SKELETAL MUSCLE SENSITIVITY TO WASTING INDUCED BY UROTHELIAL CARCINOMA

Authors

  • M. Esteves Laboratory of Biochemistry and Experimental Morphology, CIAFEL, Porto 4200-450, Portugal
  • M. Duarte Fernando Pessoa University, Porto, Portugal
  • P.A. Oliveira CITAB, University of Trás-os-Montes and Alto Douro (UTAD), Vila Real, Portugal
  • R.M. Gil da Costa CITAB, University of Trás-os-Montes and Alto Douro (UTAD), Vila Real, Portugal
  • M.P. Monteiro Clinical and Experimental Endocrinology, Unit for Multidisciplinary Research in Biomedicine, Instituto de Ciências Biomédicas Abel Salazar, University of Porto, Porto, Portugal
  • J.A. Duarte Laboratory of Biochemistry and Experimental Morphology, CIAFEL, Porto 4200-450, Portugal

DOI:

https://doi.org/10.15407/exp-oncology.2023.01.107

Keywords:

collagen deposition, cross-sectional area, histology, myonuclear domain, сancer

Abstract

Background: Skeletal muscle wasting is a common phenotypic feature of several types of cancer, and it is associated with functional impairment, respiratory complications, and fatigue. However, equivocal evidence remains regarding the impact of cancer-induced muscle wasting on the different fiber types. Aim: The aim of this study was to investigate the impact of urothelial carcinoma induced in mice on the histomorphometric features and collagen deposition in different skeletal muscles.Materials and Methods: Thirteen ICR (CD1) male mice were randomly assigned into two groups: exposed to 0.05% N-butyl-N-(4-hydroxybutyl) nitrosamine (BBN) in drinking water for 12 weeks, plus 8 weeks of tap water (BBN, n = 8) or with access to tap water for 20 weeks (CONT, n = 5). Tibialis anterior, soleus, and diaphragm muscles were collected from all animals. For cross-sectional area and myonuclear domain analysis, muscle sections were stained with hematoxylin and eosin, and for collagen deposition assessment, muscle sections were stained with picrosirius red. Results: All animals from the BBN group developed urothelial preneoplastic and neoplastic lesions, and the tibialis anterior from these animals presented a reduced cross-sectional area (p < 0.001), with a decreased proportion of fibers with a higher cross-sectional area, increased collagen deposition (p = 0.017), and higher myonuclear domain (p = 0.031). BBN mice also showed a higher myonuclear domain in the diaphragm (p = 0.015). Conclusion: Urothelial carcinoma induced muscle wasting of the tibialis anterior, expressed by a decreased cross-sectional area, higher infiltration of fibrotic tissue, and increased myonuclear domain, which also increased in the diaphragm, suggesting that fast glycolytic muscle fibers are more susceptible to be affected by cancer development.

References

Bray F, Ferlay J, Soerjomataram I, et al. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin 2018; 68: 394–424. doi: 10.3322/caac.21492

Arnold M, Rutherford MJ, Bardot A, et al. Progress in cancer survival, mortality, and incidence in seven high-income countries 1995-2014 (ICBP SURVMARK-2): a population-based study. Lancet Oncol 2019; 20: 1493–1505. doi: 10.1016/S1470-2045(19)30456-5

Fearon KC. Cancer cachexia: developing multimodal therapy for a multidimensional problem. Eur J Cancer 2008; 44: 1124–1132. doi: 10.1016/j.ejca.2008.02.033

Argiles JM, Busquets S, Stemmler B, et al. Cancer cachexia: understanding the molecular basis. Nat Rev Cancer 2014; 14: 754–762. doi: 10.1038/nrc3829

Eley HL, Tisdale MJ. Skeletal muscle atrophy, a link between depression of protein synthesis and increase in degradation. J Biol Chem 2007; 282: 7087–7097. doi: 10.1074/jbc.M610378200

Toledo M, Busquets S, Sirisi S, et al. Cancer cachexia: physical activity and muscle force in tumour-bearing rats. Oncol Rep 2011; 25: 189–193

Bower JE. Cancer-related fatigue–mechanisms, risk factors, and treatments. Nat Rev Clin Oncol 2014; 11: 597–609. doi:10.1038/nrclinonc.2014.127

Biolo G, Cederholm T, Muscaritoli M. Muscle contractile and metabolic dysfunction is a common feature of sarcopenia of aging and chronic diseases: from sarcopenic obesity to cachexia. Clin Nutr 2014; 33: 737–748. doi:10.1016/j.clnu.2014.03.007

Hardee JP, Montalvo RN, Carson JA. Linking cancer cachexia-induced anabolic resistance to skeletal muscle oxidative metabolism. Oxid Med Cell Longev 2017; 2017: 8018197. doi: 10.1155/2017/8018197

Li YP, Chen Y, Li AS, et al. Hydrogen peroxide stimulates ubiquitin-conjugating activity and expression of genes for specific E2 and E3 proteins in skeletal muscle myotubes. Am J Physiol Cell Physiol 2003; 285: C806–C812. doi: 10.1152/ajpcell.00129.2003

Ott M, Gogvadze V, Orrenius S, et al. Mitochondria, oxidative stress and cell death. Apoptosis 2007; 12: 913–922. doi: 10.1007/s10495-007-0756-2

Yu Z, Li P, Zhang M, et al. Fiber type-specific nitric oxide protects oxidative myofibers against cachectic stimuli. PLoS One 2008; 3: e2086. doi:10.1371/journal.pone.0002086

Johns N, Hatakeyama S, Stephens NA, et al. Clinical classification of cancer cachexia: phenotypic correlates in human skeletal muscle. PLoS One 2014; 9: e83618. doi: 10.1371/journal.pone.0083618

Julienne CM, Dumas JF, Goupille C, et al. Cancer cachexia is associated with a decrease in skeletal muscle mitochondrial oxidative capacities without alteration of ATP production efficiency. J Cachexia Sarcopenia Muscle 2012; 3: 265–275. doi: 10.1007/s13539-012-0071-9

Acharyya S, Ladner KJ, Nelsen LL, et al. Cancer cachexia is regulated by selective targeting of skeletal muscle gene products. J Clin Invest 2004; 114: 370–378. doi: 10.1172/JCI20174

Hiroux C, Dalle S, Koppo K, et al. Voluntary exercise does not improve muscular properties or functional capacity during C26-induced cancer cachexia in mice. J Muscle Res Cell Motil 2021; 42: 169–181. doi: 10.1007/s10974-021-09599-6

Aulino P, Berardi E, Cardillo VM, et al. Molecular, cellular and physiological characterization of the cancer cachexia-inducing C26 colon carcinoma in mouse. BMC Cancer 2010; 10: 363. doi: 10.1186/1471-2407-10-363

Monitto CL, Berkowitz D, Lee KM, et al. Differential gene expression in a murine model of cancer cachexia. Am J Physiol Endocrinol Metab 2001; 281: E289–E297. doi:10.1152/ajpendo.2001.281.2.E289

Marin-Corral J, Fontes CC, Pascual-Guardia S, et al. Redox balance and carbonylated proteins in limb and heart muscles of cachectic rats. Antioxid Redox Signal 2010; 12: 365–380. doi: 10.1089/ars.2009.2818

Fearon KC, Glass DJ, Guttridge DC. Cancer cachexia: mediators, signaling, and metabolic pathways. Cell Metab 2012; 16: 153–166. doi: 10.1016/j.cmet.2012.06.011

Li P, Waters RE, Redfern SI, et al. Oxidative phenotype protects myofibers from pathological insults induced by chronic heart failure in mice. Am J Pathol 2007; 170: 599–608. doi: 10.2353/ajpath.2007.060505

Talmadge RJ, Roy RR. Electrophoretic separation of rat skeletal muscle myosin heavy-chain isoforms. J Appl Physiol (1985) 1993; 75: 2337–2340

Caiozzo VJ, Baker MJ, Baldwin KM. Novel transitions in MHC isoforms: separate and combined effects of thyroid hormone and mechanical unloading. J Appl Physiol (1985) 1998; 85: 2237–2248. doi: 10.1152/jappl.1998.85.6.2237

Vasconcelos-Nobrega C, Pinto-Leite R, Arantes-Rodrigues R, et al. In vivo and in vitro effects of RAD001 on bladder cancer. Urol Oncol 2013; 31: 1212–1221. doi: 10.1016/j.urolonc.2011.11.002

Ferreira R, Neuparth MJ, Nogueira-Ferreira R, et al. Exercise training impacts cardiac mitochondrial proteome remodeling in murine urothelial carcinoma. Int J Mol Sci 2018; 20. doi: 10.3390/ijms20010127

Oliveira PA, Vasconcelos-Nobrega C, Gil da Costa RM, et al. The N-butyl-N-4-hydroxybutyl nitrosamine mouse urinary bladder cancer model. Methods Mol Biol 2018; 1655: 155–167. doi: 10.1007/978-1-4939-7234-0_13

Oliveira PA, Gil da Costa RM, Vasconcelos-Nobrega C, et al. Challenges with in vitro and in vivo experimental models of urinary bladder cancer for novel drug discovery. Expert Opin Drug Discov 2016; 11: 599–607. doi: 10.1080/17460441.2016.1174690

Epstein JI, Amin MB, Reuter VR, et al. The World Health Organization/International Society of Urological Pathology consensus classification of urothelial (transitional cell) neoplasms of the urinary bladder. Bladder Consensus Conference Committee. Am J Surg Pathol 1998; 22: 1435–1448. doi: 10.1097/00000478-199812000-00001

Bovolini A, Garcia J, Andrade MA, et al. Relative contribution of fat diet and physical inactivity to the development of metabolic syndrome and non-alcoholic fat liver disease in Wistar rats. Physiol Behav 2020; 225: 113040. doi: 10.1016/j.physbeh.2020.113040

Fearon K, Strasser F, Anker SD, et al. Definition and classification of cancer cachexia: an international consensus. Lancet Oncol 2011; 12: 489–495. doi: 10.1016/S1470-2045(10)70218-7

McGregor RA, Cameron-Smith D, Poppitt SD. It is not just muscle mass: a review of muscle quality, composition and metabolism during ageing as determinants of muscle function and mobility in later life. Longev Healthspan 2014; 3: 9. doi: 10.1186/2046-2395-3-9

Roberts BM, Frye GS, Ahn B, et al. Cancer cachexia decreases specific force and accelerates fatigue in limb muscle. Biochem Biophys Res Commun 2013; 435: 488–492. doi: 10.1016/j.bbrc.2013.05.018

Roberts BM, Ahn B, Smuder AJ, et al. Diaphragm and ventilatory dysfunction during cancer cachexia. FASEB J 2013; 27: 2600–2610. doi: 10.1096/fj.12-222844

Murphy KT, Chee A, Trieu J, et al. Importance of functional and metabolic impairments in the characterization of the C-26 murine model of cancer cachexia. Dis Model Mech 2012; 5: 533–545. doi: 10.1242/dmm.008839

Gransee HM, Mantilla CB, Sieck GC. Respiratory muscle plasticity. Compr Physiol 2012; 2: 1441–1462. doi: 10.1002/cphy.c110050

Aversa Z, Costelli P, Muscaritoli M. Cancer-induced muscle wasting: latest findings in prevention and treatment. Ther Adv Med Oncol 2017; 9: 369–382. doi: 10.1177/1758834017698643

Delaney K, Kasprzycka P, Ciemerych MA, et al. The role of TGF-beta1 during skeletal muscle regeneration. Cell Biol Int 2017; 41: 706–715. doi: 10.1002/cbin.10725

Lieber RL, Ward SR. Cellular mechanisms of tissue fibrosis. 4. Structural and functional consequences of skeletal muscle fibrosis. Am J Physiol Cell Physiol 2013; 305: C241–C252. doi: 10.1152/ajpcell.00173.2013

Judge SM, Nosacka RL, Delitto D, et al. Skeletal muscle fibrosis in pancreatic cancer patients with respect to survival. JNCI Cancer Spectr 2018; 2: pky043. doi: 10.1093/jncics/pky043

Mann CJ, Perdiguero E, Kharraz Y, et al. Aberrant repair and fibrosis development in skeletal muscle. Skelet Muscle 2011; 1: 21. doi: 10.1186/2044-5040-1-21

Christov C, Chretien F, Abou-Khalil R, et al. Muscle satellite cells and endothelial cells: close neighbors and privileged partners. Mol Biol Cell 2007; 18: 1397–1409. doi: 10.1091/mbc.e06-08-0693

Pallafacchina G, Blaauw B, Schiaffino S. Role of satellite cells in muscle growth and maintenance of muscle mass. Nutr Metab Cardiovasc Dis 2013; 23 Suppl 1: S12–S18. doi: 10.1016/j.numecd.2012.02.002

Gibson MC, Schultz E. The distribution of satellite cells and their relationship to specific fiber types in soleus and extensor digitorum longus muscles. Anat Rec 1982; 202: 329–337. doi: 10.1002/ar.1092020305

Liu JX, Hoglund AS, Karlsson P, et al. Myonuclear domain size and myosin isoform expression in muscle fibres from mammals representing a 100,000-fold difference in body size. Exp Physiol 2009; 94: 117–129. doi: 10.1113/expphysiol.2008.043877

Dupont-Versteegden EE, Murphy RJ, Houle JD, et al. Activated satellite cells fail to restore myonuclear number in spinal cord transected and exercised rats. Am J Physiol 1999; 277: C589–C597. doi: 10.1152/ajpcell.1999.277.3.C589

Zhong H, Roy RR, Siengthai B, et al. Effects of inactivity on fiber size and myonuclear number in rat soleus muscle. J Appl Physiol (1985) 2005; 99: 1494–1499. doi: 10.1152/japplphysiol.00394.2005

Bruusgaard JC, Gundersen K. In vivo time-lapse microscopy reveals no loss of murine myonuclei during weeks of muscle atrophy. J Clin Invest 2008; 118: 1450–1457. doi: 10.1172/JCI34022

van Wessel T, de Haan A, van der Laarse WJ, et al. The muscle fiber type-fiber size paradox: hypertrophy or oxidative metabolism? Eur J Appl Physiol 2010; 110: 665–694. doi: 10.1007/s00421-010-1545-0

Wang Y, Pessin JE. Mechanisms for fiber-type specificity of skeletal muscle atrophy. Curr Opin Clin Nutr Metab Care 2013; 16: 243–250. doi: 10.1097/MCO.0b013e328360272d

Downloads

Published

26.06.2023

How to Cite

Esteves, M., Duarte, M., Oliveira, P., Gil da Costa, R., Monteiro, M., & Duarte, J. (2023). SKELETAL MUSCLE SENSITIVITY TO WASTING INDUCED BY UROTHELIAL CARCINOMA. Experimental Oncology, 45(1), 107–119. https://doi.org/10.15407/exp-oncology.2023.01.107

Issue

Section

Original contributions