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本文引用的文献

1
NR2F1 stratifies dormant disseminated tumor cells in breast cancer patients.NR2F1 使乳腺癌患者休眠性播散肿瘤细胞发生分群。
Breast Cancer Res. 2018 Oct 16;20(1):120. doi: 10.1186/s13058-018-1049-0.
2
SOX2 regulates common and specific stem cell features in the CNS and endoderm derived organs.SOX2 调节中枢神经系统和内胚层来源器官中的常见和特定干细胞特征。
PLoS Genet. 2018 Feb 12;14(2):e1007224. doi: 10.1371/journal.pgen.1007224. eCollection 2018 Feb.
3
The dark side of SOX2: cancer - a comprehensive overview.SOX2的阴暗面:癌症——全面概述
Oncotarget. 2017 Jul 4;8(27):44917-44943. doi: 10.18632/oncotarget.16570.
4
SOX2 promotes lineage plasticity and antiandrogen resistance in TP53- and RB1-deficient prostate cancer.SOX2促进TP53和RB1缺陷型前列腺癌中的谱系可塑性和抗雄激素耐药性。
Science. 2017 Jan 6;355(6320):84-88. doi: 10.1126/science.aah4307.
5
Rb1 and Trp53 cooperate to suppress prostate cancer lineage plasticity, metastasis, and antiandrogen resistance.Rb1和Trp53协同作用以抑制前列腺癌的谱系可塑性、转移和抗雄激素耐药性。
Science. 2017 Jan 6;355(6320):78-83. doi: 10.1126/science.aah4199.
6
The Relationship Between Dormant Cancer Cells and Their Microenvironment.休眠癌细胞与其微环境之间的关系
Adv Cancer Res. 2016;132:45-71. doi: 10.1016/bs.acr.2016.07.002. Epub 2016 Aug 25.
7
SOX2 functions as a molecular rheostat to control the growth, tumorigenicity and drug responses of pancreatic ductal adenocarcinoma cells.SOX2作为一种分子变阻器,可控制胰腺导管腺癌细胞的生长、致瘤性和药物反应。
Oncotarget. 2016 Jun 7;7(23):34890-906. doi: 10.18632/oncotarget.8994.
8
Metastatic Latency and Immune Evasion through Autocrine Inhibition of WNT.通过自分泌抑制WNT实现转移潜伏期和免疫逃逸
Cell. 2016 Mar 24;165(1):45-60. doi: 10.1016/j.cell.2016.02.025.
9
SOX2 boosts major tumor progression genes in prostate cancer and is a functional biomarker of lymph node metastasis.SOX2促进前列腺癌主要肿瘤进展基因,并且是淋巴结转移的功能性生物标志物。
Oncotarget. 2016 Mar 15;7(11):12372-85. doi: 10.18632/oncotarget.6029.
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Metastasis prevention by targeting the dormant niche.通过靶向休眠微环境预防转移。
Nat Rev Cancer. 2015 Apr;15(4):238-47. doi: 10.1038/nrc3910.

Sox2 剂量: Sox2 在正常细胞和肿瘤细胞功能中的关键决定因素。

Sox2 dosage: A critical determinant in the functions of Sox2 in both normal and tumor cells.

机构信息

Eppley Institute for Research in Cancer and Allied Diseases, Fred & Pamela Buffett Cancer Center, University of Nebraska Medical Center, Omaha, Nebraska.

出版信息

J Cell Physiol. 2019 Nov;234(11):19298-19306. doi: 10.1002/jcp.28610. Epub 2019 Apr 4.

DOI:10.1002/jcp.28610
PMID:31344986
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6662612/
Abstract

The stem cell transcription factor Sox2 is widely recognized for its many roles during normal development and cancer. Over the last several years, it has become increasingly evident that Sox2 dosage plays critical roles in both normal and malignant cells. The work described in this review indicates that the dosage of Sox2 influences cell fate decisions made during normal mammalian development, as well as cell fate decisions in cancer, including those that influence the tumor cell of origin and progression of the cancer. Equally important, Sox2 dosage is a key determinant in the proliferation of both normal cells and tumor cells, where proliferation is restricted in Sox2 cells. Collectively, the studies reviewed here indicate that tumor cells utilize the fundamental effects of Sox2 dosage to suit their own needs. Finally, we speculate that elevated expression of Sox2 helps establish and maintain tumor dormancy in Sox2-positive cancers.

摘要

干细胞转录因子 Sox2 在正常发育和癌症中发挥着多种作用,这一点已得到广泛认可。在过去的几年中, Sox2 剂量在正常细胞和恶性细胞中都起着关键作用,这一点变得越来越明显。本综述中描述的工作表明, Sox2 剂量影响正常哺乳动物发育过程中细胞命运的决定,以及癌症中的细胞命运决定,包括那些影响肿瘤细胞起源和癌症进展的决定。同样重要的是, Sox2 剂量是正常细胞和肿瘤细胞增殖的关键决定因素, Sox2 细胞的增殖受到限制。总的来说,这里综述的研究表明,肿瘤细胞利用 Sox2 剂量的基本作用来满足自身的需要。最后,我们推测 Sox2 的高表达有助于 Sox2 阳性癌症中肿瘤休眠的建立和维持。