Toxic Adenoma pathophysiology: Difference between revisions

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==References==
==References==
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{{reflist|2}}
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Revision as of 19:31, 18 October 2017

Toxic Adenoma Microchapters

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] ; Associate Editor(s)-in-Chief: Aditya Ganti M.B.B.S. [2]

Overview

Thyroid-stimulating hormone (TSH) binds to its receptor on the surface of thyroid follicular cells. When TSH binds to the TSH receptor, it stimulates adenylyl cyclase conversion of adenosine triphosphate (ATP) to cyclic adenosine monophosphate (cAMP). Activation of this pathway leads to cell growth and thyroid hormone secretion. When TSH concentrations are five- to tenfold higher, TSH binding to its receptor leads to its interaction with Gq, activating phospholipase C, which in turn leads to increased intracellular calcium, diacylglycerol, and inositol phosphate. Activation of this pathway regulates iodination and thyroid hormone production. Alteration of the above pathway by activation of germline or somatic mutations in the TSH receptor or cAMP signal transduction system is believed to be responsible for the development of autonomous thyroid gland growth and hormonogenesis. The molecular alterations responsible for toxic adenomas include somatic gain-of-function mutations in the TSH receptor or the stimulatory Gsα subunit. Both result in constitutive activation of the cAMP pathway, which results in enhanced proliferation and function of thyroid follicular cells.

Pathogenesis

Thyroid-stimulating hormone (TSH) binds to its receptor on the surface of thyroid follicular cells. When TSH binds to the TSH receptor, it stimulates adenylyl cyclase conversion of adenosine triphosphate (ATP) to cyclic adenosine monophosphate (cAMP). Activation of this pathway leads to cell growth and thyroid hormone secretion. When TSH concentrations are five- to tenfold higher, TSH binding to its receptor leads to its interaction with Gq, activating phospholipase C, which in turn leads to increased intracellular calcium, diacylglycerol, and inositol phosphate. Activation of this pathway regulates iodination and thyroid hormone production. Alteration of the above pathway by activation of germline or somatic mutations in the TSH receptor or cAMP signal transduction system is believed to be responsible for the development of autonomous thyroid gland growth and hormonogenesis. The molecular alterations responsible for toxic adenomas include somatic gain-of-function mutations in the TSH receptor or the stimulatory Gsα subunit. Both result in constitutive activation of the cAMP pathway, which results in enhanced proliferation and function of thyroid follicular cells.[1][2][3][4][5]

Somatic activating GS alpha mutations

Somatic activating thyroid-stimulating hormone receptor mutations

Germline activating thyroid-stimulating hormone receptor mutations

Role of Growth Factors

Growth factors play an important role in the pathogenesis of toxic adenoma of thyroid. The following table summarizes the role of growth factors in the pathogenesis of toxic adenoma.[12][13][14][15][16][17][18][19][20]

Growth Factors (GF) Role of Growth Factors on TSH[21]
Transforming

GF-β1

  • Blocks uptake and organification of iodine
Insulin-like

GF-1

Insulin-like

GF–Binding proteins

  • Binds to IGF-1 and control its availability by stimulating IGF-I action
  • Mechanisms of their stimulatory effects include
    • Enhancing IGF-1 binding to its receptor and prolonging its intracellular half-life.
  • Insulin and epidermal growth factor (EGF) increase the productions of binding proteins
Fibroblast GF and

their receptors

Vascular endothelial

growth factor (VEGF)

Atrial natriuretic peptide

Gross Pathology

  • On macroscopic examination, a solitary toxic nodule is red and surrounded by normal thyroid tissue that is functionally suppressed and is pale in color.

Microscopic Pathology

On histological examination, toxic adenomas demonstrate following findings:

References

  1. Dumont JE, Lamy F, Roger P, Maenhaut C (1992). "Physiological and pathological regulation of thyroid cell proliferation and differentiation by thyrotropin and other factors". Physiol. Rev. 72 (3): 667–97. PMID 1320763.
  2. Van Sande J, Parma J, Tonacchera M, Swillens S, Dumont J, Vassart G (1995). "Somatic and germline mutations of the TSH receptor gene in thyroid diseases". J. Clin. Endocrinol. Metab. 80 (9): 2577–85. doi:10.1210/jcem.80.9.7673398. PMID 7673398.
  3. Parma J, Van Sande J, Swillens S, Tonacchera M, Dumont J, Vassart G (1995). "Somatic mutations causing constitutive activity of the thyrotropin receptor are the major cause of hyperfunctioning thyroid adenomas: identification of additional mutations activating both the cyclic adenosine 3',5'-monophosphate and inositol phosphate-Ca2+ cascades". Mol. Endocrinol. 9 (6): 725–33. doi:10.1210/mend.9.6.8592518. PMID 8592518.
  4. Hébrant A, van Staveren WC, Maenhaut C, Dumont JE, Leclère J (2011). "Genetic hyperthyroidism: hyperthyroidism due to activating TSHR mutations". Eur. J. Endocrinol. 164 (1): 1–9. doi:10.1530/EJE-10-0775. PMID 20926595.
  5. Trülzsch B, Krohn K, Wonerow P, Chey S, Holzapfel HP, Ackermann F, Führer D, Paschke R (2001). "Detection of thyroid-stimulating hormone receptor and Gsalpha mutations: in 75 toxic thyroid nodules by denaturing gradient gel electrophoresis". J. Mol. Med. 78 (12): 684–91. PMID 11434721.
  6. Lyons J, Landis CA, Harsh G, Vallar L, Grünewald K, Feichtinger H, Duh QY, Clark OH, Kawasaki E, Bourne HR (1990). "Two G protein oncogenes in human endocrine tumors". Science. 249 (4969): 655–9. PMID 2116665.
  7. Parma J, Duprez L, Van Sande J, Cochaux P, Gervy C, Mockel J, Dumont J, Vassart G (1993). "Somatic mutations in the thyrotropin receptor gene cause hyperfunctioning thyroid adenomas". Nature. 365 (6447): 649–51. doi:10.1038/365649a0. PMID 8413627.
  8. Weinstein LS, Shenker A, Gejman PV, Merino MJ, Friedman E, Spiegel AM (1991). "Activating mutations of the stimulatory G protein in the McCune-Albright syndrome". N. Engl. J. Med. 325 (24): 1688–95. doi:10.1056/NEJM199112123252403. PMID 1944469.
  9. Watson SG, Radford AD, Kipar A, Ibarrola P, Blackwood L (2005). "Somatic mutations of the thyroid-stimulating hormone receptor gene in feline hyperthyroidism: parallels with human hyperthyroidism". J. Endocrinol. 186 (3): 523–37. doi:10.1677/joe.1.06277. PMID 16135672.
  10. Paschke R (2011). "Molecular pathogenesis of nodular goiter". Langenbecks Arch Surg. 396 (8): 1127–36. doi:10.1007/s00423-011-0788-5. PMID 21487943.
  11. Derwahl M, Studer H (2001). "Nodular goiter and goiter nodules: Where iodine deficiency falls short of explaining the facts". Exp. Clin. Endocrinol. Diabetes. 109 (5): 250–60. doi:10.1055/s-2001-16344. PMID 11507648.
  12. Taton M, Lamy F, Roger PP, Dumont JE (1993). "General inhibition by transforming growth factor beta 1 of thyrotropin and cAMP responses in human thyroid cells in primary culture". Mol. Cell. Endocrinol. 95 (1–2): 13–21. PMID 7902304.
  13. Krohn K, Führer D, Bayer Y, Eszlinger M, Brauer V, Neumann S, Paschke R (2005). "Molecular pathogenesis of euthyroid and toxic multinodular goiter". Endocr. Rev. 26 (4): 504–24. doi:10.1210/er.2004-0005. PMID 15615818.
  14. Eszlinger M, Krohn K, Frenzel R, Kropf S, Tönjes A, Paschke R (2004). "Gene expression analysis reveals evidence for inactivation of the TGF-beta signaling cascade in autonomously functioning thyroid nodules". Oncogene. 23 (3): 795–804. doi:10.1038/sj.onc.1207186. PMID 14737114.
  15. Beere HM, Soden J, Tomlinson S, Bidey SP (1991). "Insulin-like growth factor-I production and action in porcine thyroid follicular cells in monolayer: regulation by transforming growth factor-beta". J. Endocrinol. 130 (1): 3–9. PMID 1880476.
  16. Miyakawa M, Saji M, Tsushima T, Wakai K, Shizume K (1988). "Thyroid volume and serum thyroglobulin levels in patients with acromegaly: correlation with plasma insulin-like growth factor I levels". J. Clin. Endocrinol. Metab. 67 (5): 973–8. doi:10.1210/jcem-67-5-973. PMID 3053751.
  17. Cheung NW, Lou JC, Boyages SC (1996). "Growth hormone does not increase thyroid size in the absence of thyrotropin: a study in adults with hypopituitarism". J. Clin. Endocrinol. Metab. 81 (3): 1179–83. doi:10.1210/jcem.81.3.8772597. PMID 8772597.
  18. Eszlinger M, Krohn K, Paschke R (2001). "Complementary DNA expression array analysis suggests a lower expression of signal transduction proteins and receptors in cold and hot thyroid nodules". J. Clin. Endocrinol. Metab. 86 (10): 4834–42. doi:10.1210/jcem.86.10.7933. PMID 11600550.
  19. Frautschy SA, Gonzalez AM, Martinez Murillo R, Carceller F, Cuevas P, Baird A (1991). "Expression of basic fibroblast growth factor and its receptor in the rat subfornical organ". Neuroendocrinology. 54 (1): 55–61. PMC 4237606. PMID 1656299.
  20. Sato K, Yamazaki K, Shizume K, Kanaji Y, Obara T, Ohsumi K, Demura H, Yamaguchi S, Shibuya M (1995). "Stimulation by thyroid-stimulating hormone and Grave's immunoglobulin G of vascular endothelial growth factor mRNA expression in human thyroid follicles in vitro and flt mRNA expression in the rat thyroid in vivo". J. Clin. Invest. 96 (3): 1295–302. doi:10.1172/JCI118164. PMC 185751. PMID 7657804.
  21. Kopp P (2001). "The TSH receptor and its role in thyroid disease". Cell. Mol. Life Sci. 58 (9): 1301–22. PMID 11577986.
  22. Hedinger C, Williams ED, Sobin LH (1989). "The WHO histological classification of thyroid tumors: a commentary on the second edition". Cancer. 63 (5): 908–11. PMID 2914297.

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