Dihydropyrimidine Dehydrogenase mRNA Expression in Peripheral Blood of Rectal Cancer Patients is Significantly Associated With Residual Tumor and Distant Metastases Following Resection

被引:3
作者
Hoffmann, Andreas-Claudius [1 ,2 ]
Brabender, Jan [1 ]
Metzger, Ralf [1 ]
Ling, Fredericke [1 ]
Warnecke-Eberz, Ute [1 ]
Lurje, Georg [1 ]
Hoelscher, Arnulf H. [1 ]
Schneider, Paul M. [3 ]
Vallboehmer, Daniel [1 ]
机构
[1] Univ Cologne, Dept Gen Visceral & Canc Surg, D-50931 Cologne, Germany
[2] Univ Hosp Essen, W German Canc Ctr, Dept Med Canc Res, Essen, Germany
[3] Univ Zurich Hosp, Dept Visceral & Transplantat Surg, CH-8091 Zurich, Switzerland
关键词
DPD; TS; mRNA; blood; colorectal cancer; THYMIDYLATE SYNTHASE; CARCINOMA; RHYTHM; DPD;
D O I
10.1002/jso.21233
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Background: DPD and TS expression have been shown to correlate with response of 5-FU based chemotherapy in colorectal cancer tissue. Little is known about mRNA expression levels of TS and DPD in peripheral blood. The goals of this study were to test the feasibility of DPD and TS detection in blood and their associations to TNM staging and complete surgical resection. Methods: Whole blood was drawn I day pre- and 10 days post-operatively from 23 patients with rectal cancer. Either adjuvant (n = 15) or neoadjuvant (n = 8) treatment was performed. Tumor cells were enriched from whole blood by density gradient centrifugation prior to extraction of total cellular RNA and subsequent direct quantitative reverse transcriptase-PCR assays. Results: DPD was detectable in 21/23 patients (91.3%) and TS in 14/23 (61.7%). Stepwise multiple linear regression models showed a significant association of DPD expression with distant metastases (P = 0.004) and residual tumor categories (P = 0.03). Conclusions: Quantitative analysis of TS and DPD mRNA expression in peripheral blood of rectal cancer patients is technically feasible. DPD expression levels appear to be associated with residual tumor categories and might serve as a molecular marker for complete tumor resection. Larger studies seem to be warranted to scrutinize our hypothesis. J. Surg. Oncol. 2009;99:296-301. (C) 2009 Wiley-Liss, Inc.
引用
收藏
页码:296 / 301
页数:6
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