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[前列腺癌侵袭和转移的机制]

[Mechanism of prostate cancer invasion and metastasis].

作者信息

Sakamoto Shinichi, Ichikawa Tomohiko

出版信息

Nihon Rinsho. 2014 Dec;72(12):2086-9.

PMID:25518338
Abstract

Prostate cancer cells pass through numerous steps during the process of progression and metastasis. Cancer cells from primary site undertake "epithelial-mesenchymal transition (EMT)" and migrate into neighboring site and invade into blood vessels. Migrated cancer cells will detach from extracellular matrix (ECM) and float into distant metastasis site. Those detached cells will go through either "apoptosis" or acquire "anoikis resistance" and, finally, transfer to distant metastasis site. When settle at novel metastasis site, "mesenchymal-epithelial transition (MET)" will take place. Receptor activator of nuclear factor κ-B ligand (RANKL) plays significant role in formation of bone metastasis site.

摘要

前列腺癌细胞在进展和转移过程中会经历多个步骤。来自原发部位的癌细胞进行“上皮-间质转化(EMT)”,迁移到邻近部位并侵入血管。迁移的癌细胞会从细胞外基质(ECM)脱离,漂浮到远处转移部位。那些脱离的细胞会经历“凋亡”或获得“失巢凋亡抗性”,最终转移到远处转移部位。当在新的转移部位定居时,会发生“间质-上皮转化(MET)”。核因子κ-B受体活化因子配体(RANKL)在骨转移部位的形成中起重要作用。

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引用本文的文献

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The regulatory roles of lncRNAs in the process of breast cancer invasion and metastasis.lncRNAs 在乳腺癌侵袭和转移过程中的调控作用。
Biosci Rep. 2018 Sep 28;38(5). doi: 10.1042/BSR20180772. Print 2018 Oct 31.
2
MTA1 drives malignant progression and bone metastasis in prostate cancer.MTA1 驱动前列腺癌的恶性进展和骨转移。
Mol Oncol. 2018 Sep;12(9):1596-1607. doi: 10.1002/1878-0261.12360. Epub 2018 Aug 14.
3
MicroRNA-338-3p suppresses metastasis of lung cancer cells by targeting the EMT regulator Sox4.微小RNA-338-3p通过靶向上皮-间质转化调节因子Sox4抑制肺癌细胞的转移。
Am J Cancer Res. 2016 Jan 15;6(2):127-40. eCollection 2016.