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Prevalence of IGLV3-21R110 among familial CLL: a retrospective study of 45 cases.

作者信息

Armand Marine, Verrier Patricia, Theves Floriane, Bravetti Clotilde, Le Garff-Tavernier Magali, Choquet Sylvain, Davi Frédéric

机构信息

Department of Biological Hematology, and.

Department of Clinical Hematology, Hôpital Pitié-Salpêtrière, Sorbonne Université, Assistance Publique-Hôpitaux de Paris, Paris, France.

出版信息

Blood Adv. 2022 Jun 28;6(12):3632-3635. doi: 10.1182/bloodadvances.2021006658.

DOI:10.1182/bloodadvances.2021006658
PMID:35294518
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9631562/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad54/9631562/7939a41bfbab/advancesADV2021006658f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad54/9631562/7939a41bfbab/advancesADV2021006658f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad54/9631562/7939a41bfbab/advancesADV2021006658f1.jpg

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Prevalence of IGLV3-21R110 among familial CLL: a retrospective study of 45 cases.家族性慢性淋巴细胞白血病中IGLV3-21R110的患病率:45例回顾性研究
Blood Adv. 2022 Jun 28;6(12):3632-3635. doi: 10.1182/bloodadvances.2021006658.
2
IGLV3-21R110 identifies an aggressive biological subtype of chronic lymphocytic leukemia with intermediate epigenetics.IGLV3-21R110 鉴定出具有中间表观遗传学的侵袭性慢性淋巴细胞白血病生物学亚型。
Blood. 2021 May 27;137(21):2935-2946. doi: 10.1182/blood.2020008311.
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Time to include IGLV3-21R110 status in CLL prognostication?是时候将IGLV3-21R110状态纳入慢性淋巴细胞白血病的预后评估了吗?
Blood Adv. 2023 Dec 12;7(23):7382-7383. doi: 10.1182/bloodadvances.2023011243.
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IGLV3-21R110 mutation has prognostic value in patients with treatment-naive chronic lymphocytic leukemia.IGLV3-21R110突变对未经治疗的慢性淋巴细胞白血病患者具有预后价值。
Blood Adv. 2023 Dec 12;7(23):7384-7391. doi: 10.1182/bloodadvances.2023010132.
5
is an inherited risk factor for CLL through the acquisition of a single-point mutation enabling autonomous BCR signaling.是 CLL 的遗传风险因素,通过获得允许自主 BCR 信号转导的单点突变。
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引用本文的文献

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IGLV3-21R110 mutation has prognostic value in patients with treatment-naive chronic lymphocytic leukemia.IGLV3-21R110突变对未经治疗的慢性淋巴细胞白血病患者具有预后价值。
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2
Gene and pathway based burden analyses in familial lymphoid cancer cases: Rare variants in immune pathway genes.基于基因和通路的家族性淋巴癌病例负担分析:免疫通路基因中的罕见变异。
PLoS One. 2023 Jun 28;18(6):e0287602. doi: 10.1371/journal.pone.0287602. eCollection 2023.

本文引用的文献

1
Genetic predisposition to chronic lymphocytic leukemia.慢性淋巴细胞白血病的遗传易感性。
Hemasphere. 2019 Jun 30;3(Suppl). doi: 10.1097/HS9.0000000000000194. eCollection 2019 Jun.
2
Consistent B Cell Receptor Immunoglobulin Features Between Siblings in Familial Chronic Lymphocytic Leukemia.家族性慢性淋巴细胞白血病患者兄弟姐妹间一致的B细胞受体免疫球蛋白特征
Front Oncol. 2021 Aug 26;11:740083. doi: 10.3389/fonc.2021.740083. eCollection 2021.
3
Genome-wide association study identifies risk loci for progressive chronic lymphocytic leukemia.
全基因组关联研究鉴定出进展性慢性淋巴细胞白血病的风险位点。
Nat Commun. 2021 Jan 28;12(1):665. doi: 10.1038/s41467-020-20822-9.
4
IGLV3-21R110 identifies an aggressive biological subtype of chronic lymphocytic leukemia with intermediate epigenetics.IGLV3-21R110 鉴定出具有中间表观遗传学的侵袭性慢性淋巴细胞白血病生物学亚型。
Blood. 2021 May 27;137(21):2935-2946. doi: 10.1182/blood.2020008311.
5
Celebrating 20 Years of IGHV Mutation Analysis in CLL.庆祝慢性淋巴细胞白血病IGHV突变分析20周年。
Hemasphere. 2020 Jan 22;4(1):e334. doi: 10.1097/HS9.0000000000000334. eCollection 2020 Feb.
6
is an inherited risk factor for CLL through the acquisition of a single-point mutation enabling autonomous BCR signaling.是 CLL 的遗传风险因素,通过获得允许自主 BCR 信号转导的单点突变。
Proc Natl Acad Sci U S A. 2020 Feb 25;117(8):4320-4327. doi: 10.1073/pnas.1913810117. Epub 2020 Feb 11.
7
The Light Chain IgLV3-21 Defines a New Poor Prognostic Subgroup in Chronic Lymphocytic Leukemia: Results of a Multicenter Study.轻链 IgLV3-21 定义了慢性淋巴细胞白血病的一个新的预后不良亚组:一项多中心研究的结果。
Clin Cancer Res. 2018 Oct 15;24(20):5048-5057. doi: 10.1158/1078-0432.CCR-18-0133. Epub 2018 Jun 26.
8
Distinct homotypic B-cell receptor interactions shape the outcome of chronic lymphocytic leukaemia.不同的同源 B 细胞受体相互作用塑造慢性淋巴细胞白血病的结局。
Nat Commun. 2017 Jun 9;8:15746. doi: 10.1038/ncomms15746.
9
Inherited susceptibility to chronic lymphocytic leukemia: evidence and prospects for the future.遗传性慢性淋巴细胞白血病易感性:证据与未来展望。
Ther Adv Hematol. 2013 Aug;4(4):298-308. doi: 10.1177/2040620713495639.
10
Genome-wide association study identifies a novel susceptibility locus at 6p21.3 among familial CLL.全基因组关联研究在家族性 CLL 中鉴定出位于 6p21.3 的新的易感性位点。
Blood. 2011 Feb 10;117(6):1911-6. doi: 10.1182/blood-2010-09-308205. Epub 2010 Dec 3.