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首页> 外文期刊>Integrative cancer therapies. >Xiao-Ai-Ping Injection Enhances Effect of Paclitaxel to Suppress Breast Cancer Proliferation and Metastasis via Activating Transcription Factor 3
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Xiao-Ai-Ping Injection Enhances Effect of Paclitaxel to Suppress Breast Cancer Proliferation and Metastasis via Activating Transcription Factor 3

机译:萧艾Ping注射增强了紫杉醇抑制乳腺癌增殖和转移通过激活转录因子3的作用

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Chemotherapy is an effective treatment for invasive breast cancer. Paradoxically, many recently published findings showed that the first-line chemotherapeutic agent paclitaxel (PTX) showed pro-metastatic effects in the progress of treating breast cancer. Xiao-Ai-Ping (XAP) injection, composed of a traditional herbal medicine, Marsdenia tenacissimae extract, is known to exert antitumor effects on various cancers. However, there are few experimental studies on breast cancer. The underlying mechanism of the antitumor effect of XAP combined with chemotherapy agents has not been fully understood. In the present study, we sought to find the antitumor effects of XAP combined with PTX in vitro and in vivo. The data demonstrated that the combination of XAP with PTX resulted in remarkable enhancement of the pro-apoptotic, migration-inhibiting, and anti-invasive effects of PTX in vitro. Significantly, further study showed the overexpression of ATF3 in PTX-treated cell, while XAP counteracted the change of ATF3 induced by PTX. Moreover, it showed that combination treatment could promote the inhibition of tumor growth in MDA-MB-231 cell xenograft mouse model. Compared with PTX treatment, the downregulation of ATF3 indicated that ATF3 played a pivotal role in the combination of XAP with PTX to exert a synergistic effect. Overall, it is expected that PTX combined with XAP may serve as an effective agent for antitumor treatment, and dampening ATF3 maybe a potential strategy to improve the efficacy of PTX.
机译:化疗是侵袭性乳腺癌的有效治疗方法。矛盾的是,许多最近公布的发现表明,一线化学治疗剂紫杉醇(PTX)显示出在治疗乳腺癌过程中的促型转移效应。众所周知,由传统的草药,由传统的草药组成,Xiao-Ai-ping(XAP)注射,Marsdenia Tenacissimae提取物施加对各种癌症的抗肿瘤作用。然而,乳腺癌少数实验研究。 Xap抗肿瘤效应与化疗剂结合的抗肿瘤作用的潜在机制尚未得到完全理解。在本研究中,我们试图在体外和体内发现XAP与PTX结合的抗肿瘤作用。数据表明,具有PTX的XAP的组合导致PTX体外促凋亡,迁移抑制和抗侵入作用显着提高。值得注意的是,进一步的研究表明,在PTX处理细胞中的ATF3过表达,而XAP抵消了PTX诱导的ATF3的变化。此外,它表明组合治疗可以促进MDA-MB-231细胞异种移植小鼠模型中肿瘤生长的抑制。与PTX治疗相比,ATF3的下调表明ATF3在XAP的组合中发挥了枢轴作用,具有PTX施加协同效应。总的来说,预计PTX与XAP结合可以作为抗肿瘤治疗的有效试剂,并且抑制ATF3可能是提高PTX功效的潜在策略。

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