Emodin is a Potential Drug Targeting CD44-positive Hepatocellular Cancer

Author:

Gao Yuan1ORCID,Li Youling21,zhu yunhe31,luo qiao1,Lu Yifeng1,Wen Ke1,du boyu42,xi xueyan412,Li Gang1

Affiliation:

1. Department of General Medicine, Renmin Hospital, Hubei University of Medicine, Shiyan City, Hubei Province, 442000, P.R. China

2. Department of Nuclear Medicine, Renmin Hospital, Hubei University of Medicine, Shiyan City, Hubei Province, 442000, P.R. China

3. People\'s Hospital of Shiyan Nuclear Medicine Shiyan China

4. Institute of Basic Medical Sciences, Hubei University of Medicine, Shiyan City, Hubei Province, 442000, P.R. China

Abstract

Background:: Liver cancer is one of the most prevalent forms of cancer of the digestive system in our country. The most common subtype of this disease is hepatocellular carcinoma (HCC). Currently, treatment options for HCC patients include surgical resection, liver transplantation, radiofrequency ablation, chemoembolization, and biologic-targeted therapy. However, the efficacy of these treatments is suboptimal, as they are prone to drug resistance, metastasis, spread, and recurrence. These attributes are closely related to cancer stem cells (CSCs). Therefore, the utilization of drugs targeting CSCs may effectively inhibit the development and recurrence of HCC. Methods:: HepG2 and Huh7 cells were used to analyze the antitumor activity of emodin by quantifying cell growth and metastasis, as well as to study its effect on stemness. Results:: Emodin effectively suppressed the growth and movement of HCC cells. Emodin also significantly inhibited the proliferation of CD44-positive hepatoma cells. Conclusion:: Emodin shows promise as a potential therapeutic agent for HCC by targeting CD44-- positive hepatoma cells.

Publisher

Bentham Science Publishers Ltd.

Subject

Cancer Research,Drug Discovery,Pharmacology,Oncology

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Cancer stem cells: advances in knowledge and implications for cancer therapy;Signal Transduction and Targeted Therapy;2024-07-05

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