Immunohistological expression of HIF‐1α, GLUT‐1, Bcl‐2 and Ki‐67 in consecutive biopsies during chemoradiotherapy in patients with rectal cancer |
| |
Authors: | Birgitte Mayland Havelund Flemming Brandt Sørensen John Pløen Jan Lindebjerg Karen‐Lise Garm Spindler Anders Jakobsen |
| |
Affiliation: | 1. Department of Oncology, Vejle Hospital, , Vejle;2. Institute of Regional Health Services Research, University of Southern Denmark, , Odense, Denmark;3. Department of Clinical Pathology, Vejle Hospital, , Vejle |
| |
Abstract: | The aim of this study was to describe the dynamics of HIF‐1α, GLUT‐1, Bcl‐2 and Ki‐67 during chemoradiotherapy (CRT) of rectal cancer, and to investigate the fluctuation of these biomarkers in relation to pathological response to CRT. The study included 86 patients with rectal adenocarcinoma receiving preoperative CRT (>50.4 Gy and Uracil/Tegafur). Immunohistological expressions of HIF‐1α, GLUT‐1, Bcl‐2 and Ki‐67 were investigated in biopsies taken before treatment, after 2, 4 and 6 weeks of CRT and in specimens from the operation. Decreasing expressions of HIF‐1α, Bcl‐2 and Ki‐67 were observed during CRT, whereas GLUT‐1 overall was unchanged. No significant changes of the markers were observed in the interval between CRT and surgery. A significant association was observed between the presence of residual carcinoma after 6 weeks of treatment and pathological response to CRT, but no association was seen between the fluctuations of any of the markers and response to CRT. This unique material containing specimens before, after and during CRT for rectal cancer demonstrated biological dynamics in HIF‐1α, Bcl‐2 and Ki‐67, but not GLUT‐1, expression during CRT, and a significant association was seen between the presence of residual carcinoma after 6 weeks of treatment and pathological response to CRT. |
| |
Keywords: | Bcl‐2 chemoradiotherapy glucose transporter type 1 hypoxia‐inducible factor 1 alpha Ki‐67 rectal neoplasm |
|
|