NÚÑez Jisette G, Pinheiro JordÂnia S, Padilha Gustavo L, Garcia Helana O, Porta VitÓria, Apel Miriam A, Bruno Alessandra N
Instituto Federal de Educação, Ciência e Tecnologia do Rio Grande do Sul, Campus Porto Alegre, Coronel Vicente, 281, Centro, 90030-041 Porto Alegre, RS, Brazil.
Faculdade de Farmácia da Universidade Federal do Rio Grande do Sul, Avenida Ipiranga, 2752, 90610-000 Santana, Porto Alegre, RS, Brazil.
An Acad Bras Cienc. 2020 Nov 6;92(suppl 2):e20191143. doi: 10.1590/0001-3765202020191143. eCollection 2020.
Breast and cervical cancer represent a major problem of women's global public health. Here, we investigated the chemical composition of essential oils from leaves and flowers of T. ostenii and the antineoplastic potential in a cervical cancer and breast cancer cell line, SiHa and MCF-7; and non-tumoral cells, HaCat. The chemical analysis revealed a predominance of oxygenated monoterpenes in both essential oils. The IC50 after 24 h of treatment was 72 ng/mL for EO 1 and 83 ng/mL for EO 2 in SiHa cells. For MCF-7 the IC50 was 174.3 ng/mL for EO 1. For HaCat cells it was 54.45 ng/mL for EO 1 and 20.83 ng/mL for EO 2. A synergistic effect with both essential oils and cisplatin was also verified. SiHa cells had their wound healing capacity reduced after 48 h of treatment with EO 2 and both essential oils were able to significantly inhibit the adhesion process and clonogenic ability after 24 h of treatment. Our results suggest a long-lasting inhibitory activity in SiHa cells because of the low recovery capacity of cells after treatment withdrawal. Flow cytometer with annexin V/propidium iodide demonstrated a majority cell death through late apoptosis after 24, 48 and 72 hours of treatment.
乳腺癌和宫颈癌是全球女性公共卫生领域的重大问题。在此,我们研究了峨眉香科科(Teucrium ostenii)叶和花中挥发油的化学成分,以及其对宫颈癌细胞系SiHa和乳腺癌细胞系MCF - 7,以及非肿瘤细胞HaCat的抗肿瘤潜力。化学分析表明,两种挥发油中均以氧化单萜类化合物为主。在SiHa细胞中,处理24小时后EO 1的IC50为72 ng/mL,EO 2的IC50为83 ng/mL。在MCF - 7细胞中,EO 1的IC50为174.3 ng/mL。在HaCat细胞中,EO 1的IC50为54.45 ng/mL,EO 2的IC50为20.83 ng/mL。还验证了两种挥发油与顺铂之间的协同作用。用EO 2处理48小时后,SiHa细胞的伤口愈合能力降低,两种挥发油在处理24小时后均能显著抑制细胞黏附过程和克隆形成能力。我们的结果表明,由于处理撤除后细胞恢复能力较低,SiHa细胞具有持久的抑制活性。用膜联蛋白V/碘化丙啶的流式细胞仪检测表明,处理24、48和72小时后,大多数细胞通过晚期凋亡死亡。