Evidence map›Paper›PMID 30258965›Full record

ArticleCellular and molecular gastroenterology and hepatology2018

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

Ziying Jian, Tao Cheng, Zhiheng Zhang, Susanne Raulefs, Kuangyu Shi, Katja Steiger, Nadja Maeritz, Karin Kleigrewe, Thomas Hofmann, Simone Benitz and 14 more

Open access · goldAbstract read
In one paragraph

Article in Cellular and molecular gastroenterology and hepatology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.6field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

24 citing papers in PubMed, 31 citations in OpenAlex.

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  16. Hyperinsulinemia in Obesity, Inflammation, and Cancer.Diabetes & metabolism journal · 2021
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

24 authors at 8 institutions in 2 countries.

Ziying JianDepartment of Surgery, Klinikum rechts der Isar, School of Medicine, Technical University of Munich (TUM), Munich, Germany.
Tao ChengDepartment of Surgery, Klinikum rechts der Isar, School of Medicine, Technical University of Munich (TUM), Munich, Germany.
Zhiheng ZhangDepartment of Surgery, Klinikum rechts der Isar, School of Medicine, Technical University of Munich (TUM), Munich, Germany.
Susanne RaulefsDepartment of Surgery, Klinikum rechts der Isar, School of Medicine, Technical University of Munich (TUM), Munich, Germany.
Kuangyu ShiDepartment of Nuclear Medicine, TUM, Munich, Germany.
Katja SteigerInstitute of Pathology, TUM, Munich, Germany.
Nadja MaeritzDepartment of Surgery, Klinikum rechts der Isar, School of Medicine, Technical University of Munich (TUM), Munich, Germany.
Karin KleigreweBavarian Center for Biomolecular Mass Spectrometry, Freising, Germany.
Thomas HofmannBavarian Center for Biomolecular Mass Spectrometry, Freising, Germany.
Simone BenitzDepartment of Surgery, Klinikum rechts der Isar, School of Medicine, Technical University of Munich (TUM), Munich, Germany.
Philipp BrunsDivision of Applied Bioinformatics, German Cancer Research Center, Heidelberg, Germany.
Daniel LampHelmholtz Diabetes Center, Helmholtz Zentrum München, Neuherberg, Germany.
Martin JastrochHelmholtz Diabetes Center, Helmholtz Zentrum München, Neuherberg, Germany.
Jan AkkanDepartment of Surgery, Klinikum rechts der Isar, School of Medicine, Technical University of Munich (TUM), Munich, Germany.
Carsten JägerDepartment of Surgery, Klinikum rechts der Isar, School of Medicine, Technical University of Munich (TUM), Munich, Germany.
Peilin HuangDepartment of Pathology, School of Medicine, Southeast University, Nanjing, China.
Shuang NieDepartment of Gastroenterology, Affiliated Drum Tower Hospital of Nanjing University, Medical School, Nanjing, China.
Shanshan ShenDepartment of Gastroenterology, Affiliated Drum Tower Hospital of Nanjing University, Medical School, Nanjing, China.
Xiaoping ZouDepartment of Gastroenterology, Affiliated Drum Tower Hospital of Nanjing University, Medical School, Nanjing, China.
Güralp O CeyhanDepartment of Surgery, Klinikum rechts der Isar, School of Medicine, Technical University of Munich (TUM), Munich, Germany.
Christoph W MichalskiDepartment of Visceral, Vascular and Endocrine Surgery, Martin-Luther-University Halle-Wittenberg, Halle, Germany.
Helmut FriessDepartment of Surgery, Klinikum rechts der Isar, School of Medicine, Technical University of Munich (TUM), Munich, Germany.
Jörg KleeffDepartment of Visceral, Vascular and Endocrine Surgery, Martin-Luther-University Halle-Wittenberg, Halle, Germany.
Bo KongDepartment of Surgery, Klinikum rechts der Isar, School of Medicine, Technical University of Munich (TUM), Munich, Germany.
TUM Klinikum · DENanjing Drum Tower Hospital · CNBavarian State Research Center for Agriculture · DEGerman Cancer Research Center · DEHelmholtz Zentrum München · DEMartin Luther University Halle-Wittenberg · DETechnical University of Munich · DESoutheast University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

AnimalsCarcinoma, Pancreatic DuctalCell Line, TumorCell ProliferationCollagen Type VICore Binding Factor Alpha 3 SubunitDiabetes MellitusDNA MethylationEpigenesis, GeneticGene OntologyHistonesHumansHyperglycemiaHypoglycemiaMetforminMiceCollagen Type VICore Binding Factor Alpha 3 SubunitHistonesMetforminReceptors, Retinoic Acidretinoic acid receptor betaRunx3 protein, human2DG, 2-deoxy-D-glucoseADP, adenosine diphosphateATP, adenosine triphosphateCaix, carbonic anhydrase IXCol6a1, collagenCT, computed tomographyECM, extracellular matrixEgr2, early growth response 2FBS, fetal bovine serumGlucose MetabolismIHC, immunohistochemistryMetastasisPancreatic CancerPBS, phosphate-buffered salinePCR, polymerase chain reactionPDAC, pancreatic ductal adenocarcinomaPET, positron emission tomographyqRT-PCR, quantitative real-time polymerase chain reactionRarb, retinoic acid receptor betaRA, retinoic acidRetinoic AcidRunx3, runt related transcription factor 3type VI, alpha 1

Identifiers

PMID30258965
PMCPMC6154439
OpenAlexW2883076934

What OpenQuestion holds

Texttitle and abstract
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.