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miR-205 靶基因在皮肤恶性黑色素瘤转移和生存中的转录组学鉴定

Transcriptomic identification of miR-205 target genes potentially involved in metastasis and survival of cutaneous malignant melanoma.

机构信息

Department of Pathology, Universitat de València, València, Spain.

Biomedical Research Institute INCLIVA, València, Spain.

出版信息

Sci Rep. 2020 Mar 16;10(1):4771. doi: 10.1038/s41598-020-61637-4.

DOI:10.1038/s41598-020-61637-4
PMID:32179834
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7075905/
Abstract

Cutaneous melanoma is an aggressive neoplasm and is responsible for the majority of skin cancer deaths. Several miRNAs are involved in melanoma tumor progression. One of them is miR-205, the loss of which contributes to the development of melanoma metastasis. We evaluated whole-genome mRNA expression profiling associated with different miR-205 expression levels in melanoma cells. Differential expression analysis identified 243 differentially expressed transcripts including inositol polyphosphate 5'-phosphatase-like protein-1 (INPPL1) and BTB/POZ Domain-Containing Protein 3 (BTBD3). INPPL1 and BTBD3 were downregulated when melanoma cells expressed miR-205, indicating that these genes are potential miR-205 targets. Additionally, the target prediction algorithm TargetScan revealed that INPPL1 and BTBD3 genes had predicted target sites of miR-205 in their 3'UTRs and functional analysis demonstrated that these genes were directly linked to miR-205. Interestingly, our clinical data showed that INPPL1 was significantly associated with lymph node metastasis-free survival (LNMFS), distant metastasis-free survival (DMFS) and melanoma specific survival (MSS). This study supports INPPL1 as a miR-205 target gene and, therefore, that the involvement of miR-205 in the metastatic dissemination of malignant melanoma is, at least in part, via INPPL1.

摘要

皮肤黑色素瘤是一种侵袭性肿瘤,是导致大多数皮肤癌死亡的主要原因。有几种 miRNA 参与黑色素瘤肿瘤的进展。其中之一是 miR-205,其缺失有助于黑色素瘤转移的发展。我们评估了与黑色素瘤细胞中不同 miR-205 表达水平相关的全基因组 mRNA 表达谱。差异表达分析确定了 243 个差异表达的转录本,包括肌醇多磷酸 5′-磷酸酶样蛋白-1(INPPL1)和 BTB/POZ 结构域蛋白 3(BTBD3)。当黑色素瘤细胞表达 miR-205 时,INPPL1 和 BTBD3 下调,表明这些基因是潜在的 miR-205 靶基因。此外,靶标预测算法 TargetScan 表明,INPPL1 和 BTBD3 基因在其 3'UTR 中有 miR-205 的预测靶标,功能分析表明这些基因与 miR-205 直接相关。有趣的是,我们的临床数据表明,INPPL1 与无淋巴结转移生存(LNMFS)、无远处转移生存(DMFS)和黑色素瘤特异性生存(MSS)显著相关。这项研究支持 INPPL1 作为 miR-205 的靶基因,因此 miR-205 参与恶性黑色素瘤的转移扩散至少部分是通过 INPPL1 实现的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/894f/7075905/37b58959d784/41598_2020_61637_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/894f/7075905/6985db86234c/41598_2020_61637_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/894f/7075905/f3419dbf1743/41598_2020_61637_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/894f/7075905/d1aeeae06b61/41598_2020_61637_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/894f/7075905/6027ed953831/41598_2020_61637_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/894f/7075905/32160c1956ba/41598_2020_61637_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/894f/7075905/d781cd405e2c/41598_2020_61637_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/894f/7075905/37b58959d784/41598_2020_61637_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/894f/7075905/6985db86234c/41598_2020_61637_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/894f/7075905/f3419dbf1743/41598_2020_61637_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/894f/7075905/d1aeeae06b61/41598_2020_61637_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/894f/7075905/6027ed953831/41598_2020_61637_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/894f/7075905/32160c1956ba/41598_2020_61637_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/894f/7075905/d781cd405e2c/41598_2020_61637_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/894f/7075905/37b58959d784/41598_2020_61637_Fig7_HTML.jpg

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