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Synergistic effect of a retinoid X receptor-selective ligand bexarotene (LGD1069, Targretin) and paclitaxel (Taxol) in mammary carcinoma

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Abstract

We have previously shown that the retinoid X receptor (RXR) ligand bexarotene (LGD1069, Targretin) is efficacious as a chemopreventive and chemotherapeutic agent in rat N-nitroso-N-methylurea (NMU)-induced mammary carcinomas (Cancer Res 58: 479–484, 1998). To determine additional role for bexarotene in breast cancer treatment, we evaluated the effect of bexarotene on the efficacy of paclitaxel (Taxol) treatment in a rat NMU-derived mammary tumor cell line, NMU-417,in vitro and in rat NMU-induced mammary tumors in vivo. Our growth inhibition results showed that the bexarotene/paclitaxel combination produced a concentration-dependent synergy in NMU-417 tumor cell line. Synergistic growth inhibition by the combination was associated with an increase in cell death induced by both agents. In rat NMU-induced mammary tumor model in vivo, the benefit of combination therapy was observed as early as 1 week after treatment and increased as treatment continued. At the end of 6 weeks of treatment, the bexarotene/paclitaxel combination produced an overall objective response rate of 94% compared with a rate of 12% in paclitaxel-treated and 58% in bexarotene-treated animals, an effect that was more than the additive effects produced by single agents. Although both bexarotene alone and the bexarotene/paclitaxel combination reduced tumor multiplicity to similar extent, the combination regimen produced a statistically significant decrease in total tumor burden compared to single agents and untreated controls (two-tailed, p > 0.05). Combination therapy did not further alter body weight nor increase toxicity when compared to single agents. In summary, our results demonstrated the potential of using a RXR selective ligand in combination with chemotherapy for the treatment of breast cancer.

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References

  1. Harn SM, Liebman JE, Cook J, Fisher J, Goldspiel B, Venzon D, Mitchell JB, Kaufman D: Taxol in combination with doxorubicin or etoposide. Cancer 72: 2705–2711, 1993

    Google Scholar 

  2. Tolcher AW: Paclitaxel couplets with cyclophosphamide or cisplatin in metastatic breast cancer. Semin Oncol 23 (Suppl 1): 37–43, 1996

    Google Scholar 

  3. Fornier M, Esteva FJ, Seidman AD: Trastuzumab in combination with chemotherapy for the treatment of metastatic breast cancer. Semin Oncol 27 (6 Suppl 11): 38–45, 2000

    Google Scholar 

  4. Horwitz SB, Cohen D, Rao S, Ringel I, Shen HJ, Yang CP: Taxol: mechanisms of action and resistance. J Natl Cancer Inst Monogr 15: 55–61, 1993

    Google Scholar 

  5. Sangrajrang S, Fellous A: Taxol Resistance. Chemotherapy 46: 327–334, 2000

    Google Scholar 

  6. Holmes FA, Walters RS, Theriault RL, et al: Phase II trial of Taxol, an active drug in the treatment of metastatic breast cancer. J Natl Cancer Inst 83: 1797–1805, 1991

    Google Scholar 

  7. Boehm MF, Zhang L, Badea BA, White SK, Mais DE, Berger E, Suto CM, Goldman ME, Heyman RA: Synthesis and structure-activity relationships of novel retinoid X receptor-selective retinoids. J Med Chem 37: 2930–2941, 1994

    Google Scholar 

  8. Gottardis MM, Bischoff ED, Shirley MA, Wagoner MA, Lamph WW, Heyman RA: Chemprevention of mammary carcinoma by LGD1069 (Targretin): an RXR-selective ligand. Cancer Res 56: 5566–5570, 1996

    Google Scholar 

  9. Wu K, Zhang Y, Xu X-C, Hill J, Celestino J, Kim H-T, Mohsin SK, Hilsenbeck SG, Lamph WW, Bissonnette R, Brown PH: The retinoid X receptor-selective retinoid, LGD1069, prevents the development of estrogen receptor-negative mammary tumors in transgenic mice. Cancer Res 62: 6376–6380, 2002

    Google Scholar 

  10. Wu K, Kim H-T, Rodriquez JL, Hilsenbeck SG, Mohsin SK, Xu X-C, Lamph WW, Kuhn JG, Green JE, Brown PH: Suppression of mammary tumorigenesis in transgenic mice by the RXR-selective retinoid, LGD1069. Cancer Epid Biomarker Prevention 11: 467–474, 2003

    Google Scholar 

  11. Bischoff ED, Gottardis MM, Moon TE, Heyman RA, Lamph WW: Beyond tamoxifen: the retinoid X receptorselective ligand LGD1069 (Targretin) causes complete regression of mammary carcinoma. Cancer Res. 58: 479–484, 1998

    Google Scholar 

  12. Bischoff ED, Heyman RA, Lamph WW: Effect of the retinoid X receptor-selective ligand LGD1069 on mammary carcinoma after tamoxifen failure. J Natl Cancer Inst 91: 2118–2123, 1999

    Google Scholar 

  13. Agarwal VR, Bischoff ED, Hermann T, Lamph WW: Induction of adipocyte-specific gene expression is correlated with mammary tumor regression by the retinoid X receptorligand LGD1069 (Targretin). Cancer Res 60: 6033–6038, 2000

    Google Scholar 

  14. Duvic M, Hymes K, Heald P, Breneman D, Martin AG, Myskowski P, Crowley C, Yocum RC: Bexarotene is effective and safe for treatment of refractory advancedstage cutaneous T-cell lymphoma: multinational phase II–III trail results. J Clin Oncology 19: 2456–2471, 2001

    Google Scholar 

  15. Chou TC, Talalay P: Quantitative analysis of dose-effect relationships: the combined effects of multiple drugs or enzyme inhibitors. Adv Enzyme Regul 22: 27–55, 1984

    Google Scholar 

  16. Chou TC: The median-effect principle and the combination index for quantitation of synergism and antagonism. In: Chou TC, Rideout DC (eds) Synergism and Antagonism in Chemotherapy. Academic Press, NY, 1991, pp 61–102

    Google Scholar 

  17. Blagosklonny MV, Schulte T, Nguyen P, Trepel J, Nechers LM: Taxol-induced apoptosis and phosphorylation of bcl-2 protein involves c-raf-1 and represents a novel c-raf-1 signal transduction pathway. Cancer Res. 56: 1851–1854, 1996

    Google Scholar 

  18. Lee LF, Li G, Templeton DJ, Ting JP-Y: Paclitaxel (Taxol)-induced gene expression and cell death are both mediated by the activation of c-jun NH2-terminal kinase (JNK/SAPK). J Biol Chem 273: 28253–28260, 1998

    Google Scholar 

  19. Vivat-hannah V, You D, Rizzo C, Daris J-P, Lapointe P, Zusi C, Marinier A, Lorenzi MV, Gottardis MM: Synergistic cytotoxicity exhibited by combination treatment of selective retinoid ligands with Taxol (paclitaxel). Cancer Res 61: 8703–8711, 2001

    Google Scholar 

  20. Yen A, Roberson MS, Varvayanis S, Lee AT: Retinoic acid induced mitogen-activated protein (MAP)/extracellular signal-regulated kinase (ERK) kinase-dependent MAT kinase activation needed to elicit HL-60 cell differentiation and growth arrest. Cancer Res 58: 3163–3172, 1998

    Google Scholar 

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Yen, Wc., Prudente, R.Y. & Lamph, W.W. Synergistic effect of a retinoid X receptor-selective ligand bexarotene (LGD1069, Targretin) and paclitaxel (Taxol) in mammary carcinoma. Breast Cancer Res Treat 88, 141–148 (2004). https://doi.org/10.1007/s10549-004-1426-5

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  • DOI: https://doi.org/10.1007/s10549-004-1426-5

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