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Cited by 22Metabolism, Diabetes, and CancerCancer, Hypoxia, and MetabolismCancer, Lipids, and Metabolism

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Effects of β-caryophyllene on arginine ADP-ribosyltransferase 1-mediated regulation of glycolysis in colorectal cancer under high-glucose conditions

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Zhou, Li, Zhan, Mu-Lu, Tang, Yi, Xiao, Ming, Li, Ming, Li, Qing-Shu, Yang, Lian, Li, Xian, Chen, Wen-Wen, Wang, Ya-Lan·2018·International Journal of Oncology
DOI 10.3892/ijo.2018.4506
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Abstract

Type 2 diabetes mellitus (T2DM) is associated with an increased risk of the development of colorectal cancer (CRC). A previous study revealed that the levels of arginine-specific mono-ADP-ribosyltransferase 1 (ART1) in CRC tissues from patients with T2DM were higher than in non-diabetic patients. Hyperglycemia, which is a risk factor of cancer, is a common feature of T2DM; however, the effects of ART1 on glycolysis and energy metabolism in CRC cells under high-glucose conditions remains to be elucidated. β-caryophyllene (BCP) has been reported to exert anticancer and hypoglycemic effects. In the present study, CT26 cells were cultured under a high-glucose conditions and the expression levels of relevant factors were detected by western blotting. Cell Counting Kit-8 assay, flow cytometry, Hoechst 33258 staining, ATP assay and lactic acid assay were used to detect the proliferation, apoptosis and energy metabolism of CT26 cells. To observe the effects of ART1 and BCP on tumor growth in vivo, CT26 cell tumors were successfully transplanted into BALB/c mice with T2DM. The results demonstrated that overexpression of ART1 may increase glycolysis and energy metabolism in CT26 CRC cells under high glucose conditions by regulating the protein kinase B/mammalian target of rapamycin/c‑Myc signaling pathway and the expression of glycolytic enzymes. BCP inhibited the effects induced by ART1, which may be due to a BCP-induced reduction in the expression levels of ART1 via nuclear factor-κB. Therefore, ART1 may be considered a therapeutic target for the treatment of diabetic patients with CRC.

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Metadata

Authors
Zhou, L., Zhan, M.-L., Tang, Y., Xiao, M., Li, M., Li, Q.-S., Yang, L., Li, X., Chen, W.-W., & Wang, Y.-L.
Affiliations
  • Chongqing Medical University (CN)
  • Department of Pathology, Molecular Medicine and Cancer Research Center, Chongqing Medical University, Chongqing 400016, P.R. China
ORCID
Venue
International Journal of Oncology
Publisher
Spandidos Publications
Published
2018-07-27
Volume
53
Issue
4
Pages
1613-1624
ISSN
  • 1019-6439 (ISSN-L)
  • 1791-2423
DOI
10.3892/ijo.2018.4506
OpenAlex
W2883888761
Cited by
22
References
3
Citations by year
2026: 2 · 2025: 3 · 2023: 2 · 2022: 3 · 2021: 4 · 2020: 5 · 2019: 1 · 2018: 2
FWCI
1.07
Type
journal article
Language
en
Open access
Locations
  • International Journal of Oncology (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • University of Bath
  • National Natural Science Foundation of China ((30870946))
  • Sichuan University
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer, Hypoxia, and Metabolism
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer, Lipids, and Metabolism
Keywords
β-caryophyllene, colorectal cancer, high glucose, glycolysis, energy metabolism, type 2 diabetes, hyperglycemia, NF-κB, CT26 cells, tumor growth, apoptosis, glycolytic enzymes
MeSH terms
Polycyclic Sesquiterpenes, Animals, Diabetes Mellitus, Experimental, Diabetes Mellitus, Type 2, Energy Metabolism, Glucose, Glycolysis, Humans, Male, Mice, Inbred BALB C, Sesquiterpenes, Streptozocin, Colorectal Neoplasms, Signal Transduction, Apoptosis, Xenograft Model Antitumor Assays, RNA, Small Interfering, ADP Ribose Transferases, Cell Line, Tumor, Cell Proliferation, Mice, GPI-Linked Proteins

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