Suppr超能文献

小春花提取物通过抑制 NF-κB、COX-2 和细胞周期蛋白 D1 的表达来抑制口腔癌细胞的生长和增殖,并通过上调 P53 诱导细胞凋亡。

Operculina turpethum extract inhibits growth and proliferation by inhibiting NF-κB, COX-2 and cyclin D1 and induces apoptosis by up regulating P53 in oral cancer cells.

机构信息

Department of Biotechnology, All India Institute of Medical Sciences, Ansari Nagar, New Delhi 110 029, India.

Department of Biotechnology, All India Institute of Medical Sciences, Ansari Nagar, New Delhi 110 029, India.

出版信息

Arch Oral Biol. 2017 Aug;80:1-9. doi: 10.1016/j.archoralbio.2017.03.015. Epub 2017 Mar 20.

Abstract

OBJECTIVES

Herbal drugs are popularly emerging as complementary and alternative medicines in cancer patients because of their cost effectiveness and minimal side-effects. The extract of Operculina turpethum (OT) is known to have antipyretic, anti-inflammatory and purgative properties. Since it is popularly known have antiinflammatory activity, we investigated its anti-tumor activity on four oral squamous cell carcinoma cell lines (OSCC) namely, (SCC-4, KB, SCC-9 and SCC-25).

DESIGN

Antitumor activities of Operculina turpathum extract (OTE) was investigated by MTT and clonogenic assay, effect on cell cycle and apoptosis induction by Annexin-V/propidium iodide (PI) staining and flow cytometry and invasive potential of the tumor was determined by matrigel assay. The expression of various proteins involved in these mechanisms was analysed by western blotting.

RESULTS

OTE specifically inhibited the growth and colony formation of OSCC cells in a dose-dependent manner via inhibiting NF-κB and its downstream target COX-2. It further arrested cell cycle at G0/G1 phase by inhibiting cyclin-D1 and induced early apoptosis by up-regulating P53 in OSCC cells. It also limits the invasion capacity of OSCC cells by up to 55-60%.

CONCLUSIONS

OTE shows antitumor activities in OSCC cells by inhibiting NF-κB, COX-2 and cyclin D1 and upregulation of p53 expression. It may be developed as a safe and promising alternative chemopreventive/chemotherapeutic agent for oral cancer.

摘要

目的

由于草药具有成本效益高和副作用小的特点,因此在癌症患者中作为补充和替代药物越来越受欢迎。菱角提取物(OT)已被证明具有解热、抗炎和泻下作用。由于它被广泛认为具有抗炎活性,我们研究了它对四种口腔鳞状细胞癌细胞系(OSCC)的抗肿瘤活性,即(SCC-4、KB、SCC-9 和 SCC-25)。

设计

通过 MTT 和集落形成测定法研究菱角提取物(OTE)的抗肿瘤活性,通过 Annexin-V/碘化丙啶(PI)染色和流式细胞术研究其对细胞周期和凋亡诱导的影响,以及通过基质胶测定法测定肿瘤的侵袭潜力。通过 Western blot 分析分析参与这些机制的各种蛋白质的表达。

结果

OTE 通过抑制 NF-κB 和其下游靶标 COX-2 ,以剂量依赖的方式特异性抑制 OSCC 细胞的生长和集落形成。它通过抑制细胞周期蛋白 D1 将细胞周期进一步阻滞在 G0/G1 期,并通过上调 OSCC 细胞中的 P53 诱导早期凋亡。它还将 OSCC 细胞的侵袭能力限制在 55-60%。

结论

OTE 通过抑制 NF-κB、COX-2 和细胞周期蛋白 D1 以及上调 p53 表达来抑制 OSCC 细胞中的肿瘤生长。它可能被开发为一种安全且有前途的口腔癌化学预防/化疗替代药物。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验