• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Targeting B-cell receptor signaling in leukemia and lymphoma: how and why?靶向白血病和淋巴瘤中的B细胞受体信号传导:方式与原因?
Int J Hematol Oncol. 2016 May;5(1):37-53. doi: 10.2217/ijh-2016-0003. Epub 2016 May 26.
2
B-cell receptor signaling in chronic lymphocytic leukemia and other B-cell malignancies.慢性淋巴细胞白血病及其他B细胞恶性肿瘤中的B细胞受体信号传导
Clin Adv Hematol Oncol. 2016 Jan;14(1):55-65.
3
Role of Bruton's tyrosine kinase in B cells and malignancies.布鲁顿酪氨酸激酶在 B 细胞及恶性肿瘤中的作用。
Mol Cancer. 2018 Feb 19;17(1):57. doi: 10.1186/s12943-018-0779-z.
4
Targeting Bruton's tyrosine kinase signaling as an emerging therapeutic agent of B-cell malignancies.靶向布鲁顿酪氨酸激酶信号传导作为B细胞恶性肿瘤的一种新兴治疗药物。
Oncol Lett. 2015 Dec;10(6):3339-3344. doi: 10.3892/ol.2015.3802. Epub 2015 Oct 13.
5
Targeting the B-cell receptor signaling pathway in B lymphoid malignancies.靶向B淋巴细胞恶性肿瘤中的B细胞受体信号通路。
Curr Opin Hematol. 2014 Jul;21(4):341-9. doi: 10.1097/MOH.0000000000000048.
6
Synergistic Targeting of the Regulatory and Catalytic Subunits of PI3Kδ in Mature B-cell Malignancies.协同靶向成熟 B 细胞恶性肿瘤中 PI3Kδ 的调节亚基和催化亚基。
Clin Cancer Res. 2018 Mar 1;24(5):1103-1113. doi: 10.1158/1078-0432.CCR-17-2218. Epub 2017 Dec 15.
7
CXCR4- and BCR-triggered integrin activation in B-cell chronic lymphocytic leukemia cells depends on JAK2-activated Bruton's tyrosine kinase.B细胞慢性淋巴细胞白血病细胞中CXCR4和BCR触发的整合素激活依赖于JAK2激活的布鲁顿酪氨酸激酶。
Oncotarget. 2018 Oct 12;9(80):35123-35140. doi: 10.18632/oncotarget.26212.
8
B-cell receptor signaling inhibitors for treatment of autoimmune inflammatory diseases and B-cell malignancies.B 细胞受体信号抑制剂治疗自身免疫性炎症性疾病和 B 细胞恶性肿瘤。
Int Rev Immunol. 2013 Aug;32(4):397-427. doi: 10.3109/08830185.2013.818140.
9
B-cell receptor signalling and its crosstalk with other pathways in normal and malignant cells.B细胞受体信号传导及其在正常细胞和恶性细胞中与其他信号通路的相互作用。
Eur J Haematol. 2015 Mar;94(3):193-205. doi: 10.1111/ejh.12427. Epub 2014 Sep 13.
10
Mechanisms of B Cell Receptor Activation and Responses to B Cell Receptor Inhibitors in B Cell Malignancies.B细胞受体激活机制及B细胞恶性肿瘤对B细胞受体抑制剂的反应
Cancers (Basel). 2020 May 28;12(6):1396. doi: 10.3390/cancers12061396.

引用本文的文献

1
Differential Regulation of GPVI-Induced Btk and Syk Activation by PKC, PKA and PP2A in Human Platelets.人血小板中 PKC、PKA 和 PP2A 对 GPVI 诱导的 Btk 和 Syk 激活的差异调节。
Int J Mol Sci. 2023 Apr 24;24(9):7776. doi: 10.3390/ijms24097776.
2
Structural Complementarity of Bruton's Tyrosine Kinase and Its Inhibitors for Implication in B-Cell Malignancies and Autoimmune Diseases.布鲁顿酪氨酸激酶与其抑制剂的结构互补性在B细胞恶性肿瘤和自身免疫性疾病中的意义
Pharmaceuticals (Basel). 2023 Mar 7;16(3):400. doi: 10.3390/ph16030400.
3
Parsaclisib in Japanese patients with relapsed or refractory B-cell lymphoma (CITADEL-111): A phase Ib study.帕萨昔布治疗复发或难治性 B 细胞淋巴瘤日本患者(CITADEL-111):一项 Ib 期研究。
Cancer Sci. 2022 May;113(5):1702-1711. doi: 10.1111/cas.15308. Epub 2022 Mar 15.
4
Beyond TCR Signaling: Emerging Functions of Lck in Cancer and Immunotherapy.超越 TCR 信号:Lck 在癌症和免疫疗法中的新兴功能。
Int J Mol Sci. 2019 Jul 16;20(14):3500. doi: 10.3390/ijms20143500.

本文引用的文献

1
Targeting Non-proteolytic Protein Ubiquitination for the Treatment of Diffuse Large B Cell Lymphoma.靶向非蛋白水解性蛋白质泛素化用于治疗弥漫性大B细胞淋巴瘤
Cancer Cell. 2016 Apr 11;29(4):494-507. doi: 10.1016/j.ccell.2016.03.006.
2
Acalabrutinib (ACP-196) in Relapsed Chronic Lymphocytic Leukemia.阿卡替尼(ACP-196)用于复发的慢性淋巴细胞白血病
N Engl J Med. 2016 Jan 28;374(4):323-32. doi: 10.1056/NEJMoa1509981. Epub 2015 Dec 7.
3
Ibrutinib and idelalisib target B cell receptor- but not CXCL12/CXCR4-controlled integrin-mediated adhesion in Waldenström macroglobulinemia.依鲁替尼和idelalisib靶向华氏巨球蛋白血症中B细胞受体,但不靶向CXCL12/CXCR4控制的整合素介导的黏附。
Haematologica. 2016 Mar;101(3):e111-5. doi: 10.3324/haematol.2015.137265. Epub 2015 Dec 3.
4
Cerdulatinib, a novel dual SYK/JAK kinase inhibitor, has broad anti-tumor activity in both ABC and GCB types of diffuse large B cell lymphoma.塞杜拉替尼是一种新型的SYK/JAK双重激酶抑制剂,对ABC和GCB两种类型的弥漫性大B细胞淋巴瘤均具有广泛的抗肿瘤活性。
Oncotarget. 2015 Dec 22;6(41):43881-96. doi: 10.18632/oncotarget.6316.
5
Inhibition of Lyn is a promising treatment for mantle cell lymphoma with bortezomib resistance.抑制Lyn是治疗对硼替佐米耐药的套细胞淋巴瘤的一种有前景的方法。
Oncotarget. 2015 Nov 10;6(35):38225-38. doi: 10.18632/oncotarget.5425.
6
Integration of innate into adaptive immune responses in ZAP-70-positive chronic lymphocytic leukemia.ZAP-70 阳性慢性淋巴细胞白血病中固有免疫与适应性免疫应答的整合。
Blood. 2016 Jan 28;127(4):436-48. doi: 10.1182/blood-2015-05-646935. Epub 2015 Oct 27.
7
DC-SIGN-expressing macrophages trigger activation of mannosylated IgM B-cell receptor in follicular lymphoma.表达DC-SIGN的巨噬细胞触发滤泡性淋巴瘤中甘露糖基化IgM B细胞受体的激活。
Blood. 2015 Oct 15;126(16):1911-20. doi: 10.1182/blood-2015-04-640912. Epub 2015 Aug 13.
8
A Positive Feedback Loop between Akt and mTORC2 via SIN1 Phosphorylation.通过SIN1磷酸化形成的Akt与mTORC2之间的正反馈回路。
Cell Rep. 2015 Aug 11;12(6):937-43. doi: 10.1016/j.celrep.2015.07.016. Epub 2015 Jul 30.
9
B-cell receptor signaling in the pathogenesis of lymphoid malignancies.B细胞受体信号传导在淋巴系统恶性肿瘤发病机制中的作用
Blood Cells Mol Dis. 2015 Oct;55(3):255-65. doi: 10.1016/j.bcmd.2015.06.016. Epub 2015 Jul 11.
10
Lectin binding to surface Ig variable regions provides a universal persistent activating signal for follicular lymphoma cells.凝集素与表面免疫球蛋白可变区的结合为滤泡性淋巴瘤细胞提供了一种普遍持续的激活信号。
Blood. 2015 Oct 15;126(16):1902-10. doi: 10.1182/blood-2015-04-640805. Epub 2015 Jul 20.

靶向白血病和淋巴瘤中的B细胞受体信号传导:方式与原因?

Targeting B-cell receptor signaling in leukemia and lymphoma: how and why?

作者信息

Allen John C, Talab Fatima, Slupsky Joseph R

机构信息

Department of Molecular & Clinical Pharmacology, Institute of Translational Medicine, University of Liverpool, Liverpool, L69 3GE, UK.

Redx Oncology Plc, Duncan Building, Royal Liverpool University Hospital, Daulby Street, Liverpool, L69 3GA, UK.

出版信息

Int J Hematol Oncol. 2016 May;5(1):37-53. doi: 10.2217/ijh-2016-0003. Epub 2016 May 26.

DOI:10.2217/ijh-2016-0003
PMID:30302202
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6171999/
Abstract

B-lymphocytes are dependent on B-cell receptor (BCR) signaling for the constant maintenance of their physiological function, and in many B-cell malignancies this signaling pathway is prone to aberrant activation. This understanding has led to an ever-increasing interest in the signaling networks activated following ligation of the BCR in both normal and malignant cells, and has been critical in establishing an array of small molecule inhibitors targeting BCR-induced signaling. By dissecting how different malignancies signal through BCR, researchers are contributing to the design of more customized therapeutics which have greater efficacy and lower toxicity than previous therapies. This allows clinicians access to an array of approaches to best treat patients whose malignancies have BCR signaling as a driver of pathogenesis.

摘要

B淋巴细胞的生理功能持续维持依赖于B细胞受体(BCR)信号传导,在许多B细胞恶性肿瘤中,该信号通路易于发生异常激活。这种认识使得人们对正常和恶性细胞中BCR连接后激活的信号网络越来越感兴趣,并且对于建立一系列靶向BCR诱导信号传导的小分子抑制剂至关重要。通过剖析不同恶性肿瘤如何通过BCR进行信号传导,研究人员正在为设计更具针对性的疗法做出贡献,这些疗法比以前的疗法具有更高的疗效和更低的毒性。这使临床医生能够采用一系列方法,以最佳方式治疗其恶性肿瘤由BCR信号传导作为发病机制驱动因素的患者。