Bacterially-Derived Nanocells for Tumor-Targeted Delivery of Chemotherapeutics and Cell Cycle Inhibitors

Chemotherapeutic drug therapy in cancer is seriously hampered by severe toxicity primarily due to indiscriminate drug distribution and consequent collateral damage to normal cells. Molecularly targeted drugs such as cell cycle inhibitors are being developed to achieve a higher degree of tumor cell specificity and reduce toxic side effects. Unfortunately, relative to the cytotoxics, many of the molecularly targeted drugs are less potent and the target protein is expressed only at certain stages of the cell cycle thus necessitating regimens like continuous infusion therapy to arrest a significant number of tumor cells in a heterogeneous tumor mass. Here we discuss targeted drug delivery nanovectors and a recently reported bacterially-derived 400nm sized minicell that can be packaged with therapeutically significant concentrations of chemotherapeutic drugs, targeted to tumor cell surface receptors and effect intracellular drug delivery with highly significant anti-tumor effects in-vivo. We also report that molecularly targeted drugs can also be packaged in minicells and targeted to tumor cells with highly significant tumor growth-inhibition and regression in mouse xenografts despite administration of minute amounts of drug. This targeted intracellular drug delivery may overcome many of the hurdles associated with the delivery of cytotoxic and molecularly targeted drugs.

[1]  D. Lacombe,et al.  A phase I and pharmacokinetic study of OSI-7904L, a liposomal thymidylate synthase inhibitor in combination with oxaliplatin in patients with advanced colorectal cancer , 2008, Cancer Chemotherapy and Pharmacology.

[2]  P. Delrio,et al.  Synergistic antitumour effect of raltitrexed and 5-fluorouracil plus folinic acid combination in human cancer cells , 2007, Anti-cancer drugs.

[3]  J. Lutkenhaus,et al.  Assembly dynamics of the bacterial MinCDE system and spatial regulation of the Z ring. , 2007, Annual review of biochemistry.

[4]  N. Nishiyama,et al.  In vivo antitumor activity of the folate-conjugated pH-sensitive polymeric micelle selectively releasing adriamycin in the intracellular acidic compartments. , 2007, Bioconjugate chemistry.

[5]  Bruce Stillman,et al.  Bacterially derived 400 nm particles for encapsulation and cancer cell targeting of chemotherapeutics. , 2007, Cancer cell.

[6]  M. Malumbres,et al.  Targeting cell cycle kinases for cancer therapy. , 2007, Current medicinal chemistry.

[7]  Norased Nasongkla,et al.  Functionalized Micellar Systems for Cancer Targeted Drug Delivery , 2007, Pharmaceutical Research.

[8]  G. Rabinovich,et al.  Immunosuppressive strategies that are mediated by tumor cells. , 2007, Annual review of immunology.

[9]  R. Gurny,et al.  Differential tumor cell targeting of anti-HER2 (Herceptin) and anti-CD20 (Mabthera) coupled nanoparticles. , 2007, International journal of pharmaceutics.

[10]  K. Balakin,et al.  Recent progress in discovery and development of antimitotic agents. , 2007, Anti-cancer agents in medicinal chemistry.

[11]  Hideyoshi Harashima,et al.  Effect of transferrin receptor-targeted liposomal doxorubicin in P-glycoprotein-mediated drug resistant tumor cells. , 2007, International journal of pharmaceutics.

[12]  Robert Langer,et al.  Formulation of functionalized PLGA-PEG nanoparticles for in vivo targeted drug delivery. , 2007, Biomaterials.

[13]  V. Torchilin,et al.  Micellar Nanocarriers: Pharmaceutical Perspectives , 2006, Pharmaceutical Research.

[14]  R. Diehl,et al.  An Inhibitor of the Kinesin Spindle Protein Activates the Intrinsic Apoptotic Pathway Independently of p53 and De Novo Protein Synthesis , 2006, Molecular and Cellular Biology.

[15]  P. Pisa,et al.  Tumor escape mechanisms in prostate cancer , 2006, Cancer Immunology, Immunotherapy.

[16]  Gustavo Helguera,et al.  The transferrin receptor part II: targeted delivery of therapeutic agents into cancer cells. , 2006, Clinical immunology.

[17]  S Moein Moghimi,et al.  Recent developments in polymeric nanoparticle engineering and their applications in experimental and clinical oncology. , 2006, Anti-cancer agents in medicinal chemistry.

[18]  M. Miglarese,et al.  Development of new cancer therapeutic agents targeting mitosis , 2006, Expert opinion on investigational drugs.

[19]  Stephen S. Taylor,et al.  Validating Aurora B as an anti-cancer drug target , 2006, Journal of Cell Science.

[20]  L. Piddock Multidrug-resistance efflux pumps ? not just for resistance , 2006, Nature Reviews Microbiology.

[21]  P. Gray,et al.  Tubulin-associated drug targets: Aurora kinases, Polo-like kinases, and others. , 2006, Seminars in oncology.

[22]  U. Nielsen,et al.  Antibody targeting of long-circulating lipidic nanoparticles does not increase tumor localization but does increase internalization in animal models. , 2006, Cancer research.

[23]  Robert J. Lee,et al.  A folate receptor-targeted liposomal formulation for paclitaxel. , 2006, International journal of pharmaceutics.

[24]  J. Richie,et al.  Targeted nanoparticle-aptamer bioconjugates for cancer chemotherapy in vivo. , 2006, Proceedings of the National Academy of Sciences of the United States of America.

[25]  G. Shapiro,et al.  Cyclin-dependent kinase pathways as targets for cancer treatment. , 2006, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[26]  H. Shmeeda,et al.  Intracellular uptake and intracavitary targeting of folate-conjugated liposomes in a mouse lymphoma model with up-regulated folate receptors , 2006, Molecular Cancer Therapeutics.

[27]  M. Ferrari,et al.  The Effective Dispersion of Nanovectors Within the Tumor Microvasculature , 2006, Annals of Biomedical Engineering.

[28]  L. Tamm,et al.  The Outer Membrane Protein OmpW Forms an Eight-stranded β-Barrel with a Hydrophobic Channel* , 2006, Journal of Biological Chemistry.

[29]  N. Gray,et al.  Antimitotic agents of natural origin. , 2006, Current drug targets.

[30]  C. Visintin,et al.  Aurora A and B kinases as targets for cancer: will they be selective for tumors? , 2006, Expert review of anticancer therapy.

[31]  C. Mamot,et al.  Epidermal growth factor receptor-targeted immunoliposomes significantly enhance the efficacy of multiple anticancer drugs in vivo. , 2005, Cancer research.

[32]  Ulrich Beyer,et al.  Liposomal encapsulated anti-cancer drugs. , 2005, Anti-cancer drugs.

[33]  B. Berg The FadL family: unusual transporters for unusual substrates , 2005 .

[34]  Weikang Tao,et al.  Induction of apoptosis by an inhibitor of the mitotic kinesin KSP requires both activation of the spindle assembly checkpoint and mitotic slippage. , 2005, Cancer cell.

[35]  K. Brejc,et al.  Mitotic kinesins: prospects for antimitotic drug discovery. , 2005, Current topics in medicinal chemistry.

[36]  M. Ferrari Cancer nanotechnology: opportunities and challenges , 2005, Nature Reviews Cancer.

[37]  J. Mauskopf,et al.  A guide to drug discovery: Pricing medicines: theory and practice, challenges and opportunities , 2005, Nature Reviews Drug Discovery.

[38]  Stephen S. Taylor,et al.  Aurora-kinase inhibitors as anticancer agents , 2004, Nature Reviews Cancer.

[39]  C. Benz,et al.  Future directions of liposome- and immunoliposome-based cancer therapeutics. , 2004, Seminars in oncology.

[40]  L. Rothfield,et al.  Positioning of the MinE binding site on the MinD surface suggests a plausible mechanism for activation of the Escherichia coli MinD ATPase during division site selection , 2004, Molecular microbiology.

[41]  L. Brannon-Peppas,et al.  Nanoparticle and targeted systems for cancer therapy. , 2004, Advanced drug delivery reviews.

[42]  K. Kairemo,et al.  Targeted liposomal drug delivery in cancer. , 2004, Current pharmaceutical design.

[43]  C. Benz,et al.  Development of ligand-targeted liposomes for cancer therapy , 2004, Expert opinion on therapeutic targets.

[44]  S. Nie,et al.  In vivo cancer targeting and imaging with semiconductor quantum dots , 2004, Nature Biotechnology.

[45]  T. Rapoport,et al.  Crystal Structure of the Long-Chain Fatty Acid Transporter FadL , 2004, Science.

[46]  D. Colagiovanni,et al.  Pharmacokinetics , Safety , and Efficacy of a Liposome Encapsulated Thymidylate Synthase Inhibitor , OSI-7904 L [ ( S )-2-[ 5-[ ( 1 , 2-Dihydro-3-methyl-1-oxobenzo [ f ] quinazolin-9-yl ) methyl ] amino-1-oxo-2-isoindolynl ]-glutaric Acid ] in Mice , 2004 .

[47]  Tae Gwan Park,et al.  Folate receptor targeted biodegradable polymeric doxorubicin micelles. , 2004, Journal of controlled release : official journal of the Controlled Release Society.

[48]  H. Nikaido Molecular Basis of Bacterial Outer Membrane Permeability Revisited , 2003, Microbiology and Molecular Biology Reviews.

[49]  Shizuo Akira,et al.  Toll-like Receptor Signaling* , 2003, Journal of Biological Chemistry.

[50]  T. Safra Cardiac safety of liposomal anthracyclines. , 2003, The oncologist.

[51]  P. Johnston,et al.  5-Fluorouracil: mechanisms of action and clinical strategies , 2003, Nature Reviews Cancer.

[52]  R. Duncan The dawning era of polymer therapeutics , 2003, Nature Reviews Drug Discovery.

[53]  Vladimir P. Torchilin,et al.  Immunomicelles: Targeted pharmaceutical carriers for poorly soluble drugs , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[54]  D. Farrell,et al.  Inflammatory mediator production in swine following endotoxin challenge with or without co-administration of dexamethasone. , 2003, International immunopharmacology.

[55]  Ulrik B Nielsen,et al.  Therapeutic efficacy of anti-ErbB2 immunoliposomes targeted by a phage antibody selected for cellular endocytosis. , 2002, Biochimica et biophysica acta.

[56]  M. Walton,et al.  A rationale for the clinical development of the thymidylate synthase inhibitor ZD9331 in ovarian and other solid tumours. , 2002, Biochimica et biophysica acta.

[57]  John W. Park Liposome-based drug delivery in breast cancer treatment , 2002, Breast Cancer Research.

[58]  D. Siwak,et al.  The potential of drug-carrying immunoliposomes as anticancer agents. Commentary re: J. W. Park et al., Anti-HER2 immunoliposomes: enhanced efficacy due to targeted delivery. Clin. Cancer Res., 8: 1172-1181, 2002. , 2002, Clinical cancer research : an official journal of the American Association for Cancer Research.

[59]  R. Nicholson,et al.  EGFR and cancer prognosis. , 2001, European journal of cancer.

[60]  B. Smith,et al.  A FLT3 tyrosine kinase inhibitor is selectively cytotoxic to acute myeloid leukemia blasts harboring FLT3 internal tandem duplication mutations. , 2001, Blood.

[61]  Timothy J. Mitchison,et al.  Probing Spindle Assembly Mechanisms with Monastrol, a Small Molecule Inhibitor of the Mitotic Kinesin, Eg5 , 2000, The Journal of cell biology.

[62]  D. Tzemach,et al.  Nuclear delivery of doxorubicin via folate-targeted liposomes with bypass of multidrug-resistance efflux pump. , 2000, Clinical cancer research : an official journal of the American Association for Cancer Research.

[63]  R K Jain,et al.  Openings between defective endothelial cells explain tumor vessel leakiness. , 2000, The American journal of pathology.

[64]  H. Maeda,et al.  Tumor vascular permeability and the EPR effect in macromolecular therapeutics: a review. , 2000, Journal of controlled release : official journal of the Controlled Release Society.

[65]  P. Klebba,et al.  Immune recognition of porin and lipopolysaccharide epitopes of Salmonella typhimurium in mice. , 2000, Microbial pathogenesis.

[66]  S. Haggarty,et al.  Small molecule inhibitor of mitotic spindle bipolarity identified in a phenotype-based screen. , 1999, Science.

[67]  R. Langer,et al.  Drug delivery and targeting. , 1998, Nature.

[68]  R. Jain,et al.  Regulation of transport pathways in tumor vessels: role of tumor type and microenvironment. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[69]  W. Benjamin,et al.  Immunoprotection by monoclonal antibodies to the porins and lipopolysaccharide of Salmonella typhimurium. , 1996, Microbial pathogenesis.

[70]  H. Jablonowski,et al.  Efficacy and safety of Stealth liposomal doxorubicin in AIDS-related Kaposi's sarcoma. The International SL-DOX Study Group. , 1996, British Journal of Cancer.

[71]  H. Lane,et al.  Phosphorylation by p34cdc2 regulates spindle association of human Eg5, a kinesin-related motor essential for bipolar spindle formation in vivo , 1995, Cell.

[72]  F M Muggia,et al.  Liposomal doxorubicin: antitumor activity and unique toxicities during two complementary phase I studies. , 1995, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[73]  P. Johnston,et al.  Increased thymidylate synthase protein levels are principally associated with proliferation but not cell cycle phase in asynchronous human cancer cells. , 1995, British Journal of Cancer.

[74]  T. Mitchison,et al.  Mutations in the kinesin-like protein Eg5 disrupting localization to the mitotic spindle. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[75]  T. Kuzel,et al.  Hand‐foot syndrome associated with liposome‐encapsulated doxorubicin therapy , 1995, Cancer.

[76]  J. Ross,et al.  Differential regulation of folate receptor isoforms in normal and malignant tissues in vivo and in established cell lines. Physiologic and clinical implications , 1994, Cancer.

[77]  L. Johnson Posttranscriptional regulation of thymidylate synthase gene expression , 1994, Journal of cellular biochemistry.

[78]  G. Schulz Bacterial porins: structure and function. , 1993, Current opinion in cell biology.

[79]  K. Keyomarsi,et al.  The thymidylate synthase inhibitor, ICI D1694, overcomes translational detainment of the enzyme. , 1993, The Journal of biological chemistry.

[80]  L R Coney,et al.  Distribution of the folate receptor GP38 in normal and malignant cell lines and tissues. , 1992, Cancer research.

[81]  H. Blum,et al.  Primary hepatocellular carcinoma. , 1991, The New England journal of medicine.

[82]  L. Rothfield,et al.  A division inhibitor and a topological specificity factor coded for by the minicell locus determine proper placement of the division septum in E. coli , 1989, Cell.

[83]  H. Maeda,et al.  A new concept for macromolecular therapeutics in cancer chemotherapy: mechanism of tumoritropic accumulation of proteins and the antitumor agent smancs. , 1986, Cancer research.

[84]  S. Svenson,et al.  Antibody responses to Escherichia coli J5 lipopolysaccharide and to Salmonella porin in patients with bacteremia. , 1986, Microbial pathogenesis.

[85]  A. Calvert,et al.  Modulation of anti-metabolite effects. Effects of thymidine on the efficacy of the quinazoline-based thymidylate synthetase inhibitor, CB3717. , 1984, Biochemical pharmacology.

[86]  H. Dintzis,et al.  Studies on the immunogenicity and tolerogenicity of T-independent antigens. , 1983, Journal of immunology.

[87]  M. Feldmann,et al.  THE RELATIONSHIP BETWEEN ANTIGENIC STRUCTURE AND THE REQUIREMENT FOR THYMUS-DERIVED CELLS IN THE IMMUNE RESPONSE , 1971, The Journal of experimental medicine.

[88]  W. D. Fisher,et al.  MINIATURE escherichia coli CELLS DEFICIENT IN DNA. , 1967, Proceedings of the National Academy of Sciences of the United States of America.

[89]  E. Sausville,et al.  Clinical pharmacology of UCN-01: Initial observations and comparison to preclinical models , 2009, Cancer Chemotherapy and Pharmacology.

[90]  R. Gurny,et al.  Biodegradable nanoparticles for direct or two-step tumor immunotargeting. , 2006, Bioconjugate chemistry.

[91]  W. Gmeiner,et al.  Novel chemical strategies for thymidylate synthase inhibition. , 2005, Current medicinal chemistry.

[92]  M. Lippman,et al.  Evaluation of Novel Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors , 2004, Breast Cancer Research and Treatment.

[93]  John W. Park,et al.  Immunoliposomes for cancer treatment. , 1997, Advances in pharmacology.

[94]  A. A. Gabizon Liposomal anthracyclines. , 1994, Hematology/oncology clinics of North America.