平消胶囊抑制癌症三阴性肺转移,提高癌症放疗敏感性。

Tang Wenjuan, H U Yu, Zhu Man, Dong Mingzhi, Liu Tieming, Sarwar Ammar, Zhan Yingzhuan, Zhang Yanmin
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引用次数: 0

摘要

目的:观察平消胶囊(PXC)对癌症的抗癌作用。流式细胞仪检测PXC对细胞凋亡的影响。通过室内实验研究了PXC对细胞迁移和侵袭的抑制作用。为了研究潜在的分子机制,通过Western印迹法和免疫组织化学法分析了乳腺癌症细胞中与上皮-间质转化(EMT)相关的蛋白质的表达。使用MDA-MB-231异种移植物模型和4T1转移性乳腺癌症模型评价PXC的抗癌效果。结果:三阴性癌症(TNBC)细胞系MDA-MB-231和MDA-MB-468对PXC敏感。PXC有效抑制MDA-MB-231和MDA-MB-468细胞的增殖、集落形成、迁移和侵袭。然后,MDA-MB-231异种移植物模型显示,与对照相比,PXC显著降低了肿瘤大小和重量。4T1肺转移模型显示PXC显著抑制小鼠乳腺癌症细胞向肺的扩散。从机制上讲,PXC通过降低TNBC中钙粘蛋白的周转来抑制EMT过程。PXC联合8Gy X射线治疗可明显促进细胞凋亡的诱导,抑制细胞增殖。结论:PXC可抑制TNBC的增殖和侵袭,并通过调节钙粘蛋白的转换发挥其抗转移作用,使TNBC细胞对放疗敏感。这些数据支持PXC作为TNBC辅助治疗剂的进一步发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pingxiao capsule inhibits lung metastasis of triple-negative breast cancer and sensitizes breast cancer to radiotherapy.

Objectives: To investigate the anticancer effect of Pingxiao capsule (, PXC) on the treatment of breast cancer and .

Methods: The inhibition of PXC on cell viability and proliferation was determined by cell counting kit-8, EdU assay and colony formation assay, respectively. The effect of PXC on cell apoptosis was detected by using flow cytometry. The suppression of PXC on cell migration and invasion was investigated by chamber assay. To investigate the underlying molecular mechanisms, the expression of proteins related to epithelial to mesenchymal transition (EMT) was analyzed by Western blotting in breast cancer cells and by immunohistochemistry in tumor tissues. The anticancer effect of PXC was evaluated by using MDA-MB-231 xenograft model and 4T1 metastatic breast cancer model.

Results: Our results indicated that triple-negative breast cancer (TNBC) cell lines MDA-MB-231 and MDA-MB-468 were sensitive to PXC. PXC potently inhibited the proliferation, colony formation, migration, and invasion of MDA-MB-231 and MDA-MB-468 cells . Then, MDA-MB-231 xenograft model depicted that PXC significantly reduced tumor size and weight compared with Control. 4T1 lung metastasis model showed that PXC significantly inhibited breast cancer cell spreading to lungs in mice. Mechanistically, PXC inhibited EMT process by reducing cadherin turnover in TNBC. Furthermore, PXC in combination with 8 Gy X-ray treatment obviously promoted the induction of apoptosis, and suppressed cell proliferation.

Conclusion: PXC could inhibit the proliferation and invasion of TNBC both and , and exerted its anti-metastatic effect by regulating cadherin turnover, Furthermore, it sensitized the TNBC cells to radiotherapy. The data supported further development of PXC as an adjuvant-therapy agent for TNBC.

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