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从福尔马林固定、石蜡包埋组织中提取他莫昔芬及其代谢物:一种使用液相色谱-串联质谱的创新定量方法。

Extraction of tamoxifen and its metabolites from formalin-fixed, paraffin-embedded tissues: an innovative quantitation method using liquid chromatography and tandem mass spectrometry.

机构信息

Pharmacokinetic Unit, Tom Baker Cancer Centre, Alberta Health Services, Calgary, AB, Canada.

出版信息

Cancer Chemother Pharmacol. 2014 Mar;73(3):475-84. doi: 10.1007/s00280-013-2346-z. Epub 2014 Jan 12.

Abstract

PURPOSE

Tamoxifen is a key therapeutic option for breast cancer treatment. Understanding its complex metabolism and pharmacokinetics is important for dose optimization. We examined the possibility of utilizing archival formalin-fixed paraffin-embedded (FFPE) tissue as an alternative sample source for quantification since well-annotated retrospective samples were always limited.

METHODS

Six 15 μm sections of FFPE tissues were deparaffinized with xylene and purified using solid-phase extraction. Tamoxifen and its metabolites were separated and detected by liquid chromatography-tandem mass spectrometry using multiple-reaction monitoring.

RESULTS

This method was linear between 0.4 and 200 ng/g for 4-hydroxy-tamoxifen and endoxifen, and 4-2,000 ng/g for tamoxifen and N-desmethyl-tamoxifen. Inter- and intra-assay precisions were <9 %, and mean accuracies ranged from 81 to 106 %. Extraction recoveries were between 83 and 88 %. The validated method was applied to FFPE tissues from two groups of patients, who received 20 mg/day of tamoxifen for >6 months, and were classified into breast tumor recurrence and non-recurrence. Our preliminary data show that levels of tamoxifen metabolites were significantly lower in patients with recurrent cancer, suggesting that inter-individual variability in tamoxifen metabolism might partly account for the development of cancer recurrence. Nevertheless, other causes such as non-compliance or stopping therapy of tamoxifen could possibly lead to the concentration differences.

CONCLUSIONS

The ability to successfully study tamoxifen metabolism in such tissue samples will rapidly increase our knowledge of how tamoxifen's action, metabolism and tissue distribution contribute to breast cancer control. However, larger population studies are required to understand the underlying mechanism of tamoxifen metabolism for optimization of its treatment.

摘要

目的

他莫昔芬是乳腺癌治疗的重要治疗选择。了解其复杂的代谢和药代动力学对于优化剂量很重要。我们研究了利用存档的福尔马林固定石蜡包埋(FFPE)组织作为替代样本来源的可能性,因为标记良好的回顾性样本总是有限的。

方法

用二甲苯对 6 个 15μm 的 FFPE 组织切片脱蜡并用固相萃取进行纯化。使用液质联用多反应监测法分离和检测他莫昔芬及其代谢物。

结果

该方法对 4-羟基他莫昔芬和依西美坦的线性范围为 0.4-200ng/g,对他莫昔芬和 N-去甲基他莫昔芬的线性范围为 4-2000ng/g。内和日间精密度均<9%,平均准确度在 81-106%之间。提取回收率在 83-88%之间。验证后的方法应用于两组接受 20mg/天他莫昔芬治疗>6 个月的患者的 FFPE 组织,这些患者被分为乳腺癌肿瘤复发和未复发。我们的初步数据表明,在癌症复发患者中,他莫昔芬代谢物的水平明显较低,这表明他莫昔芬代谢的个体间差异可能部分解释了癌症复发的发生。然而,其他原因如不遵医嘱或停止服用他莫昔芬也可能导致浓度差异。

结论

成功地在这些组织样本中研究他莫昔芬代谢的能力将迅速增加我们对他莫昔芬的作用、代谢和组织分布如何有助于乳腺癌控制的认识。然而,需要进行更大的人群研究,以了解他莫昔芬代谢的潜在机制,从而优化其治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7adc/3931943/041025f3d2ef/280_2013_2346_Fig1_HTML.jpg

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