发酵对紫杉介质枝叶中成分和非小细胞肺癌的影响

IF 4.4 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Frontiers in Pharmacology Pub Date : 2024-10-23 eCollection Date: 2024-01-01 DOI:10.3389/fphar.2024.1449498
Xing Guo, Rui-Sheng Wang, Zhen-Ling Zhang, Hong-Wei Zhang, Sheng-Chao Wang, Shuai Zhang, Ya-Ning Wu, Ya-Jing Li, Jun Yuan
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引用次数: 0

摘要

导言非小细胞肺癌(NSCLC)是全球常见的肺癌疾病。目前,常用的方法,如手术和放疗,都有很大的副作用。中药因其安全有效的特点成为研究热点。紫杉介质的枝叶中含有丰富的抗肿瘤活性化合物,而有关其抗肺癌分子机制的研究尚未开展:本研究旨在探讨紫杉介质发酵前后两种样品的抗肿瘤活性,并研究其抑制 NSCLC 的分子机制:方法:采用UHPLC-Q-Qrbitrap HRMS和高效液相色谱法研究了发酵前T.培养基(TM)和发酵后T.培养基qu(TMQ)的化学成分。利用 A549 诱导的肿瘤小鼠模型比较了 TM 和 TMQ 的抗肺癌活性。通过酶联免疫吸附试验(ELISA)、苏木精和伊红(H&E)染色、免疫组织化学和免疫荧光来确定TMQ的作用机制:结果表明,TM 和 TMQ 含有 83 种化合物,主要包括黄酮类、有机酸和类黄酮。TMQ 中的类黄酮和黄烷含量均高于 TM。TM 和 TMQ 均能有效抑制非小细胞肺癌(NSCLC)的肿瘤生长,且 TMQ 的抑制率(57.24%)高于 TM(49.62%)。服用 TMQ 可降低肿瘤小鼠血清中肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)和谷胱甘肽(GSH)的水平,并上调干扰素-γ(IFN-γ)、活性氧(ROS)和丙二醛(MDA)的水平。TMQ 还能增加肿瘤组织中 Bax、Caspase-3 和 Beclin-1 的蛋白表达。相反,TMQ 则抑制了 bcl-2、PI3K、Ki67、ULK1 和 mTOR 蛋白水平。蛋白质检测分析再次强调了 TMQ 比 TM 更优越的抗肿瘤效果。这些累积的研究结果表明,TMQ 的作用机制与激活癌症通路中的转录失调密切相关,它抑制了胆碱能突触、AMPK 和 PI3K/Akt/mTOR 信号通路:本研究表明,发酵增加了 T. media 的有效成分含量和抗肿瘤作用。此外,发酵后的 TMQ 作为治疗 NSCLC 的草药优于 TM。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of fermentation on the constituents in the branches and leaves of Taxus media and non-small cell lung cancer.

Introduction: Non-small cell lung cancer (NSCLC) is a prominent lung cancer disease worldwide. Currently, commonly used methods, such as surgery and radiotherapy, have significant side effects. Traditional Chinese medicine (TCM) has become a research hotspot because of its safe and effective characteristics. The branches and leaves of Taxus media are abundant in antitumor active compounds, and there has been no research conducted as yet regarding its anti-lung cancer molecular mechanism.

Objective: The aim of this study is to investigate the antitumor activity of two samples before and after fermentation of T. media, and to research the molecular mechanism of its inhibitory effect on NSCLC.

Methods: The chemical composition of pre-fermentation T. media (TM) and post-fermentation T. media qu (TMQ) were investigated using UHPLC-Q-Qrbitrap HRMS and high-performance liquid chromatography (HPLC). The anti-lung cancer activities of TM and TMQ were compared using an A549-induced tumor mouse model. An enzyme-linked immunosorbent assay (ELISA), hematoxylin and eosin (H&E) staining, immunohistochemistry, and immunofluorescence were used to determine the of TMQ mechanism of action.

Results: The results indicated that TM and TMQ contained 83 compounds, consisting primarily of flavonoids, organic acids, and taxanes. Both taxanes and flavonoids in TMQ were higher than that in TM. Both TM and TMQ effectively inhibited the tumor growth in non-small cell lung cancer (NSCLC), and the inhibition rate was greater in TMQ (57.24%) than in TM (49.62%). TMQ administration downregulated the tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6), and the glutathione (GSH) level and upregulated interferon-γ (IFN-γ), reactive oxygen species (ROS), and malondialdehyde (MDA) levels in the serum of tumor mice. TMQ treatment also increased the protein expression of Bax, Caspase-3, and Beclin-1 in tumor tissues. In contrast, the bcl-2, PI3K, Ki67, ULK1, and mTOR protein levels were suppressed by TMQ. Protein assay analyses reemphasized the superior antitumor effect of TMQ over TM. These cumulative findings demonstrated that the mechanism of action of TMQ was closely related to the activation of transcriptional misregulation in the cancer pathway that inhibited the cholinergic synaptic, AMPK, and PI3K/Akt/mTOR signaling pathways.

Conclusion: This study demonstrated that fermentation increased the active ingredient contents and antitumor effects of T. media. In addition, post-fermentation TMQ was superior to TM as a herbal medicine for NSCLC treatment.

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来源期刊
Frontiers in Pharmacology
Frontiers in Pharmacology PHARMACOLOGY & PHARMACY-
CiteScore
7.80
自引率
8.90%
发文量
5163
审稿时长
14 weeks
期刊介绍: Frontiers in Pharmacology is a leading journal in its field, publishing rigorously peer-reviewed research across disciplines, including basic and clinical pharmacology, medicinal chemistry, pharmacy and toxicology. Field Chief Editor Heike Wulff at UC Davis is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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