Faecal tumour M2 pyruvate kinase: a new, sensitive screening tool for colorectal cancer

被引:115
作者
Hardt, PD
Mazurek, S
Toepler, M
Schlierbach, P
Bretzel, RG
Eigenbrodt, E
Kloer, HU
机构
[1] Univ Giessen, Giessen Univ Hosp, Dept Med 3, D-35392 Giessen, Germany
[2] Univ Giessen, Giessen Univ Hosp, Policlin, D-35392 Giessen, Germany
[3] Univ Giessen, Fac Vet, Inst Biochem & Endocrinol, D-35392 Giessen, Germany
[4] Asklepios Clin, Dept Med, D-35423 Lich, Germany
[5] Asklepios Clin, Dept Surg, D-35423 Lich, Germany
关键词
tumour M2-PK; colorectal cancer; stool; tumour screening;
D O I
10.1038/sj.bjc.6602033
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Proliferating cells, especially tumour cells, express a special isoenzyme of pyruvate kinase, termed M2-PK, which can occur in a tetrameric form with a high affinity to its substrate, phosphoenolpyruvate (PEP), and in a dimeric form with a low PEP affinity. In tumour cells, the dimeric form is usually predominant and is therefore termed Tumour M2-PK. The levels of Tumour M2-PK within tumours and in EDTA-plasma correlate with staging and the ability of the tumour cells to metastasise. Since most colorectal tumours grow intraluminally, it appeared interesting to determine whether Tumour M2-PK is detectable in the faeces of tumour patients. Stool samples were tested by ELISA from controls without colorectal cancer and colorectal cancer patients. Whereas Tumour M2-PK levels were low in the control group (mean value+/-s.e.m.: 3.3+/-0.4, n=144), they were high in the case of colorectal cancer (56.1+/-15.3, n=60). At a cutoff value of 4 U ml(-1), the sensitivity was 73%. TNM and Dukes' classification of the tumours revealed a strong correlation between faecal Tumour M2-PK levels and staging. The determination of Tumour M2-PK in faeces provides a new promising screening tool for colorectal tumours.
引用
收藏
页码:980 / 984
页数:5
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