Literature DB >> 16633714

Trabectedin (ET-743, Yondelis) is a substrate for P-glycoprotein, but only high expression of P-glycoprotein confers the multidrug resistance phenotype.

Jan-Hendrik Beumer1, Tessa Buckle, Mariet Ouwehand, Niels E F Franke, Luis Lopez-Lazaro, Jan H M Schellens, Jos H Beijnen, Olaf van Tellingen.   

Abstract

Trabectedin (ET-743, Yondelis) is a novel anticancer drug currently undergoing phase II and III investigations. There are various and conflicting reports whether trabectedin is a substrate for P-glycoprotein (P-gp), an important factor in drug disposition and multi-drug resistance (MDR). We have now unambiguously shown that trabectedin is a P-gp substrate by investigating vectorial transport over monolayers of LLC-PK1 pig kidney and Madine-Darby Canine kidney (MDCK) cells and the mdr1a and/or MDR1 transfected subclones. We further characterized the cytotoxic effects and cellular accumulation of trabectedin in these cell lines as well as in a panel of other cell lines with high or moderate expression levels of P-gp. Trabectedin displayed the typical MDR phenotype only in highly P-gp expressing cell lines, but not in cell lines with expression levels more closely conforming to clinical samples, suggesting that P-gp will not confer resistance to trabectedin in cancer patients.

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Year:  2007        PMID: 16633714     DOI: 10.1007/s10637-006-7773-9

Source DB:  PubMed          Journal:  Invest New Drugs        ISSN: 0167-6997            Impact factor:   3.850


  29 in total

1.  Sequence-dependent synergistic cytotoxicity of ecteinascidin-743 and paclitaxel in human breast cancer cell lines in vitro and in vivo.

Authors:  Naoto Takahashi; WeiWei Li; Debabrata Banerjee; Yongbiao Guan; Yasuko Wada-Takahashi; Murray F Brennan; Ting-Chao Chou; Kathleen W Scotto; Joseph R Bertino
Journal:  Cancer Res       Date:  2002-12-01       Impact factor: 12.701

Review 2.  Role of P-glycoprotein in pharmacokinetics: clinical implications.

Authors:  Jiunn H Lin; Masayo Yamazaki
Journal:  Clin Pharmacokinet       Date:  2003       Impact factor: 6.447

3.  Extensive contribution of the multidrug transporters P-glycoprotein and Mrp1 to basal drug resistance.

Authors:  J D Allen; R F Brinkhuis; L van Deemter; J Wijnholds; A H Schinkel
Journal:  Cancer Res       Date:  2000-10-15       Impact factor: 12.701

4.  Molecular characterisation of two human cancer cell lines selected in vitro for their chemotherapeutic drug resistance to ET-743.

Authors:  S Marchini; E Marrazzo; R Bonomi; G Chiorino; M Zaffaroni; L Weissbach; F J Hornicek; M Broggini; G T Faircloth; M D'Incalci
Journal:  Eur J Cancer       Date:  2005-01       Impact factor: 9.162

5.  A new PCR MIMIC strategy to quantify low mdr1 mRNA levels in drug resistant cell lines and AML blast samples.

Authors:  T Illmer; M Schaich; U Oelschlägel; R Nowak; U Renner; B Ziegs; S Subat; A Neubauer; G Ehninger
Journal:  Leuk Res       Date:  1999-07       Impact factor: 3.156

6.  Ecteinascidin 743, a transcription-targeted chemotherapeutic that inhibits MDR1 activation.

Authors:  S Jin; B Gorfajn; G Faircloth; K W Scotto
Journal:  Proc Natl Acad Sci U S A       Date:  2000-06-06       Impact factor: 11.205

7.  P-glycoprotein in the blood-brain barrier of mice influences the brain penetration and pharmacological activity of many drugs.

Authors:  A H Schinkel; E Wagenaar; C A Mol; L van Deemter
Journal:  J Clin Invest       Date:  1996-06-01       Impact factor: 14.808

8.  Quantitative polymerase chain reaction analysis of mdr1 mRNA in multiple myeloma cell lines and clinical specimens.

Authors:  B W Futscher; L L Blake; J H Gerlach; T M Grogan; W S Dalton
Journal:  Anal Biochem       Date:  1993-09       Impact factor: 3.365

9.  A phase II study of ET-743/trabectedin ('Yondelis') for patients with advanced gastrointestinal stromal tumours.

Authors:  J-Y Blay; A Le Cesne; J Verweij; M Scurr; C Seynaeve; S Bonvalot; P Hogendoorn; J Jimeno; V Evrard; M van Glabbeke; I Judson
Journal:  Eur J Cancer       Date:  2004-06       Impact factor: 9.162

10.  Quantitative analysis of MDR1 (multidrug resistance) gene expression in human tumors by polymerase chain reaction.

Authors:  K E Noonan; C Beck; T A Holzmayer; J E Chin; J S Wunder; I L Andrulis; A F Gazdar; C L Willman; B Griffith; D D Von Hoff; I B Roninson
Journal:  Proc Natl Acad Sci U S A       Date:  1990-09       Impact factor: 11.205

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  5 in total

Review 1.  Ecteinascidins. A review of the chemistry, biology and clinical utility of potent tetrahydroisoquinoline antitumor antibiotics.

Authors:  V H Le; M Inai; R M Williams; T Kan
Journal:  Nat Prod Rep       Date:  2015-02       Impact factor: 13.423

2.  Disposition and toxicity of trabectedin (ET-743) in wild-type and mdr1 gene (P-gp) knock-out mice.

Authors:  J H Beumer; N E Franke; R Tolboom; T Buckle; H Rosing; L Lopez-Lazaro; J H M Schellens; J H Beijnen; O van Tellingen
Journal:  Invest New Drugs       Date:  2009-02-24       Impact factor: 3.850

3.  Down-regulation of the nucleotide excision repair gene XPG as a new mechanism of drug resistance in human and murine cancer cells.

Authors:  Maria Antonietta Sabatino; Mirko Marabese; Monica Ganzinelli; Elisa Caiola; Cristina Geroni; Massimo Broggini
Journal:  Mol Cancer       Date:  2010-09-24       Impact factor: 27.401

Review 4.  Trabectedin : a review of its use in the management of soft tissue sarcoma and ovarian cancer.

Authors:  Natalie J Carter; Susan J Keam
Journal:  Drugs       Date:  2007       Impact factor: 9.546

5.  Modulation of trabectedin (ET-743) hepatobiliary disposition by multidrug resistance-associated proteins (Mrps) may prevent hepatotoxicity.

Authors:  Jin Kyung Lee; Elaine M Leslie; Maciej J Zamek-Gliszczynski; Kim L R Brouwer
Journal:  Toxicol Appl Pharmacol       Date:  2007-12-03       Impact factor: 4.219

  5 in total

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