Blood coagulation factor X: molecular biology, inherited disease, and engineered therapeutics.

Blood coagulation factor X: molecular biology, inherited disease, and engineered therapeutics.
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DOI:
10.1007/s11239-021-02456-w
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发表时间:
2021-08
影响因子:
4
通讯作者:
Camire RM
Camire RM
中科院分区:
医学4区
文献类型:
--
作者:
Camire RM

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凝血因子X/Xa位于凝血级联反应的关键点,在三条主要途径(内在途径、外源性途径和共同途径)中发挥作用。由于这一中心位置,增强或抑制凝血酶的生成是一个有吸引力的治疗靶点。在这篇简短的综述中,我将总结对这一关键凝血因子的分子理解方面的关键进展,并讨论FX缺乏的分子基础,强调表达重组因子X的困难,并详细介绍两种临床评估的因子X变体。
Blood coagulation factor X/Xa sits at a pivotal point in the coagulation cascade and has a role in each of the three major pathways (intrinsic, extrinsic and the common pathway). Due to this central position, it is an attractive therapeutic target to either enhance or dampen thrombin generation. In this brief review, I will summarize key developments in the molecular understanding of this critical clotting factor and discuss the molecular basis of FX deficiency, highlight difficulties in expressing recombinant factor X, and detail two factor X variants evaluated clinically.
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