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169 related items for PubMed ID: 15634944
1. Efflux of depsipeptide FK228 (FR901228, NSC-630176) is mediated by P-glycoprotein and multidrug resistance-associated protein 1. Xiao JJ, Foraker AB, Swaan PW, Liu S, Huang Y, Dai Z, Chen J, Sadée W, Byrd J, Marcucci G, Chan KK. J Pharmacol Exp Ther; 2005 Apr; 313(1):268-76. PubMed ID: 15634944 [Abstract] [Full Text] [Related]
2. Chemoresistance to depsipeptide FK228 [(E)-(1S,4S,10S,21R)-7-[(Z)-ethylidene]-4,21-diisopropyl-2-oxa-12,13-dithia-5,8,20,23-tetraazabicyclo[8,7,6]-tricos-16-ene-3,6,9,22-pentanone] is mediated by reversible MDR1 induction in human cancer cell lines. Xiao JJ, Huang Y, Dai Z, Sadée W, Chen J, Liu S, Marcucci G, Byrd J, Covey JM, Wright J, Grever M, Chan KK. J Pharmacol Exp Ther; 2005 Jul; 314(1):467-75. PubMed ID: 15833893 [Abstract] [Full Text] [Related]
7. Histone deacetylase 1 gene expression and sensitization of multidrug-resistant neuroblastoma cell lines to cytotoxic agents by depsipeptide. Keshelava N, Davicioni E, Wan Z, Ji L, Sposto R, Triche TJ, Reynolds CP. J Natl Cancer Inst; 2007 Jul 18; 99(14):1107-19. PubMed ID: 17623797 [Abstract] [Full Text] [Related]
8. The histone deacetylase inhibitors suberoylanilide hydroxamic (Vorinostat) and valproic acid induce irreversible and MDR1-independent resistance in human colon cancer cells. Fedier A, Dedes KJ, Imesch P, Von Bueren AO, Fink D. Int J Oncol; 2007 Sep 18; 31(3):633-41. PubMed ID: 17671692 [Abstract] [Full Text] [Related]
9. Effects of FK228, a novel histone deacetylase inhibitor, on human lymphoma U-937 cells in vitro and in vivo. Sasakawa Y, Naoe Y, Inoue T, Sasakawa T, Matsuo M, Manda T, Mutoh S. Biochem Pharmacol; 2002 Oct 01; 64(7):1079-90. PubMed ID: 12234611 [Abstract] [Full Text] [Related]
10. Antitumor efficacy of FK228, a novel histone deacetylase inhibitor, depends on the effect on expression of angiogenesis factors. Sasakawa Y, Naoe Y, Noto T, Inoue T, Sasakawa T, Matsuo M, Manda T, Mutoh S. Biochem Pharmacol; 2003 Sep 15; 66(6):897-906. PubMed ID: 12963476 [Abstract] [Full Text] [Related]
12. Histone deacetylase inhibitor FK228 activates tumor suppressor Prdx1 with apoptosis induction in esophageal cancer cells. Hoshino I, Matsubara H, Hanari N, Mori M, Nishimori T, Yoneyama Y, Akutsu Y, Sakata H, Matsushita K, Seki N, Ochiai T. Clin Cancer Res; 2005 Nov 01; 11(21):7945-52. PubMed ID: 16278420 [Abstract] [Full Text] [Related]
14. Depsipeptide induces cell death in Hodgkin lymphoma-derived cell lines. Hartlapp I, Pallasch C, Weibert G, Kemkers A, Hummel M, Re D. Leuk Res; 2009 Jul 01; 33(7):929-36. PubMed ID: 19233470 [Abstract] [Full Text] [Related]
15. Reversal of multidrug resistance by two nordihydroguaiaretic acid derivatives, M4N and maltose-M3N, and their use in combination with doxorubicin or paclitaxel. Chang CC, Liang YC, Klutz A, Hsu CI, Lin CF, Mold DE, Chou TC, Lee YC, Huang RC. Cancer Chemother Pharmacol; 2006 Nov 01; 58(5):640-53. PubMed ID: 16544145 [Abstract] [Full Text] [Related]
18. FK228 (depsipeptide) as a natural prodrug that inhibits class I histone deacetylases. Furumai R, Matsuyama A, Kobashi N, Lee KH, Nishiyama M, Nakajima H, Tanaka A, Komatsu Y, Nishino N, Yoshida M, Horinouchi S. Cancer Res; 2002 Sep 01; 62(17):4916-21. PubMed ID: 12208741 [Abstract] [Full Text] [Related]
20. Reversal of P-glycoprotein-mediated multidrug resistance by protopanaxatriol ginsenosides from Korean red ginseng. Choi CH, Kang G, Min YD. Planta Med; 2003 Mar 01; 69(3):235-40. PubMed ID: 12677527 [Abstract] [Full Text] [Related] Page: [Next] [New Search]