4.5 Article

2-iodohexadecanal Inhibits thyroid cell growth in part through the induction of let-7f microRNA

Journal

MOLECULAR AND CELLULAR ENDOCRINOLOGY
Volume 414, Issue C, Pages 224-232

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.mce.2015.07.007

Keywords

Thyroid; Iodolipids; Iodine; Iodohexadecanal; miRNAs; miR-let-7f; miR-138

Funding

  1. Argentine National Research Council (CONICET) [PIC 0219]
  2. National Agency for the Promotion of Science and Technology (ANPCYT) [PICT 0038]

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It is well known that pituitary TSH exerts the major task in the regulation of thyroid function. However, this gland is capable of certain degree of autonomy, independently of TSH control. Iodine plays an important role in thyroid physiology and biochemistry. The thyroid is capable of producing afferent iodolipids such as 2-iodohexadecanal (2-IHDA). It was shown that this iodolipid mimic some of the inhibitory effects of excess iodide on several thyroid parameters. Objectives: To identify the miRNAs regulated by 2-IHDA in rat thyroid cells and likely characterize their role in thyroid cell proliferation and function. Results: FRTL-5 cells were grown in the presence of TSH and treated with 2-IHDA. Among the miRNAs up-regulated by 2-IHDA we focused on miR-let-7f and miR-138. When we transfected the miRNAs, miR-let-7f but not miR-138 overexpression inhibited proliferation of FRTL 5 cells, while miR-let-7f inhibition restored cell growth in 2-IHDA treated cultures. Analysis of cell cycle by flow cytometric DNA analysis revealed that miR-let-7f inhibition reduced the percentage of 2-IHDA treated cells in G1 phase and an increased of the percentage of cells in S phase was observed upon anti-let-7f transfection. The expresion of Cyclin D1 and Cydin D3 were reduced after the transfection of miR-let-7f and miR-138, respectively. In in vivo studies we observed that miR-let-7f and miR-138 were up regulated by 2-IHDA during goiter involution. Conclusion: These results suggest that the inhibitory effects of 2-IHDA on FRTL-5 thyroid cell proliferation are mediated in part through the induction of let-7f microRNA. (C) 2015 Elsevier Ireland Ltd. All rights reserved.

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