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隐丹参酮通过抑制转酮醇酶增强吉非替尼对非小细胞肺癌的作用。

Cryptotanshinone strengthens the effect of gefitinib against non-small cell lung cancer through inhibiting transketolase.

机构信息

School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, China.

St George and Sutherland Clinical School, Faculty of Medicine, UNSW, Sydney, Australia.

出版信息

Eur J Pharmacol. 2021 Jan 5;890:173647. doi: 10.1016/j.ejphar.2020.173647. Epub 2020 Oct 10.

Abstract

Lung cancer is the leading cause of cancer-related mortality and causes more than a million deaths per year. Gefitinib is the first-line agent of advanced lung cancer, however, resistance to gefitinib becomes a major problem in clinical application. Transketolase (TKT) is a key enzyme functioning between the oxidative arm and the non-oxidative arm of the pentose phosphate pathway. In this study, we firstly found that the expression of TKT was remarkably up-regulated in NSCLC cells, while the knockdown of TKT could inhibit cell proliferation and enhance the effect of gefitinib on NSCLC cells, which indicated the role of TKT in treating advanced lung cancer. Cryptotanshinone (CTS) is a natural active compound possessing anti-cancer effect. Here we demonstrated that CTS could strengthen the effect of gefitinib on NSCLC cells via inhibition of TKT in vitro and in vivo. Moreover, Nrf2 was involved in the repression of CTS on TKT expression. Collectively, these findings indicated the role of TKT in lung cancer progression and may provide novel therapeutic strategies to overcome resistance to gefitinib. Furthermore, CTS may serve as a new candidate in adjuvant treatment of advanced lung cancer.

摘要

肺癌是癌症相关死亡的主要原因,每年导致超过 100 万人死亡。吉非替尼是晚期肺癌的一线药物,然而,吉非替尼耐药性成为临床应用中的一个主要问题。转酮醇酶(TKT)是戊糖磷酸途径氧化臂和非氧化臂之间的关键酶。在这项研究中,我们首先发现 TKT 在非小细胞肺癌(NSCLC)细胞中的表达显著上调,而 TKT 的敲低可抑制细胞增殖并增强吉非替尼对 NSCLC 细胞的作用,这表明 TKT 在治疗晚期肺癌中的作用。隐丹参酮(CTS)是一种具有抗癌作用的天然活性化合物。我们在体外和体内证明 CTS 通过抑制 TKT 可增强吉非替尼对 NSCLC 细胞的作用。此外,Nrf2 参与了 CTS 对 TKT 表达的抑制。综上所述,这些发现表明 TKT 在肺癌进展中的作用,并可能为克服吉非替尼耐药性提供新的治疗策略。此外,CTS 可能成为辅助治疗晚期肺癌的新候选药物。

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