Identification of the miR-106b ~ 25 MicroRNA Cluster as a Proto-Oncogenic PTEN -Targeting Intron That Cooperates with Its Host Gene MCM7 in Transformation

Author:

Poliseno Laura1,Salmena Leonardo1,Riccardi Luisa1,Fornari Alessandro23,Song Min Sup1,Hobbs Robin M.1,Sportoletti Paolo1,Varmeh Shorheh1,Egia Ainara1,Fedele Giuseppe24,Rameh Lucia5,Loda Massimo24,Pandolfi Pier Paolo1

Affiliation:

1. Cancer Genetics Program, Beth Israel Deaconess Cancer Center, Departments of Medicine and Pathology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA.

2. Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02115, USA.

3. Department of Biomedical Sciences and Human Oncology, Molinette Hospital, University of Turin, 10126 Turin, Italy.

4. Department of Pathology, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA 02115, USA.

5. Boston Biomedical Research Institute, 64 Grove Street, Watertown, MA 02472, USA.

Abstract

A microRNA network regulates the tumor suppressor PTEN in prostate cancer.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference55 articles.

1. Nomenclature: PTEN human protein; PTEN human mRNA and gene; Pten mouse protein; Pten mouse mRNA and gene; DICER human protein; DICER human mRNA or gene; MCM7 human protein; MCM7 human mRNA and gene; miR-X mature miRNA; miR-X miRNA gene.

2. Biogenesis of small RNAs in animals

3. Impaired microRNA processing enhances cellular transformation and tumorigenesis

4. Up-Regulation of Dicer, a Component of the MicroRNA Machinery, in Prostate Adenocarcinoma

5. Microarray profiling of microRNAs reveals frequent coexpression with neighboring miRNAs and host genes

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