2014
Tissue profiling by nanogold-mediated mass spectrometry and artificial neural networks in the mouse model of human primary hyperoxaluria 1
HOUŠKA, Jan; Eladia María PEÑA-MÉNDEZ; Juan Ramón HERNANDEZ-FERNAUD; Eduardo SALIDO; Aleš HAMPL et al.Basic information
Original name
Tissue profiling by nanogold-mediated mass spectrometry and artificial neural networks in the mouse model of human primary hyperoxaluria 1
Authors
HOUŠKA, Jan; Eladia María PEÑA-MÉNDEZ; Juan Ramón HERNANDEZ-FERNAUD; Eduardo SALIDO; Aleš HAMPL; Josef HAVEL and Petr VAŇHARA
Edition
Journal of Applied Biomedicine, České Budějovice, Faculty of Health and Social Care, University of South Bohemia, 2014, 1214-021X
Other information
Language
English
Type of outcome
Article in a journal
Field of Study
10406 Analytical chemistry
Country of publisher
Czech Republic
Confidentiality degree
is not subject to a state or trade secret
References:
Impact factor
Impact factor: 1.302
Marked to be transferred to RIV
Yes
RIV identification code
RIV/00216224:14110/14:00073478
Organization unit
Faculty of Medicine
UT WoS
EID Scopus
Keywords in English
MALDI-TOF mass spectrometry; Primary hyperoxaluria I; Artificial neural networks; Diagnostics; Tissue profiling
Tags
International impact, Reviewed
Changed: 18/1/2015 18:52, Ing. Mgr. Věra Pospíšilíková
Abstract
In the original language
Correct assessment of tissue histopathology is a necessary prerequisite for any clinical diagnosis. Nowadays, classical methods of histochemistry and immunohistochemistry are complemented by various techniques adopted from molecular biology and bioanalytical chemistry. Mass spectrometry profiling or imaging offered a new level of tissue visualization in the last decade, revealing hidden patterns of tissue molecular organization. It can be adapted to diagnostic purposes to improve decisions on complex and morphologically not apparent diagnoses. In this work, we successfully combined tissue profiling by mass spectrometry with analysis by artificial neural networks to classify normal and diseased liver and kidney tissues in a mouse model of primary hyperoxaluria type 1. Lack of the liver L-alanine: glyoxylate aminotransferase catalyzing conversion of L-alanine and glyoxylate to pyruvate and glycine causes accumulation of oxalate salts in various tissues, especially urinary system, resulting in compromised renal function and finally end stage renal disease. As the accumulation of oxalate salts alters chemical composition of affected tissues, it makes it available for examination by bioanalytical methods. We demonstrated that the direct tissue MALDI-TOF MS combined with neural computing offers an efficient tool for diagnosis of primary hyperoxaluria type I and potentially for other metabolic disorders altering chemical composition of tissues.
Links
| GA202/07/1669, research and development project |
| ||
| MSM0021622411, plan (intention) |
| ||
| MSM0021622430, plan (intention) |
| ||
| MUNI/M/0041/2013, interní kód MU |
|