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一种新型转移诱导长链非编码RNA的鉴定,该长链非编码RNA抑制KAI1/CD82转移抑制基因并在三阴性乳腺癌中上调。

Identification of a novel metastasis inducing lncRNA which suppresses the KAI1/CD82 metastasis suppressor gene and is upregulated in triple-negative breast cancer.

作者信息

Aram Ronni, Dotan Iris, Hotz-Wagenblatt Agnes, Canaani Dan

机构信息

Department of Biochemistry and Molecular Biology, George Wise Faculty of Life Sciences, Tel Aviv University, Ramat Aviv 69978, Israel.

Bioinformatics Group, Core Facility Genomics & Proteomics, German Cancer Research Center (DKFZ), D-69120 Heidelberg, Germany.

出版信息

Oncotarget. 2017 Jun 28;8(40):67538-67552. doi: 10.18632/oncotarget.18733. eCollection 2017 Sep 15.

DOI:10.18632/oncotarget.18733
PMID:28978052
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5620192/
Abstract

Inactivation of tumor/metastasis suppressor genes via epigenetic silencing is a frequent event in human cancers. KAI1/CD82 is a metastasis suppressor gene whose normal protecting activity is deficient in twelve different solid malignancies. Here we have identified and characterized a primarily nuclear non-polyadenylated, antisense (as)-lncRNA, initiating upstream of the KAI1 human metastasis suppressor gene transcription start site; and elongating in the opposite direction to KAI1 mRNA. We show that the KAI1 promoter is bi-directional giving rise to KAI1 mRNA and its as-lncRNA. Moreover, expression of this lncRNA transcript emerges to be inversely related to the KAI1 mRNA expression, and in direct relationship to the invasiveness level of human breast cancer derived cell lines. Importantly, knockdown of the KAI1 as-lncRNA in the triple-negative breast cancer cell line MDA-MB-231 have led to increased KAI1 mRNA and protein expression, manifested in stronger adhesion to fibronectin, retardation of cell migration and reduced cell invasion . Accordingly we have named this lncRNA, SKAI1BC, standing for "Suppressor of KAI1 in Breast Cancer". These results uncover a potential way to harness tumor metastasis via targeting SKAI1BC in human breast cancer, and perhaps also in other KAI1-deficient human malignancies.

摘要

通过表观遗传沉默使肿瘤/转移抑制基因失活在人类癌症中是常见事件。KAI1/CD82是一种转移抑制基因,其正常保护活性在十二种不同的实体恶性肿瘤中存在缺陷。在此,我们鉴定并表征了一种主要位于细胞核内的非多聚腺苷酸化反义(as)-lncRNA,它在KAI1人类转移抑制基因转录起始位点上游起始;并沿与KAI1 mRNA相反的方向延伸。我们表明KAI1启动子是双向的,可产生KAI1 mRNA及其as-lncRNA。此外,这种lncRNA转录本的表达似乎与KAI1 mRNA表达呈负相关,而与源自人乳腺癌的细胞系的侵袭水平呈正相关。重要的是,在三阴性乳腺癌细胞系MDA-MB-231中敲低KAI1 as-lncRNA导致KAI1 mRNA和蛋白表达增加,表现为对纤连蛋白更强的粘附性、细胞迁移减缓以及细胞侵袭减少。因此,我们将这种lncRNA命名为SKAI1BC,代表“乳腺癌中KAI1的抑制因子”。这些结果揭示了一种通过在人乳腺癌中靶向SKAI1BC来控制肿瘤转移的潜在方法,或许在其他KAI1缺陷型人类恶性肿瘤中也是如此。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30c/5620192/35d387584c9a/oncotarget-08-67538-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30c/5620192/c3daf1443329/oncotarget-08-67538-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30c/5620192/13778d57aa3e/oncotarget-08-67538-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30c/5620192/4fd3c6c70567/oncotarget-08-67538-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30c/5620192/c3e114d5c4ff/oncotarget-08-67538-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30c/5620192/68b174d2905e/oncotarget-08-67538-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30c/5620192/0252961f98d7/oncotarget-08-67538-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30c/5620192/35d387584c9a/oncotarget-08-67538-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30c/5620192/c3daf1443329/oncotarget-08-67538-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30c/5620192/13778d57aa3e/oncotarget-08-67538-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30c/5620192/4fd3c6c70567/oncotarget-08-67538-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30c/5620192/c3e114d5c4ff/oncotarget-08-67538-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30c/5620192/68b174d2905e/oncotarget-08-67538-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30c/5620192/0252961f98d7/oncotarget-08-67538-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30c/5620192/35d387584c9a/oncotarget-08-67538-g007.jpg

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