Open Access iconOpen Access

ARTICLE

crossmark

Low-molecular-weight fucoidan inhibits the proliferation of melanoma via Bcl-2 phosphorylation and PTEN/AKT pathway

MINJI PARK1, CHULHWAN BANG2, WON-SOO YUN3, YUN-MI JEONG3,*

1 T&R Biofab Co., Ltd., Seongnam-si, 13487, Korea
2 Department of Dermatology, Seoul St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, Seoul, 02706, Korea
3 Department of Mechanical Engineering, Tech University of Korea, Si-heung City, 15073, Korea

* Corresponding Author: YUN-MI JEONG. Email: email

(This article belongs to the Special Issue: Signaling Pathway Crosstalk in Malignant Tumors: Molecular Targets and Combinatorial Therapeutics)

Oncology Research 2024, 32(2), 273-282. https://doi.org/10.32604/or.2023.044362

Abstract

Fucoidan, a sulfate polysaccharide obtained from brown seaweed, has various bioactive properties, including anti-inflammatory, anti-cancer, anti-viral, anti-oxidant, anti-coagulant, anti-thrombotic, anti-angiogenic, and anti-Helicobacter pylori properties. However, the effects of low-molecular-weight fucoidan (LMW-F) on melanoma cell lines and three dimensional (3D) cell culture models are not well understood. This study aimed to investigate the effects of LMW-F on A375 human melanoma cells and cryopreserved biospecimens derived from patients with advanced melanoma. Ultrasonic wave was used to fragment fucoidan derived from Fucus vesiculosus into smaller LMW-F. MTT and live/dead assays showed that LMW-F inhibited cell proliferation in both A375 cells and patient-derived melanoma explants in a 3D-printed collagen scaffold. The PTEN/AKT pathway was found to be involved in the anti-melanoma effects of fucoidan. Western blot analysis revealed that LMW-F reduced the phosphorylation of Bcl-2 at Thr 56, which was associated with the prevention of anti-apoptotic activity of cancer cells. Our findings suggested that LMW-F could enhance anti-melanoma chemotherapy and improve the outcomes of patients with melanoma resistance.

Keywords


Supplementary Material

Supplementary Material File

Cite This Article

APA Style
PARK, M., BANG, C., YUN, W., JEONG, Y. (2024). Low-molecular-weight fucoidan inhibits the proliferation of melanoma via bcl-2 phosphorylation and PTEN/AKT pathway. Oncology Research, 32(2), 273-282. https://doi.org/10.32604/or.2023.044362
Vancouver Style
PARK M, BANG C, YUN W, JEONG Y. Low-molecular-weight fucoidan inhibits the proliferation of melanoma via bcl-2 phosphorylation and PTEN/AKT pathway. Oncology Res . 2024;32(2):273-282 https://doi.org/10.32604/or.2023.044362
IEEE Style
M. PARK, C. BANG, W. YUN, and Y. JEONG "Low-molecular-weight fucoidan inhibits the proliferation of melanoma via Bcl-2 phosphorylation and PTEN/AKT pathway," Oncology Res. , vol. 32, no. 2, pp. 273-282. 2024. https://doi.org/10.32604/or.2023.044362



cc This work is licensed under a Creative Commons Attribution 4.0 International License , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
  • 593

    View

  • 166

    Download

  • 0

    Like

Share Link