Vitamin C induces human melanoma A375 cell apoptosis via Bax- and Bcl-2-mediated mitochondrial pathways

Xiao-Yu Chen1, Ying Chen1, Chuan-Jun Qu1

  • 1School of Integrated Traditional Chinese and Western Medicine, Binzhou Medical University, Yantai, Shandong 264003, P.R. China.

Oncology Letters
|September 14, 2019
PubMed

Insights

Vitamin C effectively inhibits melanoma cell growth by triggering programmed cell death (apoptosis). This vitamin activates key proteins and disrupts mitochondrial function, offering a potential new treatment for melanoma patients.

Area of Science:

  • Oncology
  • Cell Biology
  • Biochemistry

Background:

  • Melanoma is an aggressive skin cancer with poor prognosis due to treatment resistance.
  • Novel therapeutic strategies are needed to combat melanoma effectively.

Purpose of the Study:

  • To investigate the anti-cancer effects of Vitamin C (L-ascorbic acid) on human melanoma A375 cells.
  • To elucidate the underlying molecular mechanisms of Vitamin C's action in melanoma.

Main Methods:

  • Treatment of human melanoma A375 cells with Vitamin C.
  • Assessment of cell proliferation, apoptosis induction, and caspase activation (caspase-9, caspase-3).
  • Evaluation of mitochondrial membrane potential and expression of apoptosis-related proteins (Bax, Bcl-2).

Main Results:

  • Vitamin C significantly suppressed melanoma A375 cell proliferation.
  • Vitamin C induced apoptosis in A375 cells, evidenced by caspase-9 and caspase-3 activation.
  • A decrease in mitochondrial membrane potential and activation of the Bax/Bcl-2 pathway were observed.

Conclusions:

  • Vitamin C demonstrates potent anti-proliferative and apoptosis-inducing effects on human melanoma cells.
  • The mechanism involves the mitochondrial pathway, including caspase activation and modulation of Bax and Bcl-2.
  • Vitamin C shows potential as a clinical anti-tumor agent for melanoma treatment.

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