• We are sorry, but NCBI web applications do not support your browser and may not function properly. More information
Logo of ajcnThe American Journal of Clinical NutritionSearchSubmit ManuscriptSubscribeAll ArticlesPublished Version
Am J Clin Nutr. Jan 2010; 91(1): 258S–261S.
Published online Nov 11, 2009. doi:  10.3945/ajcn.2009.28449C
PMCID: PMC2793112

Adiponectin in insulin resistance: lessons from translational research1,2,3,4


Adiponectin is an adipose tissue–secreted endogenous insulin sensitizer, which plays a key role as a mediator of peroxisome proliferator-activated receptor γ action. Adiponectin alters glucose metabolism and insulin sensitivity, exhibits antiinflammatory and antiatherogenic properties, and has been linked to several malignancies. Circulating concentrations of adiponectin are determined primarily by genetic factors, nutrition, exercise, and abdominal adiposity. Adiponectin concentrations are lower in subjects with obesity, metabolic syndrome, and cardiovascular disease. Adiponectin knockout mice manifest glucose intolerance, insulin resistance, and hyperlipidemia and tend to develop malignancies especially when on high-fat diets. Animal studies have also shown beneficial effects of adiponectin in rodents in vivo. Circulating concentrations of adiponectin are lower in patients with diabetes, cardiovascular disease, and several malignancies. Studies to date provide promising results for the diagnostic and therapeutic role of adiponectin in obesity, insulin resistance, diabetes, cardiovascular disease, and obesity-associated malignancies.


Adiponectin [also known as Acrp30 (adipocyte complement-related protein of 30 kDa) or AdipoQ] is a 244–amino acid protein secreted mainly by the adipose tissue. It was identified almost simultaneously by 4 different groups in the mid-1990s as an adipocyte-secreted hormone but remained in obscurity until the early 2000s. Scherer et al (1) were the first to report isolating adiponectin cDNA in mice by a differential display method in adipocytes, and their data were soon thereafter confirmed by Hu et al (2). Human adiponectin cDNA was also independently identified from adipose tissue by Maeda et al (3), and human adiponectin was finally purified from plasma by Nakano et al (4) as a gelatin-binding protein. The adiponectin gene is located on chromosome 3q26, a region associated with susceptibility to developing metabolic syndrome and type 2 diabetes mellitus (5).

Adiponectin circulates in multimers, ie, as full-length or high-molecular-weight (HMW), medium-molecular-weight (or hexamer), and low-molecular-weight (or trimer) adiponectin complexes. Additionally, full-length adiponectin may be cleaved to form a smaller, globular fragment, which has been proposed to have greater potency than full-length adiponectin (1). Adiponectin contains an N-terminal collagen-like hypervariable region at the NH2 terminal and a C-terminal globular domain, which is similar in structure to tumor necrosis factor-α, another adipose tissue–secreted adipokine with an action opposite that of adiponectin (5). Adiponectin primarily circulates in human plasma as a homomultimer or full-length structure (fAd or Acrp30). Posttranslational modifications are critical determinants of activity, although consensus on the biological activity of the specific circulating forms of adiponectin is lacking. The HMW isoform was proposed to have a stronger association with insulin resistance, metabolic syndrome, and cardiovascular disease as the biologically more active form of the hormone (7). We have shown, however, that the additional predictive value provided by HMW adiponectin in humans is minimal (6, 7).


Adiponectin is synthesized primarily in white adipose tissue and, at lower concentrations, in brown adipose tissue (8). Much lower concentrations of expression have been reported in skeletal muscle, liver, colon, cardiac tissue, salivary glands, and placenta. Adiponectin is even detected in cerebrospinal fluid and breast milk at much lower concentrations (9). Normal plasma adiponectin concentrations range between 5 and 30 μg/mL (depending on the assay used), are 1000 time higher than leptin concentrations, and are inversely proportional to those of abdominal adiposity (9), insulin resistance, and type 2 diabetes. Adiponectin has also been shown to have distinct effects on lipid metabolism as well as antiinflammatory and antiatherogenic effects (10). In addition to its peripheral actions, adiponectin may act centrally to modulate food intake and energy expenditure (11). Women have higher adiponectin concentrations than do men (a measure that is independent of fat mass or distribution), which is possibly linked to differences in estrogen or androgen concentrations (12). We have reported that in growing mice adiponectin initially increases in proportion to accumulating adipose tissue until the age of ≈8–10 wk and then starts decreasing. Environmental factors act as modulators of adiponectin (13), as shown by a cross-sectional evaluation of diabetic women from the Nurses' Health Study that has linked a Mediterranean-type diet and its components, primarily whole grains, moderate alcohol consumption, and nuts, to higher adiponectin concentrations (14). A recent prospective cohort study reports that coffee consumption is associated with higher plasma adiponectin concentrations (15). In vitro and in vivo studies in mice and humans have shown that adiponectin expression and secretion is up-regulated by thiazolidinediones (1618) and/or selective peroxisome proliferator-activated receptor γ (PPARγ) modulators, predominantly the HMW form. Although head-to-head comparisons have not been performed, it appears that the selective PPARγ modulator INT131 is a relatively more potent enhancer of adiponectin secretion (19).


Two different receptor isoforms, AdipoR1 and AdipoR2, have been described to date (20). Both are 7-transmembrane proteins, and in contrast to the G protein–coupled receptor family, these receptors have internal N-terminal and external C-terminal regions (20). AdipoR1 has a high affinity for globular adiponectin and a low affinity for full-length adiponectin and is abundantly expressed in skeletal muscle and endothelial cells among other tissues. AdipoR2 has intermediate affinity for both forms of adiponectin and is predominantly expressed in the liver (21, 22). Although both receptors are present in almost every tissue, including pancreatic β cells and malignant cells, one or the other receptor usually predominates. Interestingly, HMW adiponectin has also been proposed to be a ligand for T-cadherin, but this remains to be fully elucidated.

Studies in mice link aging and high-fat feeding to increased receptor expression in muscle and liver (P < 0.001) (23). We have shown that both leptin and melanocortin agonists alter AdipoR1/R2 expression in mice (24). Low adiponectin concentrations increase the risk of developing insulin resistance and possibly diabetes (25). Yamauchi et al (26) observed in a lipoatrophic mouse model that replenishing physiologic doses of adiponectin reverses insulin resistance. Adiponectin knockout mice show increased platelet aggregation and thrombus formation, apoptosis, and tumor necrosis factor-α concentrations (27, 28). Adiponectin receptors are expressed in both fat and muscle tissues in humans (27). We have also shown that both receptors are expressed in subcutaneous and visceral adipose tissues and at significantly lower concentrations (P < 0.001) than in skeletal muscle. AdipoR1/R2 in muscle is inversely associated with circulating adiponectin concentrations whereas AdipoR2 in subcutaneous fat is positively associated with circulating adiponectin concentrations (29, 30). Receptor expression in both fat and muscle is further increased in insulin-resistant states accompanied by hypoadiponectinemia. Physical activity up-regulates adiponectin receptors (29), which suggests that the adiponectin hormone system may mediate exercise-associated improvements in insulin resistance (29, 30). Interestingly, PPARγ agonists, used as insulin sensitizers in the treatment of type 2 diabetes, stimulate adiponectin production and secretion. More specifically, these drugs (rosiglitazone, pioglitazone, and ciglitazone as well as the selective PPARγ model INT131) increase the HMW/total adiponectin concentrations (19), but further clinical studies are needed to investigate hypoadiponectimia in hyperinsulinemic states to determine the potential therapeutic effects of this hormone.


Adiponectin binding to its receptors activates several intracellular signaling pathways, mainly AMP-activated protein kinase (AMPK) but also mTOR, nuclear transcription factor-κB (NF-κB), STAT3, and JNK. AMPK phosphorylation promotes glucose utilization that results in increased fatty acid oxidation, increased glucose uptake in the muscle, and reduced gluconeogenesis in the liver. AMPK activation also regulates several downstream targets, which include enzymes (involved in regulating the synthesis of protein, fatty acids, and triglycerides such as acetyl-CoA carboxylase and fatty acid synthase) as well as transcription factors and other regulatory proteins. AMPK is an upstream regulator of mTOR and is linked with several cancers (31) by directly inhibiting this pathway that results in suppression of cell proliferation (32). The JNK- and STAT3-signaling pathways are also proposed as mediators of adiponectin's effects on the metabolic syndrome and cancer (33).


Adiponectin concentrations are low in obese patients and markedly increase after prolonged caloric restriction, such as in dieting and anorexia nervosa (34), and are significantly lower (P < 0.001) in obese subjects when compared with nonobese males and females (35). Adiponectin is more closely associated with visceral fat than with subcutaneous fat (12) and is lower in type 2 diabetes, cardiovascular disease, hypertension, and metabolic syndrome (24, 35, 36), conditions that are often associated with insulin resistance. A recent meta-analysis of prospective studies with a total of 14,598 subjects and 2623 cases of type 2 diabetes indicated that higher adiponectin concentrations were associated with a lower risk of type 2 diabetes. The estimated absolute risk difference (cases/1000 person-years)/1-log μg/mL increment in adiponectin concentrations was 3.9 for elderly Americans and 30.8 for Americans with impaired glucose tolerance (36). Furthermore, adiponectin is positively correlated with HDL cholesterol and negatively associated with serum triglycerides and apolipoprotein B-100 (37). Adiponectin shows antiinflammatory effects by enhancing nitric oxide production and activating endothelial nitric oxide synthase (38) and may act as a modulator of vascular remodeling by suppressing smooth muscle cell migration (39), which possibly plays a role in the regulation of atherosclerosis.


We have proposed that adiponectin is a link between obesity and obesity-related malignancies mainly on the basis of our original observations that adiponectin concentrations are lower in patients with these types of cancers. Case-control studies conducted by our group linked lower adiponectin concentrations to an increased risk of breast cancer (40) and these observations were later independently confirmed (42, 43). Similarly, the risk of colorectal cancer has been inversely associated with lower adiponectin in a prospective study in the context of the Health Professionals Follow-Up Study (41). Case-control studies showed that lower adiponectin concentrations are associated with a higher risk of endometrial cancer in both pre- and postmenopausal women (42, 43), and these findings were later confirmed by a larger case-control study nested within the European Prospective Investigation into Cancer and Nutrition Study (44). In addition, several groups have reported similar inverse associations with prostate cancer (45), myelodysplastic syndromes, a preleukemic condition linked with obesity (46), as well as gastric (47) and renal cancers. Lower concentrations of adiponectin were positively associated with renal cell carcinoma and tumor aggression (48) and were shown to be even lower in patients with metastasis when compared with those with localized disease (49). In contrast, a hospital-based case-control study showed that adiponectin concentrations are positively associated with pancreatic cancer, and a substudy of tissue samples showed increased expression of adiponectin receptors (50); however, further studies are needed to determine whether this is a compensatory mechanism for high adiponectin concentrations observed during cancer progression. Several single-nucleotide polymorphisms within the 5′ flanking region of the ADIPOQ gene are associated with the risk of breast and colorectal cancer (51). Adiponectin's direct effects are exerted by receptor-mediated stimulation of signaling pathways and indirectly by moderating insulin sensitivity at the level of target tissue. Adiponectin acts through receptors R1/R2 to stimulate signaling pathways, mainly AMPK, but also PPARα, MAPK, and NF-kB (52). AMPK activation regulates cell proliferation, decreases expression of transcriptional regulators, and positively regulates important proteins associated with controlling growth arrest and apoptosis (p21, p53). It is suggested that adiponectin may regulate tumor cells by directly inhibiting pro-angiogenic factors such as basic fibroblast growth factor and interleukin-8 produced by tumors or platelet-derived growth factor BB produced by endothelial cells (39). Several case-control studies showed that adiponectin receptors, especially AdipoR1, are up-regulated in malignancies that include prostate (48), breast (51), pancreatic (50), colorectal (53), and endometrial cancers (CS Mantzoros, unpublished data, 2009).

Adiponectin also exerts an indirect action through an insulin-sensitizing, antiinflammatory, and antiangiogenic effect. Hyperinsulinemia results in high concentrations of circulating insulin-like growth factor I, which leads to increased cell proliferation, decreased apoptosis, and increased inflammation (54). In vitro studies to date show that adiponectin decreases cell viability and proliferation in breast, colorectal, prostate, and endometrial cancers. Recently, in vivo studies in mice evaluated adiponectin's role in suppression of colon cancer cell proliferation and its possible therapeutic use for colon cancer (55). Although promising, further studies are needed in animals and humans to better delineate the effects of adiponectin and cell proliferation, apoptosis, inflammation, and insulin sensitization in relation to obesity-associated cancers.


Adiponectin, an endogenous insulin-sensitizing hormone and the most abundant adipokine produced by the human adipose tissue, is linked to obesity, metabolic syndrome, insulin resistance, type 2 diabetes, and inflammation as well as several types of cancers. Genetic factors such as single nucleotide polymorphism 276 in the adiponectin gene and environmental factors such as a high-fat diet and inactivity are associated with low adiponectin concentrations and may contribute to the development of insulin resistance, type 2 diabetes, and atherosclerosis. A Mediterranean-type diet, reduction of body weight, and consumption of nuts, coffee, and/or moderate amounts of alcohol have a well-established association with increased plasma adiponectin concentrations and a decreased risk of developing insulin resistance, metabolic syndrome, diabetes, and cardiovascular disease. More specifically, adiponectin could play a potential role in the treatment of insulin-resistant states, which include type 2 diabetes. Accumulating evidence from research studies conducted in both animals and humans links adiponectin and its receptors to several malignancies, which suggests a potential role in regulating cell proliferation and a possible key role in cancer prevention and/or therapy. Thus, adiponectin could prove to be an effective therapeutic agent. Alternatively, pharmacologic agents that could directly increase adiponectin's circulating concentrations (including novel or existing medications such as PPARγ agonists) and/or compounds that could directly act on specific tissue targets, such as adiponectin receptor agonists that induce signaling pathways downstream of adiponectin receptors, would be an important addition to our therapeutic armamentarium. (Other articles in this supplement to the Journal include references 5659.)


The authors' responsibilities were as follows—FZ and CSM: wrote the manuscript. FZ had no conflict of interest. CSM is the scientific cofounder and Chair of the Scientific Advisory Board of InteKrin Metabolic Therapeutics Inc, which has provided an unrestricted educational grant to support in part this symposium.


1. Scherer PE, Williams S, Fogliano M, Baldini G, Lodish HF. A novel serum protein similar to C1q, produced exclusively in adipocytes. J Biol Chem 1995;270:26746–9 [PubMed]
2. Hu E, Liang P, Spiegelman BM. AdipoQ is a novel adipose-specific gene dysregulated in obesity. J Biol Chem 1996;271:10697–703 [PubMed]
3. Maeda K, Okubo K, Shimomura I, Funahashi T, Matsuzawa Y, Matsubara K. cDNA cloning and expression of a novel adipose specific collagen-like factor, apM1 (AdiPose Most abundant Gene transcript 1). Biochem Biophys Res Commun 1996;221:286–9 [PubMed]
4. Nakano Y, Tobe T, Choi-Miura NH, Mazda T, Tomita M. Isolation and characterization of GBP28, a novel gelatin-binding protein purified from human plasma. J Biochem 1996;120:803–12 [PubMed]
5. Ruan H, Lodish HF. Insulin resistance in adipose tissue: direct and indirect effects of tumor necrosis factor-alpha. Cytokine Growth Factor Rev 2003;14:447–55 [PubMed]
6. Bluher M, Brennan AM, Kelesidis T, et al. Total and high-molecular weight adiponectin in relation to metabolic variables at baseline and in response to an exercise treatment program: comparative evaluation of three assays. Diabetes Care 2007;30:280–5 [PubMed]
7. Heidemann C, Sun Q, van Dam RM, et al. Total and high-molecular-weight adiponectin and resistin in relation to the risk for type 2 diabetes in women. Ann Intern Med 2008;149:307–16 [PMC free article] [PubMed]
8. Viengchareun S, Zennaro MC, Pascual-Le Tallec L, Lombes M. Brown adipocytes are novel sites of expression and regulation of adiponectin and resistin. FEBS Lett 2002;532:345–50 [PubMed]
9. Berg AH, Combs TP, Scherer PE. ACRP30/adiponectin: an adipokine regulating glucose and lipid metabolism. Trends Endocrinol Metab 2002;13:84–9 [PubMed]
10. Mantzoros CS, Li T, Manson JE, Meigs JB, Hu FB. Circulating adiponectin levels are associated with better glycemic control, more favorable lipid profile, and reduced inflammation in women with type 2 diabetes. J Clin Endocrinol Metab 2005;90:4542–8 [PubMed]
11. Kubota N, Yano W, Kubota T, et al. Adiponectin stimulates AMP-activated protein kinase in the hypothalamus and increases food intake. Cell Metab 2007;6:55–68 [PubMed]
12. Cnop M, Havel PJ, Utzschneider KM, et al. Relationship of adiponectin to body fat distribution, insulin sensitivity and plasma lipoproteins: evidence for independent roles of age and sex. Diabetologia 2003;46:459–69 [PubMed]
13. Pischon T, Girman CJ, Rifai N, Hotamisligil GS, Rimm EB. Association between dietary factors and plasma adiponectin concentrations in men. Am J Clin Nutr 2005;81:780–6 [PubMed]
14. Mantzoros CS, Williams CJ, Manson JE, Meigs JB, Hu FB. Adherence to the Mediterranean dietary pattern is positively associated with plasma adiponectin concentrations in diabetic women. Am J Clin Nutr 2006;84:328–35 [PubMed]
15. Williams CJ, Fargnoli JL, Hwang JJ, et al. Coffee consumption is associated with higher plasma adiponectin concentrations in women with or without type 2 diabetes: a prospective cohort study. Diabetes Care 2008;31:504–7 [PMC free article] [PubMed]
16. Combs TP, Wagner JA, Berger J, et al. Induction of adipocyte complement-related protein of 30 kilodaltons by PPARgamma agonists: a potential mechanism of insulin sensitization. Endocrinology 2002;143:998–1007 [PubMed]
17. Maeda N, Takahashi M, Funahashi T, et al. PPARgamma ligands increase expression and plasma concentrations of adiponectin, an adipose-derived protein. Diabetes 2001;50:2094–9 [PubMed]
18. Yu JG, Javorschi S, Hevener AL, et al. The effect of thiazolidinediones on plasma adiponectin levels in normal, obese, and type 2 diabetic subjects. Diabetes 2002;51:2968–74 [PubMed]
19. Higgins LS, Mantzoros CS. The development of INT131 as a selective PPARgamma modulator: approach to a safer insulin sensitizer. PPAR Res 2008;936906. [PMC free article] [PubMed]
20. Yamauchi T, Kamon J, Ito Y, et al. Cloning of adiponectin receptors that mediate antidiabetic metabolic effects. Nature 2003;423:762–9 [PubMed]
21. Goldstein BJ, Scalia R. Adiponectin: a novel adipokine linking adipocytes and vascular function. J Clin Endocrinol Metab 2004;89:2563–8 [PubMed]
22. Kadowaki T, Yamauchi T, Kubota N, Hara K, Ueki K. Adiponectin and adiponectin receptors in obesity-linked insulin resistance. Novartis Found Symp 2007;286:164–76; discussion 176–82, 200–3 [PubMed]
23. Bullen JW, Jr, Bluher S, Kelesidis T, Mantzoros CS. Regulation of adiponectin and its receptors in response to development of diet-induced obesity in mice. Am J Physiol Endocrinol Metab 2007;292:E1079–86 [PubMed]
24. Bluher S, Ziotopoulou M, Bullen JW, Jr, et al. Responsiveness to peripherally administered melanocortins in lean and obese mice. Diabetes 2004;53:82–90 [PubMed]
25. Lindsay RS, Funahashi T, Hanson RL, et al. Adiponectin and development of type 2 diabetes in the Pima Indian population. Lancet 2002;360:57–8 [PubMed]
26. Yamauchi T, Kamon J, Waki H, et al. The fat-derived hormone adiponectin reverses insulin resistance associated with both lipoatrophy and obesity. Nat Med 2001;7:941–6 [PubMed]
27. Okamoto Y, Kihara S, Ouchi N, et al. Adiponectin reduces atherosclerosis in apolipoprotein E-deficient mice. Circulation 2002;106:2767–70 [PubMed]
28. Shibata R, Sato K, Pimentel DR, et al. Adiponectin protects against myocardial ischemia-reperfusion injury through AMPK- and COX-2-dependent mechanisms. Nat Med 2005;11:1096–103 [PMC free article] [PubMed]
29. Bluher M, Bullen JW, Jr, Lee JH, et al. Circulating adiponectin and expression of adiponectin receptors in human skeletal muscle: associations with metabolic parameters and insulin resistance and regulation by physical training. J Clin Endocrinol Metab 2006;91:2310–6 [PubMed]
30. Bluher M, Williams CJ, Kloting N, et al. Gene expression of adiponectin receptors in human visceral and subcutaneous adipose tissue is related to insulin resistance and metabolic parameters and is altered in response to physical training. Diabetes Care 2007;30:3110–5 [PMC free article] [PubMed]
31. Averous J, Proud CG. When translation meets transformation: the mTOR story. Oncogene 2006;25:6423–35 [PubMed]
32. Luo Z, Saha AK, Xiang X, Ruderman NB. AMPK, the metabolic syndrome and cancer. Trends Pharmacol Sci 2005;26:69–76 [PubMed]
33. Miyazaki T, Bub JD, Uzuki M, Iwamoto Y. Adiponectin activates c-Jun NH2-terminal kinase and inhibits signal transducer and activator of transcription 3. Biochem Biophys Res Commun 2005;333:79–87 [PubMed]
34. Delporte ML, Brichard SM, Hermans MP, Beguin C, Lambert M. Hyperadiponectinaemia in anorexia nervosa. Clin Endocrinol (Oxf) 2003;58:22–9 [PubMed]
35. Arita Y, Kihara S, Ouchi N, et al. Paradoxical decrease of an adipose-specific protein, adiponectin, in obesity. Biochem Biophys Res Commun 1999;257:79–83 [PubMed]
36. Li S, Shin JJ, Ding EL, van Dam RM. Adiponectin levels and risk of type 2 diabetes: a systematic review and meta-analysis. JAMA 2009;302:179–88 [PubMed]
37. Schulze MB, Shai I, Rimm EB, Li T, Rifai N, Hu FB. Adiponectin and future coronary heart disease events among men with type 2 diabetes. Diabetes 2005;54:534–9 [PubMed]
38. Chen H, Montagnani M, Funahashi T, Shimomura I, Quon MJ. Adiponectin stimulates production of nitric oxide in vascular endothelial cells. J Biol Chem 2003;278:45021–6 [PubMed]
39. Arita Y, Kihara S, Ouchi N, et al. Adipocyte-derived plasma protein adiponectin acts as a platelet-derived growth factor-BB-binding protein and regulates growth factor-induced common postreceptor signal in vascular smooth muscle cell. Circulation 2002;105:2893–8 [PubMed]
40. Mantzoros C, Petridou E, Dessypris N, et al. Adiponectin and breast cancer risk. J Clin Endocrinol Metab 2004;89:1102–7 [PubMed]
41. Wei EK, Giovannucci E, Fuchs CS, Willett WC, Mantzoros CS. Low plasma adiponectin levels and risk of colorectal cancer in men: a prospective study. J Natl Cancer Inst 2005;97:1688–94 [PubMed]
42. Dal Maso L, Augustin LS, Karalis A, et al. Circulating adiponectin and endometrial cancer risk. J Clin Endocrinol Metab 2004;89:1160–3 [PubMed]
43. Petridou E, Mantzoros C, Dessypris N, et al. Plasma adiponectin concentrations in relation to endometrial cancer: a case-control study in Greece. J Clin Endocrinol Metab 2003;88:993–7 [PubMed]
44. Cust AE, Kaaks R, Friedenreich C, et al. Plasma adiponectin levels and endometrial cancer risk in pre- and postmenopausal women. J Clin Endocrinol Metab 2007;92:255–63 [PubMed]
45. Michalakis K, Williams CJ, Mitsiades N, et al. Serum adiponectin concentrations and tissue expression of adiponectin receptors are reduced in patients with prostate cancer: a case control study. Cancer Epidemiol Biomarkers Prev 2007;16:308–13 [PubMed]
46. Dalamaga M, Nikolaidou A, Karmaniolas K, et al. Circulating adiponectin and leptin in relation to myelodysplastic syndrome: a case-control study. Oncology 2007;73:26–32 [PubMed]
47. Ishikawa M, Kitayama J, Kazama S, Hiramatsu T, Hatano K, Nagawa H. Plasma adiponectin and gastric cancer. Clin Cancer Res 2005;11:1912–17
48. Pinthus JH, Kleinmann N, Tisdale B, et al. Lower plasma adiponectin levels are associated with larger tumor size and metastasis in clear-cell carcinoma of the kidney. Eur Urol 2008;54:866–73 [PubMed]
49. Horiguchi A, Ito K, Sumitomo M, Kimura F, Asano T, Hayakawa M. Decreased serum adiponectin levels in patients with metastatic renal cell carcinoma. Jpn J Clin Oncol 2008;38:106–11 [PubMed]
50. Dalamaga M, Migdalis I, Fargnoli JL, et al. Pancreatic cancer expresses adiponectin receptors and is associated with hypoleptinemia and hyperadiponectinemia: a case-control study. Cancer Causes Control 2009;20:625–33 [PMC free article] [PubMed]
51. Kaklamani VG, Sadim M, Hsi A, et al. Variants of the adiponectin and adiponectin receptor 1 genes and breast cancer risk. Cancer Res 2008;68:3178–84 [PMC free article] [PubMed]
52. Fenton JI, Birmingham JM, Hursting SD, Hord NG. Adiponectin blocks multiple signaling cascades associated with leptin-induced cell proliferation in Apc Min/+ colon epithelial cells. Int J Cancer 2008;122:2437–45 [PubMed]
53. Williams CJ, Mitsiades N, Sozopoulos E, et al. Adiponectin receptor expression is elevated in colorectal carcinomas but not in gastrointestinal stromal tumors. Endocr Relat Cancer 2008;15:289–99 [PubMed]
54. Ma J, Pollak M, Giovannucci E, et al. A prospective study of plasma levels of insulin-like growth factor I (IGF-I) and IGF-binding protein-3, and colorectal cancer risk among men. Growth Horm IGF Res 2000;10(suppl A):S28–9 [PubMed]
55. Fujisawa T, Endo H, Tomimoto A, et al. Adiponectin suppresses colorectal carcinogenesis under the high-fat diet condition. Gut 2008;57:1531–8 [PMC free article] [PubMed]
56. Blackburn GL. From bench to bedside: novel mechanisms and therapeutic advances through the development of selective peroxisome proliferator-activated receptor γ modulators. Am J Clin Nutr 2010;91(suppl):251S–3S [PubMed]
57. Kliewer SA, Mangelsdorf DJ. Fibroblast growth factor 21: from pharmacology to physiology. Am J Clin Nutr 2010;91(suppl):254S–7S [PMC free article] [PubMed]
58. Cheatham WW. Peroxisome proliferator-activated receptor translational research and clinical experience. Am J Clin Nutr 2010;91(suppl):262S–6S [PubMed]
59. Higgins LS, DePaoli AM. Selective peroxisome proliferator-activated receptor γ (PPARγ) modulation as a strategy for safer therapeutic PPARγ activation. Am J Clin Nutr 2010;91(suppl):267S–72S [PubMed]

Articles from The American Journal of Clinical Nutrition are provided here courtesy of American Society for Nutrition
PubReader format: click here to try


Related citations in PubMed

See reviews...See all...

Cited by other articles in PMC

See all...


  • Compound
    PubChem Compound links
  • MedGen
    Related information in MedGen
  • PubMed
    PubMed citations for these articles
  • Substance
    PubChem Substance links

Recent Activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...