Molecular confocal laser endomicroscopy: A novel technique for in vivo cellular characterization of gastrointestinal lesions

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

Molecular confocal laser endomicroscopy : A novel technique for in vivo cellular characterization of gastrointestinal lesions. / Karstensen, John Gásdal; Klausen, Pia Helene; Saftoiu, Adrian; Vilmann, Peter.

I: World Journal of Gastroenterology, Bind 20, Nr. 24, 28.06.2014, s. 7794-800.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Karstensen, JG, Klausen, PH, Saftoiu, A & Vilmann, P 2014, 'Molecular confocal laser endomicroscopy: A novel technique for in vivo cellular characterization of gastrointestinal lesions', World Journal of Gastroenterology, bind 20, nr. 24, s. 7794-800. https://doi.org/10.3748/wjg.v20.i24.7794

APA

Karstensen, J. G., Klausen, P. H., Saftoiu, A., & Vilmann, P. (2014). Molecular confocal laser endomicroscopy: A novel technique for in vivo cellular characterization of gastrointestinal lesions. World Journal of Gastroenterology, 20(24), 7794-800. https://doi.org/10.3748/wjg.v20.i24.7794

Vancouver

Karstensen JG, Klausen PH, Saftoiu A, Vilmann P. Molecular confocal laser endomicroscopy: A novel technique for in vivo cellular characterization of gastrointestinal lesions. World Journal of Gastroenterology. 2014 jun. 28;20(24):7794-800. https://doi.org/10.3748/wjg.v20.i24.7794

Author

Karstensen, John Gásdal ; Klausen, Pia Helene ; Saftoiu, Adrian ; Vilmann, Peter. / Molecular confocal laser endomicroscopy : A novel technique for in vivo cellular characterization of gastrointestinal lesions. I: World Journal of Gastroenterology. 2014 ; Bind 20, Nr. 24. s. 7794-800.

Bibtex

@article{190b8106bd714469952ec49613a7907e,
title = "Molecular confocal laser endomicroscopy: A novel technique for in vivo cellular characterization of gastrointestinal lesions",
abstract = "While flexible endoscopy is essential for macroscopic evaluation, confocal laser endomicroscopy (CLE) has recently emerged as an endoscopic method enabling visualization at a cellular level. Two systems are currently available, one based on miniprobes that can be inserted via a conventional endoscope or via a needle guided by endoscopic ultrasound. The second system has a confocal microscope integrated into the distal part of an endoscope. By adding molecular probes like fluorescein conjugated antibodies or fluorescent peptides to this procedure (either topically or systemically administered during on-going endoscopy), a novel world of molecular evaluation opens up. The method of molecular CLE could potentially be used for estimating the expression of important receptors in carcinomas, subsequently resulting in immediate individualization of treatment regimens, but also for improving the diagnostic accuracy of endoscopic procedures by identifying otherwise invisible mucosal lesions. Furthermore, studies have shown that fluorescein labelled drugs can be used to estimate the affinity of the drug to a target organ, which probably can be correlated to the efficacy of the drug. However, several of the studies in this research field have been conducted in animal facilities or in vitro, while only a limited number of trials have actually been carried out in vivo. Therefore, safety issues still needs further evaluations. This review will present an overview of the implications and pitfalls, as well as future challenges of molecular CLE in gastrointestinal diseases.",
keywords = "Biological Markers, Endoscopes, Gastrointestinal, Endoscopy, Gastrointestinal, Gastrointestinal Diseases, Gastrointestinal Tract, Humans, Individualized Medicine, Microscopy, Confocal, Molecular Imaging, Patient Selection, Predictive Value of Tests, Prognosis",
author = "Karstensen, {John G{\'a}sdal} and Klausen, {Pia Helene} and Adrian Saftoiu and Peter Vilmann",
year = "2014",
month = jun,
day = "28",
doi = "10.3748/wjg.v20.i24.7794",
language = "English",
volume = "20",
pages = "7794--800",
journal = "World Chinese Journal of Digestology",
issn = "1009-3079",
publisher = "Baishideng Publishing Group Co., Limited",
number = "24",

}

RIS

TY - JOUR

T1 - Molecular confocal laser endomicroscopy

T2 - A novel technique for in vivo cellular characterization of gastrointestinal lesions

AU - Karstensen, John Gásdal

AU - Klausen, Pia Helene

AU - Saftoiu, Adrian

AU - Vilmann, Peter

PY - 2014/6/28

Y1 - 2014/6/28

N2 - While flexible endoscopy is essential for macroscopic evaluation, confocal laser endomicroscopy (CLE) has recently emerged as an endoscopic method enabling visualization at a cellular level. Two systems are currently available, one based on miniprobes that can be inserted via a conventional endoscope or via a needle guided by endoscopic ultrasound. The second system has a confocal microscope integrated into the distal part of an endoscope. By adding molecular probes like fluorescein conjugated antibodies or fluorescent peptides to this procedure (either topically or systemically administered during on-going endoscopy), a novel world of molecular evaluation opens up. The method of molecular CLE could potentially be used for estimating the expression of important receptors in carcinomas, subsequently resulting in immediate individualization of treatment regimens, but also for improving the diagnostic accuracy of endoscopic procedures by identifying otherwise invisible mucosal lesions. Furthermore, studies have shown that fluorescein labelled drugs can be used to estimate the affinity of the drug to a target organ, which probably can be correlated to the efficacy of the drug. However, several of the studies in this research field have been conducted in animal facilities or in vitro, while only a limited number of trials have actually been carried out in vivo. Therefore, safety issues still needs further evaluations. This review will present an overview of the implications and pitfalls, as well as future challenges of molecular CLE in gastrointestinal diseases.

AB - While flexible endoscopy is essential for macroscopic evaluation, confocal laser endomicroscopy (CLE) has recently emerged as an endoscopic method enabling visualization at a cellular level. Two systems are currently available, one based on miniprobes that can be inserted via a conventional endoscope or via a needle guided by endoscopic ultrasound. The second system has a confocal microscope integrated into the distal part of an endoscope. By adding molecular probes like fluorescein conjugated antibodies or fluorescent peptides to this procedure (either topically or systemically administered during on-going endoscopy), a novel world of molecular evaluation opens up. The method of molecular CLE could potentially be used for estimating the expression of important receptors in carcinomas, subsequently resulting in immediate individualization of treatment regimens, but also for improving the diagnostic accuracy of endoscopic procedures by identifying otherwise invisible mucosal lesions. Furthermore, studies have shown that fluorescein labelled drugs can be used to estimate the affinity of the drug to a target organ, which probably can be correlated to the efficacy of the drug. However, several of the studies in this research field have been conducted in animal facilities or in vitro, while only a limited number of trials have actually been carried out in vivo. Therefore, safety issues still needs further evaluations. This review will present an overview of the implications and pitfalls, as well as future challenges of molecular CLE in gastrointestinal diseases.

KW - Biological Markers

KW - Endoscopes, Gastrointestinal

KW - Endoscopy, Gastrointestinal

KW - Gastrointestinal Diseases

KW - Gastrointestinal Tract

KW - Humans

KW - Individualized Medicine

KW - Microscopy, Confocal

KW - Molecular Imaging

KW - Patient Selection

KW - Predictive Value of Tests

KW - Prognosis

U2 - 10.3748/wjg.v20.i24.7794

DO - 10.3748/wjg.v20.i24.7794

M3 - Journal article

C2 - 24976717

VL - 20

SP - 7794

EP - 7800

JO - World Chinese Journal of Digestology

JF - World Chinese Journal of Digestology

SN - 1009-3079

IS - 24

ER -

ID: 138144462