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癌症作为一种类似重编程的疾病:对肿瘤发生和治疗的影响。

Cancer as a reprogramming-like disease: implications in tumor development and treatment.

机构信息

Instituto de Biología Molecular y Celular del Cáncer, Centro de Investigación del Cáncer, CSIC/Universidad de Salamanca, Campus M. Unamuno s/n, 37007 Salamanca, Spain.

出版信息

Semin Cancer Biol. 2010 Apr;20(2):93-7. doi: 10.1016/j.semcancer.2010.02.001. Epub 2010 Feb 24.

DOI:10.1016/j.semcancer.2010.02.001
PMID:20188174
Abstract

Cancer is a clonal malignant disease originated in a single cell and characterized by the accumulation of partially differentiated cells that are phenotypically reminiscent of normal stages of differentiation. Given the fact that human cancer is diagnosed at later stages and cannot be monitored during its natural evolution, the origin of tumors has been a subject of continuing discussion. Animal models provide a means to determine the identity of the cell-of-origin leading to malignancy and to develop new treatments. Recent findings in mice have shown that cancer stem cells could arise through a reprogramming-like mechanism, suggesting that genetic lesions that initiate the cancer process might be dispensable for tumor progression and maintenance. This review addresses the impact of these results toward a better understanding of carcinogenesis and proposes research avenues for tackling these issues in the future.

摘要

癌症是一种克隆性恶性疾病,起源于单个细胞,其特征是部分分化细胞的积累,这些细胞在表型上类似于正常的分化阶段。鉴于人类癌症在晚期才被诊断出来,而且在其自然演变过程中无法被监测到,因此肿瘤的起源一直是一个持续讨论的话题。动物模型为确定导致恶性肿瘤的起始细胞提供了一种手段,并为开发新的治疗方法提供了思路。最近在小鼠身上的发现表明,癌症干细胞可能通过类似于重编程的机制产生,这表明启动癌症进程的遗传病变对于肿瘤的进展和维持可能是可有可无的。这篇综述讨论了这些结果对更好地理解致癌作用的影响,并提出了未来解决这些问题的研究途径。

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Cancer as a reprogramming-like disease: implications in tumor development and treatment.癌症作为一种类似重编程的疾病:对肿瘤发生和治疗的影响。
Semin Cancer Biol. 2010 Apr;20(2):93-7. doi: 10.1016/j.semcancer.2010.02.001. Epub 2010 Feb 24.
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In Vivo Generation of Leukemic Stem Cells by HSC Targeting by Transgenesis.通过转基因靶向 HSC 体内生成白血病干细胞。
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Roots and stems: stem cells in cancer.根源与茎干:癌症中的干细胞
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Overlapping genes may control reprogramming of mouse somatic cells into induced pluripotent stem cells (iPSCs) and breast cancer stem cells.重叠基因可能控制小鼠体细胞重编程为诱导多能干细胞(iPSC)以及乳腺癌干细胞的过程。
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Genetically engineered mouse models of human B-cell precursor leukemias.人类B细胞前体白血病的基因工程小鼠模型。

本文引用的文献

1
Biological and molecular heterogeneity of breast cancers correlates with their cancer stem cell content.乳腺癌的生物学和分子异质性与其癌症干细胞含量相关。
Cell. 2010 Jan 8;140(1):62-73. doi: 10.1016/j.cell.2009.12.007.
2
Combinations of genetic mutations in the adult neural stem cell compartment determine brain tumour phenotypes.成人神经干细胞区室中的基因突变组合决定了脑肿瘤表型。
EMBO J. 2010 Jan 6;29(1):222-35. doi: 10.1038/emboj.2009.327. Epub 2009 Nov 19.
3
The tumor suppressor p53 regulates polarity of self-renewing divisions in mammary stem cells.
Cell Cycle. 2014;13(18):2836-46. doi: 10.4161/15384101.2014.949137.
4
Xenopatients 2.0: reprogramming the epigenetic landscapes of patient-derived cancer genomes.异种患者2.0:重编程患者来源的癌症基因组的表观遗传景观。
Cell Cycle. 2014;13(3):358-70. doi: 10.4161/cc.27770. Epub 2014 Jan 9.
5
Nuclear reprogramming of luminal-like breast cancer cells generates Sox2-overexpressing cancer stem-like cellular states harboring transcriptional activation of the mTOR pathway.腔面型乳腺癌细胞的核重编程产生 Sox2 过表达的癌症干细胞样细胞状态,其特征是 mTOR 通路的转录激活。
Cell Cycle. 2013 Sep 15;12(18):3109-24. doi: 10.4161/cc.26173. Epub 2013 Aug 21.
6
Genetic background affects susceptibility to tumoral stem cell reprogramming.遗传背景影响肿瘤干细胞重编程的易感性。
Cell Cycle. 2013 Aug 1;12(15):2505-9. doi: 10.4161/cc.25544. Epub 2013 Jul 8.
7
A New Strategy to Find Targets for Anticancer Therapy: Chemokine CXCL14/BRAK Is a Multifunctional Tumor Suppressor for Head and Neck Squamous Cell Carcinoma.一种寻找抗癌治疗靶点的新策略:趋化因子CXCL14/BRAK是头颈部鳞状细胞癌的多功能肿瘤抑制因子。
ISRN Otolaryngol. 2012 Nov 14;2012:797619. doi: 10.5402/2012/797619. Print 2012.
8
The Warburg effect version 2.0: metabolic reprogramming of cancer stem cells.Warburg 效应 2.0:肿瘤干细胞的代谢重编程。
Cell Cycle. 2013 Apr 15;12(8):1166-79. doi: 10.4161/cc.24479. Epub 2013 Apr 2.
9
Basal/HER2 breast carcinomas: integrating molecular taxonomy with cancer stem cell dynamics to predict primary resistance to trastuzumab (Herceptin).基底型/HER2 型乳腺癌:整合分子分类与癌症干细胞动力学,预测曲妥珠单抗(赫赛汀)原发性耐药。
Cell Cycle. 2013 Jan 15;12(2):225-45. doi: 10.4161/cc.23274. Epub 2012 Jan 15.
10
Loss of p53 exacerbates multiple myeloma phenotype by facilitating the reprogramming of hematopoietic stem/progenitor cells to malignant plasma cells by MafB.p53 的缺失通过促进 MafB 将造血干细胞/祖细胞重编程为恶性浆细胞,从而加剧多发性骨髓瘤的表型。
Cell Cycle. 2012 Oct 15;11(20):3896-900. doi: 10.4161/cc.22186. Epub 2012 Sep 14.
肿瘤抑制因子p53调节乳腺干细胞自我更新分裂的极性。
Cell. 2009 Sep 18;138(6):1083-95. doi: 10.1016/j.cell.2009.06.048.
4
A luminal epithelial stem cell that is a cell of origin for prostate cancer.一种作为前列腺癌起源细胞的管腔上皮干细胞。
Nature. 2009 Sep 24;461(7263):495-500. doi: 10.1038/nature08361. Epub 2009 Sep 9.
5
Direct reprogramming of human neural stem cells by OCT4.通过OCT4对人类神经干细胞进行直接重编程。
Nature. 2009 Oct 1;461(7264):649-3. doi: 10.1038/nature08436.
6
Stem cells: The promises and perils of p53.干细胞:p53的前景与风险
Nature. 2009 Aug 27;460(7259):1085-6. doi: 10.1038/4601085a.
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Differentiation stage determines potential of hematopoietic cells for reprogramming into induced pluripotent stem cells.分化阶段决定了造血细胞重编程为诱导多能干细胞的潜能。
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8
Suppression of induced pluripotent stem cell generation by the p53-p21 pathway.p53-p21 通路对诱导多能干细胞生成的抑制作用。
Nature. 2009 Aug 27;460(7259):1132-5. doi: 10.1038/nature08235. Epub 2009 Aug 9.
9
A p53-mediated DNA damage response limits reprogramming to ensure iPS cell genomic integrity.p53介导的DNA损伤反应限制重编程以确保诱导多能干细胞基因组的完整性。
Nature. 2009 Aug 27;460(7259):1149-53. doi: 10.1038/nature08287. Epub 2009 Aug 9.
10
Cancer statistics, 2009.2009年癌症统计数据。
CA Cancer J Clin. 2009 Jul-Aug;59(4):225-49. doi: 10.3322/caac.20006. Epub 2009 May 27.