Department of Chinese Medicine, China Medical University Hospital, Taichung 404, Taiwan.
School of Chinese Medicine, China Medical University, Taichung 404 Taiwan.
Int J Mol Sci. 2019 Aug 15;20(16):3978. doi: 10.3390/ijms20163978.
Hepatocellular carcinoma (HCC) is a primary malignancy of the liver. In basic studies, the regulation of autophagy has offered promising results for HCC treatment. This study aimed to address the question of whether amiodarone can improve survival rates in HCC patients associated with autophagy. Using datasets from the National Health Insurance Research Database, we enrolled patients over 18 years of age that had been diagnosed with HCC between January 1997 and December 2010. Amiodarone and non-amiodarone users were matched at a 1:1 frequency, according to all variables. Additionally, HepG2 cells treated with amiodarone were evaluated by cell viability and autophagic change. Autophagic signaling was examined by immunoblotting and tissue array immunohistochemistry. Of the 10,946 patients diagnosed with HCC, each cohort included 221 patients after 1:1 propensity score matching. The median survival was 36.70 months for the amiodarone users, and 24.48 months for the non-amiodarone users. After adjusting for age, gender, comorbidities and treatment, amiodarone users had a significantly lower risk of mortality. Amiodarone users also demonstrated an improved 3-year survival rate. Furthermore, amiodarone treatment-induced autophagy in HepG2 cells was demonstrated by autophagosome formation associated with increasing LC3B-II, P62, and Beclin-1 expression. Autophagic flux also increased following amiodarone treatment with bafilomycin A1. SiRNA of LC3B knocked down endogenous LC3B formation and restored HepG2 cell viability. This study provides epidemiologic evidence that amiodarone via autophagic degradation machinery may offer survival benefits for HCC patients with a history of arrhythmia. Further randomized, blinded, and placebo-controlled trials are warranted for patients with HCC.
肝细胞癌(HCC)是肝脏的原发性恶性肿瘤。在基础研究中,自噬的调节为 HCC 治疗提供了有希望的结果。本研究旨在探讨胺碘酮是否可以提高与自噬相关的 HCC 患者的生存率。我们使用国家健康保险研究数据库中的数据集,招募了 1997 年 1 月至 2010 年 12 月期间被诊断为 HCC 的年龄在 18 岁以上的患者。根据所有变量,将胺碘酮和非胺碘酮使用者以 1:1 的频率匹配。此外,通过细胞活力和自噬变化评估用胺碘酮处理的 HepG2 细胞。通过免疫印迹和组织阵列免疫组化检查自噬信号。在 10946 例被诊断为 HCC 的患者中,每个队列在 1:1 倾向评分匹配后包括 221 例患者。胺碘酮使用者的中位生存时间为 36.70 个月,而非胺碘酮使用者的中位生存时间为 24.48 个月。在调整年龄、性别、合并症和治疗后,胺碘酮使用者的死亡率显著降低。胺碘酮使用者的 3 年生存率也得到了提高。此外,胺碘酮治疗诱导 HepG2 细胞中的自噬,表现为自噬体形成,同时 LC3B-II、P62 和 Beclin-1 表达增加。在用巴弗洛霉素 A1 处理后,自噬通量也增加。LC3B 的 siRNA 敲低内源性 LC3B 的形成并恢复 HepG2 细胞活力。这项研究提供了流行病学证据,表明胺碘酮通过自噬降解机制可能为有心律失常史的 HCC 患者提供生存益处。需要进一步进行随机、盲法、安慰剂对照试验,以评估 HCC 患者。