Magnesium Lithospermate B Inhibits Colorectal Cancer Cell Progression Through JAK2-STAT3 Signaling.

Dan Huo, Jinpeng Zhang, Tengfei Ma, Yemao Liu, Jianqing Zhang, Bizhen Dong, Yanjun Lu, Anding Wu, Zhaoxia Jin, Yuping Li
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Abstract

Colorectal cancer (CRC) is the third most commonly diagnosed cancer and the second leading cause of cancer death worldwide. The discovery of new effective therapeutic drugs is always a priority. Magnesium lithospermate B (MLB), a native polyphenol acid, is the major component of the aqueous extracts from Danshen, a traditional Chinese medicine derived from the dry root and rhizome of Salvia miltiorrhiza. MLB has been reported to have antioxidant, anti-inflammatory, and ion channel-regulating activities in several diseases, including cardiovascular, renal, and neuronal diseases. However, the effect of MLB on cancer progression has not been reported. In this study, a series of cellular and molecular experiments were conducted on two CRC cell lines (HCT116 and SW480) to investigate the effects of. The results demonstrated that MLB exerted inhibitory effects on cell proliferation, migration, and invasion. The administration of 50 mg/kg MLB inhibited tumor growth in HCT116 cells in xenografted models. Importantly, we found that MLB treatment inhibited the Janus kinase 2 (JAK2)-signal transducer and activator of transcription 3 (STAT3) signaling pathway, and activation of JAK2-STAT3 signaling with interleukin 6 or overexpression STAT3 significantly suppressed the inhibitory effect of MLB. These findings provide evidence that MLB could inhibit CRC cell progression in vitro and might serve as a potential therapeutic drug for the treatment of CRC.

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过磷酸钙 B 镁通过 JAK2-STAT3 信号转导抑制结直肠癌细胞进展
结直肠癌(CRC)是全球第三大最常诊断出的癌症,也是第二大癌症死亡原因。发现新的有效治疗药物一直是当务之急。石甘酸镁(MLB)是一种原生多酚酸,是丹参水提取物的主要成分,丹参是从丹参的干根和根茎中提取的一种传统中药。据报道,MLB 在多种疾病(包括心血管、肾脏和神经元疾病)中具有抗氧化、抗炎和离子通道调节活性。然而,MLB 对癌症进展的影响尚未见报道。本研究对两种 CRC 细胞系(HCT116 和 SW480)进行了一系列细胞和分子实验,以研究 MLB 的作用。结果表明,MLB 对细胞增殖、迁移和侵袭有抑制作用。在异种移植模型中,50 毫克/千克的 MLB 可抑制 HCT116 细胞的肿瘤生长。重要的是,我们发现 MLB 可抑制 Janus 激酶 2(JAK2)-信号转导子和转录激活子 3(STAT3)信号通路,而用白细胞介素 6 激活 JAK2-STAT3 信号通路或过表达 STAT3 可显著抑制 MLB 的抑制作用。这些研究结果为MLB在体外抑制CRC细胞进展提供了证据,可作为治疗CRC的潜在药物。
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