In vivo molecular imaging of cervical neoplasia using acetic acid as biomarker

被引:30
作者
Balas, Costas [1 ,2 ]
Papoutsoglou, George [1 ]
Potirakis, Antonis [3 ]
机构
[1] Tech Univ Crete, Dept Elect & Comp Engn, Khania 73134, Greece
[2] IESL, FORTH, Iraklion 731110, Greece
[3] Tech Educ Inst Crete, Dept Appl Informat & Multimedia & Elect Engn, Khania 73134, Greece
关键词
cervical neoplasia; colposcopy; modeling; molecular imaging; scattering; screening;
D O I
10.1109/JSTQE.2007.913396
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
In this paper, a molecular imaging method employing acetic acid dilute solution as a biomarker is described. An interpretation of the biophysical processes that are involved in the biomarker-tissue interaction and are determining the in vivo measured dynamic scattering characteristics is presented. On the basis of this interpretation, a compartmental model of the epithelium is developed for predicting the epithelial transport phenomena that are expected to be correlated with the dynamic characteristics of the backscattered light. The model predictions have been compared with the experimental data obtained from patients with cervical neoplasia of different grade, with the aid of a specially developed imaging system. Comparisons confirmed the validity of the interpretation of the phenomenon, and particularly, the fact that dynamic scattering characteristics are largely determined by the intracellular proton concentration kinetics. In addition, the correlation of the latter with both structural and functional alterations, associated with cervical neoplasia development, has been predicted theoretically and confirmed experimentally. The established correlation enables the derivation of quantitative indices expressing disease-specific microstructural and functional alterations, from the in vivo measured dynamic optical characteristics. This highlights the potential of the developed imaging method and technology for the noninvasive diagnosis, guided therapeutics, and screening of cervical neoplasia.
引用
收藏
页码:29 / 42
页数:14
相关论文
共 66 条
[1]   The relationship between connexins, gap junctions, tissue architecture and tumour invasion, as studied in a novel in vitro model of HPV-16-associated cervical cancer progression [J].
Aasen, T ;
Hodgins, MB ;
Edward, M ;
Graham, SV .
ONCOGENE, 2003, 22 (39) :7969-7980
[2]  
ALLEMAIN GL, 1985, J BIOL CHEM, V260, P4877
[3]   A novel optical imaging method for the early detection, quantitative grading, and mapping of cancerous and precancerous lesions of cervix [J].
Balas, C .
IEEE TRANSACTIONS ON BIOMEDICAL ENGINEERING, 2001, 48 (01) :96-104
[4]  
BALAS C, 1998, SPIE OPTICAL BIOPSIE, V3568, P31
[5]   In vivo detection and staging of epithelial dysplasias and malignancies based on the quantitative assessment of acetic acid-tissue interaction kinetics [J].
Balas, CJ ;
Themelis, GC ;
Prokopakis, EP ;
Orfanudaki, I ;
Koumantakis, E ;
Helidonis, ES .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY, 1999, 53 (1-3) :153-157
[6]   Inhibition of Na+/H+ exchanger activity by an alkyl-lysophospholipid analogue in a human breast cancer cell line [J].
Besson, P ;
Gore, J ;
Vincent, E ;
Hoinard, C ;
Bougnoux, P .
BIOCHEMICAL PHARMACOLOGY, 1996, 51 (09) :1153-1158
[7]   INTRACELLULAR PH TRANSIENTS IN SQUID GIANT-AXONS CAUSED BY CO2, NH3, AND METABOLIC-INHIBITORS [J].
BORON, WF ;
DEWEER, P .
JOURNAL OF GENERAL PHYSIOLOGY, 1976, 67 (01) :91-112
[8]  
BOYER MJ, 1992, CANCER RES, V52, P4441
[10]  
Crum Christopher P, 2003, J Clin Oncol, V21, p224s, DOI 10.1200/JCO.2003.01.116