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World Health Organization (https://www.who.int/cancer/prevention/diagnosis-screening/breast-cancer/en/).https://www.who.int/cancer/prevention/diagnosis-screening/breast-cancer/en/Search in Google Scholar
Filipova A, Seifrtova M, Mokry J, Dvorak J, Rezacova M, Filip S, et al. Breast cancer and cancer stem cells: A mini-review. Tumori. 2014; 100(4): 363-369.FilipovaASeifrtovaMMokryJDvorakJRezacovaMFilipSet alBreast cancer and cancer stem cells: A mini-review2014100436336910.1177/1636.17886Search in Google Scholar
Dörfel S, Steffens CC, Meyer D, Tesch H, Kruggel L, Frank M, et al. Adjuvant chemotherapeutic treatment of 1650 patients with early breast cancer in routine care in Germany: Data from the prospective TMK cohort study. Breast Cancer. 2018; 25(3): 275-283.DörfelSSteffensCCMeyerDTeschHKruggelLFrankMet alAdjuvant chemotherapeutic treatment of 1650 patients with early breast cancer in routine care in Germany: Data from the prospective TMK cohort study201825327528310.1007/s12282-017-0823-7590652329204847Search in Google Scholar
Ribeiro JT, Macedo LT, Curigliano G, Fumagalli L, Locatelli M, Dalton M, et al. Cytotoxic drugs for patients with breast cancer in the era of targeted treatment: Back to the future? Ann Oncol. 2012; 23(3): 547-555.RibeiroJTMacedoLTCuriglianoGFumagalliLLocatelliMDaltonMet alCytotoxic drugs for patients with breast cancer in the era of targeted treatment: Back to the future?201223354755510.1093/annonc/mdr38221896541Search in Google Scholar
Duffy MJ, O’Donovan N, McDermott E, Crown J. Validated biomarkers: The key to precision treatment in patients with breast cancer. Breast. 2016; 29: 192-201.DuffyMJO’DonovanNMcDermottECrownJValidated biomarkers: The key to precision treatment in patients with breast cancer20162919220110.1016/j.breast.2016.07.00927521224Search in Google Scholar
Online Mendelian Inheritance in Man, OMIM® Mc-Kusick-Nathans Institute of Genetic Medicine, Johns Hopkins University, Baltimore, MD, USA (https://omim.org/).Johns Hopkins UniversityBaltimore, MD, USAhttps://omim.org/Search in Google Scholar
Pajer P, Pecenka V, Karafiát V, Králová J, Horejsí Z, Dvorák M. The twist gene is a common target of retroviral integration and transcriptional deregulation in experimental nephroblastoma. Oncogene. 2003; 22(5): 665-673.PajerPPecenkaVKarafiátVKrálováJHorejsíZDvorákMThe twist gene is a common target of retroviral integration and transcriptional deregulation in experimental nephroblastoma200322566567310.1038/sj.onc.120610512569359Search in Google Scholar
Yin G, Chen R, Alvero AB, Fu HH, Holmberg J, Glackin C, et al. TWISTing stemness, inflammation and proliferation of epithelial ovarian cancer cells through MIR199A2/214. Oncogene. 2010; 29(24): 3545-353.YinGChenRAlveroABFuHHHolmbergJGlackinCet alTWISTing stemness, inflammation and proliferation of epithelial ovarian cancer cells through MIR199A2/21420102924354535310.1158/0008-5472.FBCR09-B75Search in Google Scholar
Tseng JC, Chen HF, Wu KJ. A twist tale of cancer metastasis and tumor angiogenesis. Histol Histopathol. 2015; 30(11): 1283-1294.TsengJCChenHFWuKJA twist tale of cancer metastasis and tumor angiogenesis2015301112831294Search in Google Scholar
Norozi F, Ahmadzadeh A, Shahjahani M, Sharabi S, Saki N. Twist as a new prognostic marker in hematological malignancies. Clin Transl Oncol. 2016; 18(2): 113-124.NoroziFAhmadzadehAShahjahaniMSharabiSSakiNTwist as a new prognostic marker in hematological malignancies201618211312410.1007/s12094-015-1357-026203802Search in Google Scholar
Zhao Z, Rahman MA, Chen ZG, Shin DM. Multiple biological functions of Twist1 in various cancers. Oncotarget. 2017; 8(12): 20380-20393.ZhaoZRahmanMAChenZGShinDMMultiple biological functions of Twist1 in various cancers2017812203802039310.18632/oncotarget.14608538677028099910Search in Google Scholar
Qiao W, Jia Z, Liu H, Liu Q, Zhang T, Guo W, et al. Prognostic and clinicopathological value of Twist expression in breast cancer: A meta-analysis. PLoS One. 2017; 12(10): e0186191-e0186202.QiaoWJiaZLiuHLiuQZhangTGuoWet alPrognostic and clinicopathological value of Twist expression in breast cancer: A meta-analysis20171210e0186191e018620210.1371/journal.pone.0186191563319529016671Search in Google Scholar
Andreotti PE, Linder D, Hartmann DM, Cree IA, Pazzagli M, Bruckner HW. TCA-100 tumour chemo-sensitivity assay: Differences in sensitivity between cultured tumour cell lines and clinical studies. J Bio-lumin Chemilumin. 1994; 9(6): 373-378.AndreottiPELinderDHartmannDMCreeIAPazzagliMBrucknerHWTCA-100 tumour chemo-sensitivity assay: Differences in sensitivity between cultured tumour cell lines and clinical studies19949637337810.1002/bio.11700906047879653Search in Google Scholar
Cree IA, Kurbacher CM, Untch M, Sutherland LA, Hunter EM, Subedi AM, et al. Correlation of the clinical response to chemotherapy in breast cancer with ex vivo chemosensitivity. Anticancer Drugs. 1996; 7(6): 630-635.CreeIAKurbacherCMUntchMSutherlandLAHunterEMSubediAMet alCorrelation of the clinical response to chemotherapy in breast cancer with ex vivo chemosensitivity19967663063510.1097/00001813-199608000-000028913430Search in Google Scholar
Vogt U, Bielawski KP, Bosse U, Schlotter CM. Breast tumour growth inhibition in vitro through the combination of cyclophosphamide/metotrexate/5-fluorouracil, epirubicin/cyclophosphamide, epirubicin/paclitaxel, and epirubicin/docetaxel with the bisphosphonates ibandronate and zoledronic acid. Oncol Rep. 2004; 12(5): 1109-1114.VogtUBielawskiKPBosseUSchlotterCMBreast tumour growth inhibition in vitro through the combination of cyclophosphamide/metotrexate/5-fluorouracil, epirubicin/cyclophosphamide, epirubicin/paclitaxel, and epirubicin/docetaxel with the bisphosphonates ibandronate and zoledronic acid20041251109111410.3892/or.12.5.1109Search in Google Scholar
Kurbacher CM, Cree IA. Chemosensitivity testing using microplate adenosine triphosphate-based luminescence measurements. Methods Mol Med. 2005; 110: 101-120.KurbacherCMCreeIAChemosensitivity testing using microplate adenosine triphosphate-based luminescence measurements200511010112010.1385/1-59259-869-2:101Search in Google Scholar
Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. Methods. 2001; 25(4): 402-408.LivakKJSchmittgenTDAnalysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method200125440240810.1006/meth.2001.126211846609Search in Google Scholar
Zelnak A. Overcoming taxane and anthracycline resistance. Breast J. 2010; 16(3): 309-312.ZelnakAOvercoming taxane and anthracycline resistance201016330931210.1111/j.1524-4741.2010.00911.x20408821Search in Google Scholar
Hofmann D, Nitz U, Gluz O, Kates RE, Schin-koethe T, Staib T, et al. WSG ADAPT – adjuvant dynamic marker-adjusted personalized therapy trial optimizing risk assessment and therapy response prediction in early breast cancer: Study protocol for a prospective, multi-center, controlled, non-blinded, randomized, investigator initiated phase II/III trial. Trials. 2013; 14: 261. doi: 10.1186/1745- 6215-14-261.HofmannDNitzUGluzOKatesRESchin-koetheTStaibTet alWSG ADAPT – adjuvant dynamic marker-adjusted personalized therapy trial optimizing risk assessment and therapy response prediction in early breast cancer: Study protocol for a prospective, multi-center, controlled, non-blinded, randomized, investigator initiated phase II/III trial20131426110.1186/1745-6215-14-261376594023958221Open DOISearch in Google Scholar
Ayyagari VN, Hsieh TJ, Diaz-Sylvester PL, Brard L. Evaluation of the cytotoxicity of the Bithionolcisplatin combination in a panel of human ovarian cancer cell lines. BMC Cancer. 2017; 17(1): 49.AyyagariVNHsiehTJDiaz-SylvesterPLBrardLEvaluation of the cytotoxicity of the Bithionolcisplatin combination in a panel of human ovarian cancer cell lines20171714910.1186/s12885-016-3034-2523411228086831Search in Google Scholar
Smith SC, Baras AS, Lee JK, Theodorescu D. The COXEN principle: Translating signatures of in vitro chemosensitivity into tools for clinical outcome prediction and drug discovery in cancer. Cancer Res. 2010; 70(5): 1753-1758.SmithSCBarasASLeeJKTheodorescuDThe COXEN principle: Translating signatures of in vitro chemosensitivity into tools for clinical outcome prediction and drug discovery in cancer20107051753175810.1158/0008-5472.CAN-09-3562283113820160033Search in Google Scholar
Wang LF, Yin HT, Qian XP, Wei J, Zhao Y, Yu LX, et al. Beta-Tubulin III mRNA expression and docetaxel sensitivity in non-small cell lung cancer. Clin Invest Med. 2009; 32(6): E278-E284.WangLFYinHTQianXPWeiJZhaoYYuLXet alBeta-Tubulin III mRNA expression and docetaxel sensitivity in non-small cell lung cancer2009326E278E28410.25011/cim.v32i6.1066320003833Search in Google Scholar
Maestro R, Dei Tos AP, Hamamori Y, Krasnokutsky S, Sartorelli V, Kedes L, et al. Twist is a potential oncogene that inhibits apoptosis. Genes Dev. 1999; 13(17): 2207-2217.MaestroRDei TosAPHamamoriYKrasnokutskySSartorelliVKedesLet alTwist is a potential oncogene that inhibits apoptosis199913172207221710.1101/gad.13.17.220731700410485844Search in Google Scholar
Pham CG, Bubici C, Zazzeroni F, Knabb JR, Papa S, Kuntzen C, et al. Upregulation of Twist-1 by NF-kappaB blocks cytotoxicity induced by chemotherapeutic drugs. Mol Cell Biol. 2007; 27(11): 3920-3935.PhamCGBubiciCZazzeroniFKnabbJRPapaSKuntzenCet alUpregulation of Twist-1 by NF-kappaB blocks cytotoxicity induced by chemotherapeutic drugs200727113920393510.1128/MCB.01219-06190000817403902Search in Google Scholar
Wang L, Tan RZ, Zhang ZX, Yin R, Zhang YL, Cui WJ, et al. Association between Twist and multidrug resistance gene-associated proteins in Taxol®-resistantMCF-7 cells and a 293 cell model of Twist overexpression. Oncol Lett. 2018; 15(1): 1058-1066.WangLTanRZZhangZXYinRZhangYLCuiWJet alAssociation between Twist and multidrug resistance gene-associated proteins in Taxol®-resistantMCF-7 cells and a 293 cell model of Twist overexpression201815110581066Search in Google Scholar
Li QQ, Xu JD, Wang WJ, Cao XX, Chen Q, Tang F, et al. Twist1-mediated adriamycin-induced epithelial-mesenchymal transition relates to multidrug resistance and invasive potential in breast cancer cells. Clin Cancer Res. 2009; 15(8): 2657-2665.LiQQXuJDWangWJCaoXXChenQTangFet alTwist1-mediated adriamycin-induced epithelial-mesenchymal transition relates to multidrug resistance and invasive potential in breast cancer cells20091582657266510.1158/1078-0432.CCR-08-237219336515Search in Google Scholar
Saxena M, Stephens MA, Pathak H, Rangarajan A. Transcription factors that mediate epithelial-mesenchymal transition lead to multidrug resistance by upregulating ABC transporters. Cell Death Dis. 2011; 2: e179-e191.SaxenaMStephensMAPathakHRangarajanATranscription factors that mediate epithelial-mesenchymal transition lead to multidrug resistance by upregulating ABC transporters20112e179e19110.1038/cddis.2011.61319972221734725Search in Google Scholar
Hillen F, Griffioen AW. Tumour vascularization: Sprouting angiogenesis and beyond. Cancer Metastasis Rev. 2007; 26(3-4): 489-502HillenFGriffioenAWTumour vascularization: Sprouting angiogenesis and beyond2007263-448950210.1007/s10555-007-9094-7279785617717633Search in Google Scholar
Flamant L, Roegiers E, Pierre M, Hayez A, Sterpin C, De Backer O, et al. TMEM45A is essential for hypoxia-induced chemoresistance in breast and liver cancer cells. BMC Cancer. 2012; 12: 391-407.FlamantLRoegiersEPierreMHayezASterpinCDe BackerOet alTMEM45A is essential for hypoxia-induced chemoresistance in breast and liver cancer cells20121239140710.1186/1471-2407-12-391351960622954140Search in Google Scholar