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膀胱癌干细胞的起源与演变

The Origin and Evolution of Bladder Cancer Stem Cells.

作者信息

Tan Jiufeng, Wang Yao, Sun Lihui, Xu Siqi, Li Charles, Jin Xuefei

机构信息

2nd Inpatient Area of Urology Department, China-Japan Union Hospital of Jilin University, Changchun, China.

Key Laboratory of Urology Tumor of Jilin Province, Changchun, China.

出版信息

Front Cell Dev Biol. 2022 Jul 12;10:950241. doi: 10.3389/fcell.2022.950241. eCollection 2022.

DOI:10.3389/fcell.2022.950241
PMID:35903544
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9314767/
Abstract

Bladder cancer is the most common malignant tumor of the urinary system. Bladder cancer stem cells (BCSCs) play key roles in tumor initiation, metastasis, relapse and drug-resistance. Investigation of BCSCs is of great value. On the basis of a review of normal bladder stem cells and universal cancer stem cells (CSCs), we summarize the origin of BCSCs, isolation and identification of CSCs from bladder cancer, signaling pathway of BCSCs, BCSCs targeted therapy, and relationship of BCSCs with non-muscle invasiveness and muscle invasiveness. This review aims to provide better elucidation about BCSCs, and provide constructive data for classification, prognosis, treatment and early intervention of bladder cancer.

摘要

膀胱癌是泌尿系统最常见的恶性肿瘤。膀胱癌细胞(BCSCs)在肿瘤的起始、转移、复发和耐药性方面起着关键作用。对BCSCs的研究具有重要价值。在回顾正常膀胱干细胞和通用癌症干细胞(CSCs)的基础上,我们总结了BCSCs的起源、从膀胱癌中分离和鉴定CSCs、BCSCs的信号通路、BCSCs靶向治疗以及BCSCs与非肌层浸润性和肌层浸润性的关系。本综述旨在更好地阐明BCSCs,并为膀胱癌的分类、预后、治疗和早期干预提供建设性数据。

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The Origin and Evolution of Bladder Cancer Stem Cells.膀胱癌干细胞的起源与演变
Front Cell Dev Biol. 2022 Jul 12;10:950241. doi: 10.3389/fcell.2022.950241. eCollection 2022.
2
The KMT1A-GATA3-STAT3 Circuit Is a Novel Self-Renewal Signaling of Human Bladder Cancer Stem Cells.KMT1A-GATA3-STAT3 通路是人膀胱癌干细胞的一种新型自我更新信号通路。
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本文引用的文献

1
Single-cell Sequencing Reveals Variants in ARID1A, GPRC5A and MLL2 Driving Self-renewal of Human Bladder Cancer Stem Cells.单细胞测序揭示 ARID1A、GPRC5A 和 MLL2 变异驱动人类膀胱癌干细胞自我更新。
Eur Urol. 2017 Jan;71(1):8-12. doi: 10.1016/j.eururo.2016.06.025. Epub 2016 Jul 4.
2
GALNT1-Mediated Glycosylation and Activation of Sonic Hedgehog Signaling Maintains the Self-Renewal and Tumor-Initiating Capacity of Bladder Cancer Stem Cells.GALNT1 介导的糖基化和 Sonic Hedgehog 信号的激活维持膀胱癌干细胞的自我更新和肿瘤起始能力。
Cancer Res. 2016 Mar 1;76(5):1273-83. doi: 10.1158/0008-5472.CAN-15-2309. Epub 2015 Dec 16.
3
Cancer epigenetics: tumor heterogeneity, plasticity of stem-like states, and drug resistance.癌症表观遗传学:肿瘤异质性、干细胞样状态的可塑性和耐药性。
Mol Cell. 2014 Jun 5;54(5):716-27. doi: 10.1016/j.molcel.2014.05.015.
4
Tumor heterogeneity and cancer stem cell paradigm: updates in concept, controversies and clinical relevance.肿瘤异质性与癌症干细胞范式:概念更新、争议及临床相关性
Int J Cancer. 2015 May 1;136(9):1991-2000. doi: 10.1002/ijc.28804. Epub 2014 Mar 4.
5
Antibody therapy targeting the CD47 protein is effective in a model of aggressive metastatic leiomyosarcoma.抗体疗法靶向 CD47 蛋白在侵袭性转移性平滑肌肉瘤模型中有效。
Proc Natl Acad Sci U S A. 2012 Apr 24;109(17):6656-61. doi: 10.1073/pnas.1121629109. Epub 2012 Mar 26.
6
The CD47-signal regulatory protein alpha (SIRPa) interaction is a therapeutic target for human solid tumors.CD47 信号调节蛋白α(SIRPa)相互作用是人类实体瘤的治疗靶点。
Proc Natl Acad Sci U S A. 2012 Apr 24;109(17):6662-7. doi: 10.1073/pnas.1121623109. Epub 2012 Mar 26.
7
Hedgehog/Wnt feedback supports regenerative proliferation of epithelial stem cells in bladder. Hedgehog/Wnt 反馈支持膀胱上皮干细胞的再生增殖。
Nature. 2011 Apr 7;472(7341):110-4. doi: 10.1038/nature09851. Epub 2011 Mar 9.
8
A novel functional role for the oocyte-specific transcription factor newborn ovary homeobox (NOBOX) during early embryonic development in cattle.牛早期胚胎发育中卵母细胞特异性转录因子新生卵巢同源盒(NOBOX)的新功能作用。
Endocrinology. 2011 Mar;152(3):1013-23. doi: 10.1210/en.2010-1134. Epub 2010 Dec 30.
9
Molecular genetics of bladder cancer: Emerging mechanisms of tumor initiation and progression.膀胱癌的分子遗传学:肿瘤发生和进展的新机制。
Urol Oncol. 2010 Jul-Aug;28(4):429-40. doi: 10.1016/j.urolonc.2010.04.008.
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Targeting Notch to target cancer stem cells.针对 Notch 以靶向肿瘤干细胞。
Clin Cancer Res. 2010 Jun 15;16(12):3141-52. doi: 10.1158/1078-0432.CCR-09-2823. Epub 2010 Jun 8.