ApoE enhances nanodisk-mediated curcumin delivery to glioblastoma multiforme cells.

AIM To evaluate the effect of incorporating the polyphenol, curcumin, into nanodisk (ND) particles on its biological activity. MATERIALS & METHODS Curcumin-NDs formulated with different scaffold proteins were incubated with cultured glioblastoma multiforme cells. RESULTS When ApoE was employed as the ND scaffold protein, enhanced curcumin uptake was observed. Furthermore, ApoE curcumin-NDs induced greater cell death than either free curcumin or ApoAI curcumin-NDs. A total of 1 h after exposure of glioblastoma multiforme cells to ApoE curcumin-NDs, significant curcumin uptake was detected while ApoE was localized at the cell surface. After 2 h, a portion of the curcumin had migrated to the nucleus, giving rise to enhanced fluorescence intensity in discrete intranuclear sites. CONCLUSION ApoE-mediated interaction of curcumin-NDs with glioblastoma multiforme cells leads to enhanced curcumin uptake and increased biological activity.

[1]  Z. Bikádi,et al.  Circular dichroism spectroscopic studies reveal pH dependent binding of curcumin in the minor groove of natural and synthetic nucleic acids. , 2004, Organic & biomolecular chemistry.

[2]  A. Zanotto-Filho,et al.  The curry spice curcumin selectively inhibits cancer cells growth in vitro and in preclinical model of glioblastoma. , 2012, The Journal of nutritional biochemistry.

[3]  R. Béliveau,et al.  Curcumin inhibits tumor growth and angiogenesis in glioblastoma xenografts. , 2010, Molecular nutrition & food research.

[4]  Martin J. van den Bent,et al.  Radiotherapy plus concomitant and adjuvant temozolomide for glioblastoma. , 2005, The New England journal of medicine.

[5]  R. Ryan Nanodisks: hydrophobic drug delivery vehicles , 2008, Expert opinion on drug delivery.

[6]  G. Francis,et al.  Bacterial overexpression, isotope enrichment, and NMR analysis of the N-terminal domain of human apolipoprotein E. , 1997, Biochemistry and cell biology = Biochimie et biologie cellulaire.

[7]  Yi-Chiang Hsu,et al.  Curcuminoids suppress the growth and induce apoptosis through caspase-3-dependent pathways in glioblastoma multiforme (GBM) 8401 cells. , 2010, Journal of agricultural and food chemistry.

[8]  Robert A Newman,et al.  Bioavailability of curcumin: problems and promises. , 2007, Molecular pharmaceutics.

[9]  C. Brennan,et al.  Candidate pathways for promoting differentiation or quiescence of oligodendrocyte progenitor-like cells in glioma. , 2012, Cancer research.

[10]  R. Mahley,et al.  Human apolipoprotein E. Determination of the heparin binding sites of apolipoprotein E3. , 1986, The Journal of biological chemistry.

[11]  V. Seifert,et al.  The nontoxic natural compound Curcumin exerts anti-proliferative, anti-migratory, and anti-invasive properties against malignant gliomas , 2010, BMC Cancer.

[12]  T. Forte,et al.  Optimized bacterial expression of human apolipoprotein A-I. , 2003, Protein expression and purification.

[13]  M. Oda,et al.  Reconstituted high density lipoprotein enriched with the polyene antibiotic amphotericin B Published, JLR Papers in Press, November 28, 2005. , 2006, Journal of Lipid Research.

[14]  W. Yung,et al.  Altered expression and distribution of heparan sulfate proteoglycans in human gliomas. , 1989, Cancer research.

[15]  J. Zidan,et al.  Curcuma as a functional food in the control of cancer and inflammation , 2011, Current opinion in clinical nutrition and metabolic care.

[16]  E. Quinet,et al.  Human apolipoprotein A-IV. Intestinal origin and distribution in plasma. , 1980, The Journal of clinical investigation.

[17]  R. Pandey,et al.  Transport of liposomal and albumin loaded curcumin to living cells: an absorption and fluorescence spectroscopic study. , 2006, Biochimica et biophysica acta.

[18]  E. Blakely,et al.  Human glioblastoma cell lines: levels of low-density lipoprotein receptor and low-density lipoprotein receptor-related protein. , 2000, Cancer research.

[19]  Luciana Romão,et al.  Glioblastoma: therapeutic challenges, what lies ahead. , 2012, Biochimica et biophysica acta.

[20]  J. Epstein,et al.  Curcumin as a therapeutic agent: the evidence from in vitro, animal and human studies , 2010, British Journal of Nutrition.

[21]  Thanh-Son Nguyen,et al.  All-trans-retinoic acid nanodisks. , 2007, International journal of pharmaceutics.

[22]  V. Narayanaswami,et al.  Apolipoprotein E: from lipid transport to neurobiology. , 2011, Progress in lipid research.

[23]  L. Gordon,et al.  Curcumin nanodisks: formulation and characterization. , 2011, Nanomedicine : nanotechnology, biology, and medicine.

[24]  Bharat B. Aggarwal,et al.  Epigenetic changes induced by curcumin and other natural compounds , 2011, Genes & Nutrition.

[25]  L. Gordon,et al.  Curcumin nanodisk-induced apoptosis in mantle cell lymphoma , 2011, Leukemia & lymphoma.

[26]  H. Sontheimer,et al.  Inhibition of nuclear factor kappa-B signaling reduces growth in medulloblastoma in vivo , 2011, BMC Cancer.

[27]  R. Mahley,et al.  Human apolipoprotein E: the Alzheimer's disease connection , 1996, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[28]  M. Sarbolouki,et al.  Curcumin binding to DNA and RNA. , 2009, DNA and cell biology.

[29]  R. Ryan Nanobiotechnology applications of reconstituted high density lipoprotein , 2010, Journal of nanobiotechnology.