Human snoRNA-93 is processed into a microRNA-like RNA that promotes breast cancer cell invasion
RNA: Small nucleolar-derived RNA contributes to tumor invasiveness A short microRNA-like fragment excised from a small nucleolar RNA (called a snoRNA-derived RNA or sdRNA) contributes to the invasiveness of breast cancer cells. Glen Borchert from the University of South Alabama, USA, and colleagues...
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Nature Portfolio
2017
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oai:doaj.org-article:87f99f130ab34eb6904092036250f50d2021-12-02T15:18:47ZHuman snoRNA-93 is processed into a microRNA-like RNA that promotes breast cancer cell invasion10.1038/s41523-017-0032-82374-4677https://doaj.org/article/87f99f130ab34eb6904092036250f50d2017-07-01T00:00:00Zhttps://doi.org/10.1038/s41523-017-0032-8https://doaj.org/toc/2374-4677RNA: Small nucleolar-derived RNA contributes to tumor invasiveness A short microRNA-like fragment excised from a small nucleolar RNA (called a snoRNA-derived RNA or sdRNA) contributes to the invasiveness of breast cancer cells. Glen Borchert from the University of South Alabama, USA, and colleagues compared the expression of sdRNAs between a primary breast cancer cell line and a metastatic one. They identified 13 sdRNAs with markedly different abundances. Blocking the sdRNA with the biggest expression differential sdRNA-93-decreased cellular invasion, whereas increasing its abundance enhanced tumor cell invasiveness. Looking at human tissues, sdRNA-93 was routinely expressed in biopsies taken from patients with the luminal HER2-positive form of breast cancer, less often in other tumor types and almost never in healthy breast samples. Hinting at its function, the researchers showed that sdRNA-93 targets and regulates a gene contributing to specific molecular subtypes of breast cancer.Dillon G. PattersonJustin T. RobertsValeria M. KingDominika HouserovaEmmaline C. BarnhillAline CrucelloCaroline J. PolskaLucas W. BrantleyGarrett C. KaufmanMichael NguyenMegann W. SantanaIan A. SchillerJulius S. SpiccianiAnastasia K. ZapataMolly M. MillerTimothy D. ShermanRuixia MaHongyou ZhaoRitu AroraAlexander B. ColeyMelody M. ZeidanMing TanYaguang XiGlen M. BorchertNature PortfolioarticleNeoplasms. Tumors. Oncology. Including cancer and carcinogensRC254-282ENnpj Breast Cancer, Vol 3, Iss 1, Pp 1-12 (2017) |
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Neoplasms. Tumors. Oncology. Including cancer and carcinogens RC254-282 |
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Neoplasms. Tumors. Oncology. Including cancer and carcinogens RC254-282 Dillon G. Patterson Justin T. Roberts Valeria M. King Dominika Houserova Emmaline C. Barnhill Aline Crucello Caroline J. Polska Lucas W. Brantley Garrett C. Kaufman Michael Nguyen Megann W. Santana Ian A. Schiller Julius S. Spicciani Anastasia K. Zapata Molly M. Miller Timothy D. Sherman Ruixia Ma Hongyou Zhao Ritu Arora Alexander B. Coley Melody M. Zeidan Ming Tan Yaguang Xi Glen M. Borchert Human snoRNA-93 is processed into a microRNA-like RNA that promotes breast cancer cell invasion |
description |
RNA: Small nucleolar-derived RNA contributes to tumor invasiveness A short microRNA-like fragment excised from a small nucleolar RNA (called a snoRNA-derived RNA or sdRNA) contributes to the invasiveness of breast cancer cells. Glen Borchert from the University of South Alabama, USA, and colleagues compared the expression of sdRNAs between a primary breast cancer cell line and a metastatic one. They identified 13 sdRNAs with markedly different abundances. Blocking the sdRNA with the biggest expression differential sdRNA-93-decreased cellular invasion, whereas increasing its abundance enhanced tumor cell invasiveness. Looking at human tissues, sdRNA-93 was routinely expressed in biopsies taken from patients with the luminal HER2-positive form of breast cancer, less often in other tumor types and almost never in healthy breast samples. Hinting at its function, the researchers showed that sdRNA-93 targets and regulates a gene contributing to specific molecular subtypes of breast cancer. |
format |
article |
author |
Dillon G. Patterson Justin T. Roberts Valeria M. King Dominika Houserova Emmaline C. Barnhill Aline Crucello Caroline J. Polska Lucas W. Brantley Garrett C. Kaufman Michael Nguyen Megann W. Santana Ian A. Schiller Julius S. Spicciani Anastasia K. Zapata Molly M. Miller Timothy D. Sherman Ruixia Ma Hongyou Zhao Ritu Arora Alexander B. Coley Melody M. Zeidan Ming Tan Yaguang Xi Glen M. Borchert |
author_facet |
Dillon G. Patterson Justin T. Roberts Valeria M. King Dominika Houserova Emmaline C. Barnhill Aline Crucello Caroline J. Polska Lucas W. Brantley Garrett C. Kaufman Michael Nguyen Megann W. Santana Ian A. Schiller Julius S. Spicciani Anastasia K. Zapata Molly M. Miller Timothy D. Sherman Ruixia Ma Hongyou Zhao Ritu Arora Alexander B. Coley Melody M. Zeidan Ming Tan Yaguang Xi Glen M. Borchert |
author_sort |
Dillon G. Patterson |
title |
Human snoRNA-93 is processed into a microRNA-like RNA that promotes breast cancer cell invasion |
title_short |
Human snoRNA-93 is processed into a microRNA-like RNA that promotes breast cancer cell invasion |
title_full |
Human snoRNA-93 is processed into a microRNA-like RNA that promotes breast cancer cell invasion |
title_fullStr |
Human snoRNA-93 is processed into a microRNA-like RNA that promotes breast cancer cell invasion |
title_full_unstemmed |
Human snoRNA-93 is processed into a microRNA-like RNA that promotes breast cancer cell invasion |
title_sort |
human snorna-93 is processed into a microrna-like rna that promotes breast cancer cell invasion |
publisher |
Nature Portfolio |
publishDate |
2017 |
url |
https://doaj.org/article/87f99f130ab34eb6904092036250f50d |
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