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Type 1 (CDO1), three well known tumor suppressors that are frequently suppressed by hypermethylation in breast cancer [20, 21, 22].Integrative analysis of DNA methylation and gene expressionTo further investigate the biological consequences of altered DNA methylation by PD98059 dose resveratrol treatments, we correlated the epigenetic changes with gene expression variations at mRNAPLOS ONE | DOI:10.1371/journal.pone.0157866 June 29,8 /Methylation Landscape of Breast Cancer Cells in Response to ResveratrolTable 1. Cellular pathways and genes with differential DNA methylation in MDA-MB-231 cells at 24 h after treatment with resveratrol. Pathway name Cell cycle Number of genes 112 Hypermethylated (bold letters) and hypomethylated genes DKC1, AURKA, HSPA2, RCC2, HIST1H2BK, MAD1L1, TCP10, TUBB6, PRKCA,RRP1, HIST1H3A, CSNK2B, SGOL1, TUBA3C, HIST1H3D, ANKLE2, TP53, CCNB1, NUP98, DLC1, RAD17, HSP90AA1, CENPN, UBE2E2, CENPO, PSMA7, PSME3, PSMB10, NHP2, RUVBL2, APEX1, RAE1, HIST1H4F, PPP2R3B, CENPP, UBE2N, REC8, ORC1L, E2F1, TUBA1C, PSMB9, SYCP1, HIST1H2BI, TEX12, PRKAR2B, POLE, TUBA3E, SKP1, PPP2R2A, PIAS4, NCAPH, HIST1H3E, TUBA3D, UBC, INCENP, NUP210, MSH5, NUDC, RAB2A, FKBP6, BUB3, CCND1. DLG4, PYCARD, RPS6KA1, RPS6KA2, ITGB1, IL1B, SPTBN5, ASB4, GH1, GH2, HLADOB, NLRP12, EIF4G3, MRC2, EIF4G1, EIF4G2, TRAF6, CSHL1, TRAF2, EGR1, RAET1G, NFKBIE, ASB2, DUSP10, UBE2K, AKT1S1, SEC24C, IFITM2, TRAF7, RNF144B, IL17RD, LGALS3, CANX, NLRX1, RASGRF2, CD180, SEC61G, HLADMA, CARD11, MX1UBA1, FOXO1, ANGPT1, PDGFRB, PDGFRA, TNFRSF1B, ATP6V0A2, PIK3AP1, TEC,, MAPK14, KEAP1, PDGFA, GZMM, C1S, ZAP70, GHR, KIR3DL2, TLR2, ACTR3, FGF4, IFITM1, GAB1, IL6R, IKBKE, HERC5, UNC93B1, LIF, CD200R1, IL27RA, CCL17, LILRA2, NFATC2, TRIM14, FLNB, TRIM17, TCEB2, IRF4, SPTBN1, CTSL3, RAB7A, MBL2, RNF216, TRIM11, CD226, FOXO3, POLR3K, TRIM68. GTF2H4, HIST1H2BK, RRP1, XRCC5, XRCC4, TP53, Vesatolimod web PPP4R2, RAD17, GPS1, KDM4B, KDM4A, APEX1, HIST1H4F, UBE2N, FAN1, FAM175A, EYA3, ATRIP, NEIL2, NEIL3, NTHL1, RAD50, WHSC1, POLM, USP10, UBE2I, XPC, KIAA1530, XPA, HERC2, PAXIP1, REV3L, CUL4B, NFRKB, TFPT, KIAA0146, ALKBH3, CUL4A, RTEL1, ABL1, C19orf40, BACH1, ACTB, CDS1, SUMO3, INO80B, DCLRE1A, ACTR5, FANCI, CSNK1G1. ERCC6, UBC, RAD51L3, C1orf86, COPS3, DDB2, ERCC2, HIST1H2BI, POLR2J, POLE, PNKP, PIAS4. GRIN2C, DGKZ, DLG4, GRIN2D, GPR39, PRKCA, ABR, TAS1R3, RPS6KA1, ADORA3, RPS6KA2, GHRL, HTR4, SSTR2, DGKI, SHH, DGKD, NPB, GOLT1A, PLXNB1, SPTBN5, CCR10, OPRL1, PSME3, PSMB10, FGFR4, GNG12, MGLL, NPSR1, OR4F5, OR4F4, VWF,. PSMB9, PEBP1, SLA2, MLN, PROKR1, PLCB3, CXCL12, CNKSR1, GPR37, TRPC7, P2RY2, P2RY4, SST, HTR1F, SSTR3, NRG2, RGR, TAS2R4, AGT, WNT9A, ARHGEF16, ARHGEF17. DR1, BRD1, CHD3, CHD4, HIST1H2BK, KDM3A, SMARCA4, MLL, TRRAP, SMARCE1, KDM5B, KDM5C, HIST1H30A, MLL2, HIST1H3D, MLL3, PADI2, NCOR2, PHF8, EHMT1, MTA1, PRDM16, DNMT3A, PADI1, YEATS4, CSRP2BP, KDM4B, KDM4A, CREBBP, RUVBL2, EP400, SUPT3H, HIST1H4F, SETD1B, DOT1L, ACTB, MYST3, SUZ12P, AEBP2, KDM2B, WHSC1. KIAA1267, HIST1H2BI, KDM3B, SUV39H2, RBP1, SAP130, HIST1H3E, SMYD2, PADI6, HDAC10, FAM48A, MBD3. HSPA6, HSPA7, HSPA4L, GPX2, HSPA13, HSPA2, BAG5, HSPA1B, RPS6KA1, RPS6KA2, NPTXR, ETS2, NUP98, ATG16L1, IL6, DNAJB6, DLC1, HSP90AA1, UBE2E2, TXNRD1, ATG9A, RAE1, WDR45L, E2F1, PRKAG2, ACD, CBX2, RAD50, MAPKAPK2, AKT1S1, RPTOR, CCS, HIST1H1A, SOD1, WDR45, NUP62, TXNRD2, GSR, STAT3, ASF1A, TXN2, GML, NECAB3, DYNLL2. TSC2, GPX1, TNRC6C, TCEB2, TNRC6B, CEBPB, MAP1LC3B, UBC, HSPA1A, EGLN2, PRKAA1, NUP210, ATG3, MAPK14, CBX4, HSPA12B. TRADD, AKT3, PSMD2.Type 1 (CDO1), three well known tumor suppressors that are frequently suppressed by hypermethylation in breast cancer [20, 21, 22].Integrative analysis of DNA methylation and gene expressionTo further investigate the biological consequences of altered DNA methylation by resveratrol treatments, we correlated the epigenetic changes with gene expression variations at mRNAPLOS ONE | DOI:10.1371/journal.pone.0157866 June 29,8 /Methylation Landscape of Breast Cancer Cells in Response to ResveratrolTable 1. Cellular pathways and genes with differential DNA methylation in MDA-MB-231 cells at 24 h after treatment with resveratrol. Pathway name Cell cycle Number of genes 112 Hypermethylated (bold letters) and hypomethylated genes DKC1, AURKA, HSPA2, RCC2, HIST1H2BK, MAD1L1, TCP10, TUBB6, PRKCA,RRP1, HIST1H3A, CSNK2B, SGOL1, TUBA3C, HIST1H3D, ANKLE2, TP53, CCNB1, NUP98, DLC1, RAD17, HSP90AA1, CENPN, UBE2E2, CENPO, PSMA7, PSME3, PSMB10, NHP2, RUVBL2, APEX1, RAE1, HIST1H4F, PPP2R3B, CENPP, UBE2N, REC8, ORC1L, E2F1, TUBA1C, PSMB9, SYCP1, HIST1H2BI, TEX12, PRKAR2B, POLE, TUBA3E, SKP1, PPP2R2A, PIAS4, NCAPH, HIST1H3E, TUBA3D, UBC, INCENP, NUP210, MSH5, NUDC, RAB2A, FKBP6, BUB3, CCND1. DLG4, PYCARD, RPS6KA1, RPS6KA2, ITGB1, IL1B, SPTBN5, ASB4, GH1, GH2, HLADOB, NLRP12, EIF4G3, MRC2, EIF4G1, EIF4G2, TRAF6, CSHL1, TRAF2, EGR1, RAET1G, NFKBIE, ASB2, DUSP10, UBE2K, AKT1S1, SEC24C, IFITM2, TRAF7, RNF144B, IL17RD, LGALS3, CANX, NLRX1, RASGRF2, CD180, SEC61G, HLADMA, CARD11, MX1UBA1, FOXO1, ANGPT1, PDGFRB, PDGFRA, TNFRSF1B, ATP6V0A2, PIK3AP1, TEC,, MAPK14, KEAP1, PDGFA, GZMM, C1S, ZAP70, GHR, KIR3DL2, TLR2, ACTR3, FGF4, IFITM1, GAB1, IL6R, IKBKE, HERC5, UNC93B1, LIF, CD200R1, IL27RA, CCL17, LILRA2, NFATC2, TRIM14, FLNB, TRIM17, TCEB2, IRF4, SPTBN1, CTSL3, RAB7A, MBL2, RNF216, TRIM11, CD226, FOXO3, POLR3K, TRIM68. GTF2H4, HIST1H2BK, RRP1, XRCC5, XRCC4, TP53, PPP4R2, RAD17, GPS1, KDM4B, KDM4A, APEX1, HIST1H4F, UBE2N, FAN1, FAM175A, EYA3, ATRIP, NEIL2, NEIL3, NTHL1, RAD50, WHSC1, POLM, USP10, UBE2I, XPC, KIAA1530, XPA, HERC2, PAXIP1, REV3L, CUL4B, NFRKB, TFPT, KIAA0146, ALKBH3, CUL4A, RTEL1, ABL1, C19orf40, BACH1, ACTB, CDS1, SUMO3, INO80B, DCLRE1A, ACTR5, FANCI, CSNK1G1. ERCC6, UBC, RAD51L3, C1orf86, COPS3, DDB2, ERCC2, HIST1H2BI, POLR2J, POLE, PNKP, PIAS4. GRIN2C, DGKZ, DLG4, GRIN2D, GPR39, PRKCA, ABR, TAS1R3, RPS6KA1, ADORA3, RPS6KA2, GHRL, HTR4, SSTR2, DGKI, SHH, DGKD, NPB, GOLT1A, PLXNB1, SPTBN5, CCR10, OPRL1, PSME3, PSMB10, FGFR4, GNG12, MGLL, NPSR1, OR4F5, OR4F4, VWF,. PSMB9, PEBP1, SLA2, MLN, PROKR1, PLCB3, CXCL12, CNKSR1, GPR37, TRPC7, P2RY2, P2RY4, SST, HTR1F, SSTR3, NRG2, RGR, TAS2R4, AGT, WNT9A, ARHGEF16, ARHGEF17. DR1, BRD1, CHD3, CHD4, HIST1H2BK, KDM3A, SMARCA4, MLL, TRRAP, SMARCE1, KDM5B, KDM5C, HIST1H30A, MLL2, HIST1H3D, MLL3, PADI2, NCOR2, PHF8, EHMT1, MTA1, PRDM16, DNMT3A, PADI1, YEATS4, CSRP2BP, KDM4B, KDM4A, CREBBP, RUVBL2, EP400, SUPT3H, HIST1H4F, SETD1B, DOT1L, ACTB, MYST3, SUZ12P, AEBP2, KDM2B, WHSC1. KIAA1267, HIST1H2BI, KDM3B, SUV39H2, RBP1, SAP130, HIST1H3E, SMYD2, PADI6, HDAC10, FAM48A, MBD3. HSPA6, HSPA7, HSPA4L, GPX2, HSPA13, HSPA2, BAG5, HSPA1B, RPS6KA1, RPS6KA2, NPTXR, ETS2, NUP98, ATG16L1, IL6, DNAJB6, DLC1, HSP90AA1, UBE2E2, TXNRD1, ATG9A, RAE1, WDR45L, E2F1, PRKAG2, ACD, CBX2, RAD50, MAPKAPK2, AKT1S1, RPTOR, CCS, HIST1H1A, SOD1, WDR45, NUP62, TXNRD2, GSR, STAT3, ASF1A, TXN2, GML, NECAB3, DYNLL2. TSC2, GPX1, TNRC6C, TCEB2, TNRC6B, CEBPB, MAP1LC3B, UBC, HSPA1A, EGLN2, PRKAA1, NUP210, ATG3, MAPK14, CBX4, HSPA12B. TRADD, AKT3, PSMD2.

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Author: Proteasome inhibitor