Abstract
Purpose
Increasing evidence suggests that many adipokines are involved in cancer-related anorexia and cachexia syndrome (CACS), although the underlying mechanism remains to be clarify. Asprosin is a new peptide hormone mainly secreted by white adipose tissues that can increase appetite and body weight. In this cross-sectional study, we tested whether asprosin may intervene in the development of CACS.
Methods
The fasting plasma asprosin levels were determined via enzyme-linked immune-sorbent assay. Anorexia was determined using the anorexia/cachexia subscale (A/CS) of the functional assessment of anorexia/cachexia therapy (FAACT) questionnaire. The body composition was assessed using bioelectrical impedance analysis. The association of plasma asprosin with anorexia, cachexia, and nutritional status was analyzed.
Results
One hundred twenty treatment-naïve patients with pathological confirmed gastrointestinal or lung cancer and 14 mild gastritis patients were recruited. We found no significant difference in asprosin levels between subgroups of patients by age, sex, cancer types or stage. Correlation analysis suggested that asprosin levels were positively associated with body fat mass (r = 0.248, p = 0.043). No correlations were found between asprosin levels and hemoglobin, white blood cell count, blood platelet count, albumin, C-reactive protein, glucose, cholesterol, triglyceride, high density lipoprotein, low density lipoprotein, body mass index, body fat percentage, protein, skeletal muscle, muscle mass, lean body mass, and basal metabolic rate. Furthermore, asprosin levels were not significantly different between patients with or without cachexia. However, patients with anorexia had significantly lower asprosin levels compared with patients without anorexia. No significant difference in asprosin levels between gastritis and gastric cancer patients. Similarly, no significant change of asprosin levels occurred postoperatively in 10 gastric cancer patients.
Conclusions
Patients with anorexia had significantly lower asprosin levels compared with patients without anorexia. We therefore speculated that asprosin might intervene in the development of cancer anorexia and serve as a potential therapeutic target.
Similar content being viewed by others
Abbreviations
- BMI:
-
Body mass index
- CACS:
-
Cancer-related anorexia and cachexia syndrome
- ELISA:
-
Enzyme-linked immune-sorbent assay
- FAACT:
-
Functional assessment of anorexia/cachexia therapy
- NSCLC:
-
Non-small cell lung cancer
- PIF:
-
Proteolysis-inducing factor
- TNF-α:
-
Tumor necrosis factor alpha
References
Acara AC, Bolatkale M, Kiziloglu I, Ibisoglu E, Can C (2018) A novel biochemical marker for predicting the severity of ACS with unstable angina pectoris: asprosin. Am J Emerg Med 36:1504–1505
Alan M, Gurlek B, Yilmaz A, Aksit M, Aslanipour B, Gulhan I, Mehmet C, Taner CE (2019) Asprosin: a novel peptide hormone related to insulin resistance in women with polycystic ovary syndrome. Gynecol Endocrinol Off J Int Soc Gynecol Endocrinol 35:220–223
Alkahtani SA (2017) A cross-sectional study on sarcopenia using different methods: reference values for healthy Saudi young men. BMC Musculoskelet Disord 18:119
Argiles JM, Stemmler B, Lopez-Soriano FJ, Busquets S (2018) Inter-tissue communication in cancer cachexia. Nat Rev Endocrinol 15:9–20
Batista ML Jr, Olivan M, Alcantara PS, Sandoval R, Peres SB, Neves RX, Silverio R, Maximiano LF, Otoch JP, Seelaender M (2013) Adipose tissue-derived factors as potential biomarkers in cachectic cancer patients. Cytokine 61:532–539
Blauwhoff-Buskermolen S, Ruijgrok C, Ostelo RW, de Vet HCW, Verheul HMW, de van der Schueren MAE, Langius JAE (2016) The assessment of anorexia in patients with cancer: cut-off values for the FAACT-A/CS and the VAS for appetite. Suppor Care Cancer Off J Multinatl Assoc Support Care Cancer 24:661–666
Boura P, Loukides S, Grapsa D, Achimastos A, Syrigos K (2015) The diverse roles of adiponectin in non-small-cell lung cancer: current data and future perspectives. Future Oncol 11:2193–2203
Ceylan HI, Saygin O (2020) An investigation of the relationship between new fasting hormone asprosin, obesity and acute-chronic exercise: current systematic review. Arch Physiol Biochem:1–12
Del Fabbro E (2015) Current and future care of patients with the cancer anorexia-cachexia syndrome American Society of Clinical Oncology educational book American Society of Clinical Oncology Annual Meeting: e229–237
Diakowska D, Markocka-Maczka K, Szelachowski P, Grabowski K (2014) Serum levels of resistin, adiponectin, and apelin in gastroesophageal cancer patients. Dis Markers 2014:619649
Duerrschmid C, He Y, Wang C, Li C, Bournat JC, Romere C, Saha PK, Lee ME, Phillips KJ, Jain M, Jia P, Zhao Z, Farias M, Wu Q, Milewicz DM, Sutton VR, Moore DD, Butte NF, Krashes MJ, Xu Y, Chopra AR (2017) Asprosin is a centrally acting orexigenic hormone. Nat Med 23:1444–1453
Engineer DR, Garcia JM (2012) Leptin in anorexia and cachexia syndrome. Int J Pept 2012:287457
Ezeoke CC, Morley JE (2015) Pathophysiology of anorexia in the cancer cachexia syndrome. J Cachexia Sarcopenia Muscle 6:287–302
Fearon K, Strasser F, Anker SD, Bosaeus I, Bruera E, Fainsinger RL, Jatoi A, Loprinzi C, MacDonald N, Mantovani G, Davis M, Muscaritoli M, Ottery F, Radbruch L, Ravasco P, Walsh D, Wilcock A, Kaasa S, Baracos VE (2011) Definition and classification of cancer cachexia: an international consensus. Lancet Oncol 12:489–495
Ghasemi A, Saeidi J, Azimi-Nejad M, Hashemy SI (2019) Leptin-induced signaling pathways in cancer cell migration and invasion. Cell Oncol 42:243–260
Greenhill C (2016) Liver: asprosin—new hormone involved in hepatic glucose release. Nat Rev Endocrinol 12:312
Hoffmann JG, Xie W, Chopra AR (2020) Energy regulation mechanism and therapeutic potential of asprosin. Diabetes 69:559–566
Khatib MN, Shankar AH, Kirubakaran R, Gaidhane A, Gaidhane S, Simkhada P, Quazi Syed Z (2018) Ghrelin for the management of cachexia associated with cancer. Cochrane Database Syst Rev 2:CD012229
Kocaman N, Artas G (2019) Can novel adipokines, asprosin and meteorin-like, be biomarkers for malignant mesothelioma? Biotech Histochem Off Publ Biol Stain Comm:1–5
Malik JS, Yennurajalingam S (2019) Prokinetics and ghrelin for the management of cancer cachexia syndrome. Ann Palliat Med 8:80–85
Mirza KA, Tisdale MJ (2014) Functional identity of receptors for proteolysis-inducing factor on human and murine skeletal muscle. Br J Cancer 111:903–908
Muthu ML, Reinhardt DP (2020) Fibrillin-1 and fibrillin-1-derived asprosin in adipose tissue function and metabolic disorders. J Cell Commun Signal 14:159–173
Ntikoudi E, Kiagia M, Boura P, Syrigos KN (2014) Hormones of adipose tissue and their biologic role in lung cancer. Cancer Treat Rev 40:22–30
Ohnuma T, Paluri R, Adigun R (2019) Cancer, anorexia and cachexia. StatPearls, Treasure Island
Ribaudo JM, Cella D, Hahn EA, Lloyd SR, Tchekmedyian NS, Von Roenn J, Leslie WT (2000) Re-validation and shortening of the Functional Assessment of Anorexia/Cachexia Therapy (FAACT) questionnaire. Qual Life Res Int J Qual Life Asp Treat Care Rehab 9:1137–1146
Romere C, Duerrschmid C, Bournat J, Constable P, Jain M, Xia F, Saha PK, Del Solar M, Zhu B, York B, Sarkar P, Rendon DA, Gaber MW, LeMaire SA, Coselli JS, Milewicz DM, Sutton VR, Butte NF, Moore DD, Chopra AR (2016) Asprosin, a fasting-induced glucogenic protein hormone. Cell 165:566–579
Tarricone R, Ricca G, Nyanzi-Wakholi B, Medina-Lara A (2016) Impact of cancer anorexia-cachexia syndrome on health-related quality of life and resource utilisation: A systematic review. Crit Rev Oncol Hematol 99:49–62
Thissen JP, Loumaye A (2013) Role of activin A and myostatin in cancer cachexia. Ann Endocrinol 74:79–81
Ugur K, Aydin S (2019) Saliva and blood asprosin hormone concentration associated with obesity. Int J Endocrinol 2019:2521096
Wang CY, Lin TA, Liu KH, Liao CH, Liu YY, Wu VC, Wen MS, Yeh TS (2019) Serum asprosin levels and bariatric surgery outcomes in obese adults. Int J Obes 43:1019–1025
Wang Y, Qu H, Xiong X, Qiu Y, Liao Y, Chen Y, Zheng Y, Zheng H (2018) Plasma asprosin concentrations are increased in individuals with glucose dysregulation and correlated with insulin resistance and first-phase insulin secretion. Mediat Inflamm 2018:9471583
White JP (2017) IL-6, cancer and cachexia: metabolic dysfunction creates the perfect storm. Transl Cancer Res 6:S280–S285
Wiecek M, Szymura J, Maciejczyk M, Kantorowicz M, Szygula Z (2018) Acute anaerobic exercise affects the secretion of asprosin, irisin, and other cytokines—a comparison between sexes. Front Physiol 9:1782
Zhang L, Chen C, Zhou N, Fu Y, Cheng X (2019) Circulating asprosin concentrations are increased in type 2 diabetes mellitus and independently associated with fasting glucose and triglyceride. Clin Chim Acta Int J Clin Chem 489:183–188
Zhang X, Jiang H, Ma X, Wu H (2019) Increased serum level and impaired response to glucose fluctuation of asprosin is associated with type 2 diabetes mellitus. J Diabetes Investig
Funding
This work was supported by National Science Foundation of China (No. 81702423) and Chinese Postdoctoral Science Foundation (No. 2017 M623442).
Author information
Authors and Affiliations
Corresponding authors
Ethics declarations
Conflict of interest
The authors declare that they have no conflict of interest.
Ethical approval
This study was performed in line with the principles of the Declaration of Helsinki. Approval was granted by the Ethics Committee of General Hospital of Northern Theater Command.
Informed consent
Written informed consent was obtained from each participant.
Additional information
Publisher’s note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
About this article
Cite this article
Du, C., Wang, C., Guan, X. et al. Asprosin is associated with anorexia and body fat mass in cancer patients. Support Care Cancer 29, 1369–1375 (2021). https://doi.org/10.1007/s00520-020-05621-8
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00520-020-05621-8