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5-氟尿嘧啶联合小白菊内酯对人结直肠癌细胞的协同抗肿瘤作用。

Synergistic antitumor effect of 5-fluorouracil in combination with parthenolide in human colorectal cancer.

机构信息

Department of Internal Medicine of Chonbuk National University Hospital, Chonbuk National University, Jeonju 561-712, Republic of Korea.

出版信息

Cancer Lett. 2013 Jul 28;335(2):479-86. doi: 10.1016/j.canlet.2013.03.007. Epub 2013 Mar 16.

Abstract

Parthenolide (PT), a NF-κB inhibitor, has recently been demonstrated as a promising anticancer agent that promotes apoptosis of cancer cells. 5-fluorouracil (5-FU) has been a drug of choice for treatment of colorectal cancer (CRC). Unfortunately, many of the therapies that use 5-FU alone or in combination with other agents are likely to become ineffective due to drug resistance. In the present study, we investigated the antitumor effect of PT combined with 5-FU on a human CRC cell line, SW620. The results demonstrated that combination of PT and 5-FU induced apoptosis which was determined using MTT, cell cycle analysis, annexin-V assay, and Hoechst 33258 staining. Apoptosis through the mitochondrial pathway was confirmed by detecting regulation of Bcl-2 family members, cytochrome C release, and activation of caspase 3 and 9. Moreover, intra-peritoneal injection of PT and 5-FU showed significant inhibition of tumor growth in the xenograft model. These results demonstrate that PT exhibits anticancer activity in human colorectal cancer in vitro and in vivo. These findings provide an efficacious strategy to overcome 5-FU resistance in certain CRC.

摘要

小白菊内酯 (PT) 是一种 NF-κB 抑制剂,最近被证明是一种很有前途的抗癌药物,能促进癌细胞凋亡。氟尿嘧啶 (5-FU) 一直是治疗结直肠癌 (CRC) 的首选药物。不幸的是,许多单独使用 5-FU 或与其他药物联合使用的疗法可能会因耐药性而失效。在本研究中,我们研究了 PT 与 5-FU 联合对人 CRC 细胞系 SW620 的抗肿瘤作用。结果表明,PT 和 5-FU 的联合使用通过 MTT、细胞周期分析、Annexin-V 检测和 Hoechst 33258 染色来诱导细胞凋亡。通过检测 Bcl-2 家族成员的调节、细胞色素 C 的释放以及 caspase 3 和 9 的激活,证实了通过线粒体途径的凋亡。此外,PT 和 5-FU 的腹腔内注射在异种移植模型中显示出对肿瘤生长的显著抑制作用。这些结果表明,PT 在体外和体内均表现出对人结直肠癌的抗癌活性。这些发现为克服某些 CRC 中的 5-FU 耐药性提供了有效的策略。

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