References
- Bao, L., Hazari, S., Mehra, S., Kaushal, D., Moroz, K. and Dash, S. 2012. Increased expression of p-glycoprotein and doxorubicin chemoresistance of metastatic breast cancer is regulated by mir-298. Am. J. Pathol. 180, 2490-2503. https://doi.org/10.1016/j.ajpath.2012.02.024
- French, K. J., Schrecengost, R. S., Lee, B. D., Zhuang, Y., Smith, S. N., Eberly, J. L., Yun, J. K. and Smith, C. D. 2003. Discovery and evaluation of inhibitors of human sphingosine kinase. Cancer Res. 63, 5962-5969.
- Gately, D. P. and Howell, S. B. 1993. Cellular accumulation of the anticancer agent cisplatin: A review. Br. J. Cancer 67, 1171-1176. https://doi.org/10.1038/bjc.1993.221
- Giacomini, K. M., Huang, S. M., Tweedie, D. J., Benet, L. Z., Brouwer, K. L., Chu, X., Dahlin, A., Evers, R., Fischer, V., Hillgren, K. M., Hoffmaster, K. A., Ishikawa, T., Keppler, D., Kim, R. B., Lee, C. A., Niemi, M., Polli, J. W., Sugiyama, Y., Swaan, P. W., Ware, J. A., Wright, S. H., Yee, S. W., Zamek-Gliszczynski, M. J. and Zhang, L. 2010. Membrane transporters in drug development. Nat. Rev. Drug Discov. 9, 215-236. https://doi.org/10.1038/nrd3028
- Indumathy, S. and Dass, C. R. 2013. Finding chemo: The search for marine-based pharmaceutical drugs active against cancer. J. Pharm. Pharmacol. 65, 1280-1301. https://doi.org/10.1111/jphp.12097
- Ishida, S., Lee, J., Thiele, D. J. and Herskowitz, I. 2002. Uptake of the anticancer drug cisplatin mediated by the copper transporter ctr1 in yeast and mammals. Proc. Natl. Acad. Sci. USA 99, 14298-14302. https://doi.org/10.1073/pnas.162491399
- Johnson, K. R., Johnson, K. Y., Crellin, H. G., Ogretmen, B., Boylan, A. M., Harley, R. A. and Obeid, L. M. 2005. Immunohistochemical distribution of sphingosine kinase 1 in normal and tumor lung tissue. J. Histochem. Cytochem. 53, 1159-1166. https://doi.org/10.1369/jhc.4A6606.2005
- Katano, K., Kondo, A., Safaei, R., Holzer, A., Samimi, G., Mishima, M., Kuo, Y. M., Rochdi, M. and Howell, S. B. 2002. Acquisition of resistance to cisplatin is accompanied by changes in the cellular pharmacology of copper. Cancer Res. 62, 6559-6565.
- Kunkel, G. T., Maceyka, M., Milstien, S. and Spiegel, S. 2013. Targeting the sphingosine-1-phosphate axis in cancer, inflammation and beyond. Nat. Rev. Drug. Discov. 12, 688-702. https://doi.org/10.1038/nrd4099
- Kuroda, I., Musman, M., Ohtani, Ii, Ichiba, T., Tanaka, J., Gravalos, D. G. and Higa, T. 2002. Pachastrissamine, a cytotoxic anhydrophytosphingosine from a marine sponge, pachastrissa sp. J. Nat. Prod. 65, 1505-1506. https://doi.org/10.1021/np010659y
- Kuznetsov, G., Towle, M. J., Cheng, H., Kawamura, T., Tendyke, K., Liu, D., Kishi, Y., Yu, M. J. and Littlefield, B. A. 2004. Induction of morphological and biochemical apoptosis following prolonged mitotic blockage by halichondrin b macrocyclic ketone analog e7389. Cancer Res. 64, 5760-5766. https://doi.org/10.1158/0008-5472.CAN-04-1169
- Kwon, Y., Song, J., Bae, H., Kim, W. J., Lee, J. Y., Han, G. H., Lee, S. K. and Kim, S. 2015. Synthesis and biological evaluation of carbocyclic analogues of pachastrissamine. Mar. Drugs 13, 824-837. https://doi.org/10.3390/md13020824
- Lim, K. G., Gray, A. I., Pyne, S. and Pyne, N. J. 2012. Resveratrol dimers are novel sphingosine kinase 1 inhibitors and affect sphingosine kinase 1 expression and cancer cell growth and survival. Br. J. Pharmacol. 166, 1605-1616. https://doi.org/10.1111/j.1476-5381.2012.01862.x
- Lim, K. G., Tonelli, F., Li, Z., Lu, X., Bittman, R., Pyne, S. and Pyne, N. J. 2011. Fty720 analogues as sphingosine kinase 1 inhibitors: Enzyme inhibition kinetics, allosterism, proteasomal degradation, and actin rearrangement in mcf-7 breast cancer cells. J. Biol. Chem. 286, 18633-18640. https://doi.org/10.1074/jbc.M111.220756
- Maceyka, M., Payne, S. G., Milstien, S. and Spiegel, S. 2002. Sphingosine kinase, sphingosine-1-phosphate, and apoptosis. Biochim. Biophys. Acta. 1585, 193-201. https://doi.org/10.1016/S1388-1981(02)00341-4
- Mcgrath, T. and Center, M. S. 1988. Mechanisms of multidrug resistance in hl60 cells: Evidence that a surface membrane protein distinct from p-glycoprotein contributes to reduced cellular accumulation of drug. Cancer Res. 48, 3959-3963.
- Mease, K., Sane, R., Podila, L. and Taub, M. E. 2012. Differential selectivity of efflux transporter inhibitors in caco-2 and mdck-mdr1 monolayers: A strategy to assess the interaction of a new chemical entity with p-gp, bcrp, and mrp2. J. Pharm. Sci. 101, 1888-1897. https://doi.org/10.1002/jps.23069
- Pyne, S., Bittman, R. and Pyne, N. J. 2011. Sphingosine kinase inhibitors and cancer: Seeking the golden sword of hercules. Cancer Res. 71, 6576-6582. https://doi.org/10.1158/0008-5472.CAN-11-2364
- Russo, P., Nastrucci, C. and Cesario, A. 2011. From the sea to anticancer therapy. Curr. Med. Chem. 18, 3551-3562. https://doi.org/10.2174/092986711796642652
- Salma, Y., Lafont, E., Therville, N., Carpentier, S., Bonnafe, M. J., Levade, T., Genisson, Y. and Andrieu-Abadie, N. 2009. The natural marine anhydrophytosphingosine, jaspine b, induces apoptosis in melanoma cells by interfering with ceramide metabolism. Biochem. Pharmacol. 78, 477-485. https://doi.org/10.1016/j.bcp.2009.05.002
- Sato, H., Siddig, S., Uzu, M., Suzuki, S., Nomura, Y., Kashiba, T., Gushimiyagi, K., Sekine, Y., Uehara, T., Arano, Y., Yamaura, K. and Ueno, K. 2015. Elacridar enhances the cytotoxic effects of sunitinib and prevents multidrug resistance in renal carcinoma cells. Eur. J. Pharmacol. 746, 258-266. https://doi.org/10.1016/j.ejphar.2014.11.021
- Shida, D., Takabe, K., Kapitonov, D., Milstien, S. and Spiegel, S. 2008. Targeting sphk1 as a new strategy against cancer. Curr. Drug. Targets 9, 662-673. https://doi.org/10.2174/138945008785132402
- Sobue, S., Iwasaki, T., Sugisaki, C., Nagata, K., Kikuchi, R., Murakami, M., Takagi, A., Kojima, T., Banno, Y., Akao, Y., Nozawa, Y., Kannagi, R., Suzuki, M., Abe, A., Naoe, T. and Murate, T. 2006. Quantitative rt-pcr analysis of sphingolipid metabolic enzymes in acute leukemia and myelodysplastic syndromes. Leukemia 20, 2042-2046.
- Spiegel, S. and Milstien, S. 2003. Sphingosine-1-phosphate: An enigmatic signalling lipid. Nat. Rev. Mol. Cell. Biol. 4, 397-407. https://doi.org/10.1038/nrm1103
- Stoica, B. A., Movsesyan, V. A., Lea, P. M. T. and Faden, A. I. 2003. Ceramide-induced neuronal apoptosis is associated with dephosphorylation of akt, bad, fkhr, gsk-3beta, and induction of the mitochondrial-dependent intrinsic caspase pathway. Mol. Cell. Neurosci. 22, 365-382. https://doi.org/10.1016/S1044-7431(02)00028-3
- Yang, J. Y., Chang, C. J., Xia, W., Wang, Y., Wong, K. K., Engelman, J. A., Du, Y., Andreeff, M., Hortobagyi, G. N. and Hung, M. C. 2010. Activation of foxo3a is sufficient to reverse mitogen-activated protein/extracellular signal-regulated kinase kinase inhibitor chemoresistance in human cancer. Cancer Res. 70, 4709-4718. https://doi.org/10.1158/0008-5472.CAN-09-4524
- Yoo, H., Lee, Y. S., Lee, S., Kim, S. and Kim, T. Y. 2012. Pachastrissamine from pachastrissa sp. Inhibits melanoma cell growth by dual inhibition of cdk2 and erk-mediated foxo3 downregulation. Phytother. Res. 26, 1927-1933. https://doi.org/10.1002/ptr.4673
- Zhang, S., Lovejoy, K. S., Shima, J. E., Lagpacan, L. L., Shu, Y., Lapuk, A., Chen, Y., Komori, T., Gray, J. W., Chen, X., Lippard, S. J. and Giacomini, K. M. 2006. Organic cation transporters are determinants of oxaliplatin cytotoxicity. Cancer Res. 66, 8847-8857. https://doi.org/10.1158/0008-5472.CAN-06-0769
Cited by
- Pharmacokinetics of Jaspine B and Enhancement of Intestinal Absorption of Jaspine B in the Presence of Bile Acid in Rats vol.15, pp.9, 2017, https://doi.org/10.3390/md15090279