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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

High-throughput sequencing of small RNA transcriptomes reveals critical biological features targeted by microRNAs in cell models used for squamous cell cancer research

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Author(s):
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Severino, Patricia [1] ; Oliveira, Liliane Santana [2, 1] ; Torres, Natalia [1] ; Andreghetto, Flavia Maziero [1] ; Guarizo Klingbeil, Maria de Fatima [3] ; Moyses, Raquel [4] ; Wuensch-Filho, Victor [5] ; Nunes, Fabio Daumas [6] ; Mathor, Monica Beatriz [3] ; Paschoal, Alexandre Rossi [2, 7] ; Durham, Alan Mitchell [2]
Total Authors: 11
Affiliation:
[1] Hosp Israelita Albert Einstein, Albert Einstein Res & Educ Inst, Sao Paulo - Brazil
[2] Univ Sao Paulo, Inst Matemat & Estat, Sao Paulo - Brazil
[3] IPEN CNEN, Nucl & Energy Res Inst, Sao Paulo - Brazil
[4] Univ Sao Paulo, Sch Med, Dept Surg, Div Head & Neck Surg, Sao Paulo - Brazil
[5] Univ Sao Paulo, Fac Publ Hlth, Dept Epidemiol, Sao Paulo - Brazil
[6] Univ Sao Paulo, Fac Dent, Dept Stomatol, Sao Paulo - Brazil
[7] Fed Univ Technol, Cornelio Procopio, Parana - Brazil
Total Affiliations: 7
Document type: Journal article
Source: BMC Genomics; v. 14, OCT 26 2013.
Web of Science Citations: 11
Abstract

Background: The implication of post-transcriptional regulation by microRNAs in molecular mechanisms underlying cancer disease is well documented. However, their interference at the cellular level is not fully explored. Functional in vitro studies are fundamental for the comprehension of their role; nevertheless results are highly dependable on the adopted cellular model. Next generation small RNA transcriptomic sequencing data of a tumor cell line and keratinocytes derived from primary culture was generated in order to characterize the microRNA content of these systems, thus helping in their understanding. Both constitute cell models for functional studies of microRNAs in head and neck squamous cell carcinoma (HNSCC), a smoking-related cancer. Known microRNAs were quantified and analyzed in the context of gene regulation. New microRNAs were investigated using similarity and structural search, ab initio classification, and prediction of the location of mature microRNAs within would-be precursor sequences. Results were compared with small RNA transcriptomic sequences from HNSCC samples in order to access the applicability of these cell models for cancer phenotype comprehension and for novel molecule discovery. Results: Ten miRNAs represented over 70% of the mature molecules present in each of the cell types. The most expressed molecules were miR-21, miR-24 and miR-205, Accordingly; miR-21 and miR-205 have been previously shown to play a role in epithelial cell biology. Although miR-21 has been implicated in cancer development, and evaluated as a biomarker in HNSCC progression, no significant expression differences were seen between cell types. We demonstrate that differentially expressed mature miRNAs target cell differentiation and apoptosis related biological processes, indicating that they might represent, with acceptable accuracy, the genetic context from which they derive. Most miRNAs identified in the cancer cell line and in keratinocytes were present in tumor samples and cancer-free samples, respectively, with miR-21, miR-24 and miR-205 still among the most prevalent molecules at all instances. Thirteen miRNA-like structures, containing reads identified by the deep sequencing, were predicted from putative miRNA precursor sequences. Strong evidences suggest that one of them could be a new miRNA. This molecule was mostly expressed in the tumor cell line and HNSCC samples indicating a possible biological function in cancer. Conclusions: Critical biological features of cells must be fully understood before they can be chosen as models for functional studies. Expression levels of miRNAs relate to cell type and tissue context. This study provides insights on miRNA content of two cell models used for cancer research. Pathways commonly deregulated in HNSCC might be targeted by most expressed and also by differentially expressed miRNAs. Results indicate that the use of cell models for cancer research demands careful assessment of underlying molecular characteristics for proper data interpretation. Additionally, one new miRNA-like molecule with a potential role in cancer was identified in the cell lines and clinical samples. (AU)

FAPESP's process: 09/04166-5 - Characterization of microRNA regulatory networks involved in head and neck squamous cell carcinoma by means of microarray and functional studies in cell culture
Grantee:Patricia Severino
Support type: Regular Research Grants
FAPESP's process: 10/51168-0 - Environmental, clinical, histopathological and molecular factors associated with development and prognosis of head and neck squamous cell carcinomas
Grantee:Eloiza Helena Tajara da Silva
Support type: Research Projects - Thematic Grants