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A novel PPARɣ ligand, PPZ023, overcomes radioresistance via ER stress and cell death in human non-small-cell lung cancer cells.新型过氧化物酶体增殖物激活受体γ配体 PPZ023 通过内质网应激和细胞死亡克服人非小细胞肺癌细胞的放射抵抗性。
Exp Mol Med. 2020 Oct;52(10):1730-1743. doi: 10.1038/s12276-020-00511-9. Epub 2020 Oct 12.
4
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中药西黄丸通过改变多条信号通路对同基因模型中的 Lewis 肺癌产生的抑制作用与细胞毒性化疗相当。

Traditional Chinese Medicine Xihuang Wan Inhibited Lewis Lung Carcinoma in a Syngeneic Model, Equivalent to Cytotoxic Chemotherapy, by Altering Multiple Signaling Pathways.

机构信息

Graduate School, Beijing University of Chinese Medicine, Beijing, P.R. China.

Department of Oncology, Dongfang Hospital, Beijing University of Chinese Medicine, Beijing, P.R. China.

出版信息

In Vivo. 2021 Jul-Aug;35(4):2005-2014. doi: 10.21873/invivo.12469.

DOI:10.21873/invivo.12469
PMID:34182475
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8286502/
Abstract

BACKGROUND/AIM: Xihuang Wan (XHW), a traditional Chinese medicine (TCM), has been used in China for a variety of cancers including lung cancer. The present study evaluated the efficacy of XHW on a Lewis lung mouse model and explored the potential mechanism via transcriptomics.

MATERIALS AND METHODS

The mice were randomized into 6 groups: 1) untreated control (n=10); 2) low-dose XHW; 3) medium-dose XHW; 4) high-dose XHW; 5) cisplatin; and 6) untreated blank (n=4). Lewis lung carcinoma (LLC) cells were injected subcutaneously except for the 4 mice in the blank group. The body weight and tumor length and width were measured every 3 days. RNA-sequencing was performed on tumors in the high-dose XHW group and the control group.

RESULTS

XHW inhibited the growth of LLC in a syngeneic mouse model, without toxicity, with equivalent efficacy to cisplatin. RNA-sequencing demonstrated that many signaling pathways were involved in XHW-mediated inhibition of LLC, including tumor necrosis factor, estrogen, cyclic guanosine 3', 5'-monophosphate-protein kinase G, apelin and the peroxisome proliferator-activated receptor signaling pathways.

CONCLUSION

XHW inhibited LLC carcinoma through different pathways and shows clinical promise for patients who cannot tolerate platinum-based drugs.

摘要

背景/目的:西黄丸(XHW)是一种中药,已在中国用于多种癌症,包括肺癌。本研究通过转录组学评估了 XHW 对 Lewis 肺癌小鼠模型的疗效,并探讨了其潜在机制。

材料和方法

将小鼠随机分为 6 组:1)未治疗对照组(n=10);2)低剂量 XHW 组;3)中剂量 XHW 组;4)高剂量 XHW 组;5)顺铂组;6)未治疗空白组(n=4)。除空白组的 4 只小鼠外,所有小鼠均皮下注射 Lewis 肺癌细胞。每 3 天测量一次体重和肿瘤的长、宽。对高剂量 XHW 组和对照组的肿瘤进行 RNA 测序。

结果

XHW 在同基因小鼠模型中抑制 LLC 的生长,无毒性,与顺铂等效。RNA 测序表明,XHW 抑制 LLC 涉及多种信号通路,包括肿瘤坏死因子、雌激素、环鸟苷酸 3',5'-单磷酸-蛋白激酶 G、apelin 和过氧化物酶体增殖物激活受体信号通路。

结论

XHW 通过不同途径抑制 LLC 癌,为不能耐受铂类药物的患者提供了临床应用前景。