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染料木黄酮在去卵巢乳腺癌异种移植瘤模型中干扰顺铂的抗肿瘤作用。

Genistein interferes with antitumor effects of cisplatin in an ovariectomized breast cancer xenograft tumor model.

机构信息

Department of Biochemistry and Molecular Biology, School of Basic Medical Science, Nanchang University, Nanchang, 330006, China.

Department of Biochemistry and Molecular Biology, School of Basic Medical Science, Nanchang University, Nanchang, 330006, China; State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, 510060, China.

出版信息

Toxicol Lett. 2022 Feb 1;355:106-115. doi: 10.1016/j.toxlet.2021.11.013. Epub 2021 Nov 25.

Abstract

Genistein (GEN) has been demonstrated to interfere with antitumor effects of cisplatin (CIS) in vitro. To analyze whether these findings are also relevant in vivo, we examined the effects of combined GEN and CIS treatment in an ovariectomized nude mouse breast cancer xenograft model. Tumor growth and markers for antitumor activity were determined after three weeks of treatment. Furthermore, the concentrations of GEN metabolites were measured in serum, liver, and xenograft tumor tissues using liquid chromatography-tandem mass spectrometry (LC-MS/MS). Three weeks' oral exposure to GEN at a dose of 5 mg kg·d resulted in an average concentration of total GEN metabolite equivalent as high as 0.2729 nmol g wet weight in xenograft tumor tissues. At this dosage, GEN significantly antagonized the antitumor effects of CIS. Mechanistically, GEN blocked both the inhibition of cell proliferation and induction of apoptosis triggered by CIS. Moreover, GEN concentrations in xenograft tumor tissues were found to be significantly higher than in serum and liver. In conclusion, our findings suggested that oral GEN exposure at a level comparable to dietary exposure in humans could interfere with CIS chemotherapy.

摘要

染料木黄酮(GEN)已被证明会干扰顺铂(CIS)的体外抗肿瘤作用。为了分析这些发现是否在体内也具有相关性,我们在去卵巢裸鼠乳腺癌异种移植模型中检查了联合 GEN 和 CIS 治疗的效果。治疗三周后,测定肿瘤生长和抗肿瘤活性标志物。此外,使用液相色谱-串联质谱法(LC-MS/MS)在血清、肝脏和异种移植肿瘤组织中测定 GEN 代谢物的浓度。口服 GEN 5mgkg·d 治疗 3 周,导致异种移植肿瘤组织中总 GEN 代谢物当量的平均浓度高达 0.2729nmolg湿重。在此剂量下,GEN 显著拮抗 CIS 的抗肿瘤作用。从机制上讲,GEN 阻断了 CIS 引发的细胞增殖抑制和细胞凋亡诱导。此外,还发现异种移植肿瘤组织中的 GEN 浓度明显高于血清和肝脏。总之,我们的研究结果表明,与人类饮食暴露水平相当的口服 GEN 暴露可能会干扰 CIS 化疗。

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