Expression of Transketolase like gene 1 (<it>TKTL1</it>) predicts disease-free survival in patients with locally advanced rectal cancer receiving neoadjuvant chemoradiotherapy

<p>Abstract</p> <p>Background</p> <p>For patients with locally advanced rectal cancer (LARC) neoadjuvant chemoradiotherapy is recommended as standard therapy. So far, no predictive or prognostic molecular factors for patients undergoing multimodal treatment are establis...

Full description

Bibliographic Details
Main Authors: Hofmann Wolf-Karsten, Wenz Frederik, Post Stefan, Kienle Peter, Kähler Georg, Gencer Deniz, Bohn Beatrice, Ströbel Philipp, Horisberger Karoline, Schwaab Juliana, Hofheinz Ralf-Dieter, Erben Philipp
Format: Article
Language:English
Published: BMC 2011-08-01
Series:BMC Cancer
Subjects:
Online Access:http://www.biomedcentral.com/1471-2407/11/363
id doaj-0f9fba290ee54c998892f1c301393522
record_format Article
spelling doaj-0f9fba290ee54c998892f1c3013935222020-11-24T21:25:00ZengBMCBMC Cancer1471-24072011-08-0111136310.1186/1471-2407-11-363Expression of Transketolase like gene 1 (<it>TKTL1</it>) predicts disease-free survival in patients with locally advanced rectal cancer receiving neoadjuvant chemoradiotherapyHofmann Wolf-KarstenWenz FrederikPost StefanKienle PeterKähler GeorgGencer DenizBohn BeatriceStröbel PhilippHorisberger KarolineSchwaab JulianaHofheinz Ralf-DieterErben Philipp<p>Abstract</p> <p>Background</p> <p>For patients with locally advanced rectal cancer (LARC) neoadjuvant chemoradiotherapy is recommended as standard therapy. So far, no predictive or prognostic molecular factors for patients undergoing multimodal treatment are established. Increased angiogenesis and altered tumour metabolism as adaption to hypoxic conditions in cancers play an important role in tumour progression and metastasis. Enhanced expression of Vascular-endothelial-growth-factor-receptor <it>(VEGF-R</it>) and Transketolase-like-1 (<it>TKTL1</it>) are related to hypoxic conditions in tumours. In search for potential prognostic molecular markers we investigated the expression of <it>VEGFR-1</it>, <it>VEGFR-2 </it>and <it>TKTL1 </it>in patients with LARC treated with neoadjuvant chemoradiotherapy and cetuximab.</p> <p>Methods</p> <p>Tumour and corresponding normal tissue from pre-therapeutic biopsies of 33 patients (m: 23, f: 10; median age: 61 years) with LARC treated in phase-I and II trials with neoadjuvant chemoradiotherapy (cetuximab, irinotecan, capecitabine in combination with radiotherapy) were analysed by quantitative PCR.</p> <p>Results</p> <p>Significantly higher expression of <it>VEGFR-1/2 </it>was found in tumour tissue in pre-treatment biopsies as well as in resected specimen after neoadjuvant chemoradiotherapy compared to corresponding normal tissue. High <it>TKTL1 </it>expression significantly correlated with disease free survival. None of the markers had influence on early response parameters such as tumour regression grading. There was no correlation of gene expression between the investigated markers.</p> <p>Conclusion</p> <p>High <it>TKTL-1 </it>expression correlates with poor prognosis in terms of 3 year disease-free survival in patients with LARC treated with intensified neoadjuvant chemoradiotherapy and may therefore serve as a molecular prognostic marker which should be further evaluated in randomised clinical trials.</p> http://www.biomedcentral.com/1471-2407/11/363hypoxiaradiochemotherapyrectal cancer<it>TKTL1</it><it>VEGFR-1/2</it>
collection DOAJ
language English
format Article
sources DOAJ
author Hofmann Wolf-Karsten
Wenz Frederik
Post Stefan
Kienle Peter
Kähler Georg
Gencer Deniz
Bohn Beatrice
Ströbel Philipp
Horisberger Karoline
Schwaab Juliana
Hofheinz Ralf-Dieter
Erben Philipp
spellingShingle Hofmann Wolf-Karsten
Wenz Frederik
Post Stefan
Kienle Peter
Kähler Georg
Gencer Deniz
Bohn Beatrice
Ströbel Philipp
Horisberger Karoline
Schwaab Juliana
Hofheinz Ralf-Dieter
Erben Philipp
Expression of Transketolase like gene 1 (<it>TKTL1</it>) predicts disease-free survival in patients with locally advanced rectal cancer receiving neoadjuvant chemoradiotherapy
BMC Cancer
hypoxia
radiochemotherapy
rectal cancer
<it>TKTL1</it>
<it>VEGFR-1/2</it>
author_facet Hofmann Wolf-Karsten
Wenz Frederik
Post Stefan
Kienle Peter
Kähler Georg
Gencer Deniz
Bohn Beatrice
Ströbel Philipp
Horisberger Karoline
Schwaab Juliana
Hofheinz Ralf-Dieter
Erben Philipp
author_sort Hofmann Wolf-Karsten
title Expression of Transketolase like gene 1 (<it>TKTL1</it>) predicts disease-free survival in patients with locally advanced rectal cancer receiving neoadjuvant chemoradiotherapy
title_short Expression of Transketolase like gene 1 (<it>TKTL1</it>) predicts disease-free survival in patients with locally advanced rectal cancer receiving neoadjuvant chemoradiotherapy
title_full Expression of Transketolase like gene 1 (<it>TKTL1</it>) predicts disease-free survival in patients with locally advanced rectal cancer receiving neoadjuvant chemoradiotherapy
title_fullStr Expression of Transketolase like gene 1 (<it>TKTL1</it>) predicts disease-free survival in patients with locally advanced rectal cancer receiving neoadjuvant chemoradiotherapy
title_full_unstemmed Expression of Transketolase like gene 1 (<it>TKTL1</it>) predicts disease-free survival in patients with locally advanced rectal cancer receiving neoadjuvant chemoradiotherapy
title_sort expression of transketolase like gene 1 (<it>tktl1</it>) predicts disease-free survival in patients with locally advanced rectal cancer receiving neoadjuvant chemoradiotherapy
publisher BMC
series BMC Cancer
issn 1471-2407
publishDate 2011-08-01
description <p>Abstract</p> <p>Background</p> <p>For patients with locally advanced rectal cancer (LARC) neoadjuvant chemoradiotherapy is recommended as standard therapy. So far, no predictive or prognostic molecular factors for patients undergoing multimodal treatment are established. Increased angiogenesis and altered tumour metabolism as adaption to hypoxic conditions in cancers play an important role in tumour progression and metastasis. Enhanced expression of Vascular-endothelial-growth-factor-receptor <it>(VEGF-R</it>) and Transketolase-like-1 (<it>TKTL1</it>) are related to hypoxic conditions in tumours. In search for potential prognostic molecular markers we investigated the expression of <it>VEGFR-1</it>, <it>VEGFR-2 </it>and <it>TKTL1 </it>in patients with LARC treated with neoadjuvant chemoradiotherapy and cetuximab.</p> <p>Methods</p> <p>Tumour and corresponding normal tissue from pre-therapeutic biopsies of 33 patients (m: 23, f: 10; median age: 61 years) with LARC treated in phase-I and II trials with neoadjuvant chemoradiotherapy (cetuximab, irinotecan, capecitabine in combination with radiotherapy) were analysed by quantitative PCR.</p> <p>Results</p> <p>Significantly higher expression of <it>VEGFR-1/2 </it>was found in tumour tissue in pre-treatment biopsies as well as in resected specimen after neoadjuvant chemoradiotherapy compared to corresponding normal tissue. High <it>TKTL1 </it>expression significantly correlated with disease free survival. None of the markers had influence on early response parameters such as tumour regression grading. There was no correlation of gene expression between the investigated markers.</p> <p>Conclusion</p> <p>High <it>TKTL-1 </it>expression correlates with poor prognosis in terms of 3 year disease-free survival in patients with LARC treated with intensified neoadjuvant chemoradiotherapy and may therefore serve as a molecular prognostic marker which should be further evaluated in randomised clinical trials.</p>
topic hypoxia
radiochemotherapy
rectal cancer
<it>TKTL1</it>
<it>VEGFR-1/2</it>
url http://www.biomedcentral.com/1471-2407/11/363
work_keys_str_mv AT hofmannwolfkarsten expressionoftransketolaselikegene1ittktl1itpredictsdiseasefreesurvivalinpatientswithlocallyadvancedrectalcancerreceivingneoadjuvantchemoradiotherapy
AT wenzfrederik expressionoftransketolaselikegene1ittktl1itpredictsdiseasefreesurvivalinpatientswithlocallyadvancedrectalcancerreceivingneoadjuvantchemoradiotherapy
AT poststefan expressionoftransketolaselikegene1ittktl1itpredictsdiseasefreesurvivalinpatientswithlocallyadvancedrectalcancerreceivingneoadjuvantchemoradiotherapy
AT kienlepeter expressionoftransketolaselikegene1ittktl1itpredictsdiseasefreesurvivalinpatientswithlocallyadvancedrectalcancerreceivingneoadjuvantchemoradiotherapy
AT kahlergeorg expressionoftransketolaselikegene1ittktl1itpredictsdiseasefreesurvivalinpatientswithlocallyadvancedrectalcancerreceivingneoadjuvantchemoradiotherapy
AT gencerdeniz expressionoftransketolaselikegene1ittktl1itpredictsdiseasefreesurvivalinpatientswithlocallyadvancedrectalcancerreceivingneoadjuvantchemoradiotherapy
AT bohnbeatrice expressionoftransketolaselikegene1ittktl1itpredictsdiseasefreesurvivalinpatientswithlocallyadvancedrectalcancerreceivingneoadjuvantchemoradiotherapy
AT strobelphilipp expressionoftransketolaselikegene1ittktl1itpredictsdiseasefreesurvivalinpatientswithlocallyadvancedrectalcancerreceivingneoadjuvantchemoradiotherapy
AT horisbergerkaroline expressionoftransketolaselikegene1ittktl1itpredictsdiseasefreesurvivalinpatientswithlocallyadvancedrectalcancerreceivingneoadjuvantchemoradiotherapy
AT schwaabjuliana expressionoftransketolaselikegene1ittktl1itpredictsdiseasefreesurvivalinpatientswithlocallyadvancedrectalcancerreceivingneoadjuvantchemoradiotherapy
AT hofheinzralfdieter expressionoftransketolaselikegene1ittktl1itpredictsdiseasefreesurvivalinpatientswithlocallyadvancedrectalcancerreceivingneoadjuvantchemoradiotherapy
AT erbenphilipp expressionoftransketolaselikegene1ittktl1itpredictsdiseasefreesurvivalinpatientswithlocallyadvancedrectalcancerreceivingneoadjuvantchemoradiotherapy
_version_ 1725985429458518016