Abstract

Temporal dependence of changes in the morphological characteristics of cells of two cultured lines of cancer origin, HeLa and A549, induced by photodynamic treatment with Radachlorin photosensitizer, have been monitored using digital holographic microscopy during first two hours after short-term irradiation. The observed post-treatment early dynamics of the phase shift in the transmitted wavefront indicated several distinct scenarios of cell behavior depending upon the irradiation dose. In particular the phase shift increased at low doses, which can be associated with apoptosis, while at high doses it decreased, which can be associated with necrosis. As shown, the two cell types responded differently to similar irradiation doses. Although the sequence of death scenarios with the increase of the irradiation dose was the same, each scenario was realized at substantially different doses. These findings suggest that the average phase shift of the transmitted wavefront can be used for quantitative non-invasive cell death characterization. The conclusions made were cofirmed by commonly used test assays using confocal fluorescent microscopy.

© 2019 Optical Society of America under the terms of the OSA Open Access Publishing Agreement

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2019 (1)

A. A. Zhikhoreva, A. V. Belashov, D. A. Gorbenko, N. A. Avdonkina, I. A. Baldueva, A. B. Danilova, M. L. Gelfond, T. L. Nekhaeva, I. V. Semenova, and O. S. Vasyutinskii, “Morphological changes in malignant tumor cells at photodynamic treatment assessed by means of digital holographic microscopy,” Russ. J. Phys. Chem. B 13(3), 394–400 (2019).
[Crossref]

2018 (1)

D. Beltukova, V. P. Belik, O. S. Vasyutinskii, I. M. Gadzhiev, S. E. Goncharov, and I. V. Semenova, “Luminescence of Radachlorin photosensitizer in aqueous solution under excitation at 405 and 660 nm,” Opt. Spectrosc. 124(1), 49–52 (2018).
[Crossref]

2017 (4)

V. P. Belik, I. M. Gadzhiev, I. V. Semenova, and O. S. Vasyutinskii, “Time-resolved spectral analysis of Radachlorin luminescence in water,” Spectrochim. Acta, Part A 178, 181–184 (2017).
[Crossref]

A. Letai, “Apoptosis and cancer,” Annu. Rev. Cancer Biol. 1(1), 275–294 (2017).
[Crossref]

I. V. Sorokina, T. V. Denisenko, G. Imreh, P. A. Tyurin-Kuzmin, V. O. Kaminskyy, V. Gogvadze, and B. Zhivotovsky, “Involvement of autophagy in the outcome of mitotic catastrophe,” Sci. Rep. 7(1), 14571 (2017).
[Crossref]

E. Y. Kochetkova, G. I. Blinova, O. A. Bystrova, M. G. Martynova, V. A. Pospelov, and T. V. Pospelova, “Targeted elimination of senescent Ras–transformed cells by suppression of MEK/ERK pathway,” Aging 9(11), 2352–2375 (2017).
[Crossref]

2016 (3)

Z. Su, Z. Yang, L. Xie, J. P. DeWitt, and Y. Chen, “Cancer therapy in the necroptosis era,” Cell Death Differ. 23(5), 748–756 (2016).
[Crossref]

D. Beltukova, I. V. Semenova, A. G. Smolin, and O. S. Vasyutinskii, “Kinetics of photobleaching of Radachlorin photosensitizer in aqueous solutions,” Chem. Phys. Lett. 662, 127–131 (2016).
[Crossref]

A. V. Belashov, A. A. Zhikhoreva, T. N. Belyaeva, E. S. Kornilova, N. V. Petrov, A. V. Salova, I. V. Semenova, and O. S. Vasyutinskii, “Digital holographic microscopy in label-free analysis of cultured cells‘ response to photodynamic treatment,” Opt. Lett. 41(21), 5035–5038 (2016).
[Crossref]

2015 (1)

I. Fridlyanskaya, L. Alekseenko, and N. Nikolsky, “Senescence as a general cellular response to stress: A mini-review,” Exp. Gerontol. 72, 124–128 (2015).
[Crossref]

2014 (3)

A. V. Borodkina, A. N. Shatrova, N. A. Pugovkina, V. I. Zemelko, N. N. Nikolsky, and E. B. Burova, “Different protective mechanisms of human embryonic and endometrium-derived mesenchymal stem cells under oxidative stress,” Cell Tiss. Biol. 8(1), 11–21 (2014).
[Crossref]

R. Biswas, J. H. Moon, and J. C. Ahn, “Chlorin e6 derivative Radachlorin mainly accumulates in mitochondria, lysosome and endoplasmic reticulum and shows high affinity toward tumors in nude mice in photodynamic therapy,” Photochem. Photobiol. 90, 1108–1118 (2014).
[Crossref]

A. V. Belashov, N. V. Petrov, and I. V. Semenova, “Digital off-axis holographic interferometry with simulated wavefront,” Opt. Express 22(23), 28363–28376 (2014).
[Crossref]

2013 (4)

J. Kuhn, E. Shaffer, J. Mena, B. Breton, J. Parent, B. Rappaz, M. Chambon, Y. Emery, P. Magistretti, C. Depeursinge, P. Marquet, and G. Turcatti, “Label-free cytotoxicity screening assay by digital holographic microscopy,” Assay Drug Dev. Technol. 11(2), 101–107 (2013).
[Crossref]

K. Lee, K. Kim, J. Jung, J. Heo, S. Cho, S. Lee, G. Chang, Y. Jo, H. Park, and Y. Park, “Quantitative phase imaging techniques for the study of cell pathophysiology: from principles to applications,” Sensors 13(4), 4170–4191 (2013).
[Crossref]

A. I. Rybnikov, V. V. Dudenkova, M. S. Murav’eva, and Y. N. Zakharov, “Using digital off-axis holograms to investigate changes of state of living neuronal cultures,” J. Opt. Technol. 80(7), 457–462 (2013).
[Crossref]

D. DeZio, V. Cianfanelli, and F. Cecconi, “New insights into the link between DNA damage and apoptosis,” Antioxid. Redox Signaling 19(6), 559–571 (2013).
[Crossref]

2012 (1)

2011 (3)

M. Firczuk, D. Nowis, and J. Golab, “PDT-induced inflammatory and host responses,” Photochem. Photobiol. Sci. 10(5), 653–663 (2011).
[Crossref]

C. M. Brackett and S. O. Gollnick, “Photodynamic therapy enhancement of anti-tumor immunity,” Photochem. Photobiol. Sci. 10(5), 649–652 (2011).
[Crossref]

P. Mroz, A. Yaroslavsky, G. B. Kharkwal, and M. R. Hamblin, “Cell death pathways in photodynamic therapy of cancer,” Cancers 3(2), 2516–2539 (2011).
[Crossref]

2010 (1)

M. T. Silva, “Secondary necrosis: The natural outcome of the complete apoptotic program,” FEBS Lett. 584(22), 4491–4499 (2010).
[Crossref]

2009 (4)

C. A. Robertson, D. H. Evans, and H. Abrahamse, “Photodynamic therapy (PDT): A short review on cellular mechanisms and cancer research applications for PDT,” J. Photochem. Photobiol., B 96(1), 1–8 (2009).
[Crossref]

G. Kroemer, L. Galluzzi, P. Vandenabeele, J. Abrams, E. S. Alnemri, E. H. Baehrecke, M. V. Blagosklonny, W. S. El-Deiry, P. Golstein, D. R. Green, M. Hengartner, R. A. Knight, S. Kumar, S. A. Lipton, W. Malorni, G. Nunez, M. E. Peter, J. Tschopp, J. Yuan, M. Piacentini, B. Zhivotovsky, and G. Melino, “Classification of cell death: recommendations of the nomenclature committee on cell death 2009,” Cell Death Differ. 16(1), 3–11 (2009).
[Crossref]

G. Manda, M. T. Nechifor, and T.-M. Neagu, “Reactive oxygen species, cancer and anti-cancer therapies,” Curr. Chem. Biol. 3(1), 342–366 (2009).
[Crossref]

B. Rappaz, E. Cano, T. Colomb, J. Kuhn, C. D. Depeursinge, V. Simanis, P. J. Magistretti, and P. P. Marquet, “Noninvasive characterization of the fission yeast cell cycle by monitoring dry mass with digital holographic microscopy,” J. Biomed. Opt. 14(3), 034049 (2009).
[Crossref]

2008 (3)

G. Popescu, “Quantitative phase imaging of nanoscale cell structure and dynamics,” Methods Cell Biol. 90, 87–115 (2008).
[Crossref]

Y. Park, M. Diez-Silva, G. Popescu, G. Lykotrafitis, W. Choi, M. S. Feld, and S. Suresh, “Refractive index maps and membrane dynamics of human red blood cells parasitized by Plasmodium falciparum,” Proc. Natl. Acad. Sci. 105(37), 13730–13735 (2008).
[Crossref]

B. C. Wilson and M. S. Patterson, “The physics, biophysics and technology of photodynamic therapy,” Phys. Med. Biol. 53(9), R61–R109 (2008).
[Crossref]

2007 (2)

S. Elmore, “Apoptosis: A review of programmed cell death,” Toxicol. Pathol. 35(4), 495–516 (2007).
[Crossref]

M. Kemmler, M. Fratz, D. M. Giel, N. Saum, A. Brandenburg, and C. Hoffmann, “Noninvasive time-dependent cytometry monitoring by digital holography,” J. Biomed. Opt. 12(6), 064002 (2007).
[Crossref]

2006 (3)

B. Kemper, D. Carl, A. Höink, G. von Bally, I. Bredebusch, and J. Schnekenburger, “Modular digital holographic microscopy system for marker free quantitative phase contrast imaging of living cells,” Proc. SPIE 6191, 61910T (2006).
[Crossref]

N. Normanno, A. DeLuca, C. Bianco, L. Strizzi, M. Mancino, M. R. Maiello, A. Carotenuto, G. DeFeo, F. Caponigro, and D. S. Salomon, “Epidermal growth factor receptor (EGFR) signaling in cancer,” Gene 366(1), 2–16 (2006).
[Crossref]

M. Krypuy, G. M. Newnham, D. M. Thomas, M. Conron, and A. Dobrovic, “High resolution melting analysis for the rapid and sensitive detection of mutations in clinical samples: KRAS codon 12 and 13 mutations in non-small cell lung cancer,” BMC Cancer 6(1), 295 (2006).
[Crossref]

2005 (1)

D. Ribble, N. B. Goldstein, D. A. Norris, and Y. G. Shellman, “A simple technique for quantifying apoptosis in 96-well plates,” BMC Biotechnol. 5(1), 12 (2005).
[Crossref]

2004 (2)

M. Liebling, T. Blu, and M. Unser, “Complex-wave retrieval from a single off-axis hologram,” J. Opt. Soc. Am. A 21(3), 367–377 (2004).
[Crossref]

M. R. Hamblin and T. Hasan, “Photodynamic therapy: a new antimicrobial approach to infectious disease?” Photochem. Photobiol. Sci. 3(5), 436–450 (2004).
[Crossref]

1999 (1)

H. A. Aebischer and S. Waldner, “A simple and effective method for filtering speckle-interferometric phase fringe patterns,” Opt. Commun. 162(4-6), 205–210 (1999).
[Crossref]

1988 (1)

R. M. Goldstein, H. A. Zebker, and C. L. Werner, “Satellite radar interferometry: Two-dimensional phase unwrapping,” Radio Sci. 23(4), 713–720 (1988).
[Crossref]

Abrahamse, H.

C. A. Robertson, D. H. Evans, and H. Abrahamse, “Photodynamic therapy (PDT): A short review on cellular mechanisms and cancer research applications for PDT,” J. Photochem. Photobiol., B 96(1), 1–8 (2009).
[Crossref]

Abrams, J.

G. Kroemer, L. Galluzzi, P. Vandenabeele, J. Abrams, E. S. Alnemri, E. H. Baehrecke, M. V. Blagosklonny, W. S. El-Deiry, P. Golstein, D. R. Green, M. Hengartner, R. A. Knight, S. Kumar, S. A. Lipton, W. Malorni, G. Nunez, M. E. Peter, J. Tschopp, J. Yuan, M. Piacentini, B. Zhivotovsky, and G. Melino, “Classification of cell death: recommendations of the nomenclature committee on cell death 2009,” Cell Death Differ. 16(1), 3–11 (2009).
[Crossref]

Aebischer, H. A.

H. A. Aebischer and S. Waldner, “A simple and effective method for filtering speckle-interferometric phase fringe patterns,” Opt. Commun. 162(4-6), 205–210 (1999).
[Crossref]

Ahn, J. C.

R. Biswas, J. H. Moon, and J. C. Ahn, “Chlorin e6 derivative Radachlorin mainly accumulates in mitochondria, lysosome and endoplasmic reticulum and shows high affinity toward tumors in nude mice in photodynamic therapy,” Photochem. Photobiol. 90, 1108–1118 (2014).
[Crossref]

Alekseenko, L.

I. Fridlyanskaya, L. Alekseenko, and N. Nikolsky, “Senescence as a general cellular response to stress: A mini-review,” Exp. Gerontol. 72, 124–128 (2015).
[Crossref]

Alnemri, E. S.

G. Kroemer, L. Galluzzi, P. Vandenabeele, J. Abrams, E. S. Alnemri, E. H. Baehrecke, M. V. Blagosklonny, W. S. El-Deiry, P. Golstein, D. R. Green, M. Hengartner, R. A. Knight, S. Kumar, S. A. Lipton, W. Malorni, G. Nunez, M. E. Peter, J. Tschopp, J. Yuan, M. Piacentini, B. Zhivotovsky, and G. Melino, “Classification of cell death: recommendations of the nomenclature committee on cell death 2009,” Cell Death Differ. 16(1), 3–11 (2009).
[Crossref]

Avdonkina, N. A.

A. A. Zhikhoreva, A. V. Belashov, D. A. Gorbenko, N. A. Avdonkina, I. A. Baldueva, A. B. Danilova, M. L. Gelfond, T. L. Nekhaeva, I. V. Semenova, and O. S. Vasyutinskii, “Morphological changes in malignant tumor cells at photodynamic treatment assessed by means of digital holographic microscopy,” Russ. J. Phys. Chem. B 13(3), 394–400 (2019).
[Crossref]

Baehrecke, E. H.

G. Kroemer, L. Galluzzi, P. Vandenabeele, J. Abrams, E. S. Alnemri, E. H. Baehrecke, M. V. Blagosklonny, W. S. El-Deiry, P. Golstein, D. R. Green, M. Hengartner, R. A. Knight, S. Kumar, S. A. Lipton, W. Malorni, G. Nunez, M. E. Peter, J. Tschopp, J. Yuan, M. Piacentini, B. Zhivotovsky, and G. Melino, “Classification of cell death: recommendations of the nomenclature committee on cell death 2009,” Cell Death Differ. 16(1), 3–11 (2009).
[Crossref]

Baldueva, I. A.

A. A. Zhikhoreva, A. V. Belashov, D. A. Gorbenko, N. A. Avdonkina, I. A. Baldueva, A. B. Danilova, M. L. Gelfond, T. L. Nekhaeva, I. V. Semenova, and O. S. Vasyutinskii, “Morphological changes in malignant tumor cells at photodynamic treatment assessed by means of digital holographic microscopy,” Russ. J. Phys. Chem. B 13(3), 394–400 (2019).
[Crossref]

Bauwens, A.

B. Kemper, A. Bauwens, D. Bettenworth, M. Gotte, B. Greve, L. Kastl, S. Ketelhut, P. Lenz, S. Mues, J. Schnekenburger, and A. Vollmer, “Label-free quantitative in vitro live cell imaging with digital holographic microscopy, Bioanalytical Reviews (2019).

Belashov, A. V.

A. A. Zhikhoreva, A. V. Belashov, D. A. Gorbenko, N. A. Avdonkina, I. A. Baldueva, A. B. Danilova, M. L. Gelfond, T. L. Nekhaeva, I. V. Semenova, and O. S. Vasyutinskii, “Morphological changes in malignant tumor cells at photodynamic treatment assessed by means of digital holographic microscopy,” Russ. J. Phys. Chem. B 13(3), 394–400 (2019).
[Crossref]

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G. Kroemer, L. Galluzzi, P. Vandenabeele, J. Abrams, E. S. Alnemri, E. H. Baehrecke, M. V. Blagosklonny, W. S. El-Deiry, P. Golstein, D. R. Green, M. Hengartner, R. A. Knight, S. Kumar, S. A. Lipton, W. Malorni, G. Nunez, M. E. Peter, J. Tschopp, J. Yuan, M. Piacentini, B. Zhivotovsky, and G. Melino, “Classification of cell death: recommendations of the nomenclature committee on cell death 2009,” Cell Death Differ. 16(1), 3–11 (2009).
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M. Kemmler, M. Fratz, D. M. Giel, N. Saum, A. Brandenburg, and C. Hoffmann, “Noninvasive time-dependent cytometry monitoring by digital holography,” J. Biomed. Opt. 12(6), 064002 (2007).
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B. Kemper, D. Carl, A. Höink, G. von Bally, I. Bredebusch, and J. Schnekenburger, “Modular digital holographic microscopy system for marker free quantitative phase contrast imaging of living cells,” Proc. SPIE 6191, 61910T (2006).
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Ketelhut, S.

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G. Kroemer, L. Galluzzi, P. Vandenabeele, J. Abrams, E. S. Alnemri, E. H. Baehrecke, M. V. Blagosklonny, W. S. El-Deiry, P. Golstein, D. R. Green, M. Hengartner, R. A. Knight, S. Kumar, S. A. Lipton, W. Malorni, G. Nunez, M. E. Peter, J. Tschopp, J. Yuan, M. Piacentini, B. Zhivotovsky, and G. Melino, “Classification of cell death: recommendations of the nomenclature committee on cell death 2009,” Cell Death Differ. 16(1), 3–11 (2009).
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V. P. Belik, I. M. Gadzhiev, I. V. Semenova, and O. S. Vasyutinskii, “Time-resolved spectral analysis of Radachlorin luminescence in water,” Spectrochim. Acta, Part A 178, 181–184 (2017).
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Vollmer, A.

B. Kemper, A. Bauwens, D. Bettenworth, M. Gotte, B. Greve, L. Kastl, S. Ketelhut, P. Lenz, S. Mues, J. Schnekenburger, and A. Vollmer, “Label-free quantitative in vitro live cell imaging with digital holographic microscopy, Bioanalytical Reviews (2019).

von Bally, G.

B. Kemper, D. Carl, A. Höink, G. von Bally, I. Bredebusch, and J. Schnekenburger, “Modular digital holographic microscopy system for marker free quantitative phase contrast imaging of living cells,” Proc. SPIE 6191, 61910T (2006).
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H. A. Aebischer and S. Waldner, “A simple and effective method for filtering speckle-interferometric phase fringe patterns,” Opt. Commun. 162(4-6), 205–210 (1999).
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R. M. Goldstein, H. A. Zebker, and C. L. Werner, “Satellite radar interferometry: Two-dimensional phase unwrapping,” Radio Sci. 23(4), 713–720 (1988).
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B. C. Wilson and M. S. Patterson, “The physics, biophysics and technology of photodynamic therapy,” Phys. Med. Biol. 53(9), R61–R109 (2008).
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Z. Su, Z. Yang, L. Xie, J. P. DeWitt, and Y. Chen, “Cancer therapy in the necroptosis era,” Cell Death Differ. 23(5), 748–756 (2016).
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P. Mroz, A. Yaroslavsky, G. B. Kharkwal, and M. R. Hamblin, “Cell death pathways in photodynamic therapy of cancer,” Cancers 3(2), 2516–2539 (2011).
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G. Kroemer, L. Galluzzi, P. Vandenabeele, J. Abrams, E. S. Alnemri, E. H. Baehrecke, M. V. Blagosklonny, W. S. El-Deiry, P. Golstein, D. R. Green, M. Hengartner, R. A. Knight, S. Kumar, S. A. Lipton, W. Malorni, G. Nunez, M. E. Peter, J. Tschopp, J. Yuan, M. Piacentini, B. Zhivotovsky, and G. Melino, “Classification of cell death: recommendations of the nomenclature committee on cell death 2009,” Cell Death Differ. 16(1), 3–11 (2009).
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R. M. Goldstein, H. A. Zebker, and C. L. Werner, “Satellite radar interferometry: Two-dimensional phase unwrapping,” Radio Sci. 23(4), 713–720 (1988).
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A. V. Borodkina, A. N. Shatrova, N. A. Pugovkina, V. I. Zemelko, N. N. Nikolsky, and E. B. Burova, “Different protective mechanisms of human embryonic and endometrium-derived mesenchymal stem cells under oxidative stress,” Cell Tiss. Biol. 8(1), 11–21 (2014).
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A. A. Zhikhoreva, A. V. Belashov, D. A. Gorbenko, N. A. Avdonkina, I. A. Baldueva, A. B. Danilova, M. L. Gelfond, T. L. Nekhaeva, I. V. Semenova, and O. S. Vasyutinskii, “Morphological changes in malignant tumor cells at photodynamic treatment assessed by means of digital holographic microscopy,” Russ. J. Phys. Chem. B 13(3), 394–400 (2019).
[Crossref]

A. V. Belashov, A. A. Zhikhoreva, T. N. Belyaeva, E. S. Kornilova, N. V. Petrov, A. V. Salova, I. V. Semenova, and O. S. Vasyutinskii, “Digital holographic microscopy in label-free analysis of cultured cells‘ response to photodynamic treatment,” Opt. Lett. 41(21), 5035–5038 (2016).
[Crossref]

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I. V. Sorokina, T. V. Denisenko, G. Imreh, P. A. Tyurin-Kuzmin, V. O. Kaminskyy, V. Gogvadze, and B. Zhivotovsky, “Involvement of autophagy in the outcome of mitotic catastrophe,” Sci. Rep. 7(1), 14571 (2017).
[Crossref]

G. Kroemer, L. Galluzzi, P. Vandenabeele, J. Abrams, E. S. Alnemri, E. H. Baehrecke, M. V. Blagosklonny, W. S. El-Deiry, P. Golstein, D. R. Green, M. Hengartner, R. A. Knight, S. Kumar, S. A. Lipton, W. Malorni, G. Nunez, M. E. Peter, J. Tschopp, J. Yuan, M. Piacentini, B. Zhivotovsky, and G. Melino, “Classification of cell death: recommendations of the nomenclature committee on cell death 2009,” Cell Death Differ. 16(1), 3–11 (2009).
[Crossref]

Aging (1)

E. Y. Kochetkova, G. I. Blinova, O. A. Bystrova, M. G. Martynova, V. A. Pospelov, and T. V. Pospelova, “Targeted elimination of senescent Ras–transformed cells by suppression of MEK/ERK pathway,” Aging 9(11), 2352–2375 (2017).
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Annu. Rev. Cancer Biol. (1)

A. Letai, “Apoptosis and cancer,” Annu. Rev. Cancer Biol. 1(1), 275–294 (2017).
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Antioxid. Redox Signaling (1)

D. DeZio, V. Cianfanelli, and F. Cecconi, “New insights into the link between DNA damage and apoptosis,” Antioxid. Redox Signaling 19(6), 559–571 (2013).
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Assay Drug Dev. Technol. (1)

J. Kuhn, E. Shaffer, J. Mena, B. Breton, J. Parent, B. Rappaz, M. Chambon, Y. Emery, P. Magistretti, C. Depeursinge, P. Marquet, and G. Turcatti, “Label-free cytotoxicity screening assay by digital holographic microscopy,” Assay Drug Dev. Technol. 11(2), 101–107 (2013).
[Crossref]

Biomed. Opt. Express (1)

BMC Biotechnol. (1)

D. Ribble, N. B. Goldstein, D. A. Norris, and Y. G. Shellman, “A simple technique for quantifying apoptosis in 96-well plates,” BMC Biotechnol. 5(1), 12 (2005).
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BMC Cancer (1)

M. Krypuy, G. M. Newnham, D. M. Thomas, M. Conron, and A. Dobrovic, “High resolution melting analysis for the rapid and sensitive detection of mutations in clinical samples: KRAS codon 12 and 13 mutations in non-small cell lung cancer,” BMC Cancer 6(1), 295 (2006).
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Cancers (1)

P. Mroz, A. Yaroslavsky, G. B. Kharkwal, and M. R. Hamblin, “Cell death pathways in photodynamic therapy of cancer,” Cancers 3(2), 2516–2539 (2011).
[Crossref]

Cell Death Differ. (2)

Z. Su, Z. Yang, L. Xie, J. P. DeWitt, and Y. Chen, “Cancer therapy in the necroptosis era,” Cell Death Differ. 23(5), 748–756 (2016).
[Crossref]

G. Kroemer, L. Galluzzi, P. Vandenabeele, J. Abrams, E. S. Alnemri, E. H. Baehrecke, M. V. Blagosklonny, W. S. El-Deiry, P. Golstein, D. R. Green, M. Hengartner, R. A. Knight, S. Kumar, S. A. Lipton, W. Malorni, G. Nunez, M. E. Peter, J. Tschopp, J. Yuan, M. Piacentini, B. Zhivotovsky, and G. Melino, “Classification of cell death: recommendations of the nomenclature committee on cell death 2009,” Cell Death Differ. 16(1), 3–11 (2009).
[Crossref]

Cell Tiss. Biol. (1)

A. V. Borodkina, A. N. Shatrova, N. A. Pugovkina, V. I. Zemelko, N. N. Nikolsky, and E. B. Burova, “Different protective mechanisms of human embryonic and endometrium-derived mesenchymal stem cells under oxidative stress,” Cell Tiss. Biol. 8(1), 11–21 (2014).
[Crossref]

Chem. Phys. Lett. (1)

D. Beltukova, I. V. Semenova, A. G. Smolin, and O. S. Vasyutinskii, “Kinetics of photobleaching of Radachlorin photosensitizer in aqueous solutions,” Chem. Phys. Lett. 662, 127–131 (2016).
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Curr. Chem. Biol. (1)

G. Manda, M. T. Nechifor, and T.-M. Neagu, “Reactive oxygen species, cancer and anti-cancer therapies,” Curr. Chem. Biol. 3(1), 342–366 (2009).
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Exp. Gerontol. (1)

I. Fridlyanskaya, L. Alekseenko, and N. Nikolsky, “Senescence as a general cellular response to stress: A mini-review,” Exp. Gerontol. 72, 124–128 (2015).
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FEBS Lett. (1)

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Gene (1)

N. Normanno, A. DeLuca, C. Bianco, L. Strizzi, M. Mancino, M. R. Maiello, A. Carotenuto, G. DeFeo, F. Caponigro, and D. S. Salomon, “Epidermal growth factor receptor (EGFR) signaling in cancer,” Gene 366(1), 2–16 (2006).
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J. Biomed. Opt. (2)

B. Rappaz, E. Cano, T. Colomb, J. Kuhn, C. D. Depeursinge, V. Simanis, P. J. Magistretti, and P. P. Marquet, “Noninvasive characterization of the fission yeast cell cycle by monitoring dry mass with digital holographic microscopy,” J. Biomed. Opt. 14(3), 034049 (2009).
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M. Kemmler, M. Fratz, D. M. Giel, N. Saum, A. Brandenburg, and C. Hoffmann, “Noninvasive time-dependent cytometry monitoring by digital holography,” J. Biomed. Opt. 12(6), 064002 (2007).
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J. Opt. Soc. Am. A (1)

J. Opt. Technol. (1)

J. Photochem. Photobiol., B (1)

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Methods Cell Biol. (1)

G. Popescu, “Quantitative phase imaging of nanoscale cell structure and dynamics,” Methods Cell Biol. 90, 87–115 (2008).
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Opt. Commun. (1)

H. A. Aebischer and S. Waldner, “A simple and effective method for filtering speckle-interferometric phase fringe patterns,” Opt. Commun. 162(4-6), 205–210 (1999).
[Crossref]

Opt. Express (1)

Opt. Lett. (1)

Opt. Spectrosc. (1)

D. Beltukova, V. P. Belik, O. S. Vasyutinskii, I. M. Gadzhiev, S. E. Goncharov, and I. V. Semenova, “Luminescence of Radachlorin photosensitizer in aqueous solution under excitation at 405 and 660 nm,” Opt. Spectrosc. 124(1), 49–52 (2018).
[Crossref]

Photochem. Photobiol. (1)

R. Biswas, J. H. Moon, and J. C. Ahn, “Chlorin e6 derivative Radachlorin mainly accumulates in mitochondria, lysosome and endoplasmic reticulum and shows high affinity toward tumors in nude mice in photodynamic therapy,” Photochem. Photobiol. 90, 1108–1118 (2014).
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M. Firczuk, D. Nowis, and J. Golab, “PDT-induced inflammatory and host responses,” Photochem. Photobiol. Sci. 10(5), 653–663 (2011).
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C. M. Brackett and S. O. Gollnick, “Photodynamic therapy enhancement of anti-tumor immunity,” Photochem. Photobiol. Sci. 10(5), 649–652 (2011).
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M. R. Hamblin and T. Hasan, “Photodynamic therapy: a new antimicrobial approach to infectious disease?” Photochem. Photobiol. Sci. 3(5), 436–450 (2004).
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Phys. Med. Biol. (1)

B. C. Wilson and M. S. Patterson, “The physics, biophysics and technology of photodynamic therapy,” Phys. Med. Biol. 53(9), R61–R109 (2008).
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Proc. Natl. Acad. Sci. (1)

Y. Park, M. Diez-Silva, G. Popescu, G. Lykotrafitis, W. Choi, M. S. Feld, and S. Suresh, “Refractive index maps and membrane dynamics of human red blood cells parasitized by Plasmodium falciparum,” Proc. Natl. Acad. Sci. 105(37), 13730–13735 (2008).
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Proc. SPIE (1)

B. Kemper, D. Carl, A. Höink, G. von Bally, I. Bredebusch, and J. Schnekenburger, “Modular digital holographic microscopy system for marker free quantitative phase contrast imaging of living cells,” Proc. SPIE 6191, 61910T (2006).
[Crossref]

Radio Sci. (1)

R. M. Goldstein, H. A. Zebker, and C. L. Werner, “Satellite radar interferometry: Two-dimensional phase unwrapping,” Radio Sci. 23(4), 713–720 (1988).
[Crossref]

Russ. J. Phys. Chem. B (1)

A. A. Zhikhoreva, A. V. Belashov, D. A. Gorbenko, N. A. Avdonkina, I. A. Baldueva, A. B. Danilova, M. L. Gelfond, T. L. Nekhaeva, I. V. Semenova, and O. S. Vasyutinskii, “Morphological changes in malignant tumor cells at photodynamic treatment assessed by means of digital holographic microscopy,” Russ. J. Phys. Chem. B 13(3), 394–400 (2019).
[Crossref]

Sci. Rep. (1)

I. V. Sorokina, T. V. Denisenko, G. Imreh, P. A. Tyurin-Kuzmin, V. O. Kaminskyy, V. Gogvadze, and B. Zhivotovsky, “Involvement of autophagy in the outcome of mitotic catastrophe,” Sci. Rep. 7(1), 14571 (2017).
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Sensors (1)

K. Lee, K. Kim, J. Jung, J. Heo, S. Cho, S. Lee, G. Chang, Y. Jo, H. Park, and Y. Park, “Quantitative phase imaging techniques for the study of cell pathophysiology: from principles to applications,” Sensors 13(4), 4170–4191 (2013).
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Spectrochim. Acta, Part A (1)

V. P. Belik, I. M. Gadzhiev, I. V. Semenova, and O. S. Vasyutinskii, “Time-resolved spectral analysis of Radachlorin luminescence in water,” Spectrochim. Acta, Part A 178, 181–184 (2017).
[Crossref]

Toxicol. Pathol. (1)

S. Elmore, “Apoptosis: A review of programmed cell death,” Toxicol. Pathol. 35(4), 495–516 (2007).
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Other (1)

B. Kemper, A. Bauwens, D. Bettenworth, M. Gotte, B. Greve, L. Kastl, S. Ketelhut, P. Lenz, S. Mues, J. Schnekenburger, and A. Vollmer, “Label-free quantitative in vitro live cell imaging with digital holographic microscopy, Bioanalytical Reviews (2019).

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Figures (4)

Fig. 1.
Fig. 1. 3D pseudocolored phase plots of HeLa cells obtained before photodynamic treatment (a, c) and in 60 minutes after irradiation at 22.1 mW/cm$^2$ (b) and 93 mW/cm$^2$ (d).
Fig. 2.
Fig. 2. Average phase shift dynamics in HeLa (a) and A549 (b) cells at the indicated irradiation doses. (c) HeLa cells dry mass dynamics at indicated irradiation doses.(d) average phase shift dynamics in photosensitised but not irradiated HeLa cells during 6 hours of their continuous monitoring. (e) Schematics of average phase shift variation scenarios as function of fluence rate for the two cell lines. Colors in (e) correspond to those on the graphs in (a, b, c).
Fig. 3.
Fig. 3. Typical 2D phase images of HeLa and A549 cells before and after PD treatment. Irradiation doses are indicated on the left of each pair of images.
Fig. 4.
Fig. 4. Images of HeLa cells subjected to PD treatment at different irradiation doses. Images of cells before irradiation (a-c) and in 50 minutes after irradiation at the fluence rates of 15 W/cm$^2$ (d-f) and 62 mW/cm$^2$ (g-i). Left column: AO(green)/EB(red) fluorescent images; middle column: Annexin-V(green)/PI(red) fluorescent images; right column: phase contrast images.

Equations (2)

Equations on this page are rendered with MathJax. Learn more.

φ a v = 1 S c e l l S c e l l Δ φ ( x , y ) d x d y
D M = 10 λ 2 π α S c e l l Δ φ ( x , y ) d x d y