Diabetes area participation analysis: a review of companies and targets described in the 2008 – 2010 patent literature

Importance of the field: Type 2 diabetes is a chronic disease characterized by the development of insulin resistance, impaired pancreatic β-cell function and, ultimately, hyperglycemia. The disease is highly associated with obesity and it is thought that the inappropriate deposition of lipid in tissues such as liver and muscle contributes to a reduction in insulin sensitivity which, in turn, places a burden on the β-cell to secrete more insulin to achieve normoglycemia. Over an extended period of time, this can result in β-cell failure and diminished glycemic control. When poorly managed, type 2 diabetes increases the risk of developing both microvascular and macrovascular complications, including retinopathy, nephropathy and coronary artery disease. The number of Americans with diabetes has approached 24 million in 2007 and the prevalence of the disease is projected to increase with the sedentary lifestyles and high caloric diets that are common today. First-line treatment for the disease involves lifestyle modifications and, if unsuccessful, pharmacotherapy to control symptoms. Anti-diabetic drugs belonging to several mechanistic classes are available (e.g., insulin secretagogues, insulin sensitizers, insulin mimetics and DPP IV inhibitors); however, many of these drugs lose their effectiveness over time, are not well-tolerated in some patients or may have suboptimal risk:benefit ratios. The search for new anti-diabetic drugs has continued to attract considerable interest from both academia and the pharmaceutical industry. Areas covered in this review: An analysis of 2008 – 2010 patent applications claiming diabetes as an indication has been undertaken. What the reader will gain: An understanding of: i) the pharmaceutical companies that have filed patent applications in the anti-diabetes area during 2008 – 2010; ii) the different pharmacological targets under investigation and the patent activity around such targets; iii) some of the targets in the research portfolios of selected companies; iv) chemical structures of compounds that modulate emerging targets and v) the pharmacological rationale underlying several targets with the largest patent counts. Take home message: Type 2 diabetes is a complex disease with many potential points of intervention for pharmacotherapy. A majority of anti-diabetic patent applications claim chemical matter for just eight targets which include five enzymes, a GPCR, a family of nuclear hormone receptors and a class of sodium-dependent glucose co-transporters (11β-HSD1, DGAT1, DPP IV, glucokinase, GPR119, PPAR-α, -δ, -γ, SGLT1 and SGLT2, and stearoyl-CoA desaturase 1 (SCD1)). The major pharmaceutical companies are all pursuing some combination of these top eight targets. Several companies stand out for the breadth of new targets under investigation (e.g., F. Hoffmann-La Roche, Merck & Co., Pfizer, Takeda Pharmaceuticals, Sanofi-Aventis).

[1]  J. Flier,et al.  A Transgenic Model of Visceral Obesity and the Metabolic Syndrome , 2001, Science.

[2]  L. Agius,et al.  The physiological role of glucokinase binding and translocation in hepatocytes. , 1998, Advances in enzyme regulation.

[3]  R. DeFronzo,et al.  Correction of hyperglycemia with phlorizin normalizes tissue sensitivity to insulin in diabetic rats. , 1987, The Journal of clinical investigation.

[4]  T. Heise,et al.  Piragliatin (RO4389620), a novel glucokinase activator, lowers plasma glucose both in the postabsorptive state and after a glucose challenge in patients with type 2 diabetes mellitus: a mechanistic study. , 2010, The Journal of clinical endocrinology and metabolism.

[5]  S. Murray,et al.  Single‐Dose Pharmacokinetics and Pharmacodynamics of Sergliflozin Etabonate, a Novel Inhibitor of Glucose Reabsorption, in Healthy Volunteers and Patients With Type 2 Diabetes Mellitus , 2010, Journal of clinical pharmacology.

[6]  Yoshikazu Fujimori,et al.  Remogliflozin Etabonate, in a Novel Category of Selective Low-Affinity Sodium Glucose Cotransporter (SGLT2) Inhibitors, Exhibits Antidiabetic Efficacy in Rodent Models , 2008, Journal of Pharmacology and Experimental Therapeutics.

[7]  F. Matschinsky,et al.  Assessing the potential of glucokinase activators in diabetes therapy , 2009, Nature Reviews Drug Discovery.

[8]  L. P. Van den Heuvel,et al.  Autosomal recessive renal glucosuria attributable to a mutation in the sodium glucose cotransporter (SGLT2) , 2002, Human Genetics.

[9]  Peter Lindgren,et al.  Guidelines on diabetes, pre-diabetes, and cardiovascular diseases: executive summary , 2007 .

[10]  C. Reynet,et al.  Deorphanization of a G protein-coupled receptor for oleoylethanolamide and its use in the discovery of small-molecule hypophagic agents. , 2006, Cell metabolism.

[11]  C. Edwards,et al.  Human placental 11 beta-hydroxysteroid dehydrogenase: evidence for and partial purification of a distinct NAD-dependent isoform. , 1993, Endocrinology.

[12]  S. Bharate,et al.  Progress in the discovery and development of small-molecule modulators of G-protein-coupled receptor 40 (GPR40/FFA1/FFAR1): an emerging target for type 2 diabetes , 2009, Expert opinion on therapeutic patents.

[13]  S. Chirala,et al.  Glucose and fat metabolism in adipose tissue of acetyl-CoA carboxylase 2 knockout mice. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[14]  Margaret S. Wu,et al.  Role of AMP-activated protein kinase in mechanism of metformin action. , 2001, The Journal of clinical investigation.

[15]  Robert M. Jones,et al.  GPR119 agonists for the treatment of type 2 diabetes , 2009, Expert opinion on therapeutic patents.

[16]  J. Falgueyret,et al.  Synthesis and biological activity of a potent and orally bioavailable SCD inhibitor (MF-438). , 2010, Bioorganic & medicinal chemistry letters.

[17]  J. Whitworth,et al.  THE KIDNEY IS THE MAJOR SITE OF CORTISONE PRODUCTION IN MAN , 1989, Clinical endocrinology.

[18]  J. Grippo,et al.  Allosteric Activators of Glucokinase: Potential Role in Diabetes Therapy , 2003, Science.

[19]  C. Ucla,et al.  Differential expression and regulation of the glucokinase gene in liver and islets of Langerhans. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[20]  J. Seckl,et al.  Metabolic syndrome without obesity: Hepatic overexpression of 11beta-hydroxysteroid dehydrogenase type 1 in transgenic mice. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[21]  B. Walker,et al.  Effects of the 11β-Hydroxysteroid Dehydrogenase Inhibitor Carbenoxolone on Insulin Sensitivity in Men with Type 2 Diabetes , 2003 .

[22]  D. James,et al.  Acute or chronic upregulation of mitochondrial fatty acid oxidation has no net effect on whole-body energy expenditure or adiposity. , 2010, Cell metabolism.

[23]  B. Yandell,et al.  Loss of stearoyl–CoA desaturase-1 function protects mice against adiposity , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[24]  Yun-ping Zhou,et al.  Selective Small-Molecule Agonists of G Protein–Coupled Receptor 40 Promote Glucose-Dependent Insulin Secretion and Reduce Blood Glucose in Mice , 2008, Diabetes.

[25]  E. Wright,et al.  Renal Na(+)-glucose cotransporters. , 2001, American journal of physiology. Renal physiology.

[26]  E. Newsholme,et al.  The glucose fatty-acid cycle. Its role in insulin sensitivity and the metabolic disturbances of diabetes mellitus. , 1963, Lancet.

[27]  M. Miyazaki,et al.  Lack of stearoyl-CoA desaturase 1 upregulates basal thermogenesis but causes hypothermia in a cold environment Published, JLR Papers in Press, June 21, 2004. DOI 10.1194/jlr.M400039-JLR200 , 2004, Journal of Lipid Research.

[28]  B. Walker,et al.  Printed in U.S.A. Copyright © 2001 by The Endocrine Society Minireview: 11�-Hydroxysteroid Dehydrogenase Type 1— A Tissue-Specific Amplifier of Glucocorticoid Action* , 2000 .

[29]  B. Cariou The farnesoid X receptor (FXR) as a new target in non-alcoholic steatohepatitis. , 2008, Diabetes & metabolism.

[30]  A. M. Habib,et al.  Glucose Sensing in L Cells: A Primary Cell Study , 2008, Cell metabolism.

[31]  J. Corbett Review of recent acetyl-CoA carboxylase inhibitor patents: mid-2007 – 2008 , 2009, Expert opinion on therapeutic patents.

[32]  M. Bessler,et al.  Effects of Roux-en-Y gastric bypass surgery on fasting and postprandial concentrations of plasma ghrelin, peptide YY, and insulin. , 2005, The Journal of clinical endocrinology and metabolism.

[33]  M. Miyazaki,et al.  Stearoyl-CoA desaturase 1 deficiency increases insulin signaling and glycogen accumulation in brown adipose tissue. , 2005, American journal of physiology. Endocrinology and metabolism.

[34]  J. Calado,et al.  Novel compound heterozygous mutations in SLC5A2 are responsible for autosomal recessive renal glucosuria , 2004, Human Genetics.

[35]  S. Berthel,et al.  Glucokinase activators as new type 2 diabetes therapeutic agents , 2008 .

[36]  L. Abrahmsén,et al.  Selective inhibition of 11 beta-hydroxysteroid dehydrogenase type 1 improves hepatic insulin sensitivity in hyperglycemic mice strains. , 2003, Endocrinology.

[37]  D. Hargrove,et al.  Isozyme-nonselective N-Substituted Bipiperidylcarboxamide Acetyl-CoA Carboxylase Inhibitors Reduce Tissue Malonyl-CoA Concentrations, Inhibit Fatty Acid Synthesis, and Increase Fatty Acid Oxidation in Cultured Cells and in Experimental Animals* , 2003, Journal of Biological Chemistry.

[38]  T. Olsson,et al.  Tissue-specific dysregulation of cortisol metabolism in human obesity. , 2001, The Journal of clinical endocrinology and metabolism.

[39]  B. Lowell,et al.  Gene knockout of Acc2 has little effect on body weight, fat mass, or food intake , 2010, Proceedings of the National Academy of Sciences.

[40]  S. Ellard,et al.  Update on mutations in glucokinase (GCK), which cause maturity‐onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemic hypoglycemia , 2009, Human mutation.

[41]  Robert M. Jones,et al.  A role for intestinal endocrine cell-expressed g protein-coupled receptor 119 in glycemic control by enhancing glucagon-like Peptide-1 and glucose-dependent insulinotropic Peptide release. , 2008, Endocrinology.

[42]  H. Ginsberg,et al.  Regulation of plasma triglycerides in insulin resistance and diabetes. , 2005, Archives of medical research.

[43]  T. Kowalski,et al.  GPR119 is required for physiological regulation of glucagon-like peptide-1 secretion but not for metabolic homeostasis. , 2009, The Journal of endocrinology.

[44]  J. Tomlinson,et al.  11β-Hydroxysteroid dehydrogenase type 1 inhibitors for the treatment of type 2 diabetes , 2010, Expert opinion on investigational drugs.

[45]  Plamen Nikolov,et al.  Economic Costs of Diabetes in the U.S. in 2002 , 2003, Diabetes care.

[46]  C. Gui,et al.  Xenobiotic transporters of the human organic anion transporting polypeptides (OATP) family. , 2008, Xenobiotica; the fate of foreign compounds in biological systems.

[47]  B. Olde,et al.  GPR40 is expressed in glucagon producing cells and affects glucagon secretion. , 2007, Biochemical and biophysical research communications.

[48]  A. M. Habib,et al.  Nutrient-dependent secretion of glucose-dependent insulinotropic polypeptide from primary murine K cells , 2009, Diabetologia.

[49]  L. Blonde Current antihyperglycemic treatment guidelines and algorithms for patients with type 2 diabetes mellitus. , 2010, The American journal of medicine.

[50]  P. Brubaker,et al.  GPR119 Is Essential for Oleoylethanolamide-Induced Glucagon-Like Peptide-1 Secretion From the Intestinal Enteroendocrine L-Cell , 2009, Diabetes.

[51]  B. Walker,et al.  Effects of the 11 beta-hydroxysteroid dehydrogenase inhibitor carbenoxolone on insulin sensitivity in men with type 2 diabetes. , 2003, The Journal of clinical endocrinology and metabolism.

[52]  M. Erion,et al.  Liver-Targeted Drug Delivery Using HepDirect1 Prodrugs , 2005, Journal of Pharmacology and Experimental Therapeutics.

[53]  D. Webb,et al.  Carbenoxolone increases hepatic insulin sensitivity in man: a novel role for 11-oxosteroid reductase in enhancing glucocorticoid receptor activation. , 1995, The Journal of clinical endocrinology and metabolism.

[54]  S. Wakil,et al.  Acetyl-CoA carboxylase 2 mutant mice are protected against obesity and diabetes induced by high-fat/high-carbohydrate diets , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[55]  B. Walker,et al.  Minireview: 11beta-hydroxysteroid dehydrogenase type 1- a tissue-specific amplifier of glucocorticoid action. , 2001, Endocrinology.

[56]  A. Vidal-Puig,et al.  It's Not How Fat You Are, It's What You Do with It That Counts , 2008, PLoS biology.

[57]  M. Hediger,et al.  The human kidney low affinity Na+/glucose cotransporter SGLT2. Delineation of the major renal reabsorptive mechanism for D-glucose. , 1994, The Journal of clinical investigation.

[58]  John P. Overington,et al.  How many drug targets are there? , 2006, Nature Reviews Drug Discovery.

[59]  Ziwei Gu,et al.  Liver-specific deletion of acetyl-CoA carboxylase 1 reduces hepatic triglyceride accumulation without affecting glucose homeostasis. , 2006, Proceedings of the National Academy of Sciences of the United States of America.

[60]  L. Abrahmsén,et al.  Selective inhibition of 11β-hydroxysteroid dehydrogenase type 1 decreases blood glucose concentrations in hyperglycaemic mice , 2002, Diabetologia.

[61]  Didier Bagnol,et al.  A role for beta-cell-expressed G protein-coupled receptor 119 in glycemic control by enhancing glucose-dependent insulin release. , 2007, Endocrinology.

[62]  J. Fornwald,et al.  Pharmacological regulation of insulin secretion in MIN6 cells through the fatty acid receptor GPR40: identification of agonist and antagonist small molecules , 2006, British journal of pharmacology.

[63]  N. Rubins,et al.  The FFA receptor GPR40 links hyperinsulinemia, hepatic steatosis, and impaired glucose homeostasis in mouse. , 2005, Cell metabolism.

[64]  Masataka Harada,et al.  Free fatty acids regulate insulin secretion from pancreatic β cells through GPR40 , 2003, Nature.

[65]  M. Hewison,et al.  Expression of 11beta-hydroxysteroid dehydrogenase type 1 in adipose tissue is not increased in human obesity. , 2002, The Journal of clinical endocrinology and metabolism.

[66]  H. Edlund,et al.  Gpr40 Is Expressed in Enteroendocrine Cells and Mediates Free Fatty Acid Stimulation of Incretin Secretion , 2008, Diabetes.

[67]  K. Takeuchi,et al.  Overexpression of GPR40 in Pancreatic β-Cells Augments Glucose-Stimulated Insulin Secretion and Improves Glucose Tolerance in Normal and Diabetic Mice , 2009, Diabetes.

[68]  V. Routh,et al.  Glucokinase is the likely mediator of glucosensing in both glucose-excited and glucose-inhibited central neurons. , 2002, Diabetes.

[69]  L. Agius Glucokinase and molecular aspects of liver glycogen metabolism. , 2008, The Biochemical journal.

[70]  T. Asano,et al.  T-1095, an inhibitor of renal Na+-glucose cotransporters, may provide a novel approach to treating diabetes. , 1999, Diabetes.

[71]  Yoshikazu Fujimori,et al.  Sergliflozin etabonate, a selective SGLT2 inhibitor, improves glycemic control in streptozotocin-induced diabetic rats and Zucker fatty rats. , 2009, European journal of pharmacology.

[72]  H. Matsushime,et al.  Lysophosphatidylcholine enhances glucose-dependent insulin secretion via an orphan G-protein-coupled receptor. , 2005, Biochemical and biophysical research communications.

[73]  M. Cooper,et al.  11Beta-hydroxysteroid dehydrogenase type 1 and its role in the hypothalamus-pituitary-adrenal axis, metabolic syndrome, and inflammation. , 2009, The Journal of clinical endocrinology and metabolism.

[74]  P. White,et al.  The human gene for 11 beta-hydroxysteroid dehydrogenase. Structure, tissue distribution, and chromosomal localization. , 1991, The Journal of biological chemistry.

[75]  William Thomsen,et al.  Discovery of the first potent and orally efficacious agonist of the orphan G-protein coupled receptor 119. , 2008, Journal of medicinal chemistry.

[76]  L. Kaczmarek,et al.  The voltage-gated potassium channel Kv1.3 regulates peripheral insulin sensitivity. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[77]  N. Lewis,et al.  Phlorizin: a review , 2005, Diabetes/metabolism research and reviews.

[78]  C. L. Lassen,et al.  J Am Soc Nephrol 14: 2873–2882, 2003 Molecular Analysis of the SGLT2 Gene in Patients with Renal , 2022 .

[79]  S. Wakil,et al.  Continuous fat oxidation in acetyl–CoA carboxylase 2 knockout mice increases total energy expenditure, reduces fat mass, and improves insulin sensitivity , 2007, Proceedings of the National Academy of Sciences.

[80]  R. DeFronzo Insulin resistance, lipotoxicity, type 2 diabetes and atherosclerosis: the missing links. The Claude Bernard Lecture 2009 , 2010, Diabetologia.

[81]  D. Earle,et al.  Effect of diabetes and insulin of the maximum capacity of the renal tubules to reabsorb glucose. , 1951, The Journal of clinical investigation.

[82]  P. Stewart,et al.  Does central obesity reflect “Cushing's disease of the omentum”? , 1997, The Lancet.

[83]  M. Sherman,et al.  Hepatic fatty acid composition differs between chronic hepatitis C patients with and without steatosis. , 2009, The Journal of nutrition.

[84]  Edwards,et al.  11 b-Hydroxysteroid dehydrogenase type 1 knockout mice show attenuated glucocorticoid-inducible responses and resist hyperglycemia on obesity or stress , 1997 .

[85]  F. Schick,et al.  Low hepatic stearoyl-CoA desaturase 1 activity is associated with fatty liver and insulin resistance in obese humans , 2008, Diabetologia.

[86]  David M. Smith,et al.  The long-chain fatty acid receptor, GPR40, and glucolipotoxicity: investigations using GPR40-knockout mice. , 2008, Biochemical Society transactions.

[87]  Yoshikazu Fujimori,et al.  Sergliflozin, a Novel Selective Inhibitor of Low-Affinity Sodium Glucose Cotransporter (SGLT2), Validates the Critical Role of SGLT2 in Renal Glucose Reabsorption and Modulates Plasma Glucose Level , 2007, Journal of Pharmacology and Experimental Therapeutics.

[88]  John J. Mullins,et al.  Improved Lipid and Lipoprotein Profile, Hepatic Insulin Sensitivity, and Glucose Tolerance in 11β-Hydroxysteroid Dehydrogenase Type 1 Null Mice* , 2001, The Journal of Biological Chemistry.

[89]  Gaochao Zhou,et al.  AMPK: an emerging drug target for diabetes and the metabolic syndrome. , 2009, Cell metabolism.

[90]  E. Van Schaftingen,et al.  The mechanism by which rat liver glucokinase is inhibited by the regulatory protein. , 1990, European journal of biochemistry.

[91]  M. Orešič,et al.  Hepatic Stearoyl-CoA Desaturase (SCD)-1 Activity and Diacylglycerol but Not Ceramide Concentrations Are Increased in the Nonalcoholic Human Fatty Liver , 2009, Diabetes.

[92]  T. Alquier,et al.  GPR40: Good Cop, Bad Cop? , 2009, Diabetes.

[93]  J. Chambers,et al.  The Orphan G Protein-coupled Receptor GPR40 Is Activated by Medium and Long Chain Fatty Acids* , 2003, The Journal of Biological Chemistry.

[94]  D. Poirier,et al.  17β-Hydroxysteroid dehydrogenase inhibitors: a patent review , 2010, Expert opinion on therapeutic patents.

[95]  Harini Sampath,et al.  Stearoyl-CoA Desaturase-1 Mediates the Pro-lipogenic Effects of Dietary Saturated Fat* , 2007, Journal of Biological Chemistry.

[96]  Martin M. Matzuk,et al.  Continuous Fatty Acid Oxidation and Reduced Fat Storage in Mice Lacking Acetyl-CoA Carboxylase 2 , 2001, Science.

[97]  H. Ichijo,et al.  Impact of Mitochondrial Reactive Oxygen Species and Apoptosis Signal–Regulating Kinase 1 on Insulin Signaling , 2006, Diabetes.

[98]  M. Miyazaki,et al.  Stearoyl-CoA desaturase 1 deficiency elevates insulin-signaling components and down-regulates protein-tyrosine phosphatase 1B in muscle , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[99]  B. Zinman,et al.  Glycemic durability of rosiglitazone, metformin, or glyburide monotherapy. , 2006, The New England journal of medicine.

[100]  G. Marchesini,et al.  Insulin resistance in nonalcoholic fatty liver disease. , 2010, Current pharmaceutical design.

[101]  Diane M. Griffiths,et al.  THE REGENTS OF THE UNIVERSITY OF CALIFORNIA , 2007 .

[102]  Ziwei Gu,et al.  Mutant mice lacking acetyl-CoA carboxylase 1 are embryonically lethal. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[103]  M. Magnuson,et al.  Cell-specific roles of glucokinase in glucose homeostasis. , 2001, Recent progress in hormone research.

[104]  W. Washburn Evolution of sodium glucose co-transporter 2 inhibitors as anti-diabetic agents , 2009, Expert opinion on therapeutic patents.

[105]  Z. Krozowski,et al.  Cloning and tissue distribution of the human 1 lβ-hydroxysteroid dehydrogenase type 2 enzyme , 1994, Molecular and Cellular Endocrinology.

[106]  Andrew D. Steele,et al.  SIRT1 transgenic mice show phenotypes resembling calorie restriction , 2007, Aging cell.

[107]  M. Laakso,et al.  Guidelines on Diabetes, Pre-Diabetes, and Cardiovascular Diseases: Executive Summary , 2007 .

[108]  G. Schernthaner Diabetes and Cardiovascular Disease: Is intensive glucose control beneficial or deadly? Lessons from ACCORD, ADVANCE, VADT, UKPDS, PROactive, and NICE-SUGAR , 2010, Wiener Medizinische Wochenschrift.

[109]  T. Alquier,et al.  GPR40 Is Necessary but Not Sufficient for Fatty Acid Stimulation of Insulin Secretion In Vivo , 2007, Diabetes.

[110]  R. Yoshimoto,et al.  Discovery and characterization of a novel potent, selective and orally active inhibitor for mammalian ELOVL6. , 2010, European journal of pharmacology.

[111]  G. Shulman,et al.  Reversal of diet-induced hepatic steatosis and hepatic insulin resistance by antisense oligonucleotide inhibitors of acetyl-CoA carboxylases 1 and 2. , 2006, The Journal of clinical investigation.