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评估 SIRT2 抑制剂 AGK2 与紫杉醇在不同乳腺癌细胞分子亚型中的相互作用。

Assessment of Pharmacological Interactions between SIRT2 Inhibitor AGK2 and Paclitaxel in Different Molecular Subtypes of Breast Cancer Cells.

机构信息

Department of Biochemistry and Molecular Biology, Medical University of Lublin, 20-093 Lublin, Poland.

Department of Pathophysiology, Medical University of Lublin, 20-090 Lublin, Poland.

出版信息

Cells. 2022 Apr 4;11(7):1211. doi: 10.3390/cells11071211.

Abstract

Breast carcinoma (BC) is the most commonly diagnosed type of cancer in women in the world. Although the advances in the treatment of BC patients are significant, numerous side effects, severe toxicity towards normal cells as well as the multidrug resistance (MDR) phenomenon restrict the effectiveness of the therapies used. Therefore, new active compounds which decrease the MDR, extend disease-free survival, thereby ameliorating the effectiveness of the current treatment regimens, are greatly needed. Histone deacetylase inhibitors (HDIs), including sirtuin inhibitors (SIRTi), are the epigenetic antitumor agents which induce a cytotoxic effect in different types of cancer cells, including BC cells. Currently, combined forms of therapy with two or even more chemotherapeutics are promising antineoplastic tools to obtain a better response to therapy and limit adverse effects. Thus, on the one hand, much more effective chemotherapeutics, e.g., sirtuin inhibitors (SIRTi), are in demand; on the other hand, combinations of accepted cytostatics are trialed. Thus, the aim of our research was to examine the combination effects of a renowned cytotoxic drug paclitaxel (PAX) and SIRT2 inhibitor AGK2 on the proliferation and viability of the T47D, MCF7, MDA-MB-231, MDA-MB-468, BT-549 and HCC1937 BC cells. Moreover, cell cycle arrest and apoptosis induction were explored. The type of pharmacological interactions between AGK2 and PAX in different molecular subtypes of BC cells was assessed using the advanced isobolographic method. Our findings demonstrated that the tested active agents singly inhibited viability and proliferation of BC cells as well as induced cell cycle arrest and apoptosis in the cell-dependent context. Additionally, AGK2 increased the antitumor effect of PAX in most BC cell lines. We observed that, depending on the BC cell lines, the combinations of tested drugs showed synergistic, additive or antagonistic pharmacological interaction. In conclusion, our studies demonstrated that the consolidated therapy with the use of AGK2 and PAX can be considered as a potential therapeutic regimen in the personalized cure of BC patients in the future.

摘要

乳腺癌(BC)是全球女性最常见的癌症类型。尽管 BC 患者的治疗进展显著,但许多副作用、对正常细胞的严重毒性以及多药耐药(MDR)现象限制了所使用疗法的有效性。因此,迫切需要新的活性化合物来降低 MDR、延长无病生存期,从而改善当前治疗方案的效果。组蛋白去乙酰化酶抑制剂(HDIs),包括沉默调节蛋白抑制剂(SIRTi),是一种表观遗传抗肿瘤药物,可在包括 BC 细胞在内的不同类型的癌细胞中诱导细胞毒性作用。目前,两种甚至更多化疗药物联合治疗是有前途的抗肿瘤工具,可以提高对治疗的反应并限制不良反应。因此,一方面需要更有效的化疗药物,例如沉默调节蛋白抑制剂(SIRTi);另一方面,正在尝试接受的细胞抑制剂的组合。因此,我们的研究目的是研究著名细胞毒性药物紫杉醇(PAX)和 SIRT2 抑制剂 AGK2 对 T47D、MCF7、MDA-MB-231、MDA-MB-468、BT-549 和 HCC1937 BC 细胞增殖和活力的联合作用。此外,还研究了细胞周期停滞和凋亡诱导。使用先进的等效应线图法评估了 AGK2 和 PAX 在不同分子亚型的 BC 细胞中的药理相互作用类型。我们的研究结果表明,测试的活性物质单独抑制 BC 细胞的活力和增殖,并在细胞依赖性背景下诱导细胞周期停滞和凋亡。此外,AGK2 增加了 PAX 在大多数 BC 细胞系中的抗肿瘤作用。我们观察到,根据 BC 细胞系的不同,测试药物的组合表现出协同、相加或拮抗的药理相互作用。总之,我们的研究表明,使用 AGK2 和 PAX 联合治疗可以被认为是未来 BC 患者个体化治疗的潜在治疗方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d28/8998062/d7e46db80187/cells-11-01211-g001.jpg

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