Reprogramming human A375 amelanotic melanoma cells by catalase overexpression: Upregulation of antioxidant genes correlates with regression of melanoma malignancy and with malignant progression when downregulated

Reactive oxygen species (ROS) are implicated in tumor transformation. The antioxidant system (AOS) protects cells from ROS damage. However, it is also hijacked by cancers cells to proliferate within the tumor. Thus, identifying proteins altered by redox imbalance in cancer cells is an attractive pro...

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Autor principal: Bracalente, C.
Otros Autores: Ibañez, I.L, Berenstein, A., Notcovich, C., Cerda, M.B, Klamt, F., Chernomoretz, A., Durán, H.
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: Impact Journals LLC 2016
Acceso en línea:Registro en Scopus
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024 7 |2 cas  |a catalase, 9001-05-2; ubiquitin, 60267-61-0; Antioxidants; Catalase; Reactive Oxygen Species 
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100 1 |a Bracalente, C. 
245 1 0 |a Reprogramming human A375 amelanotic melanoma cells by catalase overexpression: Upregulation of antioxidant genes correlates with regression of melanoma malignancy and with malignant progression when downregulated 
260 |b Impact Journals LLC  |c 2016 
270 1 0 |m Durán, H.; Departamento de Micro y Nanotecnología, Comisión Nacional de Energía AtómicaArgentina; email: hduran@cnea.gov.ar 
506 |2 openaire  |e Política editorial 
504 |a Cakir, Y., Ballinger, S.W., Reactive species-mediated regulation of cell signaling and the cell cycle: the role of MAPK (2005) Antioxid Redox Signal, 7, pp. 726-740 
504 |a Arnold, R.S., Shi, J., Murad, E., Whalen, A.M., Sun, C.Q., Polavarapu, R., Parthasarathy, S., Lambeth, J.D., Hydrogen peroxide mediates the cell growth and transformation caused by the mitogenic oxidase Nox1 (2001) Proc Natl Acad Sci U S A, 98, pp. 5550-5555 
504 |a Meyskens, F.L., Jr., Farmer, P., Fruehauf, J.P., Redox regulation in human melanocytes and melanoma (2001) Pigment Cell Res, 14, pp. 148-154 
504 |a Condeelis, J., Singer, R.H., Segall, J.E., The great escape: when cancer cells hijack the genes for chemotaxis and motility (2005) Annu Rev Cell Dev Biol, 21, pp. 695-718 
504 |a Nishikawa, M., Reactive oxygen species in tumor metastasis (2008) Cancer Lett, 266, pp. 53-59 
504 |a Pani, G., Galeotti, T., Chiarugi, P., Metastasis: cancer cell's escape from oxidative stress (2010) Cancer Metastasis Rev, 29, pp. 351-378 
504 |a Behrend, L., Henderson, G., Zwacka, R.M., Reactive oxygen species in oncogenic transformation (2003) Biochem Soc Trans, 31, pp. 1441-1444 
504 |a Zhang, Y., Du, Y., Le, W., Wang, K., Kieffer, N., Zhang, J., Redox control of the survival of healthy and diseased cells (2011) Antioxid Redox Signal, 15, pp. 2867-2908 
504 |a da Lisboa Motta, L., Muller, C.B., De Bastiani, M.A., Behr, G.A., Franca, F.S., da Rocha, R.F., Minotto, J.B., Castro, M.A., Imbalance in redox status is associated with tumor aggressiveness and poor outcome in lung adenocarcinoma patients (2014) J Cancer Res Clin Oncol, 140, pp. 461-470 
504 |a Policastro, L., Molinari, B., Larcher, F., Blanco, P., Podhajcer, O.L., Costa, C.S., Rojas, P., Duran, H., Imbalance of antioxidant enzymes in tumor cells and inhibition of proliferation and malignant features by scavenging hydrogen peroxide (2004) Mol Carcinog, 39, pp. 103-113 
504 |a Hyoudou, K., Nishikawa, M., Ikemura, M., Kobayashi, Y., Mendelsohn, A., Miyazaki, N., Tabata, Y., Hashida, M., Prevention of pulmonary metastasis from subcutaneous tumors by binary system-based sustained delivery of catalase (2009) J Control Release, 137, pp. 110-115 
504 |a Fiaschi, T., Chiarugi, P., Oxidative stress, tumor microenvironment, and metabolic reprogramming: a diabolic liaison (2012) Int J Cell Biol, 2012 
504 |a Kim, S., Kim do, H., Jung, W.H., Koo, J.S., The expression of redox proteins in phyllodes tumor (2013) Breast Cancer Res Treat, 141, pp. 365-374 
504 |a Liu-Smith, F., Dellinger, R., Meyskens, F.L., Jr., Updates of reactive oxygen species in melanoma etiology and progression (2014) Arch Biochem Biophys, 563, pp. 51-55 
504 |a Rotblat, B., Grunewald, T.G., Leprivier, G., Melino, G., Knight, R.A., Anti-oxidative stress response genes: bioinformatic analysis of their expression and relevance in multiple cancers (2013) Oncotarget, 4, pp. 2577-2590 
504 |a Ibanez, I.L., Policastro, L.L., Tropper, I., Bracalente, C., Palmieri, M.A., Rojas, P.A., Molinari, B.L., Duran, H., H2O2 scavenging inhibits G1/S transition by increasing nuclear levels of p27KIP1 (2011) Cancer Lett, 305, pp. 58-68 
504 |a Policastro, L.L., Ibanez, I.L., Duran, H.A., Soria, G., Gottifredi, V., Podhajcer, O.L., Suppression of cancer growth by nonviral gene therapy based on a novel reactive oxygen speciesresponsive promoter (2009) Mol Ther, 17, pp. 1355-1364 
504 |a Brown, M.R., Miller, F.J., Jr., Li, W.G., Ellingson, A.N., Mozena, J.D., Chatterjee, P., Engelhardt, J.F., Weintraub, N.L., Overexpression of human catalase inhibits proliferation and promotes apoptosis in vascular smooth muscle cells (1999) Circ Res, 85, pp. 524-533 
504 |a Glorieux, C., Dejeans, N., Sid, B., Beck, R., Calderon, P.B., Verrax, J., Catalase overexpression in mammary cancer cells leads to a less aggressive phenotype and an altered response to chemotherapy (2011) Biochem Pharmacol, 82, pp. 1384-1390 
504 |a Balch, C.M., Gershenwald, J.E., Soong, S.J., Thompson, J.F., Atkins, M.B., Byrd, D.R., Buzaid, A.C., Gimotty, P.A., Final version of 2009 AJCC melanoma staging and classification (2009) J Clin Oncol, 27, pp. 6199-6206 
504 |a Hoek, K., Rimm, D.L., Williams, K.R., Zhao, H., Ariyan, S., Lin, A., Kluger, H.M., Yoshikawa, K., Expression profiling reveals novel pathways in the transformation of melanocytes to melanomas (2004) Cancer Res, 64, pp. 5270-5282 
504 |a Mohebiany, A.N., Harroch, S., Bouyain, S., New insights into the roles of the contactin cell adhesion molecules in neural development (2014) Adv Neurobiol, 8, pp. 165-194 
504 |a Hu, Q.D., Ang, B.T., Karsak, M., Hu, W.P., Cui, X.Y., Duka, T., Takeda, Y., Small, D., F3/contactin acts as a functional ligand for Notch during oligodendrocyte maturation (2003) Cell, 115, pp. 163-175 
504 |a Ghanem, G., Fabrice, J., Tyrosinase related protein 1 (TYRP1/gp75) in human cutaneous melanoma (2011) Mol Oncol, 5, pp. 150-155 
504 |a Liu, K., Wang, G., Ding, H., Chen, Y., Yu, G., Wang, J., Downregulation of metastasis suppressor 1(MTSS1) is associated with nodal metastasis and poor outcome in Chinese patients with gastric cancer (2010) BMC Cancer, 10, p. 428 
504 |a Monaghan-Benson, E., Burridge, K., Mutant B-RAF regulates a Rac-dependent cadherin switch in melanoma (2013) Oncogene, 32, pp. 4836-4844 
504 |a Yamazaki, K., Takamura, M., Masugi, Y., Mori, T., Du, W., Hibi, T., Hiraoka, N., Sakamoto, M., Adenylate cyclase-associated protein 1 overexpressed in pancreatic cancers is involved in cancer cell motility (2009) Lab Invest, 89, pp. 425-432 
504 |a Fang, D., Hallman, J., Sangha, N., Kute, T.E., Hammarback, J.A., White, W.L., Setaluri, V., Expression of microtubule-associated protein 2 in benign and malignant melanocytes: implications for differentiation and progression of cutaneous melanoma (2001) Am J Pathol, 158, pp. 2107-2115 
504 |a Subramanian, A., Tamayo, P., Mootha, V.K., Mukherjee, S., Ebert, B.L., Gillette, M.A., Paulovich, A., Mesirov, J.P., Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles (2005) Proc Natl Acad Sci U S A, 102, pp. 15545-15550 
504 |a Mootha, V.K., Lindgren, C.M., Eriksson, K.F., Subramanian, A., Sihag, S., Lehar, J., Puigserver, P., Patterson, N., PGC-1alpha-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes (2003) Nat Genet, 34, pp. 267-273 
504 |a Maresca, V., Flori, E., Briganti, S., Mastrofrancesco, A., Fabbri, C., Mileo, A.M., Paggi, M.G., Picardo, M., Correlation between melanogenic and catalase activity in in vitro human melanocytes: a synergic strategy against oxidative stress (2008) Pigment Cell Melanoma Res, 21, pp. 200-205 
504 |a Jimenez-Cervantes, C., Martinez-Esparza, M., Perez, C., Daum, N., Solano, F., Garcia-Borron, J.C., Inhibition of melanogenesis in response to oxidative stress: transient downregulation of melanocyte differentiation markers and possible involvement of microphthalmia transcription factor (2001) J Cell Sci, 114, pp. 2335-2344 
504 |a Durbec, P., Gennarini, G., Goridis, C., Rougon, G., A soluble form of the F3 neuronal cell adhesion molecule promotes neurite outgrowth (1992) J Cell Biol, 117, pp. 877-887 
504 |a Wulfanger, J., Biehl, K., Tetzner, A., Wild, P., Ikenberg, K., Meyer, S., Seliger, B., Heterogeneous expression and functional relevance of the ubiquitin carboxyl-terminal hydrolase L1 in melanoma (2013) Int J Cancer, 133, pp. 2522-2532 
504 |a Lin, J., Liu, J., Wang, Y., Zhu, J., Zhou, K., Smith, N., Zhan, X., Differential regulation of cortactin and N-WASP-mediated actin polymerization by missing in metastasis (MIM) protein (2005) Oncogene, 24, pp. 2059-2066 
504 |a Zhang, S., Qi, Q., MTSS1 suppresses cell migration and invasion by targeting CTTN in glioblastoma (2015) J Neurooncol, 121, pp. 425-431 
504 |a Zhong, J., Shaik, S., Wan, L., Tron, A.E., Wang, Z., Sun, L., Inuzuka, H., Wei, W., SCF beta-TRCP targets MTSS1 for ubiquitination-mediated destruction to regulate cancer cell proliferation and migration (2013) Oncotarget, 4, pp. 2339-2353 
504 |a Mertz, K.D., Pathria, G., Wagner, C., Saarikangas, J., Sboner, A., Romanov, J., Gschaider, M., Lappalainen, P., MTSS1 is a metastasis driver in a subset of human melanomas (2014) Nat Commun, 5, p. 3465 
504 |a Loberg, R.D., Neeley, C.K., Adam-Day, L.L., Fridman, Y., St John, L.N., Nixdorf, S., Jackson, P., Pienta, K.J., Differential expression analysis of MIM (MTSS1) splice variants and a functional role of MIM in prostate cancer cell biology (2005) Int J Oncol, 26, pp. 1699-1705 
504 |a Parr, C., Jiang, W.G., Metastasis suppressor 1 (MTSS1) demonstrates prognostic value and anti-metastatic properties in breast cancer (2009) Eur J Cancer, 45, pp. 1673-1683 
504 |a Lee, Y.G., Macoska, J.A., Korenchuk, S., Pienta, K.J., MIM, a potential metastasis suppressor gene in bladder cancer (2002) Neoplasia, 4, pp. 291-294 
504 |a Nixdorf, S., Grimm, M.O., Loberg, R., Marreiros, A., Russell, P.J., Pienta, K.J., Jackson, P., Expression and regulation of MIM (Missing In Metastasis), a novel putative metastasis suppressor gene, and MIM-B, in bladder cancer cell lines (2004) Cancer Lett, 215, pp. 209-220 
504 |a Wang, J., Li, J., Shen, J., Wang, C., Yang, L., Zhang, X., MicroRNA-182 downregulates metastasis suppressor 1 and contributes to metastasis of hepatocellular carcinoma (2012) BMC Cancer, 12, p. 227 
504 |a Dawson, J.C., Timpson, P., Kalna, G., Machesky, L.M., Mtss1 regulates epidermal growth factor signaling in head and neck squamous carcinoma cells (2012) Oncogene, 31, pp. 1781-1793 
504 |a Uhlenbrock, K., Eberth, A., Herbrand, U., Daryab, N., Stege, P., Meier, F., Friedl, P., Ahmadian, M.R., The RacGEF Tiam1 inhibits migration and invasion of metastatic melanoma via a novel adhesive mechanism (2004) J Cell Sci, 117, pp. 4863-4871 
504 |a Thomassen, M., Tan, Q., Kruse, T.A., Gene expression metaanalysis identifies chromosomal regions and candidate genes involved in breast cancer metastasis (2009) Breast Cancer Res Treat, 113, pp. 239-249 
504 |a Siritantikorn, A., Johansson, K., Ahlen, K., Rinaldi, R., Suthiphongchai, T., Wilairat, P., Morgenstern, R., Protection of cells from oxidative stress by microsomal glutathione transferase 1 (2007) Biochem Biophys Res Commun, 355, pp. 592-596 
504 |a Johansson, K., Jarvliden, J., Gogvadze, V., Morgenstern, R., Multiple roles of microsomal glutathione transferase 1 in cellular protection: a mechanistic study (2010) Free Radic Biol Med, 49, pp. 1638-1645 
504 |a Lei, K.F., Wang, Y.F., Zhu, X.Q., Lu, P.C., Sun, B.S., Jia, H.L., Ren, N., Qin, L.X., Identification of MSRA gene on chromosome 8p as a candidate metastasis suppressor for human hepatitis B virus-positive hepatocellular carcinoma (2007) BMC Cancer, 7, p. 172 
504 |a De Luca, A., Sanna, F., Sallese, M., Ruggiero, C., Grossi, M., Sacchetta, P., Rossi, C., Favaloro, B., Methionine sulfoxide reductase A down-regulation in human breast cancer cells results in a more aggressive phenotype (2010) Proc Natl Acad Sci U S A, 107, pp. 18628-18633 
504 |a Zhou, Z., Li, C.Y., Li, K., Wang, T., Zhang, B., Gao, T.W., Decreased methionine sulphoxide reductase A expression renders melanocytes more sensitive to oxidative stress: a possible cause for melanocyte loss in vitiligo (2009) Br J Dermatol, 161, pp. 504-509 
504 |a Schallreuter, K.U., Salem, M.A., Holtz, S., Panske, A., Basic evidence for epidermal H2O2/ONOO(-)-mediated oxidation/nitration in segmental vitiligo is supported by repigmentation of skin and eyelashes after reduction of epidermal H2O2 with topical NB-UVB-activated pseudocatalase PC-KUS (2013) FASEB J, 27, pp. 3113-3122 
504 |a Schallreuter, K.U., Lemke, K.R., Hill, H.Z., Wood, J.M., Thioredoxin reductase induction coincides with melanin biosynthesis in brown and black guinea pigs and in murine melanoma cells (1994) J Invest Dermatol, 103, pp. 820-824 
504 |a Tan, X., Zhai, Y., Chang, W., Hou, J., He, S., Lin, L., Yu, Y., Cao, G., Global analysis of metastasis-associated gene expression in primary cultures from clinical specimens of clear-cell renal-cell carcinoma (2008) Int J Cancer, 123, pp. 1080-1088 
504 |a Zhou, C., Nitschke, A.M., Xiong, W., Zhang, Q., Tang, Y., Bloch, M., Elliott, S., McLachlan, J.A., Proteomic analysis of tumor necrosis factor-alpha resistant human breast cancer cells reveals a MEK5/Erk5-mediated epithelial-mesenchymal transition phenotype (2008) Breast Cancer Res, 10, p. R105 
504 |a Scharlau, D., Borowicki, A., Habermann, N., Hofmann, T., Klenow, S., Miene, C., Munjal, U., Glei, M., Mechanisms of primary cancer prevention by butyrate and other products formed during gut flora-mediated fermentation of dietary fibre (2009) Mutat Res, 682, pp. 39-53 
504 |a Itoh, S., Kim, H.W., Nakagawa, O., Ozumi, K., Lessner, S.M., Aoki, H., Akram, K., Fukai, T., Novel role of antioxidant-1 (Atox1) as a copper-dependent transcription factor involved in cell proliferation (2008) J Biol Chem, 283, pp. 9157-9167 
504 |a Cai, H., Peng, F., Knockdown of copper chaperone antioxidant-1 by RNA interference inhibits copper-stimulated proliferation of non-small cell lung carcinoma cells (2013) Oncol Rep, 30, pp. 269-275 
504 |a Suh, I., Weng, J., Fernandez-Ranvier, G., Shen, W.T., Duh, Q.Y., Clark, O.H., Kebebew, E., Antineoplastic effects of decitabine, an inhibitor of DNA promoter methylation, in adrenocortical carcinoma cells (2010) Arch Surg, 145, pp. 226-232 
504 |a Nicolussi, A., D'Inzeo, S., Mincione, G., Buffone, A., Di Marcantonio, M.C., Cotellese, R., Cichella, A., Coppa, A., PRDX1 and PRDX6 are repressed in papillary thyroid carcinomas via BRAF V600E-dependent and-independent mechanisms (2014) Int J Oncol, 44, pp. 548-556 
504 |a Hendriksen, P.J., Dits, N.F., Kokame, K., Veldhoven, A., van Weerden, W.M., Bangma, C.H., Trapman, J., Jenster, G., Evolution of the androgen receptor pathway during progression of prostate cancer (2006) Cancer Res, 66, pp. 5012-5020 
504 |a Gumy-Pause, F., Pardo, B., Khoshbeen-Boudal, M., Ansari, M., Gayet-Ageron, A., Sappino, A.P., Attiyeh, E.F., Ozsahin, H., GSTP1 hypermethylation is associated with reduced protein expression, aggressive disease and prognosis in neuroblastoma (2012) Genes Chromosomes Cancer, 51, pp. 174-185 
504 |a Brabender, J., Lord, R.V., Wickramasinghe, K., Metzger, R., Schneider, P.M., Park, J.M., Holscher, A.H., Danenberg, P.V., Glutathione S-transferasepi expression is downregulated in patients with Barrett's esophagus and esophageal adenocarcinoma (2002) J Gastrointest Surg, 6, pp. 359-367 
504 |a Peng, D., Belkhiri, A., Hu, T., Chaturvedi, R., Asim, M., Wilson, K.T., Zaika, A., El-Rifai, W., Glutathione peroxidase 7 protects against oxidative DNA damage in oesophageal cells (2012) Gut, 61, pp. 1250-1260 
504 |a Peng, D.F., Hu, T.L., Soutto, M., Belkhiri, A., El-Rifai, W., Loss of glutathione peroxidase 7 promotes TNF-alphainduced NF-kappaB activation in Barrett's carcinogenesis (2014) Carcinogenesis, 35, pp. 1620-1628 
504 |a Mougiakakos, D., Okita, R., Ando, T., Durr, C., Gadiot, J., Ichikawa, J., Zeiser, R., Kiessling, R., High expression of GCLC is associated with malignant melanoma of low oxidative phenotype and predicts a better prognosis (2012) J Mol Med (Berl), 90, pp. 935-944 
504 |a Soini, Y., Karihtala, P., Mantyniemi, A., Turunen, N., Paakko, P., Kinnula, V., Glutamate-L-cysteine ligase in breast carcinomas (2004) Histopathology, 44, pp. 129-135 
504 |a Chen, L., Kwong, M., Lu, R., Ginzinger, D., Lee, C., Leung, L., Chan, J.Y., Nrf1 is critical for redox balance and survival of liver cells during development (2003) Mol Cell Biol, 23, pp. 4673-4686 
504 |a Xu, Z., Chen, L., Leung, L., Yen, T.S., Lee, C., Chan, J.Y., Liverspecific inactivation of the Nrf1 gene in adult mouse leads to nonalcoholic steatohepatitis and hepatic neoplasia (2005) Proc Natl Acad Sci U S A, 102, pp. 4120-4125 
504 |a Han, W., Ming, M., Zhao, R., Pi, J., Wu, C., He, Y.Y., Nrf1 CNCbZIP protein promotes cell survival and nucleotide excision repair through maintaining glutathione homeostasis (2012) J Biol Chem, 287, pp. 18788-18795 
504 |a Inoue, K., Imai, Y., Identification of novel transcription factors in osteoclast differentiation using genome-wide analysis of open chromatin determined by DNase-seq (2014) J Bone Miner Res, 29, pp. 1823-1832 
504 |a Kim, J., Xing, W., Wergedal, J., Chan, J.Y., Mohan, S., Targeted disruption of nuclear factor erythroid-derived 2-like 1 in osteoblasts reduces bone size and bone formation in mice (2010) Physiol Genomics, 40, pp. 100-110 
504 |a Ibanez, I.L., Bracalente, C., Notcovich, C., Tropper, I., Molinari, B.L., Policastro, L.L., Duran, H., Phosphorylation and subcellular localization of p27Kip1 regulated by hydrogen peroxide modulation in cancer cells (2012) PLoS ONE, 7 
504 |a (2011) A Language and Environment for Statistical Computing, , R Foundation for Statistical Computing 
504 |a Gentleman, R.C., Carey, V.J., Bates, D.M., Bolstad, B., Dettling, M., Dudoit, S., Ellis, B., Huber, W., Bioconductor: open software development for computational biology and bioinformatics (2004) Genome Biol, 5, p. R80 
504 |a da Huang, W., Sherman, B.T., Lempicki, R.A., Bioinformatics enrichment tools: paths toward the comprehensive functional analysis of large gene lists (2009) Nucleic Acids Res, 37, pp. 1-13 
504 |a da Huang, W., Sherman, B.T., Lempicki, R.A., Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources (2009) Nat Protoc, 4, pp. 44-57 
504 |a Ashburner, M., Ball, C.A., Blake, J.A., Botstein, D., Butler, H., Cherry, J.M., Davis, A.P., Issel-Tarver, L., Gene ontology: tool for the unification of biology. The Gene Ontology Consortium (2000) Nat Genet, 25, pp. 25-29 
504 |a Kanehisa, M., Goto, S., Sato, Y., Kawashima, M., Furumichi, M., Tanabe, M., Data, information, knowledge and principle: back to metabolism in KEGG (2014) Nucleic Acids Res, 42, pp. D199-205 
504 |a Kanehisa, M., Goto, S., Sato, Y., Furumichi, M., Tanabe, M., KEGG for integration and interpretation of large-scale molecular data sets (2012) Nucleic Acids Res, 40, pp. D109-114 
504 |a Kanehisa, M., Goto, S., KEGG: kyoto encyclopedia of genes and genomes (2000) Nucleic Acids Res, 28, pp. 27-30 
504 |a Lu, T., Finkel, T., Free radicals and senescence (2008) Exp Cell Res, 314, pp. 1918-1922 
504 |a Valko, M., Leibfritz, D., Moncol, J., Cronin, M.T., Mazur, M., Telser, J., Free radicals and antioxidants in normal physiological functions and human disease (2007) Int J Biochem Cell Biol, 39, pp. 44-84 
504 |a Allen, R.G., Tresini, M., Oxidative stress and gene regulation (2000) Free Radic Biol Med, 28, pp. 463-499 
504 |a Finkel, T., Signal transduction by reactive oxygen species (2011) J Cell Biol, 194, pp. 7-15 
504 |a Warde-Farley, D., Donaldson, S.L., Comes, O., Zuberi, K., Badrawi, R., Chao, P., Franz, M., Montojo, J., The GeneMANIA prediction server: biological network integration for gene prioritization and predicting gene function (2010) Nucleic Acids Res, 38, pp. W214-220 
504 |a Hoek, K.S., Schlegel, N.C., Brafford, P., Sucker, A., Ugurel, S., Kumar, R., Weber, B.L., Dummer, R., Metastatic potential of melanomas defined by specific gene expression profiles with no BRAF signature (2006) Pigment Cell Res, 19, pp. 290-302 
504 |a Jaeger, J., Koczan, D., Thiesen, H.J., Ibrahim, S.M., Gross, G., Spang, R., Kunz, M., Gene expression signatures for tumor progression, tumor subtype, and tumor thickness in lasermicrodissected melanoma tissues (2007) Clin Cancer Res, 13, pp. 806-815 
504 |a Jeffs, A.R., Glover, A.C., Slobbe, L.J., Wang, L., He, S., Hazlett, J.A., Awasthi, A., Eccles, M.R., A gene expression signature of invasive potential in metastatic melanoma cells (2009) PLoS One, 4 
504 |a Riker, A.I., Enkemann, S.A., Fodstad, O., Liu, S., Ren, S., Morris, C., Xi, Y., Eschrich, S., The gene expression profiles of primary and metastatic melanoma yields a transition point of tumor progression and metastasis (2008) BMC Med Genomics, 1, p. 13 
504 |a Winnepenninckx, V., Lazar, V., Michiels, S., Dessen, P., Stas, M., Alonso, S.R., Avril, M.F., Sarasin, A., Gene expression profiling of primary cutaneous melanoma and clinical outcome (2006) J Natl Cancer Inst, 98, pp. 472-482 
504 |a Smith, A.P., Hoek, K., Becker, D., Whole-genome expression profiling of the melanoma progression pathway reveals marked molecular differences between nevi/melanoma in situ and advanced-stage melanomas (2005) Cancer Biol Ther, 4, pp. 1018-1029 
504 |a Talantov, D., Mazumder, A., Yu, J.X., Briggs, T., Jiang, Y., Backus, J., Atkins, D., Wang, Y., Novel genes associated with malignant melanoma but not benign melanocytic lesions (2005) Clin Cancer Res, 11, pp. 7234-7242 
504 |a Mandruzzato, S., Callegaro, A., Turcatel, G., Francescato, S., Montesco, M.C., Chiarion-Sileni, V., Mocellin, S., Zanovello, P., A gene expression signature associated with survival in metastatic melanoma (2006) J Transl Med, 4, p. 50 
504 |a John, T., Black, M.A., Toro, T.T., Leader, D., Gedye, C.A., Davis, I.D., Guilford, P.J., Cebon, J.S., Predicting clinical outcome through molecular profiling in stage III melanoma (2008) Clin Cancer Res, 14, pp. 5173-5180 
504 |a Bogunovic, D., O'Neill, D.W., Belitskaya-Levy, I., Vacic, V., Yu, Y.L., Adams, S., Darvishian, F., Osman, I., Immune profile and mitotic index of metastatic melanoma lesions enhance clinical staging in predicting patient survival (2009) Proc Natl Acad Sci U S A, 106, pp. 20429-20434 
504 |a Schramm, S.J., Mann, G.J., Melanoma prognosis: a REMARKbased systematic review and bioinformatic analysis of immunohistochemical and gene microarray studies (2011) Mol Cancer Ther, 10, pp. 1520-1528 
504 |a Wang, L., Hurley, D.G., Watkins, W., Araki, H., Tamada, Y., Muthukaruppan, A., Ranjard, L., Print, C.G., Cell cycle gene networks are associated with melanoma prognosis (2012) PLoS ONE, 7 
504 |a Shannon, P., Markiel, A., Ozier, O., Baliga, N.S., Wang, J.T., Ramage, D., Amin, N., Ideker, T., Cytoscape: a software environment for integrated models of biomolecular interaction networks (2003) Genome Res, 13, pp. 2498-2504 
520 3 |a Reactive oxygen species (ROS) are implicated in tumor transformation. The antioxidant system (AOS) protects cells from ROS damage. However, it is also hijacked by cancers cells to proliferate within the tumor. Thus, identifying proteins altered by redox imbalance in cancer cells is an attractive prognostic and therapeutic tool. Gene expression microarrays in A375 melanoma cells with different ROS levels after overexpressing catalase were performed. Dissimilar phenotypes by differential compensation to hydrogen peroxide scavenging were generated. The melanotic A375-A7 (A7) upregulated TYRP1, CNTN1 and UCHL1 promoting melanogenesis. The metastatic A375-G10 (G10) downregulated MTSS1 and TIAM1, proteins absent in metastasis. Moreover, differential coexpression of AOS genes (EPHX2, GSTM3, MGST1, MSRA, TXNRD3, MGST3 and GSR) was found in A7 and G10. Their increase in A7 improved its AOS ability and therefore, oxidative stress response, resembling less aggressive tumor cells. Meanwhile, their decrease in G10 revealed a disruption in the AOS and therefore, enhanced its metastatic capacity. These gene signatures, not only bring new insights into the physiopathology of melanoma, but also could be relevant in clinical prognostic to classify between non aggressive and metastatic melanomas. © 2018 Impact Journals.  |l eng 
593 |a Departamento de Micro y Nanotecnología, Comisión Nacional de Energía Atómica, San Martín, Buenos Aires, Argentina 
593 |a Consejo Nacional de Investigaciones Científicas y Tecnológicas, Buenos Aires, Argentina 
593 |a Fundación Instituto Leloir and Departamento de Física, Facultad Ciencias Exactas y Naturales, Universidad de Buenos Aires, Buenos Aires, Argentina 
593 |a Laboratório de Bioquímica Celular, Departamento de Bioquímica, Instituto de Ciências Básicas da Saúde, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil 
593 |a Escuela de Ciencia y Tecnología, Universidad Nacional de San Martín, San Martín, Buenos Aires, Argentina 
690 1 0 |a AOS NETWORK 
690 1 0 |a MELANOGENESIS 
690 1 0 |a MELANOMA 
690 1 0 |a METASTASIS 
690 1 0 |a MICROARRAYS 
690 1 0 |a ANTIOXIDANT 
690 1 0 |a CATALASE 
690 1 0 |a CONTACTIN 1 
690 1 0 |a REACTIVE OXYGEN METABOLITE 
690 1 0 |a TYROSINASE RELATED PROTEIN 1 
690 1 0 |a UBIQUITIN 
690 1 0 |a CATALASE 
690 1 0 |a REACTIVE OXYGEN METABOLITE 
690 1 0 |a TRANSCRIPTOME 
690 1 0 |a A-375 CELL LINE 
690 1 0 |a ANIMAL CELL 
690 1 0 |a ANTIPROLIFERATIVE ACTIVITY 
690 1 0 |a ARTICLE 
690 1 0 |a CANCER GROWTH 
690 1 0 |a CANCER PROGNOSIS 
690 1 0 |a CANCER REGRESSION 
690 1 0 |a CNTN1 GENE 
690 1 0 |a CONTROLLED STUDY 
690 1 0 |a DOWN REGULATION 
690 1 0 |a EMBRYO 
690 1 0 |a EPHX2 GENE 
690 1 0 |a GENE 
690 1 0 |a GENE EXPRESSION PROFILING 
690 1 0 |a GENE EXPRESSION REGULATION 
690 1 0 |a GENE OVEREXPRESSION 
690 1 0 |a GSR GENE 
690 1 0 |a GSTM3 GENE 
690 1 0 |a HUMAN 
690 1 0 |a HUMAN CELL 
690 1 0 |a HYDROGEN PEROXIDE SCAVENGING ASSAY 
690 1 0 |a MELANOGENESIS 
690 1 0 |a MELANOMA 
690 1 0 |a METASTATIC MELANOMA 
690 1 0 |a MGST1 GENE 
690 1 0 |a MGST3 GENE 
690 1 0 |a MOUSE 
690 1 0 |a MSRA GENE 
690 1 0 |a NONHUMAN 
690 1 0 |a NUCLEAR REPROGRAMMING 
690 1 0 |a OXIDATIVE STRESS 
690 1 0 |a PATHOPHYSIOLOGY 
690 1 0 |a PHENOTYPE 
690 1 0 |a TUMOR CELL 
690 1 0 |a TXNRD3 GENE 
690 1 0 |a TYRP1 GENE 
690 1 0 |a UCHL1 GENE 
690 1 0 |a UPREGULATION 
690 1 0 |a AMELANOTIC MELANOMA 
690 1 0 |a CELL PROLIFERATION 
690 1 0 |a DISEASE EXACERBATION 
690 1 0 |a GENE EXPRESSION REGULATION 
690 1 0 |a GENETICS 
690 1 0 |a METABOLISM 
690 1 0 |a METASTASIS 
690 1 0 |a MICROARRAY ANALYSIS 
690 1 0 |a PATHOLOGY 
690 1 0 |a SKIN TUMOR 
690 1 0 |a TUMOR CELL LINE 
690 1 0 |a ANTIOXIDANTS 
690 1 0 |a CATALASE 
690 1 0 |a CELL LINE, TUMOR 
690 1 0 |a CELL PROLIFERATION 
690 1 0 |a DISEASE PROGRESSION 
690 1 0 |a DOWN-REGULATION 
690 1 0 |a GENE EXPRESSION PROFILING 
690 1 0 |a GENE EXPRESSION REGULATION, NEOPLASTIC 
690 1 0 |a HUMANS 
690 1 0 |a MELANOMA, AMELANOTIC 
690 1 0 |a MICROARRAY ANALYSIS 
690 1 0 |a NEOPLASM METASTASIS 
690 1 0 |a OXIDATIVE STRESS 
690 1 0 |a REACTIVE OXYGEN SPECIES 
690 1 0 |a SKIN NEOPLASMS 
690 1 0 |a TRANSCRIPTOME 
690 1 0 |a UP-REGULATION 
700 1 |a Ibañez, I.L. 
700 1 |a Berenstein, A. 
700 1 |a Notcovich, C. 
700 1 |a Cerda, M.B. 
700 1 |a Klamt, F. 
700 1 |a Chernomoretz, A. 
700 1 |a Durán, H. 
773 0 |d Impact Journals LLC, 2016  |g v. 7  |h pp. 41154-41171  |k n. 27  |p Oncotarget  |x 19492553  |t Oncotarget 
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