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World J Gastroenterol. Jan 28, 2013; 19(4): 457-462 Published online Jan 28, 2013. doi: 10.3748/WJG.v19.i4.457
Obesity and cholangiocarcinoma
Mansour A Parsi
Mansour A Parsi, Center for Endoscopy and Pancreatobiliary Disorders, Digestive Disease Institute, Cleveland Clinic, Cleveland, OH 44195, United States
Author contributions: Parsi MA is the sole contributor to this manuscript.
Correspondence to: Mansour A Parsi, MD, MPH, Center for Endoscopy and Pancreatobiliary Disorders, Digestive Disease Institute, Cleveland Clinic, Cleveland, OH 44195, United States. firstname.lastname@example.org
Telephone: +1-216-4454880 Fax: +1-216-4446284
Received: June 21, 2012 Revised: August 3, 2012 Accepted: August 14, 2012 Published online: January 28, 2013
It is estimated that about half of the population in developed countries are either overweight or obese. In some developing nations obesity rates have increased to surpass those seen in Western countries. This rate increase in obesity has many implications as obesity has been associated with numerous negative health effects including increased risks of hypertension, diabetes, cardiovascular disease, stroke, liver disease, apnea, and some cancer types. Obesity is now considered to be one of the major public health concerns facing the society. Cholangiocarcinomas (bile duct cancers) are malignant tumors arising from cholangiocytes inside or outside of the liver. Although cholangiocarcinomas are relatively rare, they are highly lethal. The low survival rate associated with cholangiocarcinoma is due to the advanced stage of the disease at the time of diagnosis. Prevention is therefore especially important in this cancer type. Some data suggest that the incidence of cholangiocarcinoma in the western world is on the rise. Increasing rate of obesity may be one of the factors responsible for this increase. Determining whether obesity is a risk factor for cholangiocarcinoma has significant clinical and societal implications as obesity is both prevalent and modifiable. This paper seeks to provide a summary of the current knowledge linking obesity and cholangiocarcinoma, and encourage further research on this topic.
Citation: Parsi MA. Obesity and cholangiocarcinoma. World J Gastroenterol 2013; 19(4): 457-462
Obesity is increasing worldwide and affects a large portion of the population in developed[1-5] and some developing nations[6-13]. In many countries obesity and its comorbidities have become a major public health concern[1,14-16]. Recently, obesity-associated cancer has attracted great attention. Epidemiological studies have provided strong evidence that obesity can increase the incidence of many cancer types including colon[18,19], breast[20,21], liver, endometrium[23,24], kidney, esophagus, stomach and pancreas.
Cholangiocarcinomas (bile duct cancers) are malignant tumors arising from cholangiocytes inside or outside of the liver. Traditionally cancers arising from the cholangiocytes inside the liver were grouped together with hepatic cancers and classified as primary liver tumors, while those arising from the cholangiocytes outside the liver were grouped together with cancers of the gallbladder and the ampulla of Vater and classified as biliary cancers. More recently, the term cholangiocarcinoma has been used to refer to cancers arising from cholangiocytes irrespective of their location.
Intrahepatic cholangiocarcinomas originate from cholangiocytes lining the small intrahepatic ductules while extrahepatic cholangiocarcinomas arise from cholangiocytes lining the larger bile ducts (right and left hepatic ducts, common hepatic duct, and common bile duct). The distinction between intrahepatic and extrahepatic cholangiocarcinomas is important, as the incidence and risk factors associated with each may be different[31-33].
In Western countries established risk factors for cholangiocarcinoma are age, sex, primary sclerosing cholangitis, and bile duct cysts. Less-established potential risk factors include cirrhosis, diabetes, obesity, alcohol, and smoking. Some data suggest that the incidence of cholangiocarcinoma in the Western world is on the rise. Increasing rate of obesity may be one of the factors responsible for this increase.
Although cholangiocarcinomas are rare in Western countries, they are highly lethal. Annual mortality associated with cholangiocarcinoma is virtually identical to its incidence throughout the world, underscoring the high case fatality rate of this cancer type. The low survival rate associated with cholangiocarcinoma is due to the advanced stage of the disease at the time of diagnosis. Prevention is therefore especially important in this cancer type. Determining whether obesity is a risk factor for cholangiocarcinoma has significant clinical and societal implications as obesity is both prevalent and modifiable.
Obesity is considered to be among the most alarming health concerns in the United States. It has been estimated that each year, more than 300 000 Americans die from illnesses related to overweight and obesity. The Centers for Disease Control and Prevention (CDC) defines obesity based on the body mass index (BMI). BMI is the ratio of weight in kilograms (kg) to height in meters squared (m2). Per CDC criteria, a BMI of 18.5-25 kg/m2 is normal, 25-30 kg/m2 is overweight and ≥ 30 kg/m2 is obese. The most recent statistics from the National Health and Nutrition Examination Surveys using BMI as a measure of overweight and obesity indicate that 35.7% of adults 20 years or older were obese in 2009-2010. Compared with the statistics for 1976-1980 this reflects a 2-fold increase in the prevalence of adult obesity[40,41]. This rate increase in obesity has many implications as obesity has been associated with numerous negative health effects including increased risks of hypertension, diabetes, cardiovascular disease, stroke, liver disease, apnea, and some cancer types possibly also cholangiocarcinoma. Therefore, as a potentially modifiable risk factor, a reduction in the prevalence of obesity among adults could have a substantial impact on morbidity, mortality, and incidence of various cancers.
The available epidemiologic data on incidence and prevalence of cholangiocarcinoma are difficult to interpret because of differing classifications and diagnostic criteria across studies[29,32,42]. For instance, some studies group intrahepatic cholangiocarcinomas with liver cancers while others group extrahepatic cholangiocarcinomas with gallbladder cancers and cancers of the ampulla of Vater. Furthermore, some studies misclassify types of cholangiocarcinomas. For example, Klatskin tumors (a type of extrahepatic cholangiocarcinoma), at times, have been misclassified as intrahepatic cholangiocarcinoma[29,30]. Finally, some studies use histology as the only diagnostic criterion while others accept other forms of diagnosis such as clinical evaluation or imaging studies.
Despite these shortcomings, the available data suggest a highly variable incidence in different parts of the world, with the highest incidence in Southeast Asia and lowest in Australia[43,44]. The incidence of cholangiocarcinoma has been reported to be as high as 96 cases per 100 000 in men and 38 per 100 000 in women in northeast Thailand. In Australia, the reported incidence is 0.2 per 100 000 among Australian men and 0.1 per 100 000 among Australian women. In other Western countries including the Unites States the incidence is close to 1 case per 100 000 population. In Western countries, approximately 80% of cholangiocarcinomas are extrahepatic. Differing exposure to risk factors is thought to account for the varying geographic incidences, with parasitic infections and hepatolithiasis being more prevalent in Asia[46-48].
Recent data show that the incidence of intrahepatic cholangiocarcinoma is increasing around the world, while the incidence of extrahepatic cholangiocarcinoma has been largely stable or even decreasing[32,43,49]. Although the exact underlying mechanism for this discrepancy is not known, it suggests that intrahepatic and extrahepatic cholangiocarcinomas may be biologically different[32,49,50].
Finally, there is evidence suggesting under-diagnosis of cholangiocarcinoma. For example among patients transplanted for liver cirrhosis of various etiologies, an incidental cholangiocarcinoma was found in approximately 12% of explanted livers. This suggests that the true incidence of cholangiocarcinoma may be higher than previously reported.
Obesity as a risk factor for cholangiocarcinoma
Data assessing the association of obesity and cholangiocarcinoma are limited. So far, four epidemiologic studies have tried to assess the link between obesity and cholangiocarcinoma (Table 1). Three of these studies were specifically designed to identify risk factors for cholangiocarcinoma[52-54].
Table 1 Epidemiologic studies assessing obesity as a potential risk factor for cholangiocarcinoma.
One of those studies using the Surveillance, Epidemiology, and End Results database that links cancer registry data and Medicare enrollment and claims files, reported a significant association between obesity and intrahepatic cholangiocarcinoma, but not between obesity and extrahepatic cholangiocarcinoma. That study however, has several limitations. The study only included patients 65 years of age and older, therefore the findings might not be generalizable to a younger population. Furthermore, because Medicare data are collected for billing rather than research purposes, completeness and accuracy of the Medicare data on prevalence of obesity and cholangiocarcinoma can be questioned. Finally, the possibility of diagnostic bias cannot be excluded because obese people with different medical conditions are more likely to undergo testing and thus have more diagnoses than other people.
Another population-based study conducted in Denmark did not find any significant association between obesity and intrahepatic cholangiocarcinoma. That study used a fairly accurate and complete national registry. Another strength of that study was histological confirmation of cholangiocarcinoma diagnosis in all cases. Extrahepatic cholangiocarcinoma, however, was not studied.
The third study, conducted in the United Kingdom by Grainge et al, found that obese patients (BMI ≥ 30 kg/m2) had 1.5 times the risk of cholangiocarcinoma compared with those with BMI < 25 kg/m2. In that study the type of cholangiocarcinoma (intrahepatic versus extrahepatic) was not specified. Another limitation of that study was that the diagnosis was not based on histology and therefore subject to misclassification.
Aside from studies looking specifically to identify risk factors for cholangiocarcinoma, a South Korean population-based study tried to assess the effect of excess weight on incidence of various cancers including cholangiocarcinoma. The study found that compared to the reference group (BMI 18.5-23 kg/m2), increasing BMI was associated with an increase in the relative risk for development of cholangiocarcinoma. That study, however, did not distinguish between intrahepatic and extrahepatic cholangiocarcinomas, included only males, and the database used was not inclusive of the entire population.
In summary, the epidemiologic data available on obesity as a risk factor for cholangiocarcinoma show conflicting results and are too limited to make any conclusions.
BIOLOGIC MECHANISMS FOR POSITIVE ASSOCIATION BETWEEN OBESITY AND CHOLANGIOCARCINOMA
Obesity is an excess of adipose tissue. Adipose tissue is a biologically active organ which in addition to adipocytes contains multiple other cell types such as pre-adipocytes, endothelial cells, macrophages and other immune cells. Adipose tissue secretes molecules into the bloodstream, which signal to other metabolic organs or to the brain to coordinate responses to altered metabolic demands. Some of these molecules, known as adipokines, have a role in modulating the risk of cancer development. Among adipokines, some of the most studied are leptin, adiponectin and pro-inflammatory molecules.
Leptin is a hormone that is primarily secreted by the adipose tissue. It acts on the hypothalamus to regulate food consumption and caloric homeostasis[58,59]. Although the major physiological site of leptin action is in the central nervous system, leptin receptors are also expressed at lower levels in peripheral tissues. Two studies have shown presence of leptin receptors on cholangiocytes[61,62]. Circulating serum leptin is increased in obesity, and has been suggested as a risk factor for cholangiocarcinoma. A recent study showed that normal and malignant intrahepatic cholangiocytes express leptin and leptin receptors. The investigators of that study also showed that leptin stimulates growth and migration, and prevents apoptosis of intrahepatic cholangiocarcinoma cells in vitro. They also showed that genetic ablation of leptin-mediated signaling inhibits cancer development and growth in an animal model of cholangiocarcinoma.
Adiponectin is another adipokine that may be involved in cancer development. It acts on a number of tissues to regulate glucose and lipid metabolism. Adiponectin levels are reduced in obesity. Several basic and epidemiological studies have suggested that adiponectin has antitumor effects[63,64]. Although the link between adiponectin and cholangiocarcinoma has not been studied, there is convincing evidence for an inverse association between adiponectin levels and cancer risk for several cancer types[59,63,65-67].
Several pro-inflammatory cytokines are secreted by monocytes and other immune cells that infiltrate adipose tissues in obesity[68,69]. Among these cytokines, interleukin-6 (IL-6) and tumor necrosis factor-α (TNF-α) have been found to have a role in development of cholangiocarcinoma. A growing body of evidence suggests that the inflammatory environment in the obese state is linked to the development of cancer through various mechanisms. IL-6 seems to have an important role in the pathogenesis and growth of cholangiocarcinoma and has been shown to act by both an autocrine and paracrine manner stimulating several intracellular pathways involved in survival and growth of malignant cholangiocytes[36,72-74]. TNF-α is a mediator of inflammation with actions directed towards both tissue destruction and recovery. Evidence suggests that TNF-α may act as an endogenous tumor promoter in addition to its role in immune responses[75,76]. Overexpression of TNF-α receptor genes has been observed in cholangiocarcinoma associated with hepatolithiasis[75-78].
Although not specifically linked to cholangiocarcinoma, there are multiple other substances that have directly or indirectly been linked to cancer in general. Research on the role of different substances on development and progression of different cancers including cholangiocarcinoma is evolving.
It is estimated that about half of the population in developed countries are either overweight or obese. In some regions of the world overweight and obesity affects more than two-thirds of the population. By 2008, an estimated 1.5 billion adults globally were overweight and 500 million adults were obese. Because of such high prevalence, establishing a clear link between excess body weight and cholangiocarcinoma can have significant effect on prevention of cholangiocarcinoma. Establishing a link may also encourage further research on identification of underlying pathophysiologic mechanisms that can potentially lead to discovery of better treatment options.
Research on obesity and cholangiocarcinoma risk should be encouraged through a variety of activities, including large cooperative initiatives, database resources, epidemiologic studies, basic science studies, and increase in funding resources.
If a link between excess weight and cholangiocarcinoma is established, multiple new questions will emerge that will need to be answered. Does reversal of obesity affect the risk for cholangiocarcinoma? Are there any differences between different modes of weight reduction (calorie restriction, exercise, drugs, bariatric surgery) in terms of cholangiocarcinoma risk reduction? Can the link between obesity and cholangiocarcinoma be somehow disrupted in the absence of weight loss (which for many individuals is a difficult task)?
Answers to these and other questions that will surely follow require well-designed studies that incorporate molecular, genetic, metabolic and nutritional factors.
P- Reviewers Hanazaki K, Quiros RM S- Editor Gou SX L- Editor A E- Editor Xiong L
Nguyen DM, El-Serag HB. The epidemiology of obesity.Gastroenterol Clin North Am. 2010;39:1-7.
Centers for Disease Control and Prevention (CDC). Vital signs: state-specific obesity prevalence among adults --- United States, 2009.MMWR Morb Mortal Wkly Rep. 2010;59:951-955.
von Ruesten A, Steffen A, Floegel A, van der A DL, Masala G, Tjønneland A, Halkjaer J, Palli D, Wareham NJ, Loos RJ. Trend in obesity prevalence in European adult cohort populations during follow-up since 1996 and their predictions to 2015.PLoS One. 2011;6:e27455.
Daigre JL, Atallah A, Boissin JL, Jean-Baptiste G, Kangambega P, Chevalier H, Balkau B, Smadja D, Inamo J. The prevalence of overweight and obesity, and distribution of waist circumference, in adults and children in the French Overseas Territories: the PODIUM survey.Diabetes Metab. 2012;38:404-411.
Sundborn G, Metcalf PA, Gentles D, Scragg R, Dyall L, Black P, Jackson R. Overweight and obesity prevalence among adult Pacific peoples and Europeans in the Diabetes Heart and Health Study (DHAHS) 2002-2003, Auckland New Zealand.N Z Med J. 2010;123:30-42.
Ayatollahi SM, Ghoreshizadeh Z. Prevalence of obesity and overweight among adults in Iran.Obes Rev. 2010;11:335-337.
Gigante DP, Moura EC, Sardinha LM. Prevalence of overweight and obesity and associated factors, Brazil, 2006.Rev Saude Publica. 2009;43 Suppl 2:83-89.
Gültekin T, Ozer BK, Akin G, Bektaş Y, Sağir M, Güleç E. Prevalence of overweight and obesity in Turkish adults.Anthropol Anz. 2009;67:205-212.
Gupta N, Goel K, Shah P, Misra A. Childhood obesity in developing countries: epidemiology, determinants, and prevention.Endocr Rev. 2012;33:48-70.
Koukoulis GN, Sakka C, Katsaros F, Goutou M, Tsirona S, Tsiapali E, Piterou A, Stefanidis I, Stathakis N. High rates of obesity prevalence in adults living in central Greece: data from the ARGOS study.Hormones (Athens). 2010;9:253-262.
Mohamud WN, Musa KI, Khir AS, Ismail AA, Ismail IS, Kadir KA, Kamaruddin NA, Yaacob NA, Mustafa N, Ali O. Prevalence of overweight and obesity among adult Malaysians: an update.Asia Pac J Clin Nutr. 2011;20:35-41.
Xi B, Liang Y, He T, Reilly KH, Hu Y, Wang Q, Yan Y, Mi J. Secular trends in the prevalence of general and abdominal obesity among Chinese adults, 1993-2009.Obes Rev. 2012;13:287-296.
Gill T. Epidemiology and health impact of obesity: an Asia Pacific perspective.Asia Pac J Clin Nutr. 2006;15 Suppl:3-14.
Orsi CM, Hale DE, Lynch JL. Pediatric obesity epidemiology.Curr Opin Endocrinol Diabetes Obes. 2011;18:14-22.
Selassie M, Sinha AC. The epidemiology and aetiology of obesity: a global challenge.Best Pract Res Clin Anaesthesiol. 2011;25:1-9.
Renehan AG, Tyson M, Egger M, Heller RF, Zwahlen M. Body-mass index and incidence of cancer: a systematic review and meta-analysis of prospective observational studies.Lancet. 2008;371:569-578.
Frezza EE, Wachtel MS, Chiriva-Internati M. Influence of obesity on the risk of developing colon cancer.Gut. 2006;55:285-291.
Larsson SC, Wolk A. Obesity and colon and rectal cancer risk: a meta-analysis of prospective studies.Am J Clin Nutr. 2007;86:556-565.
Ligibel J. Obesity and breast cancer.Oncology (Williston Park). 2011;25:994-1000.
Yang XR, Chang-Claude J, Goode EL, Couch FJ, Nevanlinna H, Milne RL, Gaudet M, Schmidt MK, Broeks A, Cox A. Associations of breast cancer risk factors with tumor subtypes: a pooled analysis from the Breast Cancer Association Consortium studies.J Natl Cancer Inst. 2011;103:250-263.
Larsson SC, Wolk A. Overweight, obesity and risk of liver cancer: a meta-analysis of cohort studies.Br J Cancer. 2007;97:1005-1008.
Kaaks R, Lukanova A, Kurzer MS. Obesity, endogenous hormones, and endometrial cancer risk: a synthetic review.Cancer Epidemiol Biomarkers Prev. 2002;11:1531-1543.
Lane G. Obesity and gynaecological cancer.Menopause Int. 2008;14:33-37.
Mathew A, George PS, Ildaphonse G. Obesity and kidney cancer risk in women: a meta-analysis (1992-2008).Asian Pac J Cancer Prev. 2009;10:471-478.
Murray L, Romero Y. Role of obesity in Barrett’s esophagus and cancer.Surg Oncol Clin N Am. 2009;18:439-452.
Yang P, Zhou Y, Chen B, Wan HW, Jia GQ, Bai HL, Wu XT. Overweight, obesity and gastric cancer risk: results from a meta-analysis of cohort studies.Eur J Cancer. 2009;45:2867-2873.
Zyromski NJ, White PB. Pancreatic cancer in obesity: epidemiology, clinical observations, and basic mechanisms.Anticancer Agents Med Chem. 2011;11:470-478.
Hammill CW, Wong LL. Intrahepatic cholangiocarcinoma: a malignancy of increasing importance.J Am Coll Surg. 2008;207:594-603.
Welzel TM, McGlynn KA, Hsing AW, O’Brien TR, Pfeiffer RM. Impact of classification of hilar cholangiocarcinomas (Klatskin tumors) on the incidence of intra- and extrahepatic cholangiocarcinoma in the United States.J Natl Cancer Inst. 2006;98:873-875.
Gatto M, Bragazzi MC, Semeraro R, Napoli C, Gentile R, Torrice A, Gaudio E, Alvaro D. Cholangiocarcinoma: update and future perspectives.Dig Liver Dis. 2010;42:253-260.
Cardinale V, Semeraro R, Torrice A, Gatto M, Napoli C, Bragazzi MC, Gentile R, Alvaro D. Intra-hepatic and extra-hepatic cholangiocarcinoma: New insight into epidemiology and risk factors.World J Gastrointest Oncol. 2010;2:407-416.
Patel T. Cholangiocarcinoma.Nat Clin Pract Gastroenterol Hepatol. 2006;3:33-42.
Mihalache F, Tantau M, Diaconu B, Acalovschi M. Survival and quality of life of cholangiocarcinoma patients: a prospective study over a 4 year period.J Gastrointestin Liver Dis. 2010;19:285-290.
Khan SA, Toledano MB, Taylor-Robinson SD. Epidemiology, risk factors, and pathogenesis of cholangiocarcinoma.HPB (Oxford). 2008;10:77-82.
Fava G, Lorenzini I. Molecular pathogenesis of cholangiocarcinoma.Int J Hepatol. 2012;2012:630543.
Shaib Y, El-Serag HB. The epidemiology of cholangiocarcinoma.Semin Liver Dis. 2004;24:115-125.
Sripa B, Pairojkul C. Cholangiocarcinoma: lessons from Thailand.Curr Opin Gastroenterol. 2008;24:349-356.
Khan SA, Emadossadaty S, Ladep NG, Thomas HC, Elliott P, Taylor-Robinson SD, Toledano MB. Rising trends in cholangiocarcinoma: is the ICD classification system misleading us?J Hepatol. 2012;56:848-854.
Sripa B, Bethony JM, Sithithaworn P, Kaewkes S, Mairiang E, Loukas A, Mulvenna J, Laha T, Hotez PJ, Brindley PJ. Opisthorchiasis and Opisthorchis-associated cholangiocarcinoma in Thailand and Laos.Acta Trop. 2011;120 Suppl 1:S158-S168.
Mulvenna J, Yonglitthipagon P, Sripa B, Brindley PJ, Loukas A, Bethony JM. Banking on the future: biobanking for “omics” approaches to biomarker discovery for Opisthorchis-induced cholangiocarcinoma in Thailand.Parasitol Int. 2012;61:173-177.
Shin HR, Oh JK, Masuyer E, Curado MP, Bouvard V, Fang YY, Wiangnon S, Sripa B, Hong ST. Epidemiology of cholangiocarcinoma: an update focusing on risk factors.Cancer Sci. 2010;101:579-585.
Patel T. Increasing incidence and mortality of primary intrahepatic cholangiocarcinoma in the United States.Hepatology. 2001;33:1353-1357.
Colmenero J, Castro-Narro G, Fleck A, Miquel R, Garcia-Valdecasas J, Navasa M. Unexpected etiologies of cryptogenic liver disease and incidental tumors in adult liver transplantation: a clinical-pathological study in 815 patients.Hepatology. 2009;50 Suppl 4:S580.
Welzel TM, Graubard BI, El-Serag HB, Shaib YH, Hsing AW, Davila JA, McGlynn KA. Risk factors for intrahepatic and extrahepatic cholangiocarcinoma in the United States: a population-based case-control study.Clin Gastroenterol Hepatol. 2007;5:1221-1228.
Welzel TM, Mellemkjaer L, Gloria G, Sakoda LC, Hsing AW, El Ghormli L, Olsen JH, McGlynn KA. Risk factors for intrahepatic cholangiocarcinoma in a low-risk population: a nationwide case-control study.Int J Cancer. 2007;120:638-641.
Grainge MJ, West J, Solaymani-Dodaran M, Aithal GP, Card TR. The antecedents of biliary cancer: a primary care case-control study in the United Kingdom.Br J Cancer. 2009;100:178-180.
Oh SW, Yoon YS, Shin SA. Effects of excess weight on cancer incidences depending on cancer sites and histologic findings among men: Korea National Health Insurance Corporation Study.J Clin Oncol. 2005;23:4742-4754.
van Kruijsdijk RC, van der Wall E, Visseren FL. Obesity and cancer: the role of dysfunctional adipose tissue.Cancer Epidemiol Biomarkers Prev. 2009;18:2569-2578.
Khandekar MJ, Cohen P, Spiegelman BM. Molecular mechanisms of cancer development in obesity.Nat Rev Cancer. 2011;11:886-895.
Mantzoros CS, Magkos F, Brinkoetter M, Sienkiewicz E, Dardeno TA, Kim SY, Hamnvik OP, Koniaris A. Leptin in human physiology and pathophysiology.Am J Physiol Endocrinol Metab. 2011;301:E567-E584.
Nock NL, Berger NA. Obesity and Cancer: Overview of Mechanisms.Cancer and Energy Balance, Epidemiology and Overview (Energy Balance and Cancer). New York: Springer; 2010;129-179.
Cohen P, Zhao C, Cai X, Montez JM, Rohani SC, Feinstein P, Mombaerts P, Friedman JM. Selective deletion of leptin receptor in neurons leads to obesity.J Clin Invest. 2001;108:1113-1121.
Sayed-Ahmed A, Rudas P, Bartha T. Partial cloning and localisation of leptin and its receptor in the one-humped camel (Camelus dromedarius).Vet J. 2005;170:264-267.
Fava G, Alpini G, Rychlicki C, Saccomanno S, DeMorrow S, Trozzi L, Candelaresi C, Venter J, Di Sario A, Marzioni M. Leptin enhances cholangiocarcinoma cell growth.Cancer Res. 2008;68:6752-6761.
Barb D, Pazaitou-Panayiotou K, Mantzoros CS. Adiponectin: a link between obesity and cancer.Expert Opin Investig Drugs. 2006;15:917-931.
Grossmann ME, Ray A, Nkhata KJ, Malakhov DA, Rogozina OP, Dogan S, Cleary MP. Obesity and breast cancer: status of leptin and adiponectin in pathological processes.Cancer Metastasis Rev. 2010;29:641-653.
An W, Bai Y, Deng SX, Gao J, Ben QW, Cai QC, Zhang HG, Li ZS. Adiponectin levels in patients with colorectal cancer and adenoma: a meta-analysis.Eur J Cancer Prev. 2012;21:126-133.
Chen X, Wang Y. Adiponectin and breast cancer.Med Oncol. 2011;28:1288-1295.
Tian YF, Chu CH, Wu MH, Chang CL, Yang T, Chou YC, Hsu GC, Yu CP, Yu JC, Sun CA. Anthropometric measures, plasma adiponectin, and breast cancer risk.Endocr Relat Cancer. 2007;14:669-677.
Weisberg SP, McCann D, Desai M, Rosenbaum M, Leibel RL, Ferrante AW. Obesity is associated with macrophage accumulation in adipose tissue.J Clin Invest. 2003;112:1796-1808.
Ruan H, Zarnowski MJ, Cushman SW, Lodish HF. Standard isolation of primary adipose cells from mouse epididymal fat pads induces inflammatory mediators and down-regulates adipocyte genes.J Biol Chem. 2003;278:47585-47593.
Braicu C, Burz C, Berindan-Neagoe I, Balacescu O, Tantau M, Cristea V, Irimie A. Molecular markers in the pathogenesis of cholangiocarcinoma: Potential for early detection and selection of appropriate treatment.GR. 2009;2:132-140.
Grivennikov SI, Greten FR, Karin M. Immunity, inflammation, and cancer.Cell. 2010;140:883-899.
Meng F, Yamagiwa Y, Ueno Y, Patel T. Over-expression of interleukin-6 enhances cell survival and transformed cell growth in human malignant cholangiocytes.J Hepatol. 2006;44:1055-1065.
Akiyama T, Hasegawa T, Sejima T, Sahara H, Seto K, Saito H, Takashima S. Serum and bile interleukin 6 after percutaneous transhepatic cholangio-drainage.Hepatogastroenterology. 1998;45:665-671.
Okada K, Shimizu Y, Nambu S, Higuchi K, Watanabe A. Interleukin-6 functions as an autocrine growth factor in a cholangiocarcinoma cell line.J Gastroenterol Hepatol. 1994;9:462-467.
Ohira S, Sasaki M, Harada K, Sato Y, Zen Y, Isse K, Kozaka K, Ishikawa A, Oda K, Nimura Y. Possible regulation of migration of intrahepatic cholangiocarcinoma cells by interaction of CXCR4 expressed in carcinoma cells with tumor necrosis factor-alpha and stromal-derived factor-1 released in stroma.Am J Pathol. 2006;168:1155-1168.
Tanimura Y, Kokuryo T, Tsunoda N, Yamazaki Y, Oda K, Nimura Y, Naing Mon N, Huang P, Nakanuma Y, Chen MF. Tumor necrosis factor alpha promotes invasiveness of cholangiocarcinoma cells via its receptor, TNFR2.Cancer Lett. 2005;219:205-213.
Blechacz B, Gores GJ. Cholangiocarcinoma: advances in pathogenesis, diagnosis, and treatment.Hepatology. 2008;48:308-321.
Sirica AE. Cholangiocarcinoma: molecular targeting strategies for chemoprevention and therapy.Hepatology. 2005;41:5-15.
Larsson SC, Wolk A. Excess body fatness: an important cause of most cancers.Lancet. 2008;371:536-537.
Swinburn BA, Sacks G, Hall KD, McPherson K, Finegood DT, Moodie ML, Gortmaker SL. The global obesity pandemic: shaped by global drivers and local environments.Lancet. 2011;378:804-814.
Finucane MM, Stevens GA, Cowan MJ, Danaei G, Lin JK, Paciorek CJ, Singh GM, Gutierrez HR, Lu Y, Bahalim AN. National, regional, and global trends in body-mass index since 1980: systematic analysis of health examination surveys and epidemiological studies with 960 country-years and 9·1 million participants.Lancet. 2011;377:557-567.