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Genome-wide CRISPR screen identifies MAD2L1BP and ANAPC15 as targets for brentuximab vedotin sensitivity in CD30+ peripheral T-cell lymphoma.

作者信息

Suto Keito, Takei Norio, Yokoyama Keito, Chiba Masahiro, Ishio Takashi, Maeda Michiyuki, Goto Hideki, Endo Tomoyuki, Teshima Takanori, Yang Yibin, Nakagawa Masao

机构信息

Department of Hematology, Hokkaido University Faculty of Medicine, Sapporo, Japan.

Institute for Animal Experimentation, Hokkaido University Faculty of Medicine, Sapporo, Japan.

出版信息

Leukemia. 2025 Jan;39(1):243-247. doi: 10.1038/s41375-024-02441-1. Epub 2024 Oct 21.

DOI:10.1038/s41375-024-02441-1
PMID:39433928
Abstract
摘要

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Genome-wide CRISPR screen identifies MAD2L1BP and ANAPC15 as targets for brentuximab vedotin sensitivity in CD30+ peripheral T-cell lymphoma.全基因组CRISPR筛选确定MAD2L1BP和ANAPC15是CD30+外周T细胞淋巴瘤中对brentuximab vedotin敏感性的靶点。
Leukemia. 2025 Jan;39(1):243-247. doi: 10.1038/s41375-024-02441-1. Epub 2024 Oct 21.
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Antibody-Drug Conjugates Targeting CD30 in T-Cell Lymphomas: Clinical Progression and Mechanism.靶向T细胞淋巴瘤中CD30的抗体药物偶联物:临床进展与机制
Cancers (Basel). 2025 Feb 2;17(3):496. doi: 10.3390/cancers17030496.

本文引用的文献

1
Principles and dynamics of spindle assembly checkpoint signalling.纺锤体组装检验点信号转导的原理与动力学。
Nat Rev Mol Cell Biol. 2023 Aug;24(8):543-559. doi: 10.1038/s41580-023-00593-z. Epub 2023 Mar 24.
2
Genome-wide CRISPR screens identify CD48 defining susceptibility to NK cytotoxicity in peripheral T-cell lymphomas.全基因组 CRISPR 筛选鉴定出外周 T 细胞淋巴瘤中 CD48 决定对 NK 细胞毒性的易感性。
Blood. 2022 Nov 3;140(18):1951-1963. doi: 10.1182/blood.2022015646.
3
The ECHELON-2 Trial: 5-year results of a randomized, phase III study of brentuximab vedotin with chemotherapy for CD30-positive peripheral T-cell lymphoma.
ECHELON-2 试验:brentuximab vedotin 联合化疗治疗 CD30 阳性外周 T 细胞淋巴瘤的随机 III 期研究的 5 年结果。
Ann Oncol. 2022 Mar;33(3):288-298. doi: 10.1016/j.annonc.2021.12.002. Epub 2021 Dec 16.
4
Genome-wide CRISPR screen identifies CDK6 as a therapeutic target in adult T-cell leukemia/lymphoma.全基因组 CRISPR 筛选鉴定 CDK6 为成人 T 细胞白血病/淋巴瘤的治疗靶点。
Blood. 2022 Mar 10;139(10):1541-1556. doi: 10.1182/blood.2021012734.
5
Mitotic slippage is determined by p31 and the weakening of the spindle-assembly checkpoint.有丝分裂滑走取决于 p31 和纺锤体装配检查点的弱化。
Oncogene. 2020 Mar;39(13):2819-2834. doi: 10.1038/s41388-020-1187-6. Epub 2020 Feb 6.
6
Systematic genetic mapping of necroptosis identifies SLC39A7 as modulator of death receptor trafficking.系统遗传作图鉴定出 SLC39A7 是死亡受体运输的调节剂。
Cell Death Differ. 2019 Jun;26(6):1138-1155. doi: 10.1038/s41418-018-0192-6. Epub 2018 Sep 20.
7
Targeting the HTLV-I-Regulated BATF3/IRF4 Transcriptional Network in Adult T Cell Leukemia/Lymphoma.靶向 HTLV-I 调节的 BATF3/IRF4 转录网络治疗成人 T 细胞白血病/淋巴瘤。
Cancer Cell. 2018 Aug 13;34(2):286-297.e10. doi: 10.1016/j.ccell.2018.06.014. Epub 2018 Jul 26.
8
CD30 Downregulation, MMAE Resistance, and MDR1 Upregulation Are All Associated with Resistance to Brentuximab Vedotin.CD30下调、MMAE耐药和MDR1上调均与对维布妥昔单抗耐药相关。
Mol Cancer Ther. 2015 Jun;14(6):1376-84. doi: 10.1158/1535-7163.MCT-15-0036. Epub 2015 Apr 3.
9
Objective responses in relapsed T-cell lymphomas with single-agent brentuximab vedotin.单药 Brentuximab vedotin 治疗复发 T 细胞淋巴瘤的客观缓解。
Blood. 2014 May 15;123(20):3095-100. doi: 10.1182/blood-2013-12-542142. Epub 2014 Mar 20.
10
Brentuximab vedotin (SGN-35) in patients with relapsed or refractory systemic anaplastic large-cell lymphoma: results of a phase II study.本妥昔单抗维迪昔(SGN-35)治疗复发或难治性系统性间变大细胞淋巴瘤患者的Ⅱ期研究结果。
J Clin Oncol. 2012 Jun 20;30(18):2190-6. doi: 10.1200/JCO.2011.38.0402. Epub 2012 May 21.