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A novel MYD88 mutation, L265RPP, in Waldenström macroglobulinemia activates the NF-κB pathway to upregulate Bcl-xL expression and enhances cell survival.

作者信息

Nagao T, Oshikawa G, Ishida S, Akiyama H, Umezawa Y, Nogami A, Kurosu T, Miura O

机构信息

Department of Hematology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan.

出版信息

Blood Cancer J. 2015 May 15;5(5):e314. doi: 10.1038/bcj.2015.36.

DOI:10.1038/bcj.2015.36
PMID:25978434
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4476015/
Abstract
摘要

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1
A novel MYD88 mutation, L265RPP, in Waldenström macroglobulinemia activates the NF-κB pathway to upregulate Bcl-xL expression and enhances cell survival.华氏巨球蛋白血症中一种新的MYD88突变L265RPP激活NF-κB途径,上调Bcl-xL表达并增强细胞存活能力。
Blood Cancer J. 2015 May 15;5(5):e314. doi: 10.1038/bcj.2015.36.
2
A mutation in MYD88 (L265P) supports the survival of lymphoplasmacytic cells by activation of Bruton tyrosine kinase in Waldenström macroglobulinemia.MYD88(L265P)突变通过激活沃尔登斯特伦巨球蛋白血症中的布鲁顿酪氨酸激酶支持淋巴浆细胞的存活。
Blood. 2013 Aug 15;122(7):1222-32. doi: 10.1182/blood-2012-12-475111. Epub 2013 Jul 8.
3
Dual NAMPT and BTK Targeting Leads to Synergistic Killing of Waldenström Macroglobulinemia Cells Regardless of MYD88 and CXCR4 Somatic Mutation Status.双重靶向NAMPT和BTK可协同杀伤华氏巨球蛋白血症细胞,无论MYD88和CXCR4体细胞突变状态如何。
Clin Cancer Res. 2016 Dec 15;22(24):6099-6109. doi: 10.1158/1078-0432.CCR-16-0630. Epub 2016 Jun 10.
4
MYD88 L265P mutation in Waldenstrom macroglobulinemia.瓦尔登斯特伦巨球蛋白血症中的 MYD88 L265P 突变。
Blood. 2013 May 30;121(22):4504-11. doi: 10.1182/blood-2012-06-436329. Epub 2013 Mar 26.
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A signal network involving coactivated NF-kappaB and STAT3 and altered p53 modulates BAX/BCL-XL expression and promotes cell survival of head and neck squamous cell carcinomas.一个涉及共激活的核因子κB和信号转导与转录激活因子3以及p53改变的信号网络调节BAX/BCL-XL表达并促进头颈部鳞状细胞癌的细胞存活。
Int J Cancer. 2008 May 1;122(9):1987-98. doi: 10.1002/ijc.23324.
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Is clinicopathological distinction of mucosa-associated lymphoid tissue lymphoma from Waldenström macroglobulinemia essential in MYD88 L265P mutation-positive cases?
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Development and characterization of a novel human Waldenström macroglobulinemia cell line: RPCI-WM1, Roswell Park Cancer Institute - Waldenström Macroglobulinemia 1.新型人 Waldenström 巨球蛋白血症细胞系的研发与特征鉴定:RPCI-WM1,罗切斯特大学癌症研究所- Waldenström 巨球蛋白血症 1 号。
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Blood. 2014 Apr 24;123(17):2673-81. doi: 10.1182/blood-2014-01-550509. Epub 2014 Mar 12.
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Cell Commun Signal. 2024 Nov 16;22(1):549. doi: 10.1186/s12964-024-01930-1.
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Waldenström Macroglobulinemia: Mechanisms of Disease Progression and Current Therapies.华氏巨球蛋白血症:疾病进展的机制和当前的治疗方法。
Int J Mol Sci. 2022 Sep 22;23(19):11145. doi: 10.3390/ijms231911145.
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Successful treatment with bortezomib for refractory fever associated with myelodysplastic syndrome with underlying lymphoplasmacytic lymphoma.

本文引用的文献

1
Role of MYD88 in lymphoplasmacytic lymphoma diagnosis and pathogenesis.MYD88在淋巴浆细胞淋巴瘤诊断和发病机制中的作用。
Hematology Am Soc Hematol Educ Program. 2014 Dec 5;2014(1):113-8. doi: 10.1182/asheducation-2014.1.113. Epub 2014 Nov 18.
2
Toll/interleukin-1 receptor (TIR) domain-mediated cellular signaling pathways.Toll/白细胞介素-1受体(TIR)结构域介导的细胞信号通路。
Apoptosis. 2015 Feb;20(2):196-209. doi: 10.1007/s10495-014-1073-1.
3
Negative regulation of RelA phosphorylation: emerging players and their roles in cancer.
硼替佐米成功治疗与潜在淋巴浆细胞淋巴瘤相关的骨髓增生异常综合征难治性发热。
Clin Case Rep. 2022 Feb 9;10(2):e05372. doi: 10.1002/ccr3.5372. eCollection 2022 Feb.
4
Detection of c.755T>C; p.L265P/c.751C>T;p.264R/* compound heterozygous mutation in a case of Waldenstrom macroglobulinemia.在一例华氏巨球蛋白血症患者中检测到c.755T>C;p.L265P/c.751C>T;p.264R/*复合杂合突变。
Indian J Hematol Blood Transfus. 2021 Oct;37(4):702-704. doi: 10.1007/s12288-021-01446-5. Epub 2021 May 20.
5
Gene expression profiling of primary vitreoretinal lymphoma.原发性玻璃体视网膜淋巴瘤的基因表达谱分析。
Cancer Sci. 2020 Apr;111(4):1417-1421. doi: 10.1111/cas.14347. Epub 2020 Mar 12.
6
Human MYD88L265P is insufficient by itself to drive neoplastic transformation in mature mouse B cells.人源 MYD88L265P 本身不足以驱动成熟鼠 B 细胞发生肿瘤转化。
Blood Adv. 2019 Nov 12;3(21):3360-3374. doi: 10.1182/bloodadvances.2019000588.
7
MYD88 and CXCR4 Mutation Profiling in Lymphoplasmacytic Lymphoma/Waldenstrom's Macroglobulinaemia.淋巴浆细胞淋巴瘤/华氏巨球蛋白血症中MYD88和CXCR4突变分析
Indian J Hematol Blood Transfus. 2019 Jan;35(1):57-65. doi: 10.1007/s12288-018-0978-1. Epub 2018 Jul 2.
8
Prognostic impact of mutation, proliferative index and cell origin in diffuse large B cell lymphoma.弥漫性大B细胞淋巴瘤中突变、增殖指数和细胞起源的预后影响
Hematol Transfus Cell Ther. 2019 Jan-Mar;41(1):50-56. doi: 10.1016/j.htct.2018.05.014. Epub 2018 Oct 24.
9
Long non-coding RNA Myd88 promotes growth and metastasis in hepatocellular carcinoma via regulating Myd88 expression through H3K27 modification.长链非编码 RNA Myd88 通过调控 H3K27 修饰影响 Myd88 表达促进肝癌的生长和转移。
Cell Death Dis. 2017 Oct 12;8(10):e3124. doi: 10.1038/cddis.2017.519.
10
Genetic characterization of MYD88-mutated lymphoplasmacytic lymphoma in comparison with MYD88-mutated chronic lymphocytic leukemia.MYD88 突变性淋巴浆细胞淋巴瘤与 MYD88 突变性慢性淋巴细胞白血病的遗传学特征比较。
Leukemia. 2017 Jun;31(6):1355-1362. doi: 10.1038/leu.2016.330. Epub 2016 Nov 14.
RelA 磷酸化的负调控:新兴的调控因子及其在癌症中的作用。
Cytokine Growth Factor Rev. 2015 Feb;26(1):7-13. doi: 10.1016/j.cytogfr.2014.09.003. Epub 2014 Oct 2.
4
Toll-Like Receptors and Cancer: MYD88 Mutation and Inflammation.Toll样受体与癌症:MYD88突变与炎症
Front Immunol. 2014 Jul 31;5:367. doi: 10.3389/fimmu.2014.00367. eCollection 2014.
5
Treatment recommendations for patients with Waldenström macroglobulinemia (WM) and related disorders: IWWM-7 consensus.华氏巨球蛋白血症(WM)及相关疾病患者的治疗建议:IWWM - 7共识
Blood. 2014 Aug 28;124(9):1404-11. doi: 10.1182/blood-2014-03-565135. Epub 2014 Jul 15.
6
Detection of MYD88 L265P in peripheral blood of patients with Waldenström's Macroglobulinemia and IgM monoclonal gammopathy of undetermined significance.检测 Waldenström 巨球蛋白血症和意义未明的单克隆免疫球蛋白血症患者外周血中的 MYD88 L265P。
Leukemia. 2014 Aug;28(8):1698-704. doi: 10.1038/leu.2014.65. Epub 2014 Feb 10.
7
The genomic landscape of Waldenstrom macroglobulinemia is characterized by highly recurring MYD88 and WHIM-like CXCR4 mutations, and small somatic deletions associated with B-cell lymphomagenesis.华氏巨球蛋白血症的基因组特征为高度重现的 MYD88 和 WHIM 样 CXCR4 突变,以及与 B 细胞淋巴瘤发生相关的小型体细胞缺失。
Blood. 2014 Mar 13;123(11):1637-46. doi: 10.1182/blood-2013-09-525808. Epub 2013 Dec 23.
8
A mutation in MYD88 (L265P) supports the survival of lymphoplasmacytic cells by activation of Bruton tyrosine kinase in Waldenström macroglobulinemia.MYD88(L265P)突变通过激活沃尔登斯特伦巨球蛋白血症中的布鲁顿酪氨酸激酶支持淋巴浆细胞的存活。
Blood. 2013 Aug 15;122(7):1222-32. doi: 10.1182/blood-2012-12-475111. Epub 2013 Jul 8.
9
MYD88 L265P is a marker highly characteristic of, but not restricted to, Waldenström's macroglobulinemia.MYD88 L265P 是一种高度特征性标志物,但不仅限于巨球蛋白血症。
Leukemia. 2013 Aug;27(8):1722-8. doi: 10.1038/leu.2013.62. Epub 2013 Feb 28.
10
Prevalence and clinical significance of the MYD88 (L265P) somatic mutation in Waldenstrom's macroglobulinemia and related lymphoid neoplasms.华氏巨球蛋白血症和相关淋巴肿瘤中 MYD88(L265P)体细胞突变的流行率及临床意义。
Blood. 2013 Mar 28;121(13):2522-8. doi: 10.1182/blood-2012-09-457101. Epub 2013 Jan 25.