World Journal of Preventive Medicine
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World Journal of Preventive Medicine. 2013, 1(2), 4-10
DOI: 10.12691/jpm-1-2-1
Open AccessArticle

Sublethal UVB Induces DNA Lesions and Pro-Apoptotic Gene Transcription in Human Keratinocytes: Attenuation by a Mixture of Plant Extracts

Rachid Ennamany1, Nadine Leconte2, Jacques Lecrlerc2, Aliza Jabès2, Hamid-Reza Rezvani3, Jérôme Rambert3, Khaled Ezzedine3 and M. Djavad Mossalayi3,

1Eurotest, Cestas-Pierroton, France

2Nuxe, Paris, France

3Inserm U1035, Dermatology group, Université Bordeaux Segalen, Bordeaux, France

Pub. Date: May 09, 2013

Cite this paper:
Rachid Ennamany, Nadine Leconte, Jacques Lecrlerc, Aliza Jabès, Hamid-Reza Rezvani, Jérôme Rambert, Khaled Ezzedine and M. Djavad Mossalayi. Sublethal UVB Induces DNA Lesions and Pro-Apoptotic Gene Transcription in Human Keratinocytes: Attenuation by a Mixture of Plant Extracts. World Journal of Preventive Medicine. 2013; 1(2):4-10. doi: 10.12691/jpm-1-2-1

Abstract

Ultraviolet B (UVB) radiation is a potent environmental factor in skin pathogenesis as it modulates oxidative burst, gene expression and proliferation/apoptosis of human normal keratinocytes. In the absence of cell apoptosis, sublethal UVB is shown to induce significant increase of mitochondrial and nuclear DNA lesions as quantified by increased apurinic/apyrimidinic sites together with transcriptomic modulation of pro-apoptosis/survival genes. These effects may be attenuated by cell pretreatment with extracts from three various plants: Papaver rhoeas, Passiflora incarnata and Anchusa arvensis or their mixture. Extracts variably decreased UVB-induced mitochondrial and nuclear DNA lesions in normal human keratincoytes. When mixed together, higher reduction of DNA lesions has been observed at lower extracts’ concentrations, compared to each extract alone which suggested their synergy. Furthermore, sublethal UVB-induced transcriptomic modulation was significantly prevented by cell preincubation with extract mixture through coordinated reduction of pro-apoptotic gene transcription while increasing pro-survival related transcripts. Finally, extract mixture protected keratinocytes against lethal UVB dose. This work reveals sublethal UVB-mediated lesions at both DNA and RNA levels in human keratinocytes and the ability of appropriate plant-derived sunscreen to reduce cell injury.

Keywords:
UVB plant extract keratinocyte photoprotection apoptosis

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References:

[1]  P. Autier, J.-F. Doré, A. M. M. Eggermont and J. W. Coebergh:  Epidemiological evidence that UVA radiation is involved in the genesis of cutaneous melanoma. Curr Opin Oncol, vol. 23, no 2, p. 189-196, mars 2011.
 
[2]  D. Kulms, E. Zeise, B. Pöppelmann and T. Schwarz:  DNA damage, death receptor activation and reactive oxygen species contribute to ultraviolet radiation-induced apoptosis in an essential and independent way. Oncogene, vol. 21, no 38, p. 5844-5851, août 2002.
 
[3]  H. R. Rezvani, N. Ali, L. J. Nissen, G. Harfouche, H. de Verneuil, A. Taïeb and F. Mazurier:  HIF-1α in epidermis: oxygen sensing, cutaneous angiogenesis, cancer and non-cancer disorders. J. Invest. Dermatol., vol. 131, no 9, p. 1793-1805, Sept. 2011.
 
[4]  Y. Aragane, D. Kulms, D. Metze, G. Wilkes, B. Pöppelmann, T. A. Luger and T. Schwarz:  Ultraviolet light induces apoptosis via direct activation of CD95 (Fas/APO-1) independently of its ligand CD95L. J. Cell Biol., vol. 140, no 1, p. 171-182, janv. 1998.
 
[5]  H. Stege, L. Roza, A. A. Vink, M. Grewe, T. Ruzicka, S. Grether-Beck and J. Krutmann:  Enzyme plus light therapy to repair DNA damage in ultraviolet-B-irradiated human skin. Proc. Natl. Acad. Sci. U.S.A., vol. 97, no 4, p. 1790-1795, févr. 2000.
 
[6]  M. F. Denning, Y. Wang, S. Tibudan, S. Alkan, B. J. Nickoloff and J.-Z. Qin:  Caspase activation and disruption of mitochondrial membrane potential during UV radiation-induced apoptosis of human keratinocytes requires activation of protein kinase C. Cell Death Differ., vol. 9, no 1, p. 40-52, janv. 2002.
 
[7]  S. Seité, A. Fourtanier, D. Moyal and A. R. Young:  Photodamage to human skin by suberythemal exposure to solar ultraviolet radiation can be attenuated by sunscreens: a review. Br. J. Dermatol., vol. 163, no 5, p. 903-914, nov. 2010.
 
[8]  M. Hillenbrand, J. Zapp and H. Becker:  Depsides from the petals of Papaver rhoeas. Planta Med., vol. 70, no 4, p. 380-382, avr. 2004.
 
[9]  K. Dhawan, S. Dhawan and A. Sharma:  Passiflora: a review update. J Ethnopharmacol, vol. 94, no 1, p. 123, sept. 2004.
 
[10]  R. H. Foster, G. Hardy and R. G. Alany:  Borage oil in the treatment of atopic dermatitis. Nutrition, vol. 26, no 7-8, p. 708-718, août 2010.
 
[11]  K. Hasplova, A. Hudecova, E. Miadokova, Z. Magdolenova, E. Galova, L. Vaculcikova, F. Gregan and M. Dusinska:  Biological activity of plant extract isolated from Papaver rhoeas on human lymfoblastoid cell line. Neoplasma, vol. 58, no 5, p. 386-391, 2011.
 
[12]  S. Schaffer, S. Schmitt-Schillig, W. E. Müller and G. P. Eckert:  Antioxidant properties of Mediterranean food plant extracts: geographical differences. J. Physiol. Pharmacol., vol. 56 Suppl 1, p. 115-124, mars 2005.
 
[13]  R. Soulimani, C. Younos, S. Jarmouni-Idrissi, D. Bousta, F. Khallouki, F. Khalouki and A. Laila:  Behavioral and pharmaco-toxicological study of Papaver rhoeas L. in mice. J Ethnopharmacol, vol. 74, no 3, p. 265-274, mars 2001.
 
[14]  H. Sahraei, Z. Faghih-Monzavi, S. M. Fatemi, S. Pashaei-Rad, S. H. Salimi and M. Kamalinejad:  Effects of Papaver rhoeas extract on the acquisition and expression of morphine-induced behavioral sensitization in mice. Phytother Res, vol. 20, no 9, p. 737-741, sept. 2006.
 
[15]  J. Rambert, M. Mamani-Matsuda, D. Moynet, P. Dubus, V. Desplat, T. Kauss, J. Dehais, T. Schaeverbeke, K. Ezzedine, D. Malvy, P. Vincendeau and M. D. Mossalayi:  Molecular blocking of CD23 supports its role in the pathogenesis of arthritis. PLoS ONE, vol. 4, no 3, p. e4834, 2009.
 
[16]  H. R. Rezvani, F. Mazurier, M. Cario-André, C. Pain, C. Ged, A. Taïeb and H. de Verneuil:  Protective effects of catalase overexpression on UVB-induced apoptosis in normal human keratinocytes. J. Biol. Chem., vol. 281, no 26, p. 17999-18007, juin 2006.
 
[17]  C. Ricci, V. Pastukh, J. Leonard, et al.  Mitochondrial DNA damage triggers mitochondrial-superoxide generation and apoptosis. Am. J. Physiol., Cell Physiol., vol. 294, no 2, p. C413-422, févr. 2008.
 
[18]  Y. G. Kim, H. J. Kim, D. S. Kim, et al.  Up-Regulation and redistribution of Bax in ultraviolet B-irradiated melanocytes. Pigment Cell Res., vol. 13, no 5, p. 352-357, oct. 2000.
 
[19]  N.-L. Wu, T.-A. Lee, T.-L. Tsai and W.-W. Lin:  TRAIL-induced keratinocyte differentiation requires caspase activation and p63 expression. J. Invest. Dermatol, vol. 131, no 4, p. 874-883, avr. 2011.
 
[20]  K. W. Cheng, J. P. Lahad, J. W. Gray and G. B. Mills:  Emerging role of RAB GTPases in cancer and human disease. Cancer Res., vol. 65, no 7, p. 2516-2519, avr. 2005.
 
[21]  S. J. Storr, N. O. Carragher, M. C. Frame, T. Parr and S. G. Martin:  The calpain system and cancer. Nat. Rev. Cancer, vol. 11, no 5, p. 364-374, mai 2011.
 
[22]  J. Zhao, S. Jitkaew, Z. Cai, S. Choksi, Q. Li, J. Luo and Z.-G. Liu:  Mixed lineage kinase domain-like is a key receptor interacting protein 3 downstream component of TNF-induced necrosis. Proc. Natl. Acad. Sci. U.S.A., vol. 109, no 14, p. 5322-5327, avr. 2012.
 
[23]  P. Miliani de Marval, S. Lutfeali, J. Y. Jin, B. Leshin, M. A. Selim and J. Y. Zhang:  CYLD inhibits tumorigenesis and metastasis by blocking JNK/AP1 signaling at multiple levels. Cancer Prev Res (Phila), vol. 4, no 6, p. 851-859, juin 2011.
 
[24]  M. J. M. Bertrand, S. Lippens, A. Staes, B. Gilbert, R. Roelandt, J. De Medts, K. Gevaert, W. Declercq and P. Vandenabeele: cIAP1/2 are direct E3 ligases conjugating diverse types of ubiquitin chains to receptor interacting proteins kinases 1 to 4 (RIP1-4). PLoS ONE, vol. 6, no 9, p. e22356, 2011.
 
[25]  L. H. Larsen, T. Lund, O. J. Vilholm and T. Plesner:  Anti-myelin associated glycoprotein neuropathy responding to lenalidomide. Leuk. Res., vol. 35, no 11, p. e198-199, nov. 2011.
 
[26]  J. Xu, T. Cheng, H. T. Feng, N. J. Pavlos and M. H. Zheng:  Structure and function of V-ATPases in osteoclasts: potential therapeutic targets for the treatment of osteolysis. Histol. Histopathol., vol. 22, no 4, p. 443-454, avr. 2007.
 
[27]  A. Sancar, L. A. Lindsey-Boltz, K. Unsal-Kaçmaz and S. Linn:  Molecular mechanisms of mammalian DNA repair and the DNA damage checkpoints. Annu. Rev. Biochem., vol. 73, p. 39-85, 2004.
 
[28]  Y. N. Kalav and G. Sariyar:  Alkaloids from Turkish Papaver rhoeas. Planta Med., vol. 55, no 5, p. 488, oct. 1989.
 
[29]  Y. Yoshihisa, M. A. Hassan, Y. Furusawa, Y. Tabuchi, T. Kondo and T. Shimizu:  Alkannin, HSP70 inducer, protects against UVB-induced apoptosis in human keratinocytes. PLoS ONE, vol. 7, no 10, p. e47903, 2012.
 
[30]  A. Mittal, C. A. Elmets and S. K. Katiyar:  Dietary feeding of proanthocyanidins from grape seeds prevents photocarcinogenesis in SKH-1 hairless mice: relationship to decreased fat and lipid peroxidation. Carcinogenesis, vol. 24, no 8, p. 1379-1388, août 2003.
 
[31]  L. Verschooten, K. Smaers, S. Van Kelst, C. Proby, D. Maes, L. Declercq, P. Agostinis and M. Garmyn:  The flavonoid luteolin increases the resistance of normal, but not malignant keratinocytes, against UVB-induced apoptosis. J. Invest. Dermatol, vol. 130, no 9, p. 2277-2285, sept. 2010.
 
[32]  H.-M. Yang, Y.-M. Ham, W.-J. Yoon, S. W. Roh, Y.-J. Jeon, T. Oda, S.-M. Kang, M.-C. Kang, E.-A. Kim, D. Kim and K.-N. Kim:  Quercitrin protects against ultraviolet B-induced cell death in vitro and in an in vivo zebrafish model. J. Photochem. Photobiol. B, Biol., vol. 114, p. 126-131, sept. 2012.