Zia Atousa, Salehghamari Ensieh, Jalali Hanieh, Taher Maryam
Department of molecular medicine, Pavia University, Pavia, Italy.
Department of Cell and Molecular Biology, Faculty of Biology, Kosar University of Bojnord, Bojnord, Iran.
Microbiologyopen. 2025 Dec;14(6):e70095. doi: 10.1002/mbo3.70095.
Triple-negative breast cancer (TNBC) is an aggressive form of breast cancer characterized by the absence of estrogen and progesterone receptors and minimal HER2 expression, restricting the available treatment options. Actinobacteria have emerged as promising sources of anticancer compounds because of their remarkable ability to produce beneficial compounds. This study aimed to evaluate the antitumor effects of the halophilic Streptomyces violaceorubidus M4 extract on TNBC both in vitro and in vivo. The extracted compounds were analyzed by LC-MS. MTT and annexin-PI assays were used to assess the apoptosis-inducing effects of the compounds on MDA-MB-231 and MCF-10A cells. The expression of apoptosis-related BAX, BCL2, P53, CASPASE-8, and CASPASE-9 genes was analyzed using Real-time PCR. A TNBC mouse model was established using 4T1 cell transplantation, and the animals received the extract intravenously for 21 days. S. violaceorubidus M4 contained bioactive compounds, including amino acids, carboxylic acids, coumarins, isoflavones, phosphatidylcholine, tetrahydroxyanthraquinone, and flavonoids. The extract demonstrated selective cytotoxicity against MDA-MB-231 cells, with an IC50 of 48.04 μg/mL after 48 h, while the IC50 for MCF-10A cells was 132 μg/mL. The reduction in Cas-9 expression alongside the elevation of Cas-8 and P53 expression suggests the participation of the extrinsic pathway in the process of apoptosis. Histopathological evaluation of tumor tissues from mouse models showed that the extract injection reduced the number of mitotic cells, nuclear pleomorphism, and angiogenesis in tumor tissue. This study suggests that S. violaceorubidus M4 has a pronounced anticancer effect on TNBC and can be considered for the production of anticancer substances.
三阴性乳腺癌(TNBC)是一种侵袭性乳腺癌,其特征是缺乏雌激素和孕激素受体且HER2表达极少,这限制了可用的治疗选择。由于放线菌具有产生有益化合物的显著能力,已成为有前景的抗癌化合物来源。本研究旨在评估嗜盐链霉菌M4提取物对TNBC的体内外抗肿瘤作用。通过液相色谱 - 质谱联用仪(LC-MS)分析提取的化合物。采用MTT法和膜联蛋白 - PI法检测化合物对MDA-MB-231和MCF-10A细胞的凋亡诱导作用。使用实时聚合酶链反应(Real-time PCR)分析凋亡相关基因BAX、BCL2、P53、CASPASE-8和CASPASE-9的表达。利用4T1细胞移植建立TNBC小鼠模型,动物静脉注射提取物21天。嗜盐链霉菌M4含有生物活性化合物,包括氨基酸、羧酸、香豆素、异黄酮、磷脂酰胆碱、四羟基蒽醌和黄酮类化合物。提取物对MDA-MB-231细胞表现出选择性细胞毒性,48小时后的半数抑制浓度(IC50)为48.04μg/mL,而MCF-10A细胞的IC50为132μg/mL。Cas-9表达的降低以及Cas-8和P53表达的升高表明外源性途径参与了凋亡过程。对小鼠模型肿瘤组织的组织病理学评估表明,注射提取物减少了肿瘤组织中的有丝分裂细胞数量、核异型性和血管生成。本研究表明,嗜盐链霉菌M4对TNBC具有显著的抗癌作用,可考虑用于生产抗癌物质。