Fluorescence spectroscopy as a potential metabonomic tool for early detection of colorectal cancer

被引:42
作者
Lawaetz, Anders Juul [1 ]
Bro, Rasmus [1 ]
Kamstrup-Nielsen, Maja [1 ]
Christensen, Ib Jarle [2 ]
Jorgensen, Lars N. [3 ]
Nielsen, Hans J. [4 ]
机构
[1] Univ Copenhagen, Fac Life Sci, Dept Food Sci Qual & Technol, DK-1958 Frederiksberg C, Denmark
[2] Rigshosp, Finsen Lab, DK-2100 Copenhagen, Denmark
[3] Univ Copenhagen, Bispebjerg Hosp, Dept Surg, Copenhagen, Denmark
[4] Copenhagen Univ Hosp Hvidovre, Dept Surg Gastroenterol, Hvidovre, Denmark
关键词
Fluorescence spectroscopy; Colorectal cancer; Chemometrics; PARAFAC; Metabonomics; BLOOD-PLASMA; ULTRAVIOLET FLUORESCENCE; TRYPTOPHAN FLUORESCENCE; SERUM; DIAGNOSIS; DISCRIMINATION; CHEMOMETRICS; TOPOGRAPHY; BIOMARKERS; COMPONENTS;
D O I
10.1007/s11306-011-0310-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Fluorescence spectroscopy Excitation Emission Matrix (EEM) measurements were applied on human blood plasma samples from a case control study on colorectal cancer. Samples were collected before large bowel endoscopy and included patients with colorectal cancer or with adenomas, and from individuals with other non malignant findings or no findings (N = 308). The objective of the study was to explore the possibilities for applying fluorescence spectroscopy as a tool for detection of colorectal cancer. Parallel Factor Analysis (PARAFAC) was applied to decompose the fluorescence EEMs into estimates of the underlying fluorophores in the sample. Both the pooled score matrix from PARAFAC, holding the relative concentrations of the derived components, and the raw unfolded spectra were used as basis for discrimination models between cancer and the various controls. Both methods gave test set validated sensitivity and specificity values around 0.75 between cancer and controls, and poor discriminations between the various controls. The PARAFAC solution gave better options for analyzing the chemical mechanisms behind the discrimination, and revealed a blue shift in tryptophan emission in the cancer patients, a result that supports previous findings. The present findings show how fluorescence spectroscopy and chemometrics can help in cancer diagnostics, and with PARAFAC fluorescence spectroscopy can be a potential metabonomic tool.
引用
收藏
页码:S111 / S121
页数:11
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