Farhoudi Sefidan Jadid Mahdi, Jahangirzadehd Gholamreza, Behroozi Javad
Department of Biology, Faculty of Basic Sciences, University of Maragheh, Maragheh, Iran.
Department of Genetics, Tabriz Branch, Islamic Azad University, Tabriz, Iran.
Horm Mol Biol Clin Investig. 2022 Sep 5;44(1):27-32. doi: 10.1515/hmbci-2022-0036. eCollection 2023 Mar 1.
Despite remarkable development of new therapeutic strategies to improve survival rates and treatment of patients with cancer, there are still many limitations in management of patients with distant metastasis breast cancer. Therefore, the aim of this study was to investigate a novel method to enhance therapeutic efficacy of Apatinib (as a chemotherapeutic agent) by co-administration of Curcumin (as a bioactive herbal compound) in breast cancer treatment.
Effects of Apatinib, Curcumin, and their combinations (Apa-Cur) was evaluated on viability and proliferation of breast cell line (MCF7) by MTT assay. Moreover, effects of Apatinib, Curcumin, and Apa-Cur was investigated on apoptosis rate in the cancer cells. Expression levels of apoptosis-related genes (, , , and ) in treated cancer cells and untreated controls were evaluated using the Real-Time PCR method.
The obtained results showed that all treatments of Apatinib, Curcumin, and Apa-Cur significantly decreased viability and proliferation of the breast cancer cells in a concentration- and time-dependent manner. However, anti-proliferation activity of Apa-Cur combination was significantly higher than Apatinib and Curcumin treatment alone. In addition, Apatinib, Curcumin, and Apa-Cur increased apoptosis percentage in the treated cancer cells through regulation of apoptosis-related genes expression.
In general, Apa-Cur combination therapy exerts more profound anti-proliferation effects on breast cancer cell than Apatinib or Curcumin monotherapy. However, further studies are required to identify other possible signaling pathways and mechanisms involved in the anticancer effects of Apatinib, Curcumin, and Apa-Cur.
尽管在提高癌症患者生存率和治疗方面新的治疗策略有了显著发展,但远处转移乳腺癌患者的管理仍存在许多局限性。因此,本研究的目的是探讨一种新方法,即通过联合使用姜黄素(一种生物活性草药化合物)来增强阿帕替尼(一种化疗药物)在乳腺癌治疗中的疗效。
通过MTT法评估阿帕替尼、姜黄素及其组合(阿帕-姜黄素)对乳腺癌细胞系(MCF7)活力和增殖的影响。此外,研究了阿帕替尼、姜黄素和阿帕-姜黄素对癌细胞凋亡率的影响。使用实时PCR法评估处理过的癌细胞和未处理对照中凋亡相关基因(、、、和)的表达水平。
所得结果表明,阿帕替尼、姜黄素和阿帕-姜黄素的所有处理均以浓度和时间依赖性方式显著降低乳腺癌细胞的活力和增殖。然而,阿帕-姜黄素组合的抗增殖活性明显高于单独使用阿帕替尼和姜黄素治疗。此外,阿帕替尼、姜黄素和阿帕-姜黄素通过调节凋亡相关基因的表达增加了处理过的癌细胞中的凋亡百分比。
总体而言,阿帕-姜黄素联合疗法对乳腺癌细胞的抗增殖作用比阿帕替尼或姜黄素单一疗法更显著。然而,需要进一步研究以确定阿帕替尼、姜黄素和阿帕-姜黄素抗癌作用中涉及的其他可能信号通路和机制。