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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Autores principales: 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
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Publicado: Nature Portfolio 2017
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Acceso en línea:https://doaj.org/article/87f99f130ab34eb6904092036250f50d
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spelling 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)
institution DOAJ
collection DOAJ
language EN
topic Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
spellingShingle 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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