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Lgr6:从干性到癌症进展

Lgr6: From Stemness to Cancer Progression.

作者信息

Cortesi Emanuela, Ventura Juan-Jose

机构信息

Translational Cell and Tissue Research, Dept. of Imaging and Pathology, KU Leuven, Belgium.

出版信息

J Lung Health Dis. 2019 Jun 18;3(1):12-15. Epub 2019 Feb 5.

Abstract

Lung cancer is the leading cause of cancer-related deaths worldwide with poor prognosis, mainly due to the delay in the diagnosis. Adenocarcinoma, a subtype of non-small cell lung cancer, has the highest incidence and significant recurrence rates. Experimental and clinical researches suggested that the presence of cancer stem cells could support the development, malignization and resistance of lung cancer. Unfortunately, our knowledge in the field is still limited. Here we report our findings regarding a cell population expressing LGR6, an epithelial stem cell marker. Under the pressure of a fine regulated p38α MAPK/mir-17-92 axis, LGR6 stem cells produce differentiated bronchioalveolar cells, in the normal lung. LGR6 is enriched in tumour cells during adenocarcinoma progression. Similar to normal stem cells, LGR6 cancer cells show self-renewal and differentiation capacities, alongside with a higher oncogenic potential. Our studies suggest a disruption in the p38α MAPK/mir-17-92 network, that enhances Wnt pathway activity, could be responsible for the selection of malignant LGR6 tumour cells. These results support the existence of a cell population with stem-like characteristics and strong oncogenic potential. This population could be useful for predictive diagnosis and a novel target for improved and more effective therapies against metastases and recurrences of lung adenocarcinomas.

摘要

肺癌是全球癌症相关死亡的主要原因,预后较差,主要是由于诊断延迟。腺癌是非小细胞肺癌的一种亚型,发病率最高且复发率显著。实验和临床研究表明,癌症干细胞的存在可能支持肺癌的发展、恶性转化和耐药性。不幸的是,我们在该领域的知识仍然有限。在此,我们报告了关于表达上皮干细胞标志物LGR6的细胞群体的研究结果。在精细调控的p38α丝裂原活化蛋白激酶/微小RNA-17-92轴的作用下,LGR6干细胞在正常肺中产生分化的支气管肺泡细胞。在腺癌进展过程中肿瘤细胞中LGR6富集。与正常干细胞相似,LGR6癌细胞表现出自我更新和分化能力,同时具有更高的致癌潜能。我们的研究表明,p38α丝裂原活化蛋白激酶/微小RNA-17-92网络的破坏增强了Wnt信号通路活性,可能是恶性LGR6肿瘤细胞被选择的原因。这些结果支持存在具有干细胞样特征和强大致癌潜能的细胞群体。该群体可能有助于预测诊断,并成为改善和更有效治疗肺腺癌转移和复发的新靶点。

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本文引用的文献

1
Cell death-based treatment of lung adenocarcinoma.
Cell Death Dis. 2018 Jan 25;9(2):117. doi: 10.1038/s41419-017-0063-y.
2
Precision Diagnosis and Treatment for Advanced Non-Small-Cell Lung Cancer.
N Engl J Med. 2017 Aug 31;377(9):849-861. doi: 10.1056/NEJMra1703413.
3
Wnt signaling in cancer.
Oncogene. 2017 Mar;36(11):1461-1473. doi: 10.1038/onc.2016.304. Epub 2016 Sep 12.
4
Lung cancer stem cells-characteristics, phenotype.
Transl Lung Cancer Res. 2016 Jun;5(3):272-9. doi: 10.21037/tlcr.2016.02.01.
5
Cancer stem cells: progress and challenges in lung cancer.
Stem Cell Investig. 2014 Apr 15;1:9. doi: 10.3978/j.issn.2306-9759.2014.03.06. eCollection 2014.
6
Cancer incidence and mortality worldwide: sources, methods and major patterns in GLOBOCAN 2012.
Int J Cancer. 2015 Mar 1;136(5):E359-86. doi: 10.1002/ijc.29210. Epub 2014 Oct 9.
8
Strategies for improving outcomes in NSCLC: a look to the future.
Lung Cancer. 2013 Dec;82(3):375-82. doi: 10.1016/j.lungcan.2013.08.025. Epub 2013 Sep 8.
9
Lung cancer stem cells: progress and prospects.
Cancer Lett. 2013 Sep 10;338(1):89-93. doi: 10.1016/j.canlet.2012.08.014. Epub 2012 Aug 17.
10
Regulation of human lung alveolar multipotent cells by a novel p38α MAPK/miR-17-92 axis.
EMBO J. 2012 Aug 15;31(16):3431-41. doi: 10.1038/emboj.2012.192. Epub 2012 Jul 24.

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