Suppr超能文献

黑色素瘤发展中的干细胞。

Stem cells in melanoma development.

作者信息

Sabatino Marianna, Stroncek David F, Klein Harvey, Marincola Francesco M, Wang Ena

机构信息

Department of Transfusion Medicine, Warren G. Magnuson Clinical Center, National Institutes of Health, 9000 Rockville Pike, Building 10 Room 1C711, Bethesda, MD 20892, United States.

出版信息

Cancer Lett. 2009 Jul 8;279(2):119-25. doi: 10.1016/j.canlet.2008.10.039. Epub 2008 Dec 17.

Abstract

Cutaneous melanoma is a significant health problem worldwide. Available treatments can induce objective tumor regression in a small percent of patients, but these responses are not always associated with improved long-term survival. The resistance of melanoma to therapy and its predestined recurrence are related to the genetic heterogeneity and genomic instability of the tumor. For many years these genetic alterations were thought to be linked to the accumulation of random mutations in functionally differentiated cells which transform them into malignant cells that have lost their ability to differentiate and have acquired drug resistance. In the last few years it has been largely demonstrated that melanoma as other solid tumors contains a subpopulation of cells (CSCs) considered the source of the primary tumor mass, of new tumor nodules and responsible for drug resistance and cancer recurrence. In this review, we provide an overview of findings and advances in CSCs research that are relevant to the initiation, natural history, and the response to treatment of malignant melanoma.

摘要

皮肤黑色素瘤是全球范围内一个重大的健康问题。现有的治疗方法能使一小部分患者出现客观的肿瘤消退,但这些反应并不总是与长期生存率的提高相关。黑色素瘤对治疗的抗性及其注定的复发与肿瘤的基因异质性和基因组不稳定性有关。多年来,这些基因改变被认为与功能分化细胞中随机突变的积累有关,这些突变将它们转化为失去分化能力并获得耐药性的恶性细胞。在过去几年中,大量研究表明,与其他实体瘤一样,黑色素瘤含有一群细胞(癌症干细胞),被认为是原发肿瘤块、新肿瘤结节的来源,也是耐药性和癌症复发的原因。在这篇综述中,我们概述了与恶性黑色素瘤的发生、自然病程及治疗反应相关的癌症干细胞研究的发现和进展。

相似文献

1
Stem cells in melanoma development.黑色素瘤发展中的干细胞。
Cancer Lett. 2009 Jul 8;279(2):119-25. doi: 10.1016/j.canlet.2008.10.039. Epub 2008 Dec 17.
2
Cancer stem cells and human malignant melanoma.癌症干细胞与人类恶性黑色素瘤
Pigment Cell Melanoma Res. 2008 Feb;21(1):39-55. doi: 10.1111/j.1755-148X.2007.00427.x.
3
Nevi and Melanoma.痣和黑素瘤。
Hematol Oncol Clin North Am. 2024 Oct;38(5):939-952. doi: 10.1016/j.hoc.2024.05.005. Epub 2024 Jun 15.
5
MITF pathway mutations in melanoma.黑色素瘤中的MITF通路突变。
Pigment Cell Melanoma Res. 2009 Aug;22(4):376-7. doi: 10.1111/j.1755-148X.2009.00599.x. Epub 2009 Jun 25.
6
Molecular pathogenesis of cutaneous melanocytic neoplasms.皮肤黑素细胞肿瘤的分子发病机制
Annu Rev Pathol. 2009;4:551-79. doi: 10.1146/annurev.pathol.3.121806.151541.
7
Oxidative stress in melanocyte senescence and melanoma transformation.黑素细胞衰老和黑色素瘤转化中的氧化应激。
Eur J Cell Biol. 2014 Jan-Feb;93(1-2):36-41. doi: 10.1016/j.ejcb.2013.11.005. Epub 2013 Nov 23.

引用本文的文献

4
Dormancy of metastatic melanoma.转移性黑色素瘤的休眠
Pigment Cell Melanoma Res. 2010 Feb;23(1):41-56. doi: 10.1111/j.1755-148X.2009.00647.x. Epub 2009 Oct 19.

本文引用的文献

3
Cancer stem cell and cancer stemloids: from biology to therapy.癌症干细胞与癌症类干细胞:从生物学到治疗
Cancer Biol Ther. 2007 Nov;6(11):1684-90. doi: 10.4161/cbt.6.11.5167. Epub 2007 Oct 10.
4
MDR1 expression identifies human melanoma stem cells.多药耐药基因1(MDR1)的表达可识别出人黑色素瘤干细胞。
Biochem Biophys Res Commun. 2008 Apr 18;368(4):930-6. doi: 10.1016/j.bbrc.2008.02.022. Epub 2008 Feb 13.
7
Systemic spread is an early step in breast cancer.全身扩散是乳腺癌的早期阶段。
Cancer Cell. 2008 Jan;13(1):58-68. doi: 10.1016/j.ccr.2007.12.003.
8
CD133: molecule of the moment.CD133:当下的热门分子。
J Pathol. 2008 Jan;214(1):3-9. doi: 10.1002/path.2283.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验