首页> 外文期刊>Clinical chemistry and laboratory medicine: CCLM >Impact of cryopreservation on serum concentration of matrix metalloproteinases (MMP)-7, TIMP-1, vascular growth factors (VEGF) and VEGF-R2 in Biobank samples.
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Impact of cryopreservation on serum concentration of matrix metalloproteinases (MMP)-7, TIMP-1, vascular growth factors (VEGF) and VEGF-R2 in Biobank samples.

机译:冷冻保存对生物库样品中基质金属蛋白酶(MMP)-7,TIMP-1,血管生长因子(VEGF)和VEGF-R2血清浓度的影响。

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摘要

BACKGROUND: Blood biomarkers are subject to pre-analytical variability. In many cases, the stability of important new tissue biomarkers during freeze cycles and storage has not been studied sufficiently. METHODS: To test the stability of matrix metalloproteinases-7 (MMP-7) and their tissue inhibitors (TIMP-1), vascular growth factors (VEGF) and VEGF-receptor, serum samples were frozen and then thawed up to six times. The impact of storage temperature was investigated using an accelerated stability testing protocol. Stability at -20 degrees C and -75 degrees C was calculated using the Arrhenius equation. RESULTS: The average concentration of TIMP-1 was stable, even after six freeze/thaw cycles. One thawing did not change the concentration of MMP-7 and VEGF-receptor. However, repeated freeze/thaw cycles increased the measured values significantly. Decreases in VEGF concentrations were dramatic, even after the first freeze/thaw cycle. According to the Arrhenius calculation, MMP-7 showed excellent stability, at least 5 years at -20 degrees C and several 100 years at -75 degrees C. The VEGF-receptor maintains 90% of its initial concentration at -20 degrees C over 3 months, and decades at -75 degrees C. TIMP-1 and VEGF showed poor stability with cryopreservation, even at -75 degrees C. CONCLUSIONS: The stability of MMP-7, TIMP-1, VEGF or VEGF-receptor in biobanking is highly variable, and this should be taken into account in the interpretation of results. A temperature -20 degrees C is unsuitable for prolonged storage of the biomarkers investigated, and repeated thawing of sera is not recommended. VEGF is especially unstable and should be quantitated using serum that has never been frozen.
机译:背景:血液生物标志物易受分析前变异性的影响。在许多情况下,尚未充分研究重要的新组织生物标志物在冷冻周期和储存过程中的稳定性。方法:为检测基质金属蛋白酶7(MMP-7)及其组织抑制剂(TIMP-1),血管生长因子(VEGF)和VEGF受体的稳定性,将血清样品冷冻并解冻至六次。使用加速稳定性测试协议研究了存储温度的影响。使用Arrhenius方程计算在-20摄氏度和-75摄氏度下的稳定性。结果:即使经过六个冻融循环,TIMP-1的平均浓度仍保持稳定。一解冻不会改变MMP-7和VEGF受体的浓度。但是,重复的冷冻/解冻循环会显着增加测量值。即使在第一个冷冻/解冻循环后,VEGF浓度的下降也是显着的。根据Arrhenius的计算,MMP-7表现出出色的稳定性,在-20摄氏度下至少5年,在-75摄氏度下至少100年。VEGF受体在-20摄氏度下保持90%的初始浓度超过3在-75摄氏度下保存数月和数十年。即使在-75摄氏度下,TIMP-1和VEGF的冷冻保存稳定性也很差。结论:MMP-7,TIMP-1,VEGF或VEGF受体在生物库中的稳定性很高变量,在解释结果时应考虑到这一点。 -20°C的温度不适合长时间保存所研究的生物标志物,不建议反复融化血清。 VEGF尤其不稳定,应使用从未冷冻的血清进行定量。

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