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硫化砷通过抑制小鼠中TLCD1的表达来缓解肝癌恶性进展。

Arsenic sulfide alleviates the progression of liver cancer malignancy by inhibiting the expression of TLCD1 in mice.

作者信息

Li Xianglu, Xing Xuehua, Wang Lin, Li Shizong

机构信息

Medical Oncology, Hainan General Hospital, Hainan Affiliated Hospital of Hainan Medical University, Haikou, Hainan Province, 570311, China.

Department of Hepatobiliary and Pancreatic Surgery, Hainan General Hospital, Hainan Affiliated Hospital of Hainan Medical University, Haikou, Hainan Province, 570311, China.

出版信息

BMC Med Genomics. 2025 Aug 9;18(1):128. doi: 10.1186/s12920-025-02195-4.

Abstract

Liver cancer is the leading cause of cancer deaths worldwide and is the only cancer type among the five deadliest cancers with an increasing incidence each year. The prognosis of liver cancer is poor and no effective treatment for this cancer to date. Arsenic sulfide has been found to be effective in the treatment of hematological malignancies but its therapeutic outcomes and associated mechanisms in liver cancer remain unknown. In this study, we found that arsenic sulfide treatment could effectively inhibit the proliferation, migration and promotion of apoptosis of hepatoma cell lines, and remarkably alleviated the progression of hepatocellular carcinoma in mouse models. Transcriptomic analysis of the HepG2 cell line treated with arsenic sulfide showed that arsenic sulfide inhibited the proliferation of hepatoma cells by inhibiting the expression of Triacylglycerol and Lipid Catabolism Deficient 1 (TLCD1), thereby alleviating the malignant progression of hepatocellular carcinoma. This study provides a molecular basis for arsenic sulfide in the treatment of liver cancer.

摘要

肝癌是全球癌症死亡的主要原因,并且是五种最致命癌症中唯一一种发病率逐年上升的癌症类型。肝癌的预后很差,迄今为止尚无针对这种癌症的有效治疗方法。已发现硫化砷在治疗血液系统恶性肿瘤方面有效,但其在肝癌中的治疗效果及相关机制仍不清楚。在本研究中,我们发现硫化砷处理可有效抑制肝癌细胞系的增殖、迁移并促进其凋亡,并且显著缓解小鼠模型中肝细胞癌的进展。对经硫化砷处理的HepG2细胞系进行转录组分析表明,硫化砷通过抑制三酰甘油和脂质分解缺陷1(TLCD1)的表达来抑制肝癌细胞的增殖,从而缓解肝细胞癌的恶性进展。本研究为硫化砷治疗肝癌提供了分子基础。

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