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Article Open Access

Potential use of compounds from sea cucumbers as MDM2 and CXCR4 inhibitors to control cancer cell growth

  • Authors:
    • Teresa Liliana Wargasetia
    • Sofy Permana
    • Nashi Widodo
  • View Affiliations / Copyright

    Affiliations: Faculty of Medicine, Maranatha Christian University, Bandung, West Java 40164, Indonesia, Biology Department, Faculty of Mathematics and Natural Sciences, The University of Brawijaya, Malang, East Java 65145, Indonesia
    Copyright: © Wargasetia et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 2985-2991
    |
    Published online on: August 7, 2018
       https://doi.org/10.3892/etm.2018.6588
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Abstract

Ineffectiveness of cancer therapy may originate in the incompatibility of the treatment with various mutations in the cancer cells. Finding novel anticancer treatments that work efficiently for varying types of cancer cells remains challenging. Previous studies have identified that compounds in sea cucumbers are capable of inhibiting the growth of cancer cells and inducing apoptosis. However, information on the underlying mechanisms controlling cancer cell growth at a molecular level remains limited. The current study analyzed the potential of colochiroside A, ds‑echinoside A, philinopside E, sphingosine and stichoposide C as inhibitors for anticancer target proteins, including mouse double minute 2 homolog (MDM2) and C‑X‑C chemokine receptor type 4 (CXCR4). Inhibition of MDM2 triggers apoptosis through regulation of tumor protein 53 and CXCR4 inhibition may prevent cancer cell proliferation and growth by affecting the Janus kinase 2/3 signal transducer and activator of transcription signaling pathway and protein tyrosine kinase 2. The results of a binding affinity analysis using molecular docking revealed that philinopside E and ds‑echinoside A may inhibit MDM2 and CXCR4. The data suggested that these active compounds may be promising inhibitors of cell growth by binding to two targets simultaneously. Furthermore, stichoposide C and colochiroside A were predicted to inhibit CXCR4. Additional research is needed to validate the in vitro activity of the aforementioned compounds.
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Copy and paste a formatted citation
Spandidos Publications style
Wargasetia TL, Permana S and Widodo N: Potential use of compounds from sea cucumbers as MDM2 and CXCR4 inhibitors to control cancer cell growth. Exp Ther Med 16: 2985-2991, 2018.
APA
Wargasetia, T.L., Permana, S., & Widodo, N. (2018). Potential use of compounds from sea cucumbers as MDM2 and CXCR4 inhibitors to control cancer cell growth. Experimental and Therapeutic Medicine, 16, 2985-2991. https://doi.org/10.3892/etm.2018.6588
MLA
Wargasetia, T. L., Permana, S., Widodo, N."Potential use of compounds from sea cucumbers as MDM2 and CXCR4 inhibitors to control cancer cell growth". Experimental and Therapeutic Medicine 16.4 (2018): 2985-2991.
Chicago
Wargasetia, T. L., Permana, S., Widodo, N."Potential use of compounds from sea cucumbers as MDM2 and CXCR4 inhibitors to control cancer cell growth". Experimental and Therapeutic Medicine 16, no. 4 (2018): 2985-2991. https://doi.org/10.3892/etm.2018.6588
Copy and paste a formatted citation
x
Spandidos Publications style
Wargasetia TL, Permana S and Widodo N: Potential use of compounds from sea cucumbers as MDM2 and CXCR4 inhibitors to control cancer cell growth. Exp Ther Med 16: 2985-2991, 2018.
APA
Wargasetia, T.L., Permana, S., & Widodo, N. (2018). Potential use of compounds from sea cucumbers as MDM2 and CXCR4 inhibitors to control cancer cell growth. Experimental and Therapeutic Medicine, 16, 2985-2991. https://doi.org/10.3892/etm.2018.6588
MLA
Wargasetia, T. L., Permana, S., Widodo, N."Potential use of compounds from sea cucumbers as MDM2 and CXCR4 inhibitors to control cancer cell growth". Experimental and Therapeutic Medicine 16.4 (2018): 2985-2991.
Chicago
Wargasetia, T. L., Permana, S., Widodo, N."Potential use of compounds from sea cucumbers as MDM2 and CXCR4 inhibitors to control cancer cell growth". Experimental and Therapeutic Medicine 16, no. 4 (2018): 2985-2991. https://doi.org/10.3892/etm.2018.6588
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