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High-dose ascorbate exerts anti-tumor activities and improves inhibitory effect of carboplatin through the pro-oxidant function pathway in uterine serous carcinoma cell lines.

Publication ,  Journal Article
Shen, X; Wang, J; Deng, B; Chen, S; John, C; Zhao, Z; Sinha, N; Haag, J; Sun, W; Kong, W; Spasojevic, I; Batinic-Haberle, I; Secord, AA ...
Published in: Gynecol Oncol
April 2024

OBJECTIVE: Uterine serous carcinoma is a highly aggressive non-endometrioid subtype of endometrial cancer with poor survival rates overall, creating a strong need for new therapeutic strategies to improve outcomes. High-dose ascorbate (vitamin C) has been shown to inhibit cell proliferation and tumor growth in multiple preclinical models and has shown promising anti-tumor activity in combination with chemotherapy, with a favorable safety profile. We aimed to study the anti-tumor effects of ascorbate and its synergistic effect with carboplatin on uterine serous carcinoma cells. METHODS: Cell proliferation was evaluated by MTT and colony formation assays in ARK1, ARK2 and SPEC2 cells. Cellular stress, antioxidant ability, cleaved caspase 3 activity and adhesion were measured by ELISA assays. Cell cycle was detected by Cellometer. Invasion was measured using a wound healing assay. Changes in protein expression were determined by Western immunoblotting. RESULTS: High-dose ascorbate significantly inhibited cell proliferation, caused cell cycle arrest, induced cellular stress, and apoptosis, increased DNA damage, and suppressed cell invasion in ARK1 and SPEC2 cells. Treatment of both cells with 1 mM N-acetylcysteine reversed ascorbate-induced apoptosis and inhibition of cell proliferation. The combination of ascorbate and carboplatin produced significant synergistic effects in inhibiting cell proliferation and invasion, inducing cellular stress, causing DNA damage, and enhancing cleaved caspase 3 levels compared to each compound alone in both cells. CONCLUSIONS: Ascorbate has potent antitumor activity and acts synergistically with carboplatin through its pro-oxidant effects. Clinical trials of ascorbate combined with carboplatin as adjuvant treatment of uterine serous carcinoma are worth exploring.

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Published In

Gynecol Oncol

DOI

EISSN

1095-6859

Publication Date

April 2024

Volume

183

Start / End Page

93 / 102

Location

United States

Related Subject Headings

  • Uterine Neoplasms
  • Reactive Oxygen Species
  • Oncology & Carcinogenesis
  • Humans
  • Female
  • Drug Synergism
  • DNA Damage
  • Cystadenocarcinoma, Serous
  • Cell Proliferation
  • Cell Line, Tumor
 

Citation

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Shen, X., Wang, J., Deng, B., Chen, S., John, C., Zhao, Z., … Bae-Jump, V. L. (2024). High-dose ascorbate exerts anti-tumor activities and improves inhibitory effect of carboplatin through the pro-oxidant function pathway in uterine serous carcinoma cell lines. Gynecol Oncol, 183, 93–102. https://doi.org/10.1016/j.ygyno.2024.03.021
Shen, Xiaochang, Jiandong Wang, Boer Deng, Shuning Chen, Catherine John, Ziyi Zhao, Nikita Sinha, et al. “High-dose ascorbate exerts anti-tumor activities and improves inhibitory effect of carboplatin through the pro-oxidant function pathway in uterine serous carcinoma cell lines.Gynecol Oncol 183 (April 2024): 93–102. https://doi.org/10.1016/j.ygyno.2024.03.021.
Shen, Xiaochang, et al. “High-dose ascorbate exerts anti-tumor activities and improves inhibitory effect of carboplatin through the pro-oxidant function pathway in uterine serous carcinoma cell lines.Gynecol Oncol, vol. 183, Apr. 2024, pp. 93–102. Pubmed, doi:10.1016/j.ygyno.2024.03.021.
Shen X, Wang J, Deng B, Chen S, John C, Zhao Z, Sinha N, Haag J, Sun W, Kong W, Spasojevic I, Batinic-Haberle I, Secord AA, Zhou C, Bae-Jump VL. High-dose ascorbate exerts anti-tumor activities and improves inhibitory effect of carboplatin through the pro-oxidant function pathway in uterine serous carcinoma cell lines. Gynecol Oncol. 2024 Apr;183:93–102.
Journal cover image

Published In

Gynecol Oncol

DOI

EISSN

1095-6859

Publication Date

April 2024

Volume

183

Start / End Page

93 / 102

Location

United States

Related Subject Headings

  • Uterine Neoplasms
  • Reactive Oxygen Species
  • Oncology & Carcinogenesis
  • Humans
  • Female
  • Drug Synergism
  • DNA Damage
  • Cystadenocarcinoma, Serous
  • Cell Proliferation
  • Cell Line, Tumor