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Correlation of Global MicroRNA Expression With Basal Cell Carcinoma Subtype

Basal cell carcinomas (BCCs) are the most common cancers in the United States. The histologic appearance distinguishes several subtypes, each of which can have a different biologic behavior. In this study, global miRNA expression was quantified by high-throughput sequencing in nodular BCCs, a subtyp...

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Autores principales: Heffelfinger, Christopher, Ouyang, Zhengqing, Engberg, Anna, Leffell, David J., Hanlon, Allison M., Gordon, Patricia B., Zheng, Wei, Zhao, Hongyu, Snyder, Michael P., Bale, Allen E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3284335/
https://www.ncbi.nlm.nih.gov/pubmed/22384406
http://dx.doi.org/10.1534/g3.111.001115
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author Heffelfinger, Christopher
Ouyang, Zhengqing
Engberg, Anna
Leffell, David J.
Hanlon, Allison M.
Gordon, Patricia B.
Zheng, Wei
Zhao, Hongyu
Snyder, Michael P.
Bale, Allen E.
author_facet Heffelfinger, Christopher
Ouyang, Zhengqing
Engberg, Anna
Leffell, David J.
Hanlon, Allison M.
Gordon, Patricia B.
Zheng, Wei
Zhao, Hongyu
Snyder, Michael P.
Bale, Allen E.
author_sort Heffelfinger, Christopher
collection PubMed
description Basal cell carcinomas (BCCs) are the most common cancers in the United States. The histologic appearance distinguishes several subtypes, each of which can have a different biologic behavior. In this study, global miRNA expression was quantified by high-throughput sequencing in nodular BCCs, a subtype that is slow growing, and infiltrative BCCs, aggressive tumors that extend through the dermis and invade structures such as cutaneous nerves. Principal components analysis correctly classified seven of eight infiltrative tumors on the basis of miRNA expression. The remaining tumor, on pathology review, contained a mixture of nodular and infiltrative elements. Nodular tumors did not cluster tightly, likely reflecting broader histopathologic diversity in this class, but trended toward forming a group separate from infiltrative BCCs. Quantitative polymerase chain reaction assays were developed for six of the miRNAs that showed significant differences between the BCC subtypes, and five of these six were validated in a replication set of four infiltrative and three nodular tumors. The expression level of miR-183, a miRNA that inhibits invasion and metastasis in several types of malignancies, was consistently lower in infiltrative than nodular tumors and could be one element underlying the difference in invasiveness. These results represent the first miRNA profiling study in BCCs and demonstrate that miRNA gene expression may be involved in tumor pathogenesis and particularly in determining the aggressiveness of these malignancies.
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spelling pubmed-32843352012-03-01 Correlation of Global MicroRNA Expression With Basal Cell Carcinoma Subtype Heffelfinger, Christopher Ouyang, Zhengqing Engberg, Anna Leffell, David J. Hanlon, Allison M. Gordon, Patricia B. Zheng, Wei Zhao, Hongyu Snyder, Michael P. Bale, Allen E. G3 (Bethesda) Investigations Basal cell carcinomas (BCCs) are the most common cancers in the United States. The histologic appearance distinguishes several subtypes, each of which can have a different biologic behavior. In this study, global miRNA expression was quantified by high-throughput sequencing in nodular BCCs, a subtype that is slow growing, and infiltrative BCCs, aggressive tumors that extend through the dermis and invade structures such as cutaneous nerves. Principal components analysis correctly classified seven of eight infiltrative tumors on the basis of miRNA expression. The remaining tumor, on pathology review, contained a mixture of nodular and infiltrative elements. Nodular tumors did not cluster tightly, likely reflecting broader histopathologic diversity in this class, but trended toward forming a group separate from infiltrative BCCs. Quantitative polymerase chain reaction assays were developed for six of the miRNAs that showed significant differences between the BCC subtypes, and five of these six were validated in a replication set of four infiltrative and three nodular tumors. The expression level of miR-183, a miRNA that inhibits invasion and metastasis in several types of malignancies, was consistently lower in infiltrative than nodular tumors and could be one element underlying the difference in invasiveness. These results represent the first miRNA profiling study in BCCs and demonstrate that miRNA gene expression may be involved in tumor pathogenesis and particularly in determining the aggressiveness of these malignancies. Genetics Society of America 2012-02-01 /pmc/articles/PMC3284335/ /pubmed/22384406 http://dx.doi.org/10.1534/g3.111.001115 Text en Copyright © 2012 Heffelfinger et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Unported License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Investigations
Heffelfinger, Christopher
Ouyang, Zhengqing
Engberg, Anna
Leffell, David J.
Hanlon, Allison M.
Gordon, Patricia B.
Zheng, Wei
Zhao, Hongyu
Snyder, Michael P.
Bale, Allen E.
Correlation of Global MicroRNA Expression With Basal Cell Carcinoma Subtype
title Correlation of Global MicroRNA Expression With Basal Cell Carcinoma Subtype
title_full Correlation of Global MicroRNA Expression With Basal Cell Carcinoma Subtype
title_fullStr Correlation of Global MicroRNA Expression With Basal Cell Carcinoma Subtype
title_full_unstemmed Correlation of Global MicroRNA Expression With Basal Cell Carcinoma Subtype
title_short Correlation of Global MicroRNA Expression With Basal Cell Carcinoma Subtype
title_sort correlation of global microrna expression with basal cell carcinoma subtype
topic Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3284335/
https://www.ncbi.nlm.nih.gov/pubmed/22384406
http://dx.doi.org/10.1534/g3.111.001115
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