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Chemoprotective Effect of Daphnetin in Doxorubicin Treated Esophageal Cancer Stem Cell Xenograft Tumor Mouse

  • BIOCHEMISTRY, BIOPHYSICS, AND MOLECULAR BIOLOGY
  • Published:
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Abstract

Background: Chemotherapy drugs commonly used for cancer therapy, but chemotherapy has limitation due to side effects. Current studies suggest natural products are reducing the side effects of chemotherapy medicines. In this study, we examined the side effects of doxorubicin (Dox) in esophageal cancer cells (CSCs) derived tumors in vivo. Methods: Esophageal cancer cells (YMI) were treated in vitro with daphnetin (DAP) along with DOX. The MTT assay was used for estimating the cell viability and Annexin/7-AAD was used for the determination of apoptosis. Cell cycle arrest was conducted using the PI-staining method. The potential effect of DAP was evaluated by the estimation of oxidative stress such as total antioxidant capacity (TAC), malondialdehyde (MDA) and superoxide dismutase (SOD) and body weight in the xenograft mice. Results: DAP can protect Dox cell toxicity by suppressing cell apoptosis of ESCC. DAP arrest the cells as S-phase. In vivo experimental study showed that Dox simultaneously with DAP decreases the tumor size along with increased body weight in the nude mice compared to Dox alone treated group mice. Dox along with the DAP exhibited less systemic toxicity and reduced oxidative stress fraction circulation. Conclusion: The result suggests that daphnetin may be used as an adjuvant therapy to reduce the systemic toxicity of chemotherapeutic agents, such as DOX, in stem cell treatment with ESCC cancer.

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Abbreviations

DOX:

=Doxorubicin

CSCs:

=Esophageal cancer cells

YMI:

=Esophageal cancer cells

DAP:

=Daphnetin

TAC:

=Total antioxidant capacity

MDA:

=Malondialdehyde

SOD:

=Superoxide dismutase

EC:

=Esophageal cancer

TNF-α:

=Tumor necrosis factor-α

IL-1:

=Interleukin-1

DMEM:

=Dulbecco’s modified eagle medium

bFGF:

=Basic fibroblast growth factor

XTT:

=2,3-bis (2-methoxy-4-nitro-5-sulfophenyl)−5-[(phenylamino) carbonyl]−2H-tetrazolium hydroxide

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Funding

The project supported by the Foundation of Medical Scientific Research (Grant no. YWJKJJHKYJJ-F116113).

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Correspondence to Qianxi Deng.

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The authors declare that they have no conflict of interest.

COMPLIANCE WITH ETHICAL STANDARDS

The whole animal study was approved from the institution on 22 Dec 2019 with approval number SC20190821F.

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Deng, Q., Wu, L., Li, Y. et al. Chemoprotective Effect of Daphnetin in Doxorubicin Treated Esophageal Cancer Stem Cell Xenograft Tumor Mouse. Dokl Biochem Biophys 499, 273–281 (2021). https://doi.org/10.1134/S1607672921040128

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  • DOI: https://doi.org/10.1134/S1607672921040128

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