Yao Wanxin, Liu Chen, Zhang Ningyin, Zhang Yanmei, Qian Yong
Affiliated Yongkang First People's Hospital and School of Pharmacy, Hangzhou Medical College, Hangzhou, Zhejiang 310014, P.R. China.
School of Laboratory Medicine and Bioengineering, Hangzhou Medical College, Hangzhou, Zhejiang 310013, P.R. China.
Oncol Lett. 2024 Jul 30;28(4):466. doi: 10.3892/ol.2024.14599. eCollection 2024 Oct.
Atractyloside is a traditional Chinese medicine used to treat nasal congestion, and allergic rhinitis; however, its effects on cancer are unknown. Non-small cell lung cancer (NSCLC) is associated with high mortality rates worldwide, and relapse due to epidermal growth factor receptor mutations is a problem in clinical therapy. Therefore, novel biomarkers are required for the diagnosis and treatment of NSCLC. Brother of the regulator of imprinted sites (; also known as ) is a potential therapeutic target in NSCLC. promotes cisplatin resistance and it has been suggested that it may account for multidrug resistance. The present study examined expression in tyrosine kinase inhibitor (TKI)-resistant NSCLC cells. Subsequently, small interfering RNA was used to knock down expression, and the effects of this knockdown were assessed on TKI-resistant NSCLC cell viability. The present study also investigated the effect of atractyloside on the proliferation of NSCLC cells using MTT assay. The results of the present study indicated that the inhibition of BORIS or its related downstream pathways may have potential for the treatment of TKI-resistant NSCLC. In addition, atractyloside mimicked knockdown, regulated its downstream genes and inhibited the proliferation of TKI-resistant NSCLC cells. In conclusion, the findings of the present study supported the potential application of atractyloside in TKI-resistant NSCLC therapy.
白术内酯是一种用于治疗鼻塞和过敏性鼻炎的传统中药;然而,其对癌症的影响尚不清楚。非小细胞肺癌(NSCLC)在全球范围内具有较高的死亡率,并且由于表皮生长因子受体突变导致的复发是临床治疗中的一个问题。因此,NSCLC的诊断和治疗需要新的生物标志物。印记位点调控因子的兄弟(;也称为 )是NSCLC中的一个潜在治疗靶点。 促进顺铂耐药性,有人认为它可能是多药耐药的原因。本研究检测了酪氨酸激酶抑制剂(TKI)耐药的NSCLC细胞中 的表达。随后,使用小干扰RNA敲低 表达,并评估这种敲低对TKI耐药的NSCLC细胞活力的影响。本研究还使用MTT法研究了白术内酯对NSCLC细胞增殖的影响。本研究结果表明,抑制BORIS或其相关下游途径可能对TKI耐药的NSCLC治疗具有潜力。此外,白术内酯模拟 敲低,调节其下游基因并抑制TKI耐药的NSCLC细胞的增殖。总之,本研究结果支持白术内酯在TKI耐药的NSCLC治疗中的潜在应用。