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夏枯草 D. 唐通过调节 PI3K/AKT 通路抑制结直肠癌细胞对 5-氟尿嘧啶的耐药性。

Scutellaria barbata D. Don inhibits 5-fluorouracil resistance in colorectal cancer by regulating PI3K/AKT pathway.

机构信息

Academy of Integrative Medicine Biomedical Research Center, Fujian University of Traditional Chinese Medicine, Fuzhou, Fujian 350122, P.R. China.

出版信息

Oncol Rep. 2017 Oct;38(4):2293-2300. doi: 10.3892/or.2017.5892. Epub 2017 Aug 9.

Abstract

5-Fluorouracil (5-FU) resistance or multidrug resistance (MDR) has become a major obstacle in clinical treatment of cancers including colorectal cancer (CRC). Aberrant activation of phosphatidylinositol 3 kinase (PI3K)/protein kinase B (AKT) pathway may lead to unlimited growth and chemoresistance in CRC cells, which thus could be a promising therapeutic target. As a long-term used traditional Chinese folk-medicine, Scutellaria barbata D. Don (SB) processes specific anticancer activity, but its activity against cancer chemoresistance is less known. Therefore, using a 5-FU-resistant CRC cell line HCT-8/5-FU, in this study we evaluated the therapeutic efficacy of the ethanol extracts of SB (EESB) against 5-FU resistance and explored the possible molecular mechanisms. We found that EESB significantly suppressed proliferation and promoted apoptosis in HCT-8/5-FU cells. Additionally, EESB displayed remarkable effect enhancing the retention of the ATP-binding cassette (ABC) transporter substrate, rhodamine‑123 (Rh‑123) in HCT-8/5-FU cells. Furthermore, EESB obviously downregulated the expression of cyclin D1, Bcl-2 and ABCG2, while upregulated p21 and Bax expression. Moreover, EESB showed a prominent suppressive effect on the activation of PI3K/AKT pathway. The findings suggested that Scutellaria barbata D. Don was able to inhibit chemoresistance in colorectal cancer by suppression of the PI3K/AKT pathway.

摘要

5-氟尿嘧啶(5-FU)耐药或多药耐药(MDR)已成为包括结直肠癌(CRC)在内的癌症临床治疗的主要障碍。磷脂酰肌醇 3 激酶(PI3K)/蛋白激酶 B(AKT)通路的异常激活可能导致 CRC 细胞的无限生长和化疗耐药,因此可能成为有前途的治疗靶点。作为一种长期使用的传统中药,半枝莲(SB)具有特定的抗癌活性,但对癌症耐药性的活性知之甚少。因此,本研究使用 5-FU 耐药 CRC 细胞系 HCT-8/5-FU 评估了 SB 乙醇提取物(EESB)对 5-FU 耐药的治疗效果,并探讨了可能的分子机制。我们发现 EESB 可显著抑制 HCT-8/5-FU 细胞的增殖并促进其凋亡。此外,EESB 显示出显著增强 ATP 结合盒(ABC)转运体底物罗丹明 123(Rh-123)在 HCT-8/5-FU 细胞中保留的作用。此外,EESB 明显下调了细胞周期蛋白 D1、Bcl-2 和 ABCG2 的表达,同时上调了 p21 和 Bax 的表达。此外,EESB 对 PI3K/AKT 通路的激活显示出显著的抑制作用。研究结果表明,半枝莲能够通过抑制 PI3K/AKT 通路抑制结直肠癌的化疗耐药性。

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