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Glycemic Variability Promotes Both Local Invasion and Metastatic Colonization by Pancreatic Ductal Adenocarcinoma

BACKGROUND & AIMS: Although nearly half of pancreatic ductal adenocarcinoma (PDAC) patients have diabetes mellitus with episodes of hyperglycemia, its tumor microenvironment is hypoglycemic. Thus, it is crucial for PDAC cells to develop adaptive mechanisms dealing with oscillating glucose levels...

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Autores principales: Jian, Ziying, Cheng, Tao, Zhang, Zhiheng, Raulefs, Susanne, Shi, Kuangyu, Steiger, Katja, Maeritz, Nadja, Kleigrewe, Karin, Hofmann, Thomas, Benitz, Simone, Bruns, Philipp, Lamp, Daniel, Jastroch, Martin, Akkan, Jan, Jäger, Carsten, Huang, Peilin, Nie, Shuang, Shen, Shanshan, Zou, Xiaoping, Ceyhan, Güralp O., Michalski, Christoph W., Friess, Helmut, Kleeff, Jörg, Kong, Bo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6154439/
https://www.ncbi.nlm.nih.gov/pubmed/30258965
http://dx.doi.org/10.1016/j.jcmgh.2018.07.003
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author Jian, Ziying
Cheng, Tao
Zhang, Zhiheng
Raulefs, Susanne
Shi, Kuangyu
Steiger, Katja
Maeritz, Nadja
Kleigrewe, Karin
Hofmann, Thomas
Benitz, Simone
Bruns, Philipp
Lamp, Daniel
Jastroch, Martin
Akkan, Jan
Jäger, Carsten
Huang, Peilin
Nie, Shuang
Shen, Shanshan
Zou, Xiaoping
Ceyhan, Güralp O.
Michalski, Christoph W.
Friess, Helmut
Kleeff, Jörg
Kong, Bo
author_facet Jian, Ziying
Cheng, Tao
Zhang, Zhiheng
Raulefs, Susanne
Shi, Kuangyu
Steiger, Katja
Maeritz, Nadja
Kleigrewe, Karin
Hofmann, Thomas
Benitz, Simone
Bruns, Philipp
Lamp, Daniel
Jastroch, Martin
Akkan, Jan
Jäger, Carsten
Huang, Peilin
Nie, Shuang
Shen, Shanshan
Zou, Xiaoping
Ceyhan, Güralp O.
Michalski, Christoph W.
Friess, Helmut
Kleeff, Jörg
Kong, Bo
author_sort Jian, Ziying
collection PubMed
description BACKGROUND & AIMS: Although nearly half of pancreatic ductal adenocarcinoma (PDAC) patients have diabetes mellitus with episodes of hyperglycemia, its tumor microenvironment is hypoglycemic. Thus, it is crucial for PDAC cells to develop adaptive mechanisms dealing with oscillating glucose levels. So far, the biological impact of such glycemic variability on PDAC biology remains unknown. METHODS: Murine PDAC cells were cultured in low- and high-glucose medium to investigate the molecular, biochemical, and metabolic influence of glycemic variability on tumor behavior. A set of in vivo functional assays including orthotopic implantation and portal and tail vein injection were used. Results were further confirmed on tissues from PDAC patients. RESULTS: Glycemic variability has no significant effect on PDAC cell proliferation. Hypoglycemia is associated with local invasion and angiogenesis, whereas hyperglycemia promotes metastatic colonization. Increased metastatic colonization under hyperglycemia is due to increased expression of runt related transcription factor 3 (Runx3), which further activates expression of collagen, type VI, alpha 1 (Col6a1), forming a glycemic pro-metastatic pathway. Through epigenetic machinery, retinoic acid receptor beta (Rarb) expression fluctuates according to glycemic variability, acting as a critical sensor relaying the glycemic signal to Runx3/Col6a1. Moreover, the signal axis of Rarb/Runx3/Col6a1 is pharmaceutically accessible to a widely used antidiabetic substance, metformin, and Rar modulator. Finally, PDAC tissues from patients with diabetes show an increased expression of COL6A1. CONCLUSIONS: Glycemic variability promotes both local invasion and metastatic colonization of PDAC. A pro-metastatic signal axis Rarb/Runx3/Col6a1 whose activity is controlled by glycemic variability is identified. The therapeutic relevance of this pathway needs to be explored in PDAC patients, especially in those with diabetes.
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spelling pubmed-61544392018-09-26 Glycemic Variability Promotes Both Local Invasion and Metastatic Colonization by Pancreatic Ductal Adenocarcinoma Jian, Ziying Cheng, Tao Zhang, Zhiheng Raulefs, Susanne Shi, Kuangyu Steiger, Katja Maeritz, Nadja Kleigrewe, Karin Hofmann, Thomas Benitz, Simone Bruns, Philipp Lamp, Daniel Jastroch, Martin Akkan, Jan Jäger, Carsten Huang, Peilin Nie, Shuang Shen, Shanshan Zou, Xiaoping Ceyhan, Güralp O. Michalski, Christoph W. Friess, Helmut Kleeff, Jörg Kong, Bo Cell Mol Gastroenterol Hepatol Original Research BACKGROUND & AIMS: Although nearly half of pancreatic ductal adenocarcinoma (PDAC) patients have diabetes mellitus with episodes of hyperglycemia, its tumor microenvironment is hypoglycemic. Thus, it is crucial for PDAC cells to develop adaptive mechanisms dealing with oscillating glucose levels. So far, the biological impact of such glycemic variability on PDAC biology remains unknown. METHODS: Murine PDAC cells were cultured in low- and high-glucose medium to investigate the molecular, biochemical, and metabolic influence of glycemic variability on tumor behavior. A set of in vivo functional assays including orthotopic implantation and portal and tail vein injection were used. Results were further confirmed on tissues from PDAC patients. RESULTS: Glycemic variability has no significant effect on PDAC cell proliferation. Hypoglycemia is associated with local invasion and angiogenesis, whereas hyperglycemia promotes metastatic colonization. Increased metastatic colonization under hyperglycemia is due to increased expression of runt related transcription factor 3 (Runx3), which further activates expression of collagen, type VI, alpha 1 (Col6a1), forming a glycemic pro-metastatic pathway. Through epigenetic machinery, retinoic acid receptor beta (Rarb) expression fluctuates according to glycemic variability, acting as a critical sensor relaying the glycemic signal to Runx3/Col6a1. Moreover, the signal axis of Rarb/Runx3/Col6a1 is pharmaceutically accessible to a widely used antidiabetic substance, metformin, and Rar modulator. Finally, PDAC tissues from patients with diabetes show an increased expression of COL6A1. CONCLUSIONS: Glycemic variability promotes both local invasion and metastatic colonization of PDAC. A pro-metastatic signal axis Rarb/Runx3/Col6a1 whose activity is controlled by glycemic variability is identified. The therapeutic relevance of this pathway needs to be explored in PDAC patients, especially in those with diabetes. Elsevier 2018-07-26 /pmc/articles/PMC6154439/ /pubmed/30258965 http://dx.doi.org/10.1016/j.jcmgh.2018.07.003 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Research
Jian, Ziying
Cheng, Tao
Zhang, Zhiheng
Raulefs, Susanne
Shi, Kuangyu
Steiger, Katja
Maeritz, Nadja
Kleigrewe, Karin
Hofmann, Thomas
Benitz, Simone
Bruns, Philipp
Lamp, Daniel
Jastroch, Martin
Akkan, Jan
Jäger, Carsten
Huang, Peilin
Nie, Shuang
Shen, Shanshan
Zou, Xiaoping
Ceyhan, Güralp O.
Michalski, Christoph W.
Friess, Helmut
Kleeff, Jörg
Kong, Bo
Glycemic Variability Promotes Both Local Invasion and Metastatic Colonization by Pancreatic Ductal Adenocarcinoma
title Glycemic Variability Promotes Both Local Invasion and Metastatic Colonization by Pancreatic Ductal Adenocarcinoma
title_full Glycemic Variability Promotes Both Local Invasion and Metastatic Colonization by Pancreatic Ductal Adenocarcinoma
title_fullStr Glycemic Variability Promotes Both Local Invasion and Metastatic Colonization by Pancreatic Ductal Adenocarcinoma
title_full_unstemmed Glycemic Variability Promotes Both Local Invasion and Metastatic Colonization by Pancreatic Ductal Adenocarcinoma
title_short Glycemic Variability Promotes Both Local Invasion and Metastatic Colonization by Pancreatic Ductal Adenocarcinoma
title_sort glycemic variability promotes both local invasion and metastatic colonization by pancreatic ductal adenocarcinoma
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6154439/
https://www.ncbi.nlm.nih.gov/pubmed/30258965
http://dx.doi.org/10.1016/j.jcmgh.2018.07.003
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