Literature DB >> 27895979

Optical redox ratio identifies metastatic potential-dependent changes in breast cancer cell metabolism.

Kinan Alhallak1, Lisa G Rebello1, Timothy J Muldoon1, Kyle P Quinn1, Narasimhan Rajaram1.   

Abstract

The development of prognostic indicators of breast cancer metastatic risk could reduce the number of patients receiving chemotherapy for tumors with low metastatic potential. Recent evidence points to a critical role for cell metabolism in driving breast cancer metastasis. Endogenous fluorescence intensity of nicotinamide adenine dinucleotide (NADH) and flavin adenine dinucleotide (FAD) can provide a label-free method for assessing cell metabolism. We report the optical redox ratio of FAD/(FAD + NADH) of four isogenic triple-negative breast cancer cell lines with varying metastatic potential. Under normoxic conditions, the redox ratio increases with increasing metastatic potential (168FARN>4T07>4T1), indicating a shift to more oxidative metabolism in cells capable of metastasis. Reoxygenation following acute hypoxia increased the redox ratio by 43 ± 9% and 33 ± 4% in the 4T1 and 4T07 cells, respectively; in contrast, the redox ratio decreased 14 ± 7% in the non-metastatic 67NR cell line. These results demonstrate that the optical redox ratio is sensitive to the metabolic adaptability of breast cancer cells with high metastatic potential and could potentially be used to measure dynamic functional changes that are indicative of invasive or metastatic potential.

Entities:  

Keywords:  (170.1530) Cell analysis; (170.2520) Fluorescence microscopy; (170.2655) Functional monitoring and imaging

Year:  2016        PMID: 27895979      PMCID: PMC5119579          DOI: 10.1364/BOE.7.004364

Source DB:  PubMed          Journal:  Biomed Opt Express        ISSN: 2156-7085            Impact factor:   3.732


  46 in total

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  31 in total

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Review 4.  Evaluating Cell Metabolism Through Autofluorescence Imaging of NAD(P)H and FAD.

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9.  Optical Redox Imaging Detects the Effects of DEK Oncogene Knockdown on the Redox State of MDA-MB-231 Breast Cancer Cells.

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Authors:  David E Lee; Jacob L Brown; Megan E Rosa-Caldwell; Richard A Perry; Lemuel A Brown; Wesley S Haynie; Tyrone A Washington; Michael P Wiggs; Narasimhan Rajaram; Nicholas P Greene
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