Laurine Verset1, Joke Tommelein2, Xavier Moles Lopez3, Christine Decaestecker3, Tom Boterberg2, Elly De Vlieghere2, Isabelle Salmon4, Marc Mareel2, Marc Bracke2, Olivier De Wever5, Pieter Demetter6. 1. Department of Pathology, Erasme University Hospital, Université Libre de Bruxelles (ULB), Brussels, Belgium. 2. Laboratory of Experimental Cancer Research, Department of Radiation Oncology and Experimental Cancer Research, Universiteit Gent (UG), Ghent, Belgium. 3. DIAPATH-CMMI Center for Microscopy and Molecular Imaging, Gosselies, Belgium; Laboratories of Image, Signal Processing and Acoustics (LISA), ULB, Brussels, Belgium. 4. Department of Pathology, Erasme University Hospital, Université Libre de Bruxelles (ULB), Brussels, Belgium; DIAPATH-CMMI Center for Microscopy and Molecular Imaging, Gosselies, Belgium. 5. Laboratory of Experimental Cancer Research, Department of Radiation Oncology and Experimental Cancer Research, Universiteit Gent (UG), Ghent, Belgium. Electronic address: olivier.dewever@ugent.be. 6. Department of Pathology, Erasme University Hospital, Université Libre de Bruxelles (ULB), Brussels, Belgium. Electronic address: pieter.demetter@erasme.ulb.ac.be.
Abstract
BACKGROUND AND PURPOSE: Cancer-associated fibroblasts (CAFs) are increasingly recognised as promoters of tumour progression. It is poorly investigated whether cancer management protocols, such as neoadjuvant radio(chemo)therapy, have an impact on CAFs and, by consequence, on tumour progression. This prompted us to study the impact of neoadjuvant radio(chemo)therapy on the α-SMA/epithelial area ratio in rectal cancer, and the impact of this ratio on recurrence-free survival. MATERIAL AND METHODS: Immunohistochemistry for the CAF marker α-SMA and the proliferation marker Ki67 was performed on sections from 98 rectal cancers of which 62 had undergone neoadjuvant radio(chemo)therapy. RESULTS: Computer-assisted quantitative analysis showed that the α-SMA/neoplastic epithelial area ratio was higher after neoadjuvant therapy, and that rectal cancers with high α-SMA/epithelial area ratio had low proliferation rates. Interestingly, the α-SMA/epithelial area ratio was an adverse prognostic factor with regard to recurrence-free survival in univariate analysis. In addition, multivariate analysis showed that an α-SMA/epithelial area ratio above 1 provides an independent prognostic value associated with a poor recurrence-free survival. CONCLUSION: These results suggest that neoadjuvant treatment has an impact on CAFs in rectal cancer. The correlation of CAFs with decreased recurrence-free survival and abundant experimental data in the literature suggest that under certain circumstances, not yet very well understood, CAFs may favour tumour progression.
BACKGROUND AND PURPOSE:Cancer-associated fibroblasts (CAFs) are increasingly recognised as promoters of tumour progression. It is poorly investigated whether cancer management protocols, such as neoadjuvant radio(chemo)therapy, have an impact on CAFs and, by consequence, on tumour progression. This prompted us to study the impact of neoadjuvant radio(chemo)therapy on the α-SMA/epithelial area ratio in rectal cancer, and the impact of this ratio on recurrence-free survival. MATERIAL AND METHODS: Immunohistochemistry for the CAF marker α-SMA and the proliferation marker Ki67 was performed on sections from 98 rectal cancers of which 62 had undergone neoadjuvant radio(chemo)therapy. RESULTS: Computer-assisted quantitative analysis showed that the α-SMA/neoplastic epithelial area ratio was higher after neoadjuvant therapy, and that rectal cancers with high α-SMA/epithelial area ratio had low proliferation rates. Interestingly, the α-SMA/epithelial area ratio was an adverse prognostic factor with regard to recurrence-free survival in univariate analysis. In addition, multivariate analysis showed that an α-SMA/epithelial area ratio above 1 provides an independent prognostic value associated with a poor recurrence-free survival. CONCLUSION: These results suggest that neoadjuvant treatment has an impact on CAFs in rectal cancer. The correlation of CAFs with decreased recurrence-free survival and abundant experimental data in the literature suggest that under certain circumstances, not yet very well understood, CAFs may favour tumour progression.
Authors: Natacha Leroi; François Lallemand; Philippe Coucke; Agnès Noel; Philippe Martinive Journal: Front Pharmacol Date: 2016-03-30 Impact factor: 5.810
Authors: Thomas Gevaert; Yves-Rémi Van Eycke; Thomas Vanden Broeck; Hein Van Poppel; Isabelle Salmon; Sandrine Rorive; Frank Claessens; Dirk De Ridder; Christine Decaestecker; Steven Joniau Journal: Sci Rep Date: 2018-09-25 Impact factor: 4.379