Correction: Inhibition of p38 MAPK signaling augments skin tumorigenesis via NOX2 driven ROS generation (PLoS ONE (2014) 9:5 (e97245) DOI: 10.1371/journal.pone.0097245);Inhibition of p38 MAPK signaling augments skin tumorigenesis via NOX2 driven ROS generation

PLoS ONE

Volumn 9, Issue 5, 2014, Pages

  Liu, Liang ^a   Rezvani, Hamid Reza ^b,c   Back, Jung Ho ^a   Hosseini, Mohsen ^b,c   Tang, Xiuwei ^a   Zhu, Yucui ^a   Mahfouf, Walid ^b,c   Raad, Houssam ^b,c   Raji, Grace ^a   Athar, Mohammad ^d   Kim, Arianna L ^a   Bickers, David R ^a  

^a Och Spine at New York Presbyterian Hospitals   (United States)

^b UNIVERSITÉ DE BORDEAUX   (France)

^c INSERM   (France)

^d UNIVERSITY OF ALABAMA AT BIRMINGHAM   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

4 (4 FLUOROPHENYL) 2 (4 METHYLSULFINYLPHENYL) 5 (4 PYRIDYL)IMIDAZOLE; ISOPROTEIN; MITOGEN ACTIVATED PROTEIN KINASE P38; PROTEIN P53; REACTIVE OXYGEN METABOLITE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE OXIDASE 2; CYBB PROTEIN, HUMAN; IMIDAZOLE DERIVATIVE; MEMBRANE PROTEIN; PYRIDINE DERIVATIVE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE OXIDASE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CANCER INHIBITION; CELL CULTURE; CELL PROLIFERATION; ENZYME ACTIVITY; ENZYME INHIBITION; FEMALE; HUMAN; HUMAN CELL; KERATINOCYTE; MALE; MOUSE; NONHUMAN; PROTEIN EXPRESSION; PROTEIN SUBUNIT; SIGNAL TRANSDUCTION; SKIN CARCINOGENESIS; SKIN CARCINOMA; TISSUE MICROARRAY; TUMOR XENOGRAFT; ULTRAVIOLET IRRADIATION; ANIMAL; CARCINOGENESIS; DEFICIENCY; DRUG EFFECTS; GENE EXPRESSION REGULATION; KNOCKOUT MOUSE; METABOLISM; MICROARRAY ANALYSIS; PHYSIOLOGY; RADIATION RESPONSE; SKIN TUMOR; SQUAMOUS CELL CARCINOMA; TUMOR CELL LINE; ULTRAVIOLET RADIATION;

ANIMALS; CARCINOGENESIS; CARCINOMA, SQUAMOUS CELL; CELL LINE, TUMOR; CELL PROLIFERATION; CELLS, CULTURED; GENE EXPRESSION REGULATION, ENZYMOLOGIC; HUMANS; IMIDAZOLES; KERATINOCYTES; MAP KINASE SIGNALING SYSTEM; MEMBRANE GLYCOPROTEINS; MICE; MICE, KNOCKOUT; MICROARRAY ANALYSIS; NADPH OXIDASE; PYRIDINES; REACTIVE OXYGEN SPECIES; SKIN NEOPLASMS; TUMOR SUPPRESSOR PROTEIN P53; ULTRAVIOLET RAYS;

EID: 84901261855     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0172451     Document Type: Erratum

References (45)

1. Bito T, Nishigori C (2012) Impact of reactive oxygen species on keratinocyte signaling pathways. Journal of Dermatological Science 68: 3-8.
2. Bossi O, Gartsbein M, Leitges M, Kuroki T, Grossman S, et al. (2008) UV irradiation increases ROS production via PKCdelta signaling in primary murine fibroblasts. J Cell Biochem 105: 194-207.
3. Scharffetter-Kochanek K, Wlaschek M, Brenneisen P, Schauen M, Blaudschun R, et al. (1997) UV-induced reactive oxygen species in photocarcinogenesis and photoaging. Biol Chem 378: 1247-1257. (Pubitemid 27507540)
4. Bedard K, Krause KH (2007) The NOX family of ROS-generating NADPH oxidases: physiology and pathophysiology. Physiol Rev 87: 245-313. (Pubitemid 46209993)
5. Kang MA, So EY, Simons AL, Spitz DR, Ouchi T (2012) DNA damage induces reactive oxygen species generation through the H2AX-Nox1/Rac1 pathway. Cell Death Dis 3: e249.
6. Maraldi T, Prata C, Vieceli Dalla Sega F, Caliceti C, Zambonin L, et al. (2009) NAD(P)H oxidase isoform Nox2 plays a prosurvival role in human leukaemia cells. Free Radic Res 43: 1111-1121.
7. Block K, Gorin Y (2012) Aiding and abetting roles of NOX oxidases in cellular transformation. Nat Rev Cancer 12: 627-637.
8. Kamata T (2009) Roles of Nox1 and other Nox isoforms in cancer development. Cancer Sci 100: 1382-1388.
9. Mitsushita J, Lambeth JD, Kamata T (2004) The superoxide-generating oxidase Nox1 is functionally required for Ras oncogene transformation. Cancer Res 64: 3580-3585. (Pubitemid 38657935)
10. Rezvani HR, Rossignol R, Ali N, Benard G, Tang X, et al. (2011) XPC silencing in normal human keratinocytes triggers metabolic alterations through NOX-1 activation-mediated reactive oxygen species. Biochim Biophys Acta 1807: 609-619.
11. Rezvani HR, Kim AL, Rossignol R, Ali N, Daly M, et al. (2011) XPC silencing in normal human keratinocytes triggers metabolic alterations that drive the formation of squamous cell carcinomas. J Clin Invest 121: 195-211.
12. Cuadrado A, Nebreda AR (2010) Mechanisms and functions of p38 MAPK signalling. Biochem J 429: 403-417.
13. Wagner EF, Nebreda AR (2009) Signal integration by JNK and p38 MAPK pathways in cancer development. Nat Rev Cancer 9: 537-549.
14. Cuenda A, Rousseau S (2007) p38 MAP-kinases pathway regulation, function and role in human diseases. Biochim Biophys Acta 1773: 1358-1375. (Pubitemid 47125981)
15. Junttila MR, Ala-Aho R, Jokilehto T, Peltonen J, Kallajoki M, et al. (2007) p38alpha and p38delta mitogen-activated protein kinase isoforms regulate invasion and growth of head and neck squamous carcinoma cells. Oncogene 26: 5267-5279. (Pubitemid 47237627)
16. Dashti SR, Efimova T, Eckert RL (2001) MEK7-dependent activation of p38 MAP kinase in keratinocytes. J Biol Chem 276: 8059-8063.
17. Tan G, Niu J, Shi Y, Ouyang H, Wu ZH (2012) NF-kappaB-dependent microRNA-125b up-regulation promotes cell survival by targeting p38alpha upon ultraviolet radiation. J Biol Chem 287: 33036-33047.
18. Ambrosino C, Nebreda AR (2001) Cell cycle regulation by p38 MAP kinases. Biol Cell 93: 47-51. (Pubitemid 33040859)
19. Thornton TM, Rincon M (2009) Non-classical p38 map kinase functions: cell cycle checkpoints and survival. Int J Biol Sci 5: 44-51.
20. Phong MS, Van Horn RD, Li S, Tucker-Kellogg G, Surana U, et al. (2010) p38 mitogen-activated protein kinase promotes cell survival in response to DNA damage but is not required for the G(2) DNA damage checkpoint in human cancer cells. Mol Cell Biol 30: 3816-3826.
21. Aguirre-Ghiso JA (2007) Models, mechanisms and clinical evidence for cancer dormancy. Nat Rev Cancer 7: 834-846.
22. Qiang L, Wu C, Ming M, Viollet B, He YY (2013) Autophagy controls p38 activation to promote cell survival under genotoxic stress. J Biol Chem 288: 1603-1611.
23. Liu K, Yu D, Cho YY, Bode AM, Ma W, et al. (2013) Sunlight UV-induced skin cancer relies upon activation of the p38alpha signaling pathway. Cancer Res.
24. Cuadrado A, Nebreda AR (2010) Mechanisms and functions of p38 MAPK signalling. Biochemical Journal 429: 403-417.
25. Chen Y, Miao Z-H, Zhao W-M, Ding J (2005) The p53 pathway is synergized by p38 MAPK signaling to mediate 11,11 9-dideoxyverticillin-induced G2/M arrest. FEBS Letters 579: 3683-3690. (Pubitemid 40897709)
26. Raingeaud J, Gupta S, Rogers JS, Dickens M, Han J, et al. (1995) Proinflammatory Cytokines and Environmental Stress Cause p38 Mitogen-activated Protein Kinase Activation by Dual Phosphorylation on Tyrosine and Threonine. Journal of Biological Chemistry 270: 7420-7426.
27. Xu J, Clark RA, Parks WC (2001) p38 mitogen-activated kinase is a bidirectional regulator of human fibroblast collagenase-1 induction by three-dimensional collagen lattices. Biochem J 355: 437-447. (Pubitemid 32397804)
28. Cuenda A, Rouse J, Doza YN, Meier R, Cohen P, et al. (1995) SB 203580 is a specific inhibitor of a MAP kinase homologue which is stimulated by cellular stresses and interleukin-1. FEBS Lett 364: 229-233.
29. Kim H, Casta A, Tang X, Luke CT, Kim AL, et al. (2012) Loss of hairless confers susceptibility to UVB-induced tumorigenesis via disruption of NFkappaB signaling. PLoS One 7: e39691.
30. Kim AL, Athar M, Bickers DR, Gautier J (2002) Stage-specific alterations of cyclin expression during UVB-induced murine skin tumor development. Photochem Photobiol 75: 58-67.
31. Kim KH, Back JH, Zhu Y, Arbesman J, Athar M, et al. (2011) Resveratrol targets transforming growth factor-beta2 signaling to block UV-induced tumor progression. J Invest Dermatol 131: 195-202.
32. Kim AL, Labasi JM, Zhu Y, Tang X, McClure K, et al. (2005) Role of p38 MAPK in UVB-induced inflammatory responses in the skin of SKH-1 hairless mice. J Invest Dermatol 124: 1318-1325. (Pubitemid 40847422)
33. Brash DE, Rudolph JA, Simon JA, Lin A, McKenna GJ, et al. (1991) A role for sunlight in skin cancer: UV-induced p53 mutations in squamous cell carcinoma. Proc Natl Acad Sci U S A 88: 10124-10128. (Pubitemid 21915787)
34. Black AP, Ogg GS (2003) The role of p53 in the immunobiology of cutaneous squamous cell carcinoma. Clin Exp Immunol 132: 379-384. (Pubitemid 36713942)
35. Hui L, Bakiri L, Mairhorfer A, Schweifer N, Haslinger C, et al. (2007) p38alpha suppresses normal and cancer cell proliferation by antagonizing the JNK-c-Jun pathway. Nat Genet 39: 741-749. (Pubitemid 46848584)
36. Ming M, Feng L, Shea CR, Soltani K, Zhao B, et al. (2011) PTEN positively regulates UVB-induced DNA damage repair. Cancer Res 71: 5287-5295.
37. Dickinson SE, Olson ER, Zhang J, Cooper SJ, Melton T, et al. (2011) p38 MAP kinase plays a functional role in UVB-induced mouse skin carcinogenesis. Mol Carcinog 50: 469-478.
38. Liu K, Yu D, Cho YY, Bode AM, Ma W, et al. (2013) Sunlight UV-induced skin cancer relies upon activation of the p38alpha signaling pathway. Cancer Res 73: 2181-2188.
39. Schindler EM, Hindes A, Gribben EL, Burns CJ, Yin Y, et al. (2009) p38d Mitogen-Activated Protein Kinase Is Essential for Skin Tumor Development in Mice. Cancer Research 69: 4648-4655.
40. Haider AS, Peters SB, Kaporis H, Cardinale I, Fei J, et al. (2006) Genomic analysis defines a cancer-specific gene expression signature for human squamous cell carcinoma and distinguishes malignant hyperproliferation from benign hyperplasia. J Invest Dermatol 126: 869-881.
41. Trempolec N, Dave-Coll N, Nebreda AR (2013) SnapShot: p38 MAPK Substrates. Cell 152: 924-924.e921.
42. Zhong SP, Ma WY, Dong Z (2000) ERKs and p38 kinases mediate ultraviolet B-induced phosphorylation of histone H3 at serine 10. J Biol Chem 275: 20980-20984.
43. Zhong S, Zhang Y, Jansen C, Goto H, Inagaki M, et al. (2001) MAP kinases mediate UVB-induced phosphorylation of histone H3 at serine 28. J Biol Chem 276: 12932-12937.
44. Nowak SJ, Corces VG (2004) Phosphorylation of histone H3: a balancing act between chromosome condensation and transcriptional activation. Trends Genet 20: 214-220. (Pubitemid 38369193)
45. James TT, Aroor AR, Lim RW, Shukla SD (2012) Histone H3 phosphorylation (Ser10, Ser28) and phosphoacetylation (K9S10) are differentially associated with gene expression in liver of rats treated in vivo with acute ethanol. J Pharmacol Exp Ther 340: 237-247.