• 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

靶向 SOX2 在癌症治疗中的应用。

Targeting SOX2 in anticancer therapy.

机构信息

a Skin Cancer Unit, German Cancer Research Center (DKFZ), Heidelberg and Department of Dermatology, Venereology and Allergology , University Medical Center Mannheim, Ruprecht-Karl University of Heidelberg , Mannheim , Germany.

出版信息

Expert Opin Ther Targets. 2018 Dec;22(12):983-991. doi: 10.1080/14728222.2018.1538359. Epub 2018 Oct 26.

DOI:10.1080/14728222.2018.1538359
PMID:30366514
Abstract

SOX2 is a transcription factor that is important in the development and maintenance of the stem cell state. Furthermore, SOX2 is associated with cancer progression because it promotes the migration, invasion, and proliferation of cancer cells. SOX2 is also expressed in cancer stem cells and appears to be involved in the resistance toward anticancer therapies. These features render SOX2 an attractive target for cancer therapy. Areas covered: In this review, we highlight the role of SOX2 in cancer and in the resistance toward anticancer therapies. We summarize recent studies dealing with SOX2 as a direct or indirect therapeutic target in cancer. Expert opinion: SOX2 is an attractive target in cancer therapy because of its role in cancer progression and therapy resistance. SOX2 is a transcription factor, hence direct targeting is difficult. Studies aimed at a functional depletion, for example by knock-down with siRNAs, are difficult to translate into clinical settings. Alternatively, the identification of SOX2 upstream or downstream regulators that are easier to target is of paramount importance.

摘要

SOX2 是一种转录因子,在干细胞状态的发育和维持中起着重要作用。此外,SOX2 与癌症进展有关,因为它促进癌细胞的迁移、侵袭和增殖。SOX2 也在癌症干细胞中表达,似乎参与了对癌症治疗的耐药性。这些特征使 SOX2 成为癌症治疗的一个有吸引力的靶点。

涵盖领域

在这篇综述中,我们强调了 SOX2 在癌症中和在对抗癌治疗的耐药性中的作用。我们总结了最近关于 SOX2 作为癌症的直接或间接治疗靶点的研究。

专家意见

SOX2 是癌症治疗中一个有吸引力的靶点,因为它在癌症进展和治疗耐药性中起作用。SOX2 是一种转录因子,因此直接靶向治疗很困难。旨在通过 siRNA 敲低等方法实现功能耗竭的研究很难转化为临床环境。另一方面,确定更容易靶向的 SOX2 上游或下游调节剂至关重要。

相似文献

1
Targeting SOX2 in anticancer therapy.靶向 SOX2 在癌症治疗中的应用。
Expert Opin Ther Targets. 2018 Dec;22(12):983-991. doi: 10.1080/14728222.2018.1538359. Epub 2018 Oct 26.
2
Silencing SOX2 Expression by RNA Interference Inhibits Proliferation, Invasion and Metastasis, and Induces Apoptosis through MAP4K4/JNK Signaling Pathway in Human Laryngeal Cancer TU212 Cells.通过RNA干扰沉默SOX2表达可抑制人喉癌TU212细胞的增殖、侵袭和转移,并通过MAP4K4/JNK信号通路诱导细胞凋亡。
J Histochem Cytochem. 2015 Sep;63(9):721-33. doi: 10.1369/0022155415590829. Epub 2015 May 22.
3
SOX2 promotes the migration and invasion of laryngeal cancer cells by induction of MMP-2 via the PI3K/Akt/mTOR pathway.SOX2 通过 PI3K/Akt/mTOR 通路诱导 MMP-2 的表达促进喉癌细胞的迁移和侵袭。
Oncol Rep. 2014 Jun;31(6):2651-9. doi: 10.3892/or.2014.3120. Epub 2014 Apr 2.
4
SOX2 in development and cancer biology.发育与癌症生物学中的SOX2
Semin Cancer Biol. 2020 Dec;67(Pt 1):74-82. doi: 10.1016/j.semcancer.2019.08.007. Epub 2019 Aug 11.
5
SOX2-RNAi attenuates S-phase entry and induces RhoA-dependent switch to protease-independent amoeboid migration in human glioma cells.SOX2-RNAi 减弱 S 期进入并诱导 RhoA 依赖性向非依赖蛋白酶的阿米巴样迁移在人神经胶质瘤细胞中。
Mol Cancer. 2011 Nov 9;10:137. doi: 10.1186/1476-4598-10-137.
6
SOX2-mediated upregulation of CD24 promotes adaptive resistance toward targeted therapy in melanoma.SOX2介导的CD24上调促进黑色素瘤对靶向治疗的适应性耐药。
Int J Cancer. 2018 Dec 15;143(12):3131-3142. doi: 10.1002/ijc.31609. Epub 2018 Oct 16.
7
XIAP Limits Autophagic Degradation of Sox2 and Is A Therapeutic Target in Nasopharyngeal Carcinoma Stem Cells.XIAP 限制 Sox2 的自噬降解,是鼻咽癌干细胞的治疗靶点。
Theranostics. 2018 Feb 5;8(6):1494-1510. doi: 10.7150/thno.21717. eCollection 2018.
8
LncRNA SOX2-OT is a novel prognostic biomarker for osteosarcoma patients and regulates osteosarcoma cells proliferation and motility through modulating SOX2.LncRNA SOX2-OT 是骨肉瘤患者的一种新型预后生物标志物,通过调节 SOX2 来调节骨肉瘤细胞的增殖和迁移。
IUBMB Life. 2017 Nov;69(11):867-876. doi: 10.1002/iub.1681. Epub 2017 Sep 29.
9
Linking Pluripotency Reprogramming and Cancer.连接多能性重编程与癌症。
Stem Cells Transl Med. 2017 Feb;6(2):335-339. doi: 10.5966/sctm.2015-0225. Epub 2016 Sep 20.
10
FoxM1 Promotes Stemness and Radio-Resistance of Glioblastoma by Regulating the Master Stem Cell Regulator Sox2.FoxM1通过调控主要干细胞调节因子Sox2促进胶质母细胞瘤的干性和放射抗性。
PLoS One. 2015 Oct 7;10(10):e0137703. doi: 10.1371/journal.pone.0137703. eCollection 2015.

引用本文的文献

1
The role of SOX transcription factors in prostate cancer: Focusing on SOX2.SOX转录因子在前列腺癌中的作用:聚焦于SOX2
Genes Dis. 2025 May 21;12(6):101692. doi: 10.1016/j.gendis.2025.101692. eCollection 2025 Nov.
2
Elevated SNHG1 promotes invasion and migration of Cd(II)-transformed cells through Sox2, Rac1, and Slug.升高的SNHG1通过Sox2、Rac1和Slug促进镉(II)转化细胞的侵袭和迁移。
Toxicol Appl Pharmacol. 2025 Sep;502:117452. doi: 10.1016/j.taap.2025.117452. Epub 2025 Jun 24.
3
Dihydrotanshinone I enhanced BRAF mutant melanoma treatment efficacy by inhibiting the STAT3/SOX2 signaling pathway.
二氢丹参酮I通过抑制STAT3/SOX2信号通路增强BRAF突变型黑色素瘤的治疗效果。
Front Oncol. 2025 Jan 29;15:1429018. doi: 10.3389/fonc.2025.1429018. eCollection 2025.
4
IMPA1-derived inositol maintains stemness in castration-resistant prostate cancer via IMPDH2 activation.IMP A1 衍生的肌醇通过 IMPDH2 的激活来维持去势抵抗性前列腺癌的干性。
J Exp Med. 2024 Nov 4;221(11). doi: 10.1084/jem.20231832. Epub 2024 Oct 29.
5
Blood-, Tissue- and Urine-Based Prognostic Biomarkers of Upper Tract Urothelial Carcinoma.基于血液、组织和尿液的上尿路尿路上皮癌预后生物标志物
Diagnostics (Basel). 2024 Aug 31;14(17):1927. doi: 10.3390/diagnostics14171927.
6
Dexamethasone-tamoxifen combination exerts synergistic therapeutic effects in tamoxifen-resistance breast cancer cells.地塞米松-他莫昔芬联合用药对他莫昔芬耐药乳腺癌细胞发挥协同治疗作用。
Biosci Rep. 2024 Jul 31;44(7). doi: 10.1042/BSR20240367.
7
Morphological and Molecular Biological Characteristics of Experimental Rat Glioblastoma Tissue Strains Induced by Different Carcinogenic Chemicals.不同致癌化学物质诱导的实验性大鼠胶质母细胞瘤组织株的形态学和分子生物学特征
Biomedicines. 2024 Mar 22;12(4):713. doi: 10.3390/biomedicines12040713.
8
STIM1/SOX2 proteins are co-expressed in the tumor and microenvironmental stromal cells of pancreatic ductal adenocarcinoma and ampullary carcinoma.STIM1/SOX2 蛋白在胰腺导管腺癌和壶腹癌的肿瘤和微环境基质细胞中共同表达。
World J Surg Oncol. 2024 Mar 26;22(1):84. doi: 10.1186/s12957-024-03356-y.
9
SOX2 and OCT4 mediate radiation and drug resistance in pancreatic tumor organoids.SOX2和OCT4介导胰腺肿瘤类器官的放射和耐药性。
Cell Death Discov. 2024 Mar 1;10(1):106. doi: 10.1038/s41420-024-01871-1.
10
Significance of OCT3/4 and SOX2 antigens expression by leukemic blast cells in adult acute leukemia.成人急性白血病中白血病原始细胞OCT3/4和SOX2抗原表达的意义
J Egypt Natl Canc Inst. 2024 Feb 12;36(1):5. doi: 10.1186/s43046-024-00209-3.