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DOI 10.1111/j.1601-0825.2011.01855.x

Медицинская библиотека · Oral diseases · 2012

A preliminary study on the FAM5C expression in generalized chronic periodontitis.

Ribeiro F V, Santos V R, Bastos M F, De Miranda T S, Vieira A R, De Figueiredo L C, Duarte P M

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

OBJECTIVE

The Family with sequence similarity 5 member C (FAM5C) has been suggested to contribute in aggressive periodontitis. However, there is no data regarding its role in chronic periodontitis. The aim of this study was to evaluate the FAM5C expression in chronic periodontitis and to study association of FAM5C with key immunoinflammatory markers.

MATERIAL AND

METHODS

Gingival biopsies were harvested from periodontally healthy subjects (n = 10) and chronic periodontitis subjects (n = 15). The levels of mRNA of FAM5C, interleukin (IL)-17, IL-6, IL-23, IL-10, IL-4, interferon-c, toll-like receptor (TLR)-2, TLR-4, osteoprotegerin (OPG), receptor activator of NF-κB ligand (RANKL), tumor necrosis factor (TNF)-a, transforming growth factor-b, transcription factor forkhead box p3, and transcription factor orphan nuclear receptor C2 were evaluated by real-time polymerase chain reaction.

RESULTS

FAM5C mRNA levels were not different between periodontally healthy and diseased tissues (P > 0.05). Gene expressions of IL-17, TNF-a, OPG, RANKL, TLR-2, and TLR-4 were higher in periodontitis, when compared to periodontally healthy sites (P < 0.05), while no differences between groups were observed for the other genes evaluated (P > 0.05). There were no correlations between the gene expression of FAM5C and the other immunoinflammatory markers (P > 0.05).

CONCLUSION

Within the limits of this study, it seems that FAM5C expression does not contribute to chronic periodontitis.

Для цитирования: Ribeiro F V, Santos V R, Bastos M F, De Miranda T S, Vieira A R, De Figueiredo L C, Duarte P M. A preliminary study on the FAM5C expression in generalized chronic periodontitis.. Oral diseases. 2012. DOI: 10.1111/j.1601-0825.2011.01855.x.

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