Hou Yuhang, Hao Hongyun, Yuan Yan, Zhang Jing, Liu Zhengrui, Nie Yimin, Zhang Shichang, Yuan Shengtao, Yang Mei
New Drug Screening and Pharmacodynamics Evaluation Center, National Key Laboratory for Multi-Target Natural Drugs, China Pharmaceutical University, Nanjing 210000, China.
Key Laboratory of Straw Comprehensive Utilization and Black Soil Conservation, Ministry of Education, College of Life Sciences, Jilin Agricultural University, Changchun 130118, China.
Pharmaceuticals (Basel). 2024 Sep 26;17(10):1269. doi: 10.3390/ph17101269.
(1) Background: Nifuratel (NF113), derived from nitrofuran, has a specific anti-tumor effect. However, the potential mechanisms of NF113 in triple-negative breast cancer remain unknown. (2) Methods: In the study, CCK8 assay and colony formation assays were used to evaluate the inhibition effect of NF113 on cell proliferation. Apoptosis and cell cycle distribution were tested by flow cytometry. The mechanism of NF113's anti-tumor effect was predicted by transcriptome sequencing and verified by using PCR and Western blot experiments. Breast cancer organoids constructed from the patient-derived tumor xenograft model and the MDA-MB-468 xenograft mouse model were established to evaluate the effect of NF113. (3) Results: Our study showed that NF113 had an anti-tumor effect on triple-negative breast cancer both in vitro and in vivo. NF113 also induced apoptosis and G2/M phase arrest in triple-negative breast cancer cells. Our experimental data further verified that NF113 reduced GADD5A mRNA and protein expression, which were significantly upregulated in breast cancer, with downstream CDC25C and AKT phosphorylation changes. (4) Conclusions: Our data provided compelling evidence that NF113 inhibited breast cancer growth via upregulating GADD45A. Conclusion: NF113 was able to exert inhibitory effects on the proliferation of triple-negative breast cancer in vivo and in vitro, which may induce G2/M phase arrest via the GADD45A/CyclinB/CDK1 pathway and apoptosis via GADD45A/JNK/P38.
(1) 背景:硝呋太尔(NF113)源自硝基呋喃,具有特定的抗肿瘤作用。然而,NF113在三阴性乳腺癌中的潜在机制仍不清楚。(2) 方法:在本研究中,采用CCK8法和集落形成试验评估NF113对细胞增殖的抑制作用。通过流式细胞术检测细胞凋亡和细胞周期分布。通过转录组测序预测NF113抗肿瘤作用的机制,并通过PCR和蛋白质印迹实验进行验证。建立了由患者来源的肿瘤异种移植模型构建的乳腺癌类器官和MDA-MB-468异种移植小鼠模型,以评估NF113的作用。(3) 结果:我们的研究表明,NF113在体外和体内对三阴性乳腺癌均具有抗肿瘤作用。NF113还诱导三阴性乳腺癌细胞凋亡和G2/M期阻滞。我们的实验数据进一步证实,NF113降低了在乳腺癌中显著上调的GADD5A mRNA和蛋白表达,并伴有下游CDC25C和AKT磷酸化的变化。(4) 结论:我们的数据提供了令人信服的证据,表明NF113通过上调GADD45A抑制乳腺癌生长。结论:NF113能够在体内和体外对三阴性乳腺癌的增殖发挥抑制作用,其可能通过GADD45A/CyclinB/CDK1途径诱导G2/M期阻滞,并通过GADD45A/JNK/P38诱导凋亡。