Albahri Ghosoon, Badran Adnan, Hellany Heba, Baydoun Serine, Abdallah Rola, Alame Mohamad, Hijazi Akram, Maresca Marc, Baydoun Elias
Doctoral School of Science and Technology-Platform of Research and Analysis in Environmental Sciences (EDST-PRASE), Beirut 1107, Lebanon.
Department of Biology, Faculty of Arts and Sciences, American University of Beirut, Riad El Solh, Beirut 1107, Lebanon.
Int J Mol Sci. 2025 Sep 1;26(17):8506. doi: 10.3390/ijms26178506.
Breast cancer is a common and chronic condition, and despite improvements in diagnosis, treatment, and prevention, the number of cases of breast cancer is rising annually. New therapeutic drugs that target specific checkpoints should be created to fight breast cancer. possesses substantial cultural value as a herb and is regarded as one of the most significant medicinal plants; however, little is known about its anticancerous biological activity and chemopreventive molecular pathways against the triple-negative breast cancer (MDA-MB-231) cell line. In this study, the antioxidant, anticancer, and underlying molecular mechanisms of the ethanolic leaves extract (MAE) were evaluated, and its phytochemical composition was determined. Results indicated that MAE diminished the viability of MDA-MB-231 cells in a concentration- and time-dependent manner. Although MAE exhibited 55% radical scavenging activity at higher concentrations in the 2,2-diphenyl-1-picrylhydrazyl (DPPH) assay, the attenuation of its cytotoxic effects in MDA-MB-231 cells with N-acetylcysteine (NAC) co-treatment suggests a potential role of oxidative stress. Additionally, MAE caused an increase in the tumor suppressor p53. Moreover, this extract caused a significant decrease in the expression of Ki-67 (a cellular proliferation marker), MMP-9 (matrix metalloproteinase-9, an enzyme involved in extracellular matrix degradation and metastasis), and STAT-3 (a transcription factor regulating cell growth and survival). Also, MAE altered cell cycle, cell migration, angiogenesis, invasion, aggregation, and adhesion to suppress cellular processes linked to metastasis. All of our research points to MAE's potential to function as an anticancer agent and opens up new possibilities for the development of innovative triple-negative breast cancer treatments.
乳腺癌是一种常见的慢性疾病,尽管在诊断、治疗和预防方面有所改善,但乳腺癌病例数仍在逐年上升。应研发针对特定检查点的新型治疗药物来对抗乳腺癌。作为一种草药,它具有重要的文化价值,被视为最重要的药用植物之一;然而,关于其对三阴性乳腺癌(MDA-MB-231)细胞系的抗癌生物活性和化学预防分子途径却知之甚少。在本研究中,评估了乙醇叶提取物(MAE)的抗氧化、抗癌及潜在分子机制,并确定了其植物化学成分。结果表明,MAE以浓度和时间依赖性方式降低了MDA-MB-231细胞的活力。尽管在2,2-二苯基-1-苦基肼(DPPH)试验中,MAE在较高浓度下表现出55%的自由基清除活性,但N-乙酰半胱氨酸(NAC)共处理减弱其对MDA-MB-231细胞的细胞毒性作用,提示氧化应激可能发挥了作用。此外,MAE使肿瘤抑制因子p53增加。而且,该提取物使细胞增殖标志物Ki-67、基质金属蛋白酶-9(参与细胞外基质降解和转移的一种酶)和信号转导与转录激活因子-3(一种调节细胞生长和存活的转录因子)的表达显著降低。此外,MAE改变细胞周期、细胞迁移、血管生成、侵袭、聚集和黏附,以抑制与转移相关的细胞过程。我们所有的研究都表明MAE有潜力作为一种抗癌剂发挥作用,并为开发创新的三阴性乳腺癌治疗方法开辟了新的可能性。