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SLFN11 专题研讨会报告:从功能到作为癌症标志物的作用。

Report on the first SLFN11 monothematic workshop: from function to role as a biomarker in cancer.

机构信息

Istituto di Ricovero e Cura a Carattere Scientifico, Policlinico San Martino IST-Istituto Nazionale Tumori, Genoa, Italy.

Università degli Studi di Genova, Viale Benedetto XV, 6, 16132, Genoa, Italy.

出版信息

J Transl Med. 2017 Oct 2;15(1):199. doi: 10.1186/s12967-017-1296-3.

DOI:10.1186/s12967-017-1296-3
PMID:28969705
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5625715/
Abstract

SLFN11 is a recently discovered protein with a putative DNA/RNA helicase function. First identified in association with the maturation of thymocytes, SLFN11 was later causally associated, by two independent groups, with the resistance to DNA damaging agents such as topoisomerase I and II inhibitors, platinum compounds, and other alkylators, making it an attractive molecule for biomarker development. Later, SLFN11 was linked to antiviral response in human cells and interferon production, establishing a potential bond between immunity and chemotherapy. Recently, we demonstrated the potential role of SLN11 as a biomarker to predict sensitivity to the carboplatin/taxol combination in ovarian cancer. The present manuscript reports on the first international monothematic workshop on SLFN11. Several researchers from around the world, directly and actively involved in the discovery, functional characterization, and study of SLFN11 for its biomarker and medicinal properties gathered to share their views on the current knowledge advances concerning SLFN11. The aim of the manuscript is to summarize the authors' interventions and the main take-home messages resulting from the workshop.

摘要

SLFN11 是一种新发现的具有潜在 DNA/RNA 解旋酶功能的蛋白质。最初在胸腺细胞成熟过程中被发现,后来有两个独立的研究小组发现 SLFN11 与 DNA 损伤剂(如拓扑异构酶 I 和 II 抑制剂、铂化合物和其他烷化剂)的耐药性有关,这使得它成为生物标志物开发的有吸引力的分子。后来,SLFN11 与人细胞的抗病毒反应和干扰素产生有关,在免疫和化疗之间建立了潜在的联系。最近,我们证明了 SLN11 作为一种生物标志物预测卵巢癌对卡铂/紫杉醇联合化疗敏感性的潜力。本文报道了首次关于 SLFN11 的国际专题研讨会。来自世界各地的几位直接和积极参与 SLFN11 的发现、功能特征以及针对其生物标志物和药物特性进行研究的研究人员聚集在一起,分享他们对 SLFN11 的当前知识进展的看法。本文的目的是总结作者的干预措施以及研讨会得出的主要结论。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbac/5625715/f6cf177942fa/12967_2017_1296_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbac/5625715/b8a1d16f39ed/12967_2017_1296_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbac/5625715/93a2791fbe9f/12967_2017_1296_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbac/5625715/1c2040915030/12967_2017_1296_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbac/5625715/f6cf177942fa/12967_2017_1296_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbac/5625715/b8a1d16f39ed/12967_2017_1296_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbac/5625715/93a2791fbe9f/12967_2017_1296_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbac/5625715/1c2040915030/12967_2017_1296_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbac/5625715/f6cf177942fa/12967_2017_1296_Fig4_HTML.jpg

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Identification of genetic determinants of breast cancer immune phenotypes by integrative genome-scale analysis.通过整合全基因组规模分析鉴定乳腺癌免疫表型的遗传决定因素。
Oncoimmunology. 2017 Feb 6;6(2):e1253654. doi: 10.1080/2162402X.2016.1253654. eCollection 2017.
3
Resistance to PARP inhibitors by SLFN11 inactivation can be overcome by ATR inhibition.
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J Pathol Clin Res. 2025 Mar;11(2):e70025. doi: 10.1002/2056-4538.70025.
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Circulating tumor cells: advancing personalized therapy in small cell lung cancer patients.循环肿瘤细胞:推动小细胞肺癌患者的个性化治疗
Mol Oncol. 2024 Jul 2. doi: 10.1002/1878-0261.13696.
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Therapeutic Targeting of DNA Repair Pathways in Pediatric Extracranial Solid Tumors: Current State and Implications for Immunotherapy.小儿颅外实体瘤中DNA修复途径的治疗靶点:现状及对免疫治疗的影响
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