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AR420626, a selective agonist of GPR41/FFA3, suppresses growth of hepatocellular carcinoma cells by inducing apoptosis via HDAC inhibition
Therapeutic Advances in Medical Oncology ( IF 4.9 ) Pub Date : 2020-03-20 , DOI: 10.1177/1758835920913432
Daisuke Mikami 1 , Mamiko Kobayashi 2 , Junsuke Uwada 3 , Takashi Yazawa 3 , Kazuko Kamiyama 2 , Kazuhisa Nishimori 2 , Yudai Nishikawa 2 , Sho Nishikawa 2 , Seiji Yokoi 2 , Takanobu Taniguchi 3 , Masayuki Iwano 2
Affiliation  

Hepatocellular carcinoma (HCC) is a common malignant cancer worldwide and the third leading cause of cancer death.1,2 Surgical resection followed by liver transplantation is a curative treatment for early stage HCC, but the tumor is prone to recurrence.3 Furthermore, the clinical symptoms of early stage HCC are frequently unclear, and diagnosis may be delayed until an advanced stage, resulting in a high mortality rate.4 Sorafenib, a multikinase inhibitor, is used as first-line treatment for patients with advanced-stage HCC, but may only provide a three-month survival benefit in comparison with a placebo.5 Thus, establishment of new chemotherapy is urgently needed, especially for patients with advanced HCC.

中文翻译:

AR420626 是 GPR41/FFA3 的选择性激动剂,通过抑制 HDAC 诱导细胞凋亡来抑制肝细胞癌细胞的生长

肝细胞癌(HCC)是世界范围内常见的恶性肿瘤,也是癌症死亡的第三大原因。1,2手术切除后肝移植是早期 HCC 的治愈性治疗方法,但肿瘤容易复发。3此外,早期 HCC 的临床症状往往不明确,诊断可能会延迟到晚期,导致高死亡率。4索拉非尼是一种多激酶抑制剂,被用作晚期 HCC 患者的一线治疗,但与安慰剂相比,可能仅能提供三个月的生存获益。5因此,迫切需要建立新的化疗方案,尤其是对于晚期 HCC 患者。
更新日期:2020-04-21
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