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肌球蛋白重链 9:癌基因还是抑癌基因?

Myosin Heavy Chain 9: Oncogene or Tumor Suppressor Gene?

机构信息

Shaanxi Provincial Cancer Hospital Affiliated to Medical School, Xi'an Jiao Tong University, Xi'an, Shaanxi, China (mainland).

Hong Hui Hospital, The Affiliated Hospital, School of Medicine, Xi'an Jiao Tong University, Xi'an, Shaanxi, China (mainland).

出版信息

Med Sci Monit. 2019 Jan 31;25:888-892. doi: 10.12659/MSM.912320.

DOI:10.12659/MSM.912320
PMID:30739906
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6366299/
Abstract

MYH9 was first discovered due to thrombocytopenia caused by MYH9 mutation-related abnormalities. In recent years, researchers have increasingly found that MYH9 plays an important role in cancer as a cytokine involved in cytoskeletal reorganization, cellular pseudopodia formation, and migration. MYH9 is closely related to the progress and poor prognosis of most solid tumors, and it is now accepted that MYH9 is a suppressor gene and plays an important role on the re-Rho pathway. Recent research has been limited to the study of tissues. However, it would be more direct and informative to be able to use hematology to assess tumor prognosis and changes in MYH9 levels and NMMHC-IIA. This article summarizes recent research on MYH9 and provides a reference for future clinical research.

摘要

MYH9 最初是由于 MYH9 突变相关异常导致的血小板减少而被发现的。近年来,研究人员越来越发现 MYH9 作为一种参与细胞骨架重排、细胞伪足形成和迁移的细胞因子,在癌症中起着重要作用。MYH9 与大多数实体瘤的进展和不良预后密切相关,现在人们认为 MYH9 是一个抑癌基因,在再 Rho 途径中发挥着重要作用。最近的研究仅限于组织研究。然而,能够利用血液学来评估肿瘤的预后以及 MYH9 水平和 NMMHC-IIA 的变化将更加直接和有信息。本文总结了 MYH9 的最新研究成果,为未来的临床研究提供了参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6674/6366299/8b80ddfcc983/medscimonit-25-888-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6674/6366299/8b80ddfcc983/medscimonit-25-888-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6674/6366299/8b80ddfcc983/medscimonit-25-888-g001.jpg

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1
Myosin Heavy Chain 9: Oncogene or Tumor Suppressor Gene?肌球蛋白重链 9:癌基因还是抑癌基因?
Med Sci Monit. 2019 Jan 31;25:888-892. doi: 10.12659/MSM.912320.
2
Altered cytoskeleton organization in platelets from patients with MYH9-related disease.MYH9相关疾病患者血小板中细胞骨架组织的改变。
J Thromb Haemost. 2005 May;3(5):1026-35. doi: 10.1111/j.1538-7836.2005.01244.x.
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Mutations responsible for MYH9-related thrombocytopenia impair SDF-1-driven migration of megakaryoblastic cells.导致 MYH9 相关性血小板减少症的突变可损害巨核细胞前体细胞的 SDF-1 驱动迁移。
Thromb Haemost. 2011 Oct;106(4):693-704. doi: 10.1160/TH11-02-0126. Epub 2011 Aug 11.
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Haematological characteristics of MYH9 disorders due to MYH9 R702 mutations.由MYH9 R702突变引起的MYH9相关疾病的血液学特征。
Eur J Haematol. 2007 Mar;78(3):220-6. doi: 10.1111/j.1600-0609.2006.00806.x. Epub 2007 Jan 16.
5
Analysis of clinical manifestations, mutant gene and encoded protein in two Chinese MYH9-related disease families.两个中国MYH9相关疾病家系的临床表现、突变基因及编码蛋白分析
Clin Chim Acta. 2006 Nov;373(1-2):49-54. doi: 10.1016/j.cca.2006.04.027. Epub 2006 May 16.
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Advances in the understanding of MYH9 disorders.对 MYH9 相关疾病的认识进展。
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Pathogenetic mechanisms of hematological abnormalities of patients with MYH9 mutations.MYH9突变患者血液学异常的发病机制。
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Nonmuscle Myosin Heavy Chain IIA Mutation Predicts Severity and Progression of Sensorineural Hearing Loss in Patients With MYH9-Related Disease.非肌肉肌球蛋白重链IIA突变可预测MYH9相关疾病患者感音神经性听力损失的严重程度和进展情况。
Ear Hear. 2016 Jan-Feb;37(1):112-20. doi: 10.1097/AUD.0000000000000198.
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MYH9-Related Thrombocytopenia: Four Novel Variants Affecting the Tail Domain of the Non-Muscle Myosin Heavy Chain IIA Associated with a Mild Clinical Evolution of the Disorder.MYH9 相关性血小板减少症:四种新的变异影响非肌肉肌球蛋白重链 IIA 的尾部结构,与该疾病的轻度临床演变相关。
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MYH9: Structure, functions and role of non-muscle myosin IIA in human disease.MYH9:非肌肉肌球蛋白 IIA 在人类疾病中的结构、功能和作用。
Gene. 2018 Jul 20;664:152-167. doi: 10.1016/j.gene.2018.04.048. Epub 2018 Apr 19.

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本文引用的文献

1
MYH9: Structure, functions and role of non-muscle myosin IIA in human disease.MYH9:非肌肉肌球蛋白 IIA 在人类疾病中的结构、功能和作用。
Gene. 2018 Jul 20;664:152-167. doi: 10.1016/j.gene.2018.04.048. Epub 2018 Apr 19.
2
Hereditary thrombocytopenias: a growing list of disorders.遗传性血小板减少症:不断增加的疾病种类。
Hematology Am Soc Hematol Educ Program. 2017 Dec 8;2017(1):385-399. doi: 10.1182/asheducation-2017.1.385.
3
Activation of ROCK and MLCK tunes regional stress fiber formation and mechanics via preferential myosin light chain phosphorylation.
肺癌中机械生物学机制的相关性最新进展
Transl Oncol. 2025 May;55:102375. doi: 10.1016/j.tranon.2025.102375. Epub 2025 Mar 24.
4
Exploring the nexus between MYH9 and tumors: novel insights and new therapeutic opportunities.探索MYH9与肿瘤之间的联系:新见解与新治疗机遇。
Front Cell Dev Biol. 2024 Aug 1;12:1421763. doi: 10.3389/fcell.2024.1421763. eCollection 2024.
5
A novel role for KIFC1-MYH9 interaction in triple-negative breast cancer aggressiveness and racial disparity.KIFC1-MYH9 相互作用在三阴性乳腺癌侵袭性和种族差异中的新作用。
Cell Commun Signal. 2024 Jun 6;22(1):312. doi: 10.1186/s12964-024-01664-0.
6
Pan-cancer and single-cell analysis of actin cytoskeleton genes related to disulfidptosis.与二硫键介导的程序性坏死相关的肌动蛋白细胞骨架基因的泛癌和单细胞分析
Open Med (Wars). 2024 Mar 30;19(1):20240929. doi: 10.1515/med-2024-0929. eCollection 2024.
7
Single molecule imaging of the central dogma reveals myosin-2A gene expression is regulated by contextual translational buffering.中心法则的单分子成像揭示肌球蛋白-2A基因表达受上下文翻译缓冲调控。
bioRxiv. 2024 Feb 18:2024.02.11.579797. doi: 10.1101/2024.02.11.579797.
8
Analysis of myosin genes in HNSCC and identify MYL1 as a specific poor prognostic biomarker, promotes tumor metastasis and correlates with tumor immune infiltration in HNSCC.分析头颈鳞状细胞癌中的肌球蛋白基因,并鉴定 MYL1 作为一个特定的不良预后生物标志物,促进头颈鳞状细胞癌中的肿瘤转移,并与肿瘤免疫浸润相关。
BMC Cancer. 2023 Sep 7;23(1):840. doi: 10.1186/s12885-023-11349-5.
9
Comprehensive landscape of the miRNA-regulated prognostic marker LAYN with immune infiltration and stemness in pan-cancer.miRNA 调控的预后标志物 LAYN 在泛癌中的免疫浸润和干性的综合全景。
J Cancer Res Clin Oncol. 2023 Oct;149(13):10989-11011. doi: 10.1007/s00432-023-04986-7. Epub 2023 Jun 19.
10
Identification of MYH9 as a key regulator for synoviocyte migration and invasion through secretome profiling.通过分泌组谱分析鉴定 MYH9 作为滑膜细胞迁移和侵袭的关键调节因子。
Ann Rheum Dis. 2023 Aug;82(8):1035-1048. doi: 10.1136/ard-2022-223625. Epub 2023 May 15.
ROCK和肌球蛋白轻链激酶(MLCK)的激活通过优先使肌球蛋白轻链磷酸化来调节局部应力纤维的形成和力学特性。
Mol Biol Cell. 2017 Dec 15;28(26):3832-3843. doi: 10.1091/mbc.E17-06-0401. Epub 2017 Oct 18.
4
MYBPH inhibits vascular smooth muscle cell migration and attenuates neointimal hyperplasia in a rat carotid balloon-injury model.在大鼠颈动脉球囊损伤模型中,MYBPH抑制血管平滑肌细胞迁移并减轻内膜增生。
Exp Cell Res. 2017 Oct 1;359(1):154-162. doi: 10.1016/j.yexcr.2017.07.036. Epub 2017 Aug 8.
5
LIM kinase 1 interacts with myosin-9 and alpha-actinin-4 and promotes colorectal cancer progression.LIM激酶1与肌球蛋白-9和α-辅肌动蛋白-4相互作用,并促进结直肠癌进展。
Br J Cancer. 2017 Aug 8;117(4):563-571. doi: 10.1038/bjc.2017.193. Epub 2017 Jun 29.
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MYH9 gene mutations associated with bleeding.与出血相关的MYH9基因突变。
Platelets. 2017 May;28(3):312-315. doi: 10.1080/09537104.2017.1294250. Epub 2017 Apr 3.
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Myosin IIA-related Actomyosin Contractility Mediates Oxidative Stress-induced Neuronal Apoptosis.肌球蛋白IIA相关的肌动球蛋白收缩性介导氧化应激诱导的神经元凋亡。
Front Mol Neurosci. 2017 Mar 14;10:75. doi: 10.3389/fnmol.2017.00075. eCollection 2017.
8
Clinical and genetic diagnosis of familial hypertrophic cardiomyopathy: Results in pediatric cardiology.家族性肥厚型心肌病的临床与基因诊断:儿科心脏病学的研究结果
Rev Port Cardiol. 2017 Mar;36(3):155-165. doi: 10.1016/j.repc.2016.09.009. Epub 2017 Feb 15.
9
The tumor suppressor capability of p53 is dependent on non-muscle myosin IIA function in head and neck cancer.在头颈癌中,p53的肿瘤抑制能力依赖于非肌肉肌球蛋白IIA的功能。
Oncotarget. 2017 Apr 4;8(14):22991-23007. doi: 10.18632/oncotarget.14967.
10
MYH9 binds to lncRNA gene PTCSC2 and regulates FOXE1 in the 9q22 thyroid cancer risk locus.MYH9与长链非编码RNA基因PTCSC2结合,并在9q22甲状腺癌风险位点调控FOXE1。
Proc Natl Acad Sci U S A. 2017 Jan 17;114(3):474-479. doi: 10.1073/pnas.1619917114. Epub 2017 Jan 3.