Genetic variability of the ABCC2 gene and clinical outcomes in pancreatic cancer patients. (9th January 2019)
- Record Type:
- Journal Article
- Title:
- Genetic variability of the ABCC2 gene and clinical outcomes in pancreatic cancer patients. (9th January 2019)
- Main Title:
- Genetic variability of the ABCC2 gene and clinical outcomes in pancreatic cancer patients
- Authors:
- Gentiluomo, Manuel
Puchalt García, Paula
Galeotti, Alice Alessandra
Talar-Wojnarowska, Renata
Tjaden, Christine
Tavano, Francesca
Strobel, Oliver
Kupcinskas, Juozas
Neoptolemos, John
Hegyi, Péter
Costello, Eithne
Pezzilli, Raffaele
Sperti, Cosimo
Lawlor, Rita T
Capurso, Gabriele
Szentesi, Andrea
Soucek, Pavel
Vodicka, Pavel
Lovecek, Martin
Hackert, Thilo
Cavestro, Giulia Martina
Milanetto, Anna Caterina
Canzian, Federico
Campa, Daniele - Abstract:
- Abstract: Pancreatic ductal adenocarcinoma (PDAC) has an extremely poor prognosis, caused by various factors, such as the aggressiveness of the disease, the limited therapeutic options and the lack of early detection and risk markers. The ATP binding cassette subfamily C member 2 (ABCC2) protein plays a critical role in response to various drugs and is differentially expressed in gemcitabine sensitive and resistant cells. Moreover, single nucleotide polymorphisms (SNPs) in the gene have been associated with differential outcomes and prognosis in several tumour types. The aim of this study was to investigate the possible association between SNPs in the ABCC2 gene and overall survival (OS) in PDAC patients. We analysed 12 polymorphisms, including tagging-SNPs covering all the genetic variability of the ABCC2 gene and genotyped them in 1415 PDAC patients collected within the Pancreatic Disease ReseArch (PANDoRA) consortium. We tested the association between ABCC2 SNPs and PDAC OS using Cox proportional hazard models. We analysed PDAC patients dividing them by stage and observed that the minor alleles of three SNPs showed an association with worse OS [rs3740067: hazard ratio (HR) = 3.29, 95% confidence interval (CI) = 1.56–6.97, P = 0.002; rs3740073: HR = 3.11, 95% CI = 1.52–6.38, P = 0.002 and rs717620: HR = 2.90, 95% CI = 1.41–5.95, P = 0.004, respectively] in stage I patients. In patients with more advanced PDAC, we did not observe any statistically significant association.Abstract: Pancreatic ductal adenocarcinoma (PDAC) has an extremely poor prognosis, caused by various factors, such as the aggressiveness of the disease, the limited therapeutic options and the lack of early detection and risk markers. The ATP binding cassette subfamily C member 2 (ABCC2) protein plays a critical role in response to various drugs and is differentially expressed in gemcitabine sensitive and resistant cells. Moreover, single nucleotide polymorphisms (SNPs) in the gene have been associated with differential outcomes and prognosis in several tumour types. The aim of this study was to investigate the possible association between SNPs in the ABCC2 gene and overall survival (OS) in PDAC patients. We analysed 12 polymorphisms, including tagging-SNPs covering all the genetic variability of the ABCC2 gene and genotyped them in 1415 PDAC patients collected within the Pancreatic Disease ReseArch (PANDoRA) consortium. We tested the association between ABCC2 SNPs and PDAC OS using Cox proportional hazard models. We analysed PDAC patients dividing them by stage and observed that the minor alleles of three SNPs showed an association with worse OS [rs3740067: hazard ratio (HR) = 3.29, 95% confidence interval (CI) = 1.56–6.97, P = 0.002; rs3740073: HR = 3.11, 95% CI = 1.52–6.38, P = 0.002 and rs717620: HR = 2.90, 95% CI = 1.41–5.95, P = 0.004, respectively] in stage I patients. In patients with more advanced PDAC, we did not observe any statistically significant association. Our results suggest that rs3740067, rs3740073 and rs717620 could be promising prognostic markers in stage I PDAC patients. Abstract : We investigated the possible association between single nucleotide polymorphisms (SNPs) in the ABCC2 gene and overall survival (OS) in pancreatic ductal adenocarcinoma patients and observed that the minor alleles of three SNPs showed an association with worse OS in stage I patients. … (more)
- Is Part Of:
- Carcinogenesis. Volume 40:Number 4(2019)
- Journal:
- Carcinogenesis
- Issue:
- Volume 40:Number 4(2019)
- Issue Display:
- Volume 40, Issue 4 (2019)
- Year:
- 2019
- Volume:
- 40
- Issue:
- 4
- Issue Sort Value:
- 2019-0040-0004-0000
- Page Start:
- 544
- Page End:
- 550
- Publication Date:
- 2019-01-09
- Subjects:
- Carcinogenesis -- Periodicals
Cancer -- Genetic aspects -- Periodicals
Cancer -- Prevention -- Periodicals
Cancer -- Periodicals
616.994071 - Journal URLs:
- http://carcin.oupjournals.org ↗
http://carcin.oxfordjournals.org ↗
http://www.ingenta.com/journals/browse/oup/carcin?mode=direct ↗
http://ukcatalogue.oup.com/ ↗
http://firstsearch.oclc.org ↗ - DOI:
- 10.1093/carcin/bgz006 ↗
- Languages:
- English
- ISSNs:
- 0143-3334
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3051.007000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 25088.xml