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三氟尿苷/替匹嘧啶联合瑞戈非尼在人结直肠癌细胞中的序贯联合化疗作用。

Effective Sequential Combined Chemotherapy with Trifluridine/Tipiracil and Regorafenib in Human Colorectal Cancer Cells.

机构信息

Translational Research Laboratory, Taiho Pharmaceutical Co., Ltd., 224-2, Ebisuno Hiraishi, Kawauchi-Cho Tokushima, Tokushima 771-0194, Japan.

Applied Pharmacology Laboratory, Taiho Pharmaceutical Co., Ltd., 224-2, Ebisuno Hiraishi, Kawauchi-Cho Tokushima, Tokushima 771-0194, Japan.

出版信息

Int J Mol Sci. 2018 Sep 25;19(10):2915. doi: 10.3390/ijms19102915.

DOI:10.3390/ijms19102915
PMID:30257515
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6213129/
Abstract

Salvage chemotherapy for refractory metastatic colorectal cancer using trifluridine/tipiracil (FTD/TPI) and regorafenib has shown survival benefits. We evaluated the antitumor effects of FTD or FTD/TPI combined with regorafenib in vitro and in vivo. SW620, HCT 116, and HT-29 human colorectal cancer cell lines were treated with FTD and regorafenib simultaneously and sequentially. Cell death, incorporation of FTD into DNA, and molecules related to FTD and regorafenib-associated cell death were investigated. The antitumor effects of FTD combined with regorafenib in SW620 and COLO205 xenografts were also evaluated. Cell death was greater after sequential treatment with FTD followed by regorafenib in SW620 cells, but not in HCT 116 and HT-29 cells, than after treatment with FTD alone, which was attributable to thymidylate synthase reduction with the induction of apoptosis. In contrast, simultaneous and sequential exposure to regorafenib followed by FTD, but not FTD alone, attenuated the cell death effect. Furthermore, combined FTD/TPI treatment followed by regorafenib had greater antitumor activity than either monotherapy in SW620 and COLO205 xenograft models. Treatment results following regorafenib administration subsequent to FTD or FTD/TPI suggest that sequential therapy with FTD/TPI prior to regorafenib may be effective in a clinical setting.

摘要

使用三氟尿苷/替匹嘧啶(FTD/TPI)和瑞戈非尼对难治性转移性结直肠癌进行挽救化疗显示出生存获益。我们评估了 FTD 或 FTD/TPI 联合瑞戈非尼在体外和体内的抗肿瘤作用。SW620、HCT116 和 HT-29 人结直肠癌细胞系同时和顺序用 FTD 和瑞戈非尼处理。研究了细胞死亡、FTD 掺入 DNA 以及与 FTD 和瑞戈非尼相关细胞死亡相关的分子。还评估了 FTD 联合瑞戈非尼在 SW620 和 COLO205 异种移植中的抗肿瘤作用。SW620 细胞中 FTD 序贯治疗后细胞死亡大于 FTD 单药治疗,而 HCT116 和 HT-29 细胞中则无,这归因于胸苷酸合成酶减少诱导细胞凋亡。相比之下,瑞戈非尼同时和序贯暴露于 FTD 后,而不是 FTD 单药治疗,会减弱细胞死亡作用。此外,FTD/TPI 联合治疗后序贯应用瑞戈非尼在 SW620 和 COLO205 异种移植模型中比单药治疗具有更强的抗肿瘤活性。FTD 或 FTD/TPI 后给予瑞戈非尼的治疗结果表明,FTD/TPI 序贯治疗后给予瑞戈非尼可能在临床环境中有效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d43/6213129/de9eb80fa738/ijms-19-02915-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d43/6213129/86735ce72464/ijms-19-02915-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d43/6213129/71f9da82ce96/ijms-19-02915-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d43/6213129/12c49d2c782a/ijms-19-02915-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d43/6213129/de9eb80fa738/ijms-19-02915-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d43/6213129/86735ce72464/ijms-19-02915-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d43/6213129/71f9da82ce96/ijms-19-02915-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d43/6213129/12c49d2c782a/ijms-19-02915-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d43/6213129/de9eb80fa738/ijms-19-02915-g004.jpg

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本文引用的文献

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