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Therapeutic potential of targeting sphingosine kinases and sphingosine 1-phosphate in hematological malignancies

机译:靶向鞘氨醇激酶和1-磷酸鞘氨醇在血液系统恶性肿瘤中的治疗潜力

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摘要

Sphingolipids, such as ceramide, sphingosine and sphingosine 1-phosphate (S1P) are bioactive molecules that have important functions in a variety of cellular processes, which include proliferation, survival, differentiation and cellular responses to stress. Sphingolipids have a major impact on the determination of cell fate by contributing to either cell survival or death. Although ceramide and sphingosine are usually considered to induce cell death, S1P promotes survival of cells. Sphingosine kinases (SPHKs) are the enzymes that catalyze the conversion of sphingosine to S1P. There are two isoforms, SPHK1 and SPHK2, which are encoded by different genes. SPHK1 has recently been implicated in contributing to cell transformation, tumor angiogenesis and metastatic spread, as well as cancer cell multidrug-resistance. More recent findings suggest that SPHK2 also has a role in cancer progression. This review is an overview of our understanding of the role of SPHKs and S1P in hematopoietic malignancies and provides information on the current status of SPHK inhibitors with respect to their therapeutic potential in the treatment of haematological cancers.
机译:鞘脂,例如神经酰胺,鞘氨醇和鞘氨醇1-磷酸(S1P)是在多种细胞过程中具有重要功能的生物活性分子,这些过程包括增殖,存活,分化和细胞对应激的反应。鞘脂通过有助于细胞存活或死亡而对确定细胞命运具有重大影响。尽管通常认为神经酰胺和鞘氨醇可诱导细胞死亡,但S1P可促进细胞存活。鞘氨醇激酶(SPHK)是催化鞘氨醇向S1P转化的酶。有两个同种型,SPHK1和SPHK2,由不同的基因编码。 SPHK1最近与细胞转化,肿瘤血管生成和转移扩散以及癌细胞多药耐药性有关。最近的发现表明SPHK2在癌症进展中也起作用。这篇综述概述了我们对SPHK和S1P在造血系统恶性肿瘤中的作用的理解,并提供了有关SPHK抑制剂在血液癌症治疗中的治疗潜力的当前状态的信息。

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