{"title":"SMYD2在白血病中的研究进展","authors":"Teresa Rubio-Tomás","doi":"10.23937/2469-5696/1410067","DOIUrl":null,"url":null,"abstract":"SMYD2 is one of the five members (SMYD1-5) of the Su(Var)3-9, Enhancer-of-zeste and Trithorax (SET) and Myeloid, Nervy, and DEAF-1 (MYND) domain-containing (SMYD) protein family and is it known to methylate histone and non-histone substrates. By methylating a wide range of targets, SMYD2 acts as an oncogene in most cancer types. In this review I will comment on the last publications related to the role of SMYD2 in leukemia and I will refer to more extensive reviews if the reader aims to have a broader picture of the state of the art. *Corresponding author: Teresa Rubio-Tomás, Institut d’Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain; School of Medicine, University of Crete, Crete, Greece Check for updates SMYD2 Promotes Leukemia Progression Remarkably, SMYD2 is not only involved in leukemia, but also normal lineage differentiation of hematopoietic stem cells, since mice lacking SMYD2 specifically in hematopoietic stem cells displayed aberrant lymphocyte development. Regarding leukemia, these SMYD2 knockout mice had a high rate of apoptosis and showed loss of anchorage-independent transformation of leukemia cells [1]. In line with these observations, the authors detected overexpression of SMYD2 in many types of human leukemia [1]. Even residual expression of SMYD2 (and SMYD3) can promote chronic lymphocytic leukemia, probably due to the acquisition of complex karyotype [2]. Zipin-Roitman, et al. observed that decreased expression of SMYD2 leads to overexpression of SET7/9, indicating some kind of interplay between these two methyl transferases, that results in higher resistance to DNA damage of leukemia cells [3]. In addition, SMYD2 seemed to be downstream of MYC in acute myeloid leukemia [4]. ISSN: 2469-5696 DOI: 10.23937/2469-5696/1410067 Tomás. Int J Blood Res Disord 2021, 8:067 • Page 2 of 2 • 5. Ping Z, Ruan JF, Weng W, Tang Y (2020) Overexpression of SET and MYND domain-containing protein 2 (SMYD2) is associated with poor prognosis in pediatric b lineage acute lymphoblastic leukemia. Leuk Lymphoma 61: 437-444. 6. Sakamoto LHT, Andrade RV, Felipe MSS, Motoyama AB, Silva FP, et al. (2014) SMYD2 is highly expressed in pediatric acute lymphoblastic leukemia and constitutes a bad prognostic factor. Leuk Res 38: 496-502. 7. Xin Y, Jiang XJ, Fang ZM (2019) HSistone methyltransferase SMYD2: Ubiquitous regulator of disease. Clinical Epigenetics 11: 112. 8. Edoardo F, Manoni E, Ferroni C, Del Rio A, Bartolini M (2019) Small-molecule inhibitors of lysine methyltransferases SMYD2 and SMYD3: Current trends. Future Medicinal Chemistry 11: 901-921. 9. Teresa R-T (2021) The SMYD family proteins in immunology: An update of their obvious and non-obvious relations with the immune system. 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In this review I will comment on the last publications related to the role of SMYD2 in leukemia and I will refer to more extensive reviews if the reader aims to have a broader picture of the state of the art. *Corresponding author: Teresa Rubio-Tomás, Institut d’Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain; School of Medicine, University of Crete, Crete, Greece Check for updates SMYD2 Promotes Leukemia Progression Remarkably, SMYD2 is not only involved in leukemia, but also normal lineage differentiation of hematopoietic stem cells, since mice lacking SMYD2 specifically in hematopoietic stem cells displayed aberrant lymphocyte development. Regarding leukemia, these SMYD2 knockout mice had a high rate of apoptosis and showed loss of anchorage-independent transformation of leukemia cells [1]. In line with these observations, the authors detected overexpression of SMYD2 in many types of human leukemia [1]. Even residual expression of SMYD2 (and SMYD3) can promote chronic lymphocytic leukemia, probably due to the acquisition of complex karyotype [2]. Zipin-Roitman, et al. observed that decreased expression of SMYD2 leads to overexpression of SET7/9, indicating some kind of interplay between these two methyl transferases, that results in higher resistance to DNA damage of leukemia cells [3]. In addition, SMYD2 seemed to be downstream of MYC in acute myeloid leukemia [4]. ISSN: 2469-5696 DOI: 10.23937/2469-5696/1410067 Tomás. Int J Blood Res Disord 2021, 8:067 • Page 2 of 2 • 5. Ping Z, Ruan JF, Weng W, Tang Y (2020) Overexpression of SET and MYND domain-containing protein 2 (SMYD2) is associated with poor prognosis in pediatric b lineage acute lymphoblastic leukemia. Leuk Lymphoma 61: 437-444. 6. Sakamoto LHT, Andrade RV, Felipe MSS, Motoyama AB, Silva FP, et al. (2014) SMYD2 is highly expressed in pediatric acute lymphoblastic leukemia and constitutes a bad prognostic factor. 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引用次数: 1
摘要
SMYD2是Su(Var)3-9的五个成员(SMYD1-5)之一,它是组氨酸和三酮的增强剂(SET)和含髓、Nervy和DEAF-1(MYND)结构域(SMYD)蛋白家族的成员之一,已知它能使组蛋白和非组蛋白底物甲基化。SMYD2通过甲基化多种靶点,在大多数癌症类型中起到癌基因的作用。在这篇综述中,我将评论与SMYD2在白血病中的作用有关的最新出版物,如果读者想更广泛地了解最新技术,我将参考更广泛的综述。*通讯作者:Teresa Rubio Tomás,Institut d’Investigacions Biomèdiques August Pi I Sunyer(IDIPAPS),西班牙巴塞罗那;希腊克里特岛克里特大学医学院查看最新消息SMYD2促进白血病进展值得注意的是,SMYD2不仅与白血病有关,而且与造血干细胞的正常谱系分化有关,因为在造血干细胞中缺乏SMYD2的小鼠表现出异常的淋巴细胞发育。关于白血病,这些SMYD2敲除小鼠具有高的细胞凋亡率,并且显示出白血病细胞的锚定非依赖性转化的丧失[1]。根据这些观察结果,作者在许多类型的人类白血病中检测到SMYD2的过度表达[1]。即使SMYD2(和SMYD3)的残留表达也可能促进慢性淋巴细胞白血病,这可能是由于获得了复杂的核型[2]。Zipin Roitman等人观察到,SMYD2表达的减少导致SET7/9的过度表达,表明这两种甲基转移酶之间存在某种相互作用,从而导致白血病细胞对DNA损伤具有更高的抵抗力[3]。此外,在急性髓系白血病中,SMYD2似乎是MYC的下游[4]。ISSN:2469-5696 DOI:10.23937/2469-5696/141067托马斯。Int J Blood Res Disord 2021,8:067•第2页,共2页•5。Ping Z,Ruan JF,Weng W,Tang Y(2020)SET和MYND结构域含蛋白2(SMYD2)的过表达与儿童b谱系急性淋巴细胞白血病的不良预后相关。白血病61:437-444。6.Sakamoto LHT、Andrade RV、Felipe MSS、Motoyama AB、Silva FP等人(2014)SMYD2在儿童急性淋巴细胞白血病中高度表达,并构成不良预后因素。Leuk Res 38:496-502。7、辛勇,姜新军,方ZM(2019)高丝氨酸甲基转移酶SMYD2:疾病的普遍调节因子。临床表观遗传学11:112。8.Edoardo F,Manoni E,Ferroni C,Del Rio A,Bartolini M(2019)赖氨酸甲基转移酶SMYD2和SMYD3的小分子抑制剂:当前趋势。《未来药物化学》11:901-921。9.Teresa R-T(2021)免疫学中的SMYD家族蛋白:它们与免疫系统的明显和非明显关系的更新。Heliyon 7:e07387。
SMYD2 is one of the five members (SMYD1-5) of the Su(Var)3-9, Enhancer-of-zeste and Trithorax (SET) and Myeloid, Nervy, and DEAF-1 (MYND) domain-containing (SMYD) protein family and is it known to methylate histone and non-histone substrates. By methylating a wide range of targets, SMYD2 acts as an oncogene in most cancer types. In this review I will comment on the last publications related to the role of SMYD2 in leukemia and I will refer to more extensive reviews if the reader aims to have a broader picture of the state of the art. *Corresponding author: Teresa Rubio-Tomás, Institut d’Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain; School of Medicine, University of Crete, Crete, Greece Check for updates SMYD2 Promotes Leukemia Progression Remarkably, SMYD2 is not only involved in leukemia, but also normal lineage differentiation of hematopoietic stem cells, since mice lacking SMYD2 specifically in hematopoietic stem cells displayed aberrant lymphocyte development. Regarding leukemia, these SMYD2 knockout mice had a high rate of apoptosis and showed loss of anchorage-independent transformation of leukemia cells [1]. In line with these observations, the authors detected overexpression of SMYD2 in many types of human leukemia [1]. Even residual expression of SMYD2 (and SMYD3) can promote chronic lymphocytic leukemia, probably due to the acquisition of complex karyotype [2]. Zipin-Roitman, et al. observed that decreased expression of SMYD2 leads to overexpression of SET7/9, indicating some kind of interplay between these two methyl transferases, that results in higher resistance to DNA damage of leukemia cells [3]. In addition, SMYD2 seemed to be downstream of MYC in acute myeloid leukemia [4]. ISSN: 2469-5696 DOI: 10.23937/2469-5696/1410067 Tomás. Int J Blood Res Disord 2021, 8:067 • Page 2 of 2 • 5. Ping Z, Ruan JF, Weng W, Tang Y (2020) Overexpression of SET and MYND domain-containing protein 2 (SMYD2) is associated with poor prognosis in pediatric b lineage acute lymphoblastic leukemia. Leuk Lymphoma 61: 437-444. 6. Sakamoto LHT, Andrade RV, Felipe MSS, Motoyama AB, Silva FP, et al. (2014) SMYD2 is highly expressed in pediatric acute lymphoblastic leukemia and constitutes a bad prognostic factor. Leuk Res 38: 496-502. 7. Xin Y, Jiang XJ, Fang ZM (2019) HSistone methyltransferase SMYD2: Ubiquitous regulator of disease. Clinical Epigenetics 11: 112. 8. Edoardo F, Manoni E, Ferroni C, Del Rio A, Bartolini M (2019) Small-molecule inhibitors of lysine methyltransferases SMYD2 and SMYD3: Current trends. Future Medicinal Chemistry 11: 901-921. 9. Teresa R-T (2021) The SMYD family proteins in immunology: An update of their obvious and non-obvious relations with the immune system. Heliyon 7: e07387.