Lack of association of CD44-rs353630 and CHI3L2-rs684559 with pancreatic ductal adenocarcinoma survival
Jazyk angličtina Země Anglie, Velká Británie Médium electronic
Typ dokumentu časopisecké články, multicentrická studie, práce podpořená grantem
PubMed
33828170
PubMed Central
PMC8027406
DOI
10.1038/s41598-021-87130-0
PII: 10.1038/s41598-021-87130-0
Knihovny.cz E-zdroje
- MeSH
- antigeny CD44 genetika MeSH
- chitinasy genetika MeSH
- duktální karcinom slinivky břišní genetika mortalita MeSH
- jednonukleotidový polymorfismus MeSH
- Kaplanův-Meierův odhad MeSH
- lidé středního věku MeSH
- lidé MeSH
- nádorové biomarkery genetika MeSH
- nádory slinivky břišní genetika mortalita MeSH
- senioři MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- multicentrická studie MeSH
- práce podpořená grantem MeSH
- Názvy látek
- antigeny CD44 MeSH
- CD44 protein, human MeSH Prohlížeč
- CHI3L2 protein, human MeSH Prohlížeč
- chitinasy MeSH
- nádorové biomarkery MeSH
Although pancreatic ductal adenocarcinoma (PDAC) survival is poor, there are differences in patients' response to the treatments. Detection of predictive biomarkers explaining these differences is of the utmost importance. In a recent study two genetic markers (CD44-rs353630 and CHI3L2-rs684559) were reported to be associated with survival after PDAC resection. We attempted to replicate the associations in 1856 PDAC patients (685 resected with stage I/II) from the PANcreatic Disease ReseArch (PANDoRA) consortium. We also analysed the combined effect of the two genotypes in order to compare our results with what was previously reported. Additional stratified analyses considering TNM stage of the disease and whether the patients received surgery were also performed. We observed no statistically significant associations, except for the heterozygous carriers of CD44-rs353630, who were associated with worse OS (HR = 5.01; 95% CI 1.58-15.88; p = 0.006) among patients with stage I disease. This association is in the opposite direction of those reported previously, suggesting that data obtained in such small subgroups are hardly replicable and should be considered cautiously. The two polymorphisms combined did not show any statistically significant association. Our results suggest that the effect of CD44-rs353630 and CHI3L2-rs684559 cannot be generalized to all PDAC patients.
1st Department of Medicine University of Szeged Szeged Hungary
ARC Net Research Centre University of Verona Verona Italy
Department of Biology University of Pisa Via Derna 1 56126 Pisa Italy
Department of Digestive Tract Diseases Medical University of Lodz Lodz Poland
Department of Medicine Herlev and Gentofte Hospital Copenhagen University Hospital Herlev Denmark
Department of Medicine Medicina Di Laboratorio University of Padua Padua Italy
Department of Oncology Herlev and Gentofte Hospital Copenhagen University Hospital Herlev Denmark
Department of Surgery Erasmus Medical Center Erasmus University Rotterdam The Netherlands
Department of Surgery Gastroenterology Oncology Clinica Chirurgica University of Padua Padua Italy
Department of Surgery Rigshospitalet Copenhagen University Hospital Copenhagen Denmark
Gastroenterology Unit San Carlo Hospital Potenza Italy
Genomic Epidemiology Group German Cancer Research Center Heidelberg Germany
Institute for Translational Medicine Medical School University of Pécs Pecs Hungary
Laboratory of Biology Medical School National and Kapodistrian University of Athens Athens Greece
Sant'Andrea Hospital Faculty of Medicine and Psychology Sapienza University of Rome Rome Italy
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