A novel long non-coding RNA SLNCR1 promotes proliferation, migration, and invasion of melanoma via transcriptionally regulating SOX5

Abstract Steroid receptor RNA activator (SRA)-like non-coding RNA (SLNCR1) has been implicated in various tumorigenic processes, but the precise regulatory role in melanoma progression remains uncertain. We performed a comprehensive analysis to investigate the prognostic value of SLNCR1 expression i...

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Main Authors: Lele Cong, Qing Zhao, Hongyan Sun, Zilong Zhou, Yue Hu, Chunyi Li, Miao Hao, Xianling Cong
Format: Article
Language:English
Published: Nature Publishing Group 2024-04-01
Series:Cell Death Discovery
Online Access:https://doi.org/10.1038/s41420-024-01922-7
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author Lele Cong
Qing Zhao
Hongyan Sun
Zilong Zhou
Yue Hu
Chunyi Li
Miao Hao
Xianling Cong
author_facet Lele Cong
Qing Zhao
Hongyan Sun
Zilong Zhou
Yue Hu
Chunyi Li
Miao Hao
Xianling Cong
author_sort Lele Cong
collection DOAJ
description Abstract Steroid receptor RNA activator (SRA)-like non-coding RNA (SLNCR1) has been implicated in various tumorigenic processes, but the precise regulatory role in melanoma progression remains uncertain. We performed a comprehensive analysis to investigate the prognostic value of SLNCR1 expression in patients with melanoma by TCGA database and melanoma tissue samples via the Kaplan–Meier method. Subsequently, we conducted qRT-PCR and Fluorescence in Situ Hybridization (FISH) assays to identify SLNCR1 expression levels and localization in tissues and cells, respectively. Loss-of-function assays utilizing shRNAs vectors were used to investigate the potential impact of SLNCR1. Our data showed that SLNCR1 is significantly up-regulated in human malignant melanoma tissues and cell lines and functions as an oncogene. Silencing of SLNCR1 suppressed melanoma cell proliferation, migration, invasion, and inhibited tumorigenesis in a mouse xenograft model. Additionally, we employed bioinformatic predictive analysis, combined with dual-luciferase reporter analysis and functional rescue assays, to elucidate the mechanistic target of the SLNCR1/SOX5 axis in melanoma. Mechanistically, we discovered that SLNCR1 promotes EMT of human melanoma by targeting SOX5, as downregulation of SLNCR1 expression leads to a decrease in SOX5 protein levels and inhibits melanoma tumorigenesis. Our research offers promising insights for more precise diagnosis and treatment of human melanoma.
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spelling doaj.art-7167a52d4c424b5a90d3ffad51a0c47d2024-04-07T11:08:32ZengNature Publishing GroupCell Death Discovery2058-77162024-04-0110111110.1038/s41420-024-01922-7A novel long non-coding RNA SLNCR1 promotes proliferation, migration, and invasion of melanoma via transcriptionally regulating SOX5Lele Cong0Qing Zhao1Hongyan Sun2Zilong Zhou3Yue Hu4Chunyi Li5Miao Hao6Xianling Cong7Department of Dermatology, China-Japan Union Hospital of Jilin UniversityDepartment of Neurology, China-Japan Union Hospital of Jilin UniversityDepartment of Biobank, China-Japan Union Hospital of Jilin UniversityDepartment of Biobank, China-Japan Union Hospital of Jilin UniversityDepartment of Biobank, China-Japan Union Hospital of Jilin UniversityInstitute of Antler Science and Product Technology, Changchun Sci-Tech UniversityScientific Research Center, China-Japan Union Hospital of Jilin UniversityDepartment of Biobank, China-Japan Union Hospital of Jilin UniversityAbstract Steroid receptor RNA activator (SRA)-like non-coding RNA (SLNCR1) has been implicated in various tumorigenic processes, but the precise regulatory role in melanoma progression remains uncertain. We performed a comprehensive analysis to investigate the prognostic value of SLNCR1 expression in patients with melanoma by TCGA database and melanoma tissue samples via the Kaplan–Meier method. Subsequently, we conducted qRT-PCR and Fluorescence in Situ Hybridization (FISH) assays to identify SLNCR1 expression levels and localization in tissues and cells, respectively. Loss-of-function assays utilizing shRNAs vectors were used to investigate the potential impact of SLNCR1. Our data showed that SLNCR1 is significantly up-regulated in human malignant melanoma tissues and cell lines and functions as an oncogene. Silencing of SLNCR1 suppressed melanoma cell proliferation, migration, invasion, and inhibited tumorigenesis in a mouse xenograft model. Additionally, we employed bioinformatic predictive analysis, combined with dual-luciferase reporter analysis and functional rescue assays, to elucidate the mechanistic target of the SLNCR1/SOX5 axis in melanoma. Mechanistically, we discovered that SLNCR1 promotes EMT of human melanoma by targeting SOX5, as downregulation of SLNCR1 expression leads to a decrease in SOX5 protein levels and inhibits melanoma tumorigenesis. Our research offers promising insights for more precise diagnosis and treatment of human melanoma.https://doi.org/10.1038/s41420-024-01922-7
spellingShingle Lele Cong
Qing Zhao
Hongyan Sun
Zilong Zhou
Yue Hu
Chunyi Li
Miao Hao
Xianling Cong
A novel long non-coding RNA SLNCR1 promotes proliferation, migration, and invasion of melanoma via transcriptionally regulating SOX5
Cell Death Discovery
title A novel long non-coding RNA SLNCR1 promotes proliferation, migration, and invasion of melanoma via transcriptionally regulating SOX5
title_full A novel long non-coding RNA SLNCR1 promotes proliferation, migration, and invasion of melanoma via transcriptionally regulating SOX5
title_fullStr A novel long non-coding RNA SLNCR1 promotes proliferation, migration, and invasion of melanoma via transcriptionally regulating SOX5
title_full_unstemmed A novel long non-coding RNA SLNCR1 promotes proliferation, migration, and invasion of melanoma via transcriptionally regulating SOX5
title_short A novel long non-coding RNA SLNCR1 promotes proliferation, migration, and invasion of melanoma via transcriptionally regulating SOX5
title_sort novel long non coding rna slncr1 promotes proliferation migration and invasion of melanoma via transcriptionally regulating sox5
url https://doi.org/10.1038/s41420-024-01922-7
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