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多糖通过S1PR1-STAT3信号通路对肺癌前转移微环境的抑制作用

Inhibitory Effect of Polysaccharide on Premetastatic Niche of Lung Cancer through the S1PR1-STAT3 Signaling Pathway.

作者信息

Shen Ming, Wang Yan-Jun, Liu Zhao-Hua, Chen Yan-Wen, Liang Qian-Kun, Li Yang, Ming Hai-Xia

机构信息

School of Basic Medicine, Gansu University of Chinese Medicine, Lanzhou, China.

Basic Discipline of Integrative Traditional Chinese and Western Medicine, Gansu University of Chinese Medicine, Lanzhou, China.

出版信息

Evid Based Complement Alternat Med. 2023 Jan 20;2023:4010797. doi: 10.1155/2023/4010797. eCollection 2023.

Abstract

As a common malignant tumor, the morbidity and mortality of lung cancer have been rising in recent years. The concept of "premetastatic niche" may lead to a revolutionary change in antitumor metastasis therapeutic strategies. Traditional Chinese medicine with multitargets and lower poisonous agents may be a potentially effective means to intervene in the "premetastatic niche (PMN)" to prevent and treat tumor metastasis. polysaccharide (APS) is a substance with strong immune activity in that has excellent biological activities such as immunomodulation, anti-inflammatory, and antitumor. In this study, we constructed a tumor lung metastasis animal model to explore the intervention mechanism of APS on the premetastatic niche. We found that APS inhibited the formation of the lung premetastatic niche and inhibited the recruitment of myeloid-derived suppressor cells (MDSCs) in the lung. Mechanistically, we showed that the proteins and gene expression of S1PR1, STAT3, and p-STAT3 in the S1PR1/STAT3 signaling pathway were suppressed by APS. In line with the above findings, our results confirmed that APS may inhibit the accumulation of MDSCs in the premetastatic niche through the intervention of the S1PR1-STAT3 signaling pathway to achieve the antitumor effect.

摘要

作为一种常见的恶性肿瘤,近年来肺癌的发病率和死亡率一直在上升。“前转移生态位”的概念可能会导致抗肿瘤转移治疗策略发生革命性变化。具有多靶点和低毒副作用的中药可能是干预“前转移生态位(PMN)”以预防和治疗肿瘤转移的一种潜在有效手段。黄芪多糖(APS)是黄芪中具有强大免疫活性的物质,具有免疫调节、抗炎和抗肿瘤等优异的生物学活性。在本研究中,我们构建了肿瘤肺转移动物模型,以探讨APS对前转移生态位的干预机制。我们发现APS抑制了肺前转移生态位的形成,并抑制了肺中髓源性抑制细胞(MDSCs)的募集。机制上,我们表明APS抑制了S1PR1/STAT3信号通路中S1PR1、STAT3和p-STAT3的蛋白和基因表达。与上述发现一致,我们的结果证实APS可能通过干预S1PR1-STAT3信号通路来抑制前转移生态位中MDSCs的积累,从而实现抗肿瘤作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94ff/9883101/2ae3ec8ee9f9/ECAM2023-4010797.001.jpg

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