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Experimental and population-based studies on colorectal cancer - Thymidine phosphorylase as a potential biomarker

Abstract
Background: Colorectal cancer (CRC) is one of the most common malignancies, and the only reliable treatment option for cure is surgery. Method: Quantitative real-time polymerase chain reaction was used to analyze the gene expression of the enzyme thymidine phosphorylase (TP), which was related to prognostic factors (paper I, n=254), evaluated as a predictive factor (paper III, n=125), and assessed by change of treatment (paper II, n=28). Data from the Swedish Colorectal Cancer Registry were retrieved and analyzed in order to assess adherence to present clinical guidelines (n=34,000). Results: In stage III CRC, TP analyzed in tumor tissue correlated with lymph node staging, with higher expression levels relating to a greater number of positive nodes and a worse N-stage. Higher TP expression was also associated with a worse histological tumor grade. Rectal cancer exhibited significantly higher TP expression in mucosa and tumor tissue compared to colon cancer. There was a significant increase of TP gene expression when comparing rectal cancer biopsies before and after radiotherapy. In addition, a decrease in TP levels was noted after chemotherapy. In patients with metastatic CRC, time to progression was significantly longer in patients with high TP expression, but there was no correlation to tumor response rate or palliative survival. The factors associated with adherence to guideline treatment in colon cancer stage III patients were lower age, less comorbidity, worse N-stage, and presence of a multidisciplinary team conference. One-third of the patients started their adjuvant chemotherapy more than eight weeks after surgery. Conclusion: TP may be useful in prognostic and predictive situations. TP is affected by radiotherapy, which might be used in clinical settings. However, there are conflicting results, and TP and the methods of analyzing TP need to be evaluated further in larger studies. The adherence to guideline treatment in colon cancer stage III is acceptable in younger and healthier patients. In addition, there is scope for shortening the waiting time until the start of chemotherapy.
Parts of work
I. Elinor Bexe Lindskog, Yvonne Wettergren , Elisabeth Odin , Bengt Gustavsson, Kristoffer Derwinger Thymidine phosphorylase gene expression in stage III colorectal cancer Clin Med Insights Oncol. 2012; 6: 347-353 ::PMID::23115484
 
II. Kristoffer Derwinger, Elinor Bexe Lindskog, Erik Palmqvist, Yvonne Wettergren Changes in thymidine phosphorylase gene expression related to treatment of rectal cancer Anticancer Res. 2013; 33(6): 2447-51 ::PMID::23749894
 
III. Elinor Bexe Lindskog, Kristoffer Derwinger, Bengt Gustavsson, Peter Falk, Yvonne Wettergren Thymidine phosphorylase expression is associated with time to progression in patients with metastatic colorectal cancer BMC Clin Pathol. 2014; 14: 25 ::PMID::24936150
 
IV. Elinor Bexe Lindskog, Katrín Ásta Gunnarsdóttir, Kristoffer Derwinger, Yvonne Wettergren, Bengt Glimelius, Karl Kodeda A population-based cohort study on adherence to practice guidelines for adjuvant chemotherapy in colorectal cancer Submitted for publication
 
Degree
Doctor of Philosophy (Medicine)
University
University of Gothenburg. Sahlgrenska Academy
Institution
Institute of Clincial Sciences. Department of Surgery
Disputation
Fredagen 26 september 2014 kl 09.00, stora aulan, centralkliniken, Sahlgrenska Universitetssjukhus/Östra.
Date of defence
2014-09-26
E-mail
elinor.bexe-lindskog@surgery.gu.se
URI
http://hdl.handle.net/2077/35950
Collections
  • Doctoral Theses / Doktorsavhandlingar Institutionen för kliniska vetenskaper
  • Doctoral Theses from Sahlgrenska Academy
  • Doctoral Theses from University of Gothenburg / Doktorsavhandlingar från Göteborgs universitet
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Thesis frame (32.43Mb)
Abstract (194.6Kb)
Date
2014-09-05
Author
Bexe Lindskog, Elinor
Keywords
colorectal cancer
thymidine phosphorylase
chemotherapy, adjuvant
biological markers
prognosis
practice guidelines
radiotherapy
Publication type
Doctoral thesis
ISBN
978-91-628-9086-5 (tryckt)
978-91-628-9092-6 (pdf)
Language
eng
Metadata
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