High throughput assessment of cells and tissues: Bayesian classification of spectral metrics from infrared vibrational spectroscopic imaging data

被引:111
作者
Bhargava, Rohit
Fernandez, Daniel C.
Hewitt, Stephen M.
Levin, Ira W. [1 ]
机构
[1] NIDDK, Chem Phys Lab, NIH, Bethesda, MD 20892 USA
[2] Univ Illinois, Dept Bioengn, Urbana, IL 61801 USA
[3] Univ Illinois, Beckman Inst Adv Sci & Technol, Urbana, IL 61801 USA
[4] NCI, Tissue Array Res Program, Pathol Lab, Ctr Canc Res,NIH, Bethesda, MD 20892 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 2006年 / 1758卷 / 07期
关键词
Fourier transform infrared (FTIR) spectroscopy; imaging; biophotonics; prostate; tissue microarray; Bayesian statistics; likelihood classification; discriminant; cancer; histology; pathology; ROC;
D O I
10.1016/j.bbamem.2006.05.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Vibrational spectroscopy allows a visualization of tissue constituents based on intrinsic chemical composition and provides a potential route to obtaining diagnostic markers of diseases. Characterizations utilizing infrared vibrational spectroscopy, in particular, are conventionally low throughput in data acquisition, generally lacking in spatial resolution with the resulting data requiring intensive numerical computations to extract information. These factors impair the ability of infrared spectroscopic measurements to represent accurately the spatial heterogeneity in tissue, to incorporate robustly the diversity introduced by patient cohorts or preparative artifacts and to validate developed protocols in large population studies. In this manuscript, we demonstrate a combination of Fourier transform infrared (FTIR) spectroscopic imaging, tissue microarrays (TMAs) and fast numerical analysis as a paradigm for the rapid analysis, development and validation of high throughput spectroscopic characterization protocols. We provide an extended description of the data treatment algorithm and a discussion of various factors that may influence decision-making using this approach. Finally, a number of prostate tissue biopsies, arranged in an array modality, are employed to examine the efficacy of this approach in histologic recognition of epithelial cell polarization in patients displaying a variety of normal, malignant and hyperplastic conditions. An index of epithelial cell polarization, derived from a combined spectral and morphological analysis, is determined to be a potentially useful diagnostic marker. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:830 / 845
页数:16
相关论文
共 49 条
[11]   Resolution limits for infrared microspectroscopy explored with synchrotron radiation [J].
Carr, GL .
REVIEW OF SCIENTIFIC INSTRUMENTS, 2001, 72 (03) :1613-1619
[12]  
CARR GL, 2005, MULTICHANNEL DETECTI, P56
[13]  
Caspers PJ, 1998, BIOSPECTROSCOPY, V4, pS31, DOI 10.1002/(SICI)1520-6343(1998)4:5+<S31::AID-BSPY4>3.0.CO
[14]  
2-M
[15]   A decade of vibrational micro-spectroscopy of human cells and tissue (1994-2004) [J].
Diem, M ;
Romeo, M ;
Boydston-White, S ;
Miljkovic, M ;
Matthäus, C .
ANALYST, 2004, 129 (10) :880-885
[16]  
Eysel HH, 1997, BIOSPECTROSCOPY, V3, P161, DOI 10.1002/(SICI)1520-6343(1997)3:2<161::AID-BSPY9>3.0.CO
[17]  
2-A
[18]   Infrared spectroscopic imaging for histopathologic recognition [J].
Fernandez, DC ;
Bhargava, R ;
Hewitt, SM ;
Levin, IW .
NATURE BIOTECHNOLOGY, 2005, 23 (04) :469-474
[19]   A study of cytokinetic and motile prostate cancer cells using synchrotron-based FTIR micro spectroscopic imaging [J].
Gazi, E ;
Dwyer, J ;
Lockyer, NP ;
Miyan, J ;
Gardner, P ;
Hart, CA ;
Brown, MD ;
Clarke, NW .
VIBRATIONAL SPECTROSCOPY, 2005, 38 (1-2) :193-201
[20]   Water and protein structure in photoaged and chronically aged skin [J].
Gniadecka, M ;
Nielsen, OF ;
Wessel, S ;
Heidenheim, M ;
Christensen, DH ;
Wulf, HC .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1998, 111 (06) :1129-1133