Literature DB >> 19663784

Reduced nicotinamide adenine dinucleotide (NADH) fluorescence for the detection of cell death.

Hsing-Wen Wang1, Yau-Huei Wei, Han-Wen Guo.   

Abstract

NADH/FAD fluorescence spectroscopy/imaging is an extremely useful tool to probe cellular metabolism and has been applied in the clinic such as early cancer detection. Recently, the potential of using NADH/FAD fluorescence as a biomarker to detect cell death has been investigated for development of cancer treatments with higher efficacy. This review aims to provide the updated information in cell death detection using the NADH/FAD fluorescence spectroscopy and imaging based on measurement of the intensity or lifetime of NADH or FAD fluorescence. The response of NADH fluorescence lifetime to metabolic perturbation, hypoxic environment, and anaerobic glycolysis (e.g., in precancerous tissues and stem cells) is also reviewed to discuss the nature and implications of the lifetime change of NADH fluorescence. Further studies are required to understand the actual site and mechanism of NADH binding of a specific death pathway for future successful in vivo detection of cell death using the NADH fluorescence lifetime.

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Year:  2009        PMID: 19663784     DOI: 10.2174/187152009789377718

Source DB:  PubMed          Journal:  Anticancer Agents Med Chem        ISSN: 1871-5206            Impact factor:   2.505


  14 in total

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Journal:  Tissue Eng Part C Methods       Date:  2011-12-14       Impact factor: 3.056

3.  Clinical research device for ovarian cancer detection by optical spectroscopy in the ultraviolet C-visible.

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Journal:  J Biomed Opt       Date:  2010 Sep-Oct       Impact factor: 3.170

4.  Mechanistic Analysis of Fluorescence Quenching of Reduced Nicotinamide Adenine Dinucleotide by Oxamate in Lactate Dehydrogenase Ternary Complexes.

Authors:  Huo-Lei Peng; Robert Callender
Journal:  Photochem Photobiol       Date:  2017-06-22       Impact factor: 3.421

5.  Wide-field medium-repetition-rate multiphoton microscopy reduces photodamage of living cells.

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Journal:  Biomed Opt Express       Date:  2016-03-24       Impact factor: 3.732

6.  Quantification of the Metabolic State in Cell-Model of Parkinson's Disease by Fluorescence Lifetime Imaging Microscopy.

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Journal:  Sci Rep       Date:  2016-01-13       Impact factor: 4.379

7.  Loss of function of miR-342-3p results in MCT1 over-expression and contributes to oncogenic metabolic reprogramming in triple negative breast cancer.

Authors:  Sandra L Romero-Cordoba; Sergio Rodriguez-Cuevas; Veronica Bautista-Pina; Antonio Maffuz-Aziz; Elvira D'Ippolito; Giulia Cosentino; Sara Baroni; Marilena V Iorio; Alfredo Hidalgo-Miranda
Journal:  Sci Rep       Date:  2018-08-16       Impact factor: 4.379

8.  Endogenous fluorescence signatures in living pluripotent stem cells change with loss of potency.

Authors:  Jayne M Squirrell; Jimmy J Fong; Carlos A Ariza; Amber Mael; Kassondra Meyer; Nirupama K Shevde; Avtar Roopra; Gary E Lyons; Timothy J Kamp; Kevin W Eliceiri; Brenda M Ogle
Journal:  PLoS One       Date:  2012-08-29       Impact factor: 3.240

9.  Protein-bound NAD(P)H Lifetime is Sensitive to Multiple Fates of Glucose Carbon.

Authors:  Joe T Sharick; Peter F Favreau; Amani A Gillette; Sophia M Sdao; Matthew J Merrins; Melissa C Skala
Journal:  Sci Rep       Date:  2018-04-03       Impact factor: 4.379

10.  A complex morphofunctional approach for zinc toxicity evaluation in rats.

Authors:  Gennadii Piavchenko; Alexander Alekseev; Olga Stelmashchuk; Evgeniya Seryogina; Evgeny Zherebtsov; Elena Kuznetsova; Andrey Dunaev; Yuri Volkov; Sergey Kuznetsov
Journal:  Heliyon       Date:  2020-04-21
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