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微小 RNA-107 是一种新型的肿瘤抑制因子,靶向黑色素瘤中的 POU3F2。

MicroRNA-107 is a novel tumor suppressor targeting POU3F2 in melanoma.

机构信息

Department of Dermatology, Daqing Oilfield General Hospital, No. 9 Zhongkang Road, Saertu District, Daqing, 163000, Heilongjiang, China.

Department of Stomatology, Daqing Oilfield General Hospital, No. 9 Zhongkang Road, Saertu District, Daqing, 163000, Heilongjiang, China.

出版信息

Biol Res. 2020 Mar 14;53(1):11. doi: 10.1186/s40659-020-00278-3.

DOI:10.1186/s40659-020-00278-3
PMID:32169117
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7071777/
Abstract

BACKGROUND

Melanoma is one of the major types of skin cancer. The metastatic melanoma is among the most lethal forms of malignant skin tumors. We hereby aimed to characterize a novel microRNA (miR) in the metastatic melanoma model.

METHODS

First, we evaluated the expression of miR-107 in melanoma cells and tumor tissues. The comparison between primary and metastatic cancer tissues was also accessed. Next, we examined the impact of miR-107 on melanoma cell proliferation, cell cycle, colony formation, apoptotic activity, migration and matrix invasion. A downstream target of miR-107 was also predicted and validated functionally in melanoma cells.

RESULTS

Our findings showed miR-107 was significantly downregulated in melanoma. Its expression was lowest in metastatic form. Over-expression of miR-107 reduced melanoma cell proliferation, migration and invasion. POU3F2 was identified as the downstream target of miR-107. Over-expression of POU3F2 antagonized miR-107-mediated inhibitory effect on melanoma cells.

CONCLUSION

Our study has reported miR-107 as a novel tumor suppressive factor in the metastatic melanoma model. It has provided new avenue to manage melanoma and improve the survival rate in the advanced stage.

摘要

背景

黑色素瘤是皮肤癌的主要类型之一。转移性黑色素瘤是最致命的恶性皮肤肿瘤之一。本研究旨在对转移性黑色素瘤模型中的一种新型 microRNA(miR)进行特征分析。

方法

首先,我们评估了 miR-107 在黑色素瘤细胞和肿瘤组织中的表达。还比较了原发性和转移性癌组织之间的差异。接下来,我们研究了 miR-107 对黑色素瘤细胞增殖、细胞周期、集落形成、凋亡活性、迁移和基质侵袭的影响。miR-107 的下游靶标也在黑色素瘤细胞中进行了预测和功能验证。

结果

我们的研究结果表明 miR-107 在黑色素瘤中显著下调,在转移性黑色素瘤中表达最低。过表达 miR-107 可降低黑色素瘤细胞的增殖、迁移和侵袭。POU3F2 被鉴定为 miR-107 的下游靶标。过表达 POU3F2 拮抗了 miR-107 对黑色素瘤细胞的抑制作用。

结论

本研究报道了 miR-107 作为转移性黑色素瘤模型中的一种新型肿瘤抑制因子。它为管理黑色素瘤提供了新的途径,并提高了晚期患者的生存率。

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LINC00662 promotes melanoma progression by competitively binding miR-107 and activating the β-catenin signaling pathway.LINC00662 通过竞争性结合 miR-107 并激活 β-catenin 信号通路促进黑色素瘤进展。
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YO2 Induces Melanoma Cell Apoptosis through p53-Mediated LRP1 Downregulation.YO2通过p53介导的低密度脂蛋白受体相关蛋白1(LRP1)下调诱导黑色素瘤细胞凋亡。
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