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本文引用的文献

1
A Mesenchymal Tumor Cell State Confers Increased Dependency on the BCL-XL Antiapoptotic Protein in Kidney Cancer.间质肿瘤细胞状态赋予肾癌细胞对 BCL-XL 抗凋亡蛋白的依赖性增加。
Clin Cancer Res. 2022 Nov 1;28(21):4689-4701. doi: 10.1158/1078-0432.CCR-22-0669.
2
A Targetable Myeloid Inflammatory State Governs Disease Recurrence in Clear-Cell Renal Cell Carcinoma.靶向髓系炎症状态可控制透明细胞肾细胞癌的疾病复发。
Cancer Discov. 2022 Oct 5;12(10):2308-2329. doi: 10.1158/2159-8290.CD-21-0925.
3
Addition of Navitoclax to Ongoing Ruxolitinib Therapy for Patients With Myelofibrosis With Progression or Suboptimal Response: Phase II Safety and Efficacy.纳武利尤单抗联合芦可替尼治疗进展或应答不足的骨髓纤维化患者的Ⅱ期安全性和有效性。
J Clin Oncol. 2022 May 20;40(15):1671-1680. doi: 10.1200/JCO.21.02188. Epub 2022 Feb 18.
4
Development of a BCL-xL and BCL-2 dual degrader with improved anti-leukemic activity.开发一种具有增强抗白血病活性的 BCL-xL 和 BCL-2 双降解剂。
Nat Commun. 2021 Nov 25;12(1):6896. doi: 10.1038/s41467-021-27210-x.
5
Dual targeting of the DNA damage response pathway and BCL-2 in diffuse large B-cell lymphoma.双重靶向弥漫性大 B 细胞淋巴瘤的 DNA 损伤反应通路和 BCL-2。
Leukemia. 2022 Jan;36(1):197-209. doi: 10.1038/s41375-021-01347-6. Epub 2021 Jul 24.
6
Lenvatinib plus Pembrolizumab or Everolimus for Advanced Renal Cell Carcinoma.仑伐替尼联合帕博利珠单抗或依维莫司治疗晚期肾细胞癌。
N Engl J Med. 2021 Apr 8;384(14):1289-1300. doi: 10.1056/NEJMoa2035716. Epub 2021 Feb 13.
7
Integrative molecular characterization of sarcomatoid and rhabdoid renal cell carcinoma.肉瘤样和横纹肌样肾细胞癌的综合分子特征。
Nat Commun. 2021 Feb 5;12(1):808. doi: 10.1038/s41467-021-21068-9.
8
Therapeutic development and current uses of BCL-2 inhibition.BCL-2 抑制的治疗开发和当前用途。
Hematology Am Soc Hematol Educ Program. 2020 Dec 4;2020(1):1-9. doi: 10.1182/hematology.2020000154.
9
Sarcomatoid renal cell carcinoma: biology, natural history and management.肉瘤样肾细胞癌:生物学、自然史与治疗。
Nat Rev Urol. 2020 Dec;17(12):659-678. doi: 10.1038/s41585-020-00382-9. Epub 2020 Oct 13.
10
Efficacy and Safety of Nivolumab Plus Ipilimumab versus Sunitinib in First-line Treatment of Patients with Advanced Sarcomatoid Renal Cell Carcinoma.纳武利尤单抗联合伊匹单抗对比舒尼替尼用于晚期肉瘤样肾细胞癌患者一线治疗的疗效和安全性。
Clin Cancer Res. 2021 Jan 1;27(1):78-86. doi: 10.1158/1078-0432.CCR-20-2063. Epub 2020 Sep 1.

通过抑制 BCL-XL 诱导肾癌细胞凋亡。

XL-ing at Induction of Apoptosis in Kidney Cancer through Inhibition of BCL-XL.

机构信息

Human Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, New York.

Department of Surgery, Urology Service, Memorial Sloan Kettering Cancer Center, New York, New York.

出版信息

Clin Cancer Res. 2022 Nov 1;28(21):4600-4602. doi: 10.1158/1078-0432.CCR-22-2104.

DOI:10.1158/1078-0432.CCR-22-2104
PMID:35984355
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9633424/
Abstract

Through analysis of the cancer dependency map of CRISPR and short hairpin RNA datasets, the antiapoptotic BCL-XL was found to be a selective dependency in kidney cancer. Among kidney cancers, BCL-XL inhibition is most active in those with a mesenchymal gene signature, which portends a poor prognosis and response to current therapies. See related article by Grubb et al., p. 4689.

摘要

通过对 CRISPR 和短发夹 RNA 数据集的癌症依赖图谱进行分析,发现抗凋亡蛋白 BCL-XL 是肾癌的一个选择性依赖性。在肾癌中,具有间充质基因特征的肿瘤对 BCL-XL 抑制最为活跃,这预示着预后不良且对当前治疗方法无反应。详见 Grubb 等人的相关文章,第 4689 页。