College of Chemistry and Environmental Engineering, Sichuan University of Science and Engineering, Zigong 643000, China.
Department of Medicinal Chemistry, School of Pharmacy, Third Military Medical University, Chongqing 40038, China.
Bioorg Med Chem Lett. 2021 Jun 1;41:127997. doi: 10.1016/j.bmcl.2021.127997. Epub 2021 Mar 26.
Resistance phenomena during chemotherapy of tumor has been severely hampering the applications of chemotherapeutics. Due to advantage of drug repurposing, discovery of new chemosensitizers based on approved drugs is an effect strategy to find new candidates. Herein, we found antidepressant drug - sertraline, could sensitize drug-resistant gastric cancer cell (SGC-7901/DDP) with the IC value of 18.73 μM. To understand the structure-activity relationship and improve the activity, 30 derivatives were synthesized and evaluated. The IC value of the best compound was improved to 5.2 μM. Moreover, we found apoptosis induction and cell cycle arrest was the reason for the cell death of the drug-resistant cells after treatment of sertraline and derivatives, and PI3K/Akt/mTOR pathway was involved.
肿瘤化疗过程中的耐药现象严重阻碍了化疗药物的应用。由于药物再利用的优势,基于已批准药物发现新的化疗增敏剂是寻找新候选药物的有效策略。在此,我们发现抗抑郁药 - 舍曲林能够以 18.73 μM 的 IC 值敏化耐药胃癌细胞(SGC-7901/DDP)。为了了解构效关系并提高活性,合成并评价了 30 个衍生物。最佳化合物的 IC 值提高到 5.2 μM。此外,我们发现舍曲林及其衍生物处理耐药细胞后诱导细胞凋亡和细胞周期停滞是耐药细胞死亡的原因,涉及 PI3K/Akt/mTOR 通路。