Cited by 20Cancer, Hypoxia, and MetabolismPancreatic and Hepatic Oncology ResearchChemokine receptors and signaling

The DOI matches its Crossref record; the references it cites are not checked yet.

The CX3CL1/CX3CR1 reprograms glucose metabolism through HIF-1 pathway in pancreatic adenocarcinoma: The CX3CL1/CX3CR1/HIF-1 Pathway Reprogrammes Glucose Metabolism

Ren, He, Zhao, Tiansuo, Sun, Junwei, Wang, Xiuchao, Liu, Jingcheng, Gao, Song, Yu, Ming, Hao, Jihui·2013·Journal of Cellular Biochemistry

Abstract

One of the hallmarks of cancer is revised glucose metabolism that promotes cell survival and proliferation. In pancreatic cancer, the regulatory mechanism of glucose metabolism remains to be elucidated. In this study, we found that CX3CR1 is expressed in pancreatic cancer cells lines. Exogenous or transfected CX3CL1 increased glucose uptake and lactate secretion. CX3CL1 stimulated HIF-1 expression through PI3K/Akt and MAPK pathways. Furthermore, knockdown of HIF-1 blocked CX3CL1-modified glucose metabolism in pancreatic adenocarcinoma cells. In conclusion, the CX3CL1/CX3CR1 reprograms glucose metabolism through HIF-1 pathway in pancreatic cancer cells.

Overview

Integrity signals

Registry

Crossref · 10.1002/jcb.24608

Cites

Statistics

Recomputing p-values needs the paper’s full text.

Verification

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Citations

The citation lists haven’t been fetched yet

References 26 · Cited by 20

Research works printed but not linked: 24

  1. Chen, 2003, Dominant-negative hypoxia-inducible factor-1 alpha reduces tumorigenicity of pancreatic cancer cells through the suppression of glucose metabolism, Am J Pathol, 162, 1283, 10.1016/S0002-9440(10)63924-7 · DOI
  2. Deberardinis, 2008, Brick by brick: Metabolism and tumor cell growth, Curr Opin Genet Dev, 18, 54, 10.1016/j.gde.2008.02.003 · DOI · Paper page
  3. Dores, 2012, Ubiquitination of G protein-coupled receptors: Functional implications and drug discovery, Mol Pharmacol, 82, 563, 10.1124/mol.112.079418 · DOI
  4. Farrow, 2002, Inflammation and the development of pancreatic cancer, Surg Oncol, 10, 153, 10.1016/S0960-7404(02)00015-4 · DOI · Paper page
  5. Gaudin, 2011, Identification of the chemokine CX3CL1 as a new regulator of malignant cell proliferation in epithelial ovarian cancer, PLoS ONE, 6, e21546, 10.1371/journal.pone.0021546 · DOI
  6. Imai, 1997, Identification and molecular characterization of fractalkine receptor CX3CR1, which mediates both leukocyte migration and adhesion, Cell, 91, 521, 10.1016/S0092-8674(00)80438-9 · DOI
  7. Koppenol, 2011, Otto Warburg's contributions to current concepts of cancer metabolism, Nat Rev Cancer, 11, 325, 10.1038/nrc3038 · DOI · Paper page
  8. Koukourakis, 2006, Comparison of metabolic pathways between cancer cells and stromal cells in colorectal carcinomas: A metabolic survival role for tumor-associated stroma, Cancer Res, 66, 632, 10.1158/0008-5472.CAN-05-3260 · DOI
  9. Liao, 2007, Hypoxia: A key regulator of angiogenesis in cancer, Cancer Metastasis Rev, 26, 281, 10.1007/s10555-007-9066-y · DOI
  10. Marchese, 2001, Agonist-promoted ubiquitination of the G protein-coupled receptor CXCR4 mediates lysosomal sorting, J Biol Chem, 7, 45509, 10.1074/jbc.C100527200 · DOI
  11. Marchesi, 2008, The chemokine receptor CX3CR1 is involved in the neural tropism and malignant behavior of pancreatic ductal adenocarcinoma, Cancer Res, 68, 9060, 10.1158/0008-5472.CAN-08-1810 · DOI
  12. Ransohoff, 2009, Chemokines and chemokine receptors: Standing at the crossroads of immunobiology and neurobiology, Immunity, 31, 711, 10.1016/j.immuni.2009.09.010 · DOI
  13. Rodriguez-Enriquez, 2009, Targeting of cancer energy metabolism, Mol Nutr Food Res, 53, 29, 10.1002/mnfr.200700470 · DOI
  14. Ryu, 2008, Activation of fractalkine/CX3CR1 by vascular endothelial cells induces angiogenesis through VEGF-A/KDR and reverses hindlimb ischaemia, Cardiovasc Res, 78, 333, 10.1093/cvr/cvm067 · DOI
  15. Semenza, 2011, Regulation of metabolism by hypoxia-inducible factor 1, Cold Spring Harb Symp Quant Biol, 76, 347, 10.1101/sqb.2011.76.010678 · DOI · Paper page
  16. Shulby, 2004, CX3CR1-fractalkine expression regulates cellular mechanisms involved in adhesion, migration, and survival of human prostate cancer cells, Cancer Res, 64, 4693, 10.1158/0008-5472.CAN-03-3437 · DOI
  17. Sun, 2010, CXCL12/CXCR4/CXCR7 chemokine axis and cancer progression, Cancer Metastasis Rev, 29, 709, 10.1007/s10555-010-9256-x · DOI
  18. Tanimoto, 2010, Role of glucose metabolism and cellularity for tumor malignancy evaluation using FDG-PET/CT and MRI, Nucl Med Commun, 31, 604, 10.1097/MNM.0b013e328339350c · DOI
  19. Tsao, 2000, Down-regulation of G protein-coupled receptors, Curr Opin Neurobiol, 10, 365, 10.1016/S0959-4388(00)00096-9 · DOI
  20. Vander Heiden, 2009, Understanding the Warburg effect: The metabolic requirements of cell proliferation, Science, 324, 1029, 10.1126/science.1160809 · DOI · Paper page
  21. Wang, 2011, Polymorphisms in the hypoxia-inducible factor-1alpha gene confer susceptibility to pancreatic cancer, Cancer Biol Ther, 12, 383, 10.4161/cbt.12.5.15982 · DOI
  22. Warburg, 1956, On the origin of cancer cells, Science, 123, 309, 10.1126/science.123.3191.309 · DOI · Paper page
  23. White, 2010, Fractalkine has anti-apoptotic and proliferative effects on human vascular smooth muscle cells via epidermal growth factor receptor signalling, Cardiovasc Res, 85, 825, 10.1093/cvr/cvp341 · DOI
  24. Xu, 2012, High expression of CX3CL1/CX3CR1 axis predicts a poor prognosis of pancreatic ductal adenocarcinoma, J Gastrointest Surg, 16, 1493, 10.1007/s11605-012-1921-7 · DOI

Metadata

Authors
Ren, H., Zhao, T., Sun, J., Wang, X., Liu, J., Gao, S., Yu, M., & Hao, J.
Affiliations
Tianjin Medical University Cancer Institute and Hospital (CN)
Corresponding author
Hao, Jihui
Venue
Journal of Cellular Biochemistry
Publisher
Wiley
Published
2013-09-13
Volume
114
Issue
11
Pages
2603-2611
ISSN
0730-2312 (ISSN-L)
OpenAlex
W1841453023
Cited by
20
References
26
Citations by year
2025: 2 · 2024: 2 · 2023: 1 · 2022: 3 · 2021: 3 · 2020: 3 · 2019: 1 · 2017: 2 · 2015: 2 · 2014: 1
FWCI
0.35
Type
journal article
Language
en
Open access
closed
Locations
  • Journal of Cellular Biochemistry (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer, Hypoxia, and Metabolism
  • Health Sciences › Medicine › Oncology › Pancreatic and Hepatic Oncology Research
  • Health Sciences › Medicine › Oncology › Chemokine receptors and signaling
Keywords
fractalkine, CX3CR1, pancreatic ductal adenocarcinoma, glucose metabolism, HIF-1, PI3K/Akt signaling, MAPK signaling, lactate secretion, glucose uptake, cancer metabolism
MeSH terms
CX3C Chemokine Receptor 1, Glucose, Humans, Pancreatic Neoplasms, Gene Expression Regulation, Neoplastic, Receptors, Chemokine, Cell Line, Tumor, Hypoxia-Inducible Factor 1, Chemokine CX3CL1, HEK293 Cells

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review