Tumour‐specific and organ‐specific protein synthesis rates in patients with pancreatic cancer

Abstract Background Living tissues maintain a fine balance between protein synthesis and protein breakdown rates. Animal studies indicate that protein synthesis rates are higher in organs when compared with skeletal muscle tissue. As such, organ and tumour protein synthesis could have major effects...

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Main Authors: David P.J. vanDijk, Astrid M.H. Horstman, Joey S.J. Smeets, Marcel denDulk, Heike I. Grabsch, Cornelis H.C. Dejong, Sander S. Rensen, Steven W.M. Olde Damink, Luc J.C. vanLoon
Format: Article
Language:English
Published: Wiley 2019-06-01
Series:Journal of Cachexia, Sarcopenia and Muscle
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Online Access:https://doi.org/10.1002/jcsm.12419
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spelling doaj-c878c9acc08c4f1fa5d6b39793b9c9452020-11-25T02:22:45ZengWileyJournal of Cachexia, Sarcopenia and Muscle2190-59912190-60092019-06-0110354955610.1002/jcsm.12419Tumour‐specific and organ‐specific protein synthesis rates in patients with pancreatic cancerDavid P.J. vanDijk0Astrid M.H. Horstman1Joey S.J. Smeets2Marcel denDulk3Heike I. Grabsch4Cornelis H.C. Dejong5Sander S. Rensen6Steven W.M. Olde Damink7Luc J.C. vanLoon8Department of Surgery Maastricht University Maastricht The NetherlandsNUTRIM School of Nutrition and Translational Research in Metabolism Maastricht University Maastricht The NetherlandsNUTRIM School of Nutrition and Translational Research in Metabolism Maastricht University Maastricht The NetherlandsDepartment of Surgery Maastricht University Maastricht The NetherlandsDepartment of Pathology Maastricht University Maastricht The NetherlandsDepartment of Surgery Maastricht University Maastricht The NetherlandsDepartment of Surgery Maastricht University Maastricht The NetherlandsDepartment of Surgery Maastricht University Maastricht The NetherlandsNUTRIM School of Nutrition and Translational Research in Metabolism Maastricht University Maastricht The NetherlandsAbstract Background Living tissues maintain a fine balance between protein synthesis and protein breakdown rates. Animal studies indicate that protein synthesis rates are higher in organs when compared with skeletal muscle tissue. As such, organ and tumour protein synthesis could have major effects on whole‐body protein metabolism in wasting disorders such as cancer cachexia. We aimed to assess protein synthesis rates in pancreatic tumour tissue and healthy pancreas, liver, and skeletal muscle tissue in vivo in humans. Methods In eight patients with pancreatic cancer undergoing pancreaticoduodenectomy, primed continuous infusions with L‐[ring‐13C6]phenylalanine and L‐[3,5‐2H2]tyrosine were started prior to surgery and continued throughout the surgical procedures. During surgery, plasma samples and biopsies from the pancreas, pancreatic tumour, liver, and vastus lateralis muscle were taken. Post‐absorptive fractional protein synthesis rates were determined by measuring incorporation of labelled L‐[ring‐13C6]phenylalanine in tissue protein using the weighed plasma L‐[ring‐13C6]phenylalanine enrichments as the precursor pool. Results Five male patients and three female patients with a mean age of 67 ± 2 years were included into this study. Plasma L‐[ring‐13C6]phenylalanine enrichments (6–9 mole per cent excess) did not change during surgery (P = 0.60). Pancreatic tumour protein synthesis rates were 2.6‐fold lower than surrounding pancreatic tissue protein synthesis rates (0.268 ± 0.053 vs. 0.694 ± 0.228%/h, respectively; P = 0.028) and 1.7‐fold lower than liver protein synthesis rates (0.268 ± 0.053 vs. 0.448 ± 0.043%/h, respectively; P = 0.046). Among healthy organ samples, protein synthesis rates were 20‐fold and 13‐fold higher in pancreas and liver, respectively, compared with skeletal muscle tissue (0.694 ± 0.228 and 0.448 ± 0.043 vs. 0.035 ± 0.005%/h, respectively; P < 0.05). Conclusions Liver and pancreas tissue protein synthesis rates are higher when compared with pancreatic tumour and skeletal muscle tissue protein synthesis rates and can, therefore, strongly impact whole‐body protein metabolism in vivo in humans.https://doi.org/10.1002/jcsm.12419Protein metabolismPancreatic cancerPancreasLiver
collection DOAJ
language English
format Article
sources DOAJ
author David P.J. vanDijk
Astrid M.H. Horstman
Joey S.J. Smeets
Marcel denDulk
Heike I. Grabsch
Cornelis H.C. Dejong
Sander S. Rensen
Steven W.M. Olde Damink
Luc J.C. vanLoon
spellingShingle David P.J. vanDijk
Astrid M.H. Horstman
Joey S.J. Smeets
Marcel denDulk
Heike I. Grabsch
Cornelis H.C. Dejong
Sander S. Rensen
Steven W.M. Olde Damink
Luc J.C. vanLoon
Tumour‐specific and organ‐specific protein synthesis rates in patients with pancreatic cancer
Journal of Cachexia, Sarcopenia and Muscle
Protein metabolism
Pancreatic cancer
Pancreas
Liver
author_facet David P.J. vanDijk
Astrid M.H. Horstman
Joey S.J. Smeets
Marcel denDulk
Heike I. Grabsch
Cornelis H.C. Dejong
Sander S. Rensen
Steven W.M. Olde Damink
Luc J.C. vanLoon
author_sort David P.J. vanDijk
title Tumour‐specific and organ‐specific protein synthesis rates in patients with pancreatic cancer
title_short Tumour‐specific and organ‐specific protein synthesis rates in patients with pancreatic cancer
title_full Tumour‐specific and organ‐specific protein synthesis rates in patients with pancreatic cancer
title_fullStr Tumour‐specific and organ‐specific protein synthesis rates in patients with pancreatic cancer
title_full_unstemmed Tumour‐specific and organ‐specific protein synthesis rates in patients with pancreatic cancer
title_sort tumour‐specific and organ‐specific protein synthesis rates in patients with pancreatic cancer
publisher Wiley
series Journal of Cachexia, Sarcopenia and Muscle
issn 2190-5991
2190-6009
publishDate 2019-06-01
description Abstract Background Living tissues maintain a fine balance between protein synthesis and protein breakdown rates. Animal studies indicate that protein synthesis rates are higher in organs when compared with skeletal muscle tissue. As such, organ and tumour protein synthesis could have major effects on whole‐body protein metabolism in wasting disorders such as cancer cachexia. We aimed to assess protein synthesis rates in pancreatic tumour tissue and healthy pancreas, liver, and skeletal muscle tissue in vivo in humans. Methods In eight patients with pancreatic cancer undergoing pancreaticoduodenectomy, primed continuous infusions with L‐[ring‐13C6]phenylalanine and L‐[3,5‐2H2]tyrosine were started prior to surgery and continued throughout the surgical procedures. During surgery, plasma samples and biopsies from the pancreas, pancreatic tumour, liver, and vastus lateralis muscle were taken. Post‐absorptive fractional protein synthesis rates were determined by measuring incorporation of labelled L‐[ring‐13C6]phenylalanine in tissue protein using the weighed plasma L‐[ring‐13C6]phenylalanine enrichments as the precursor pool. Results Five male patients and three female patients with a mean age of 67 ± 2 years were included into this study. Plasma L‐[ring‐13C6]phenylalanine enrichments (6–9 mole per cent excess) did not change during surgery (P = 0.60). Pancreatic tumour protein synthesis rates were 2.6‐fold lower than surrounding pancreatic tissue protein synthesis rates (0.268 ± 0.053 vs. 0.694 ± 0.228%/h, respectively; P = 0.028) and 1.7‐fold lower than liver protein synthesis rates (0.268 ± 0.053 vs. 0.448 ± 0.043%/h, respectively; P = 0.046). Among healthy organ samples, protein synthesis rates were 20‐fold and 13‐fold higher in pancreas and liver, respectively, compared with skeletal muscle tissue (0.694 ± 0.228 and 0.448 ± 0.043 vs. 0.035 ± 0.005%/h, respectively; P < 0.05). Conclusions Liver and pancreas tissue protein synthesis rates are higher when compared with pancreatic tumour and skeletal muscle tissue protein synthesis rates and can, therefore, strongly impact whole‐body protein metabolism in vivo in humans.
topic Protein metabolism
Pancreatic cancer
Pancreas
Liver
url https://doi.org/10.1002/jcsm.12419
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