deals with identification of differences in N-glycosylation of proteins in tissue and serum samples from the individuals showing sensitivity or resistance to platinum/taxane-based chemotherapy. The detection sensitivity to chemotherapy is vitally important for these patients.
Links
EF15_003/0000469, research and development project |
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EF17_050/0008496, research and development project |
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LM2018121, research and development project |
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LM2018127, research and development project |
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90127, large research infrastructures |
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