Abstract
Type 1 iodothyronine deiodinase (D1) is a crucial enzyme which converts the prohormone thyroxine (T4) into active tri-iodothyronine (T3). There has been strong evidence that the metabolism of thyroid hormones is disturbed in some neoplastic tissues such as thyroid, renal, and breast cancer. However, there are few available data about D1 enzyme activity in benign tumors such as hemangioma, which is the most common primary liver tumor. Hence this study aimed to determine the enzymatic activity of D1 in hemangiomas in relation to healthy liver tissue. Seven tumors and healthy control tissues were obtained from patients who had liver resection due to hemangioma. The activity was assessed by measurement of radioactive iodine released by deiodination catalyzed by D1. It was found that D1 activity was significantly lower in the hemagiomas than in the healthy surrounding tissue (p = 0.0017). The results indicated that thyroid hormones play important roles not only in the regulation of cell metabolism, but also in cell growth, division, and apoptosis. The active form T3 acts through its nuclear receptors and influences the up- and down-regulation of target genes. Healthy liver tissue expresses a high level of D1, but disturbed D1 activity may result in changes in the local concentration of T3 which may impair gene transcription. These finding demonstrate a low enzymatic activity of D1 in liver hemangioma and suggest an as yet unknown role of thyroid hormones in this type of benign liver tumor.
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Introduction
The role of thyroid hormones in carcinogenesis has been postulated for many years. However, existing data are not sufficient for a complete understanding of the process. Thyroxin (T4), which is the main product of the thyroid gland, is considered a pro-hormone and must be converted to the active form, tri-iodothyronine (T3). T3 acts through its nuclear receptors, i.e., thyroid hormone receptors (TRs), and has significant influence on transcription, translation, and cell division and differentiation. T3 is produced by monodeiodination catalyzed by type 1 iodothyronine deiodinase (D1). This enzyme is present in almost all human cells, but the highest concentrations were found in the thyroid, liver, and kidneys (Bianco et al. 2002). Both its enzymatic activity and its gene expression have been examined in some cancers tissues. Significant decreases in gene expression and enzyme activity were found in papillary thyroid cancer tissue (Ambroziak et al. 2005; De Souza Meyer et al. 2005) as well as in papillary and follicular thyroid cancer cell lines (Arnaldi et al. 2005; Schreck et al. 1994), renal clear cell cancer (Pachucki et al. 2001), lung cancer (Wawrzynska et al. 2003), and pituitary adenomas (Baur et al. 2002; Tannahill et al. 2002). Surprisingly, elevated D1 enzyme activity and mRNA expression were described in human breast cancer tissue (Debski et al. 2007; García-Solís and Aceves 2003).
There has been strong evidence that the metabolism of thyroid hormones is disturbed in some of neoplastic tissues (Gonzalez-Sancho et al. 2003; Jakobs et al. 2002). However, there are few available data about D1’s enzymatic activity in benign tumors such as hemangiomas, which are the most common primary liver tumors. Interestingly, in this type of benign lesion an elevated level of deiodinase type 3 (D3), which inactivates thyroid hormones, was reported (Ho et al. 2005; Huang et al. 2005; Konrad et al. 2003).
The aim of this study was to determine the enzymatic activity of D1 in liver hemangioma in comparison with healthy liver tissue.
Materials and Methods
Seven tumor samples and an equal number of healthy liver control samples were obtained from patients who underwent liver resection for hemangioma, which is now a very rare indication for surgical intervention. Liver resection is limited to a very selected group of patients. There were neither postoperative deaths nor major complications. The group consisted of three men and four women with a mean age of 50 years. Five patients had extended liver resection (more than three segments). In two cases the resection included two segments. The mean tumor size was 7.86 cm (Table 1). The samples were taken from the tumor as well as from a site far from it, which was macroscopically normal liver tissue. These noncancerous tissues were assigned as controls. Immediately after the surgical procedures, the samples were frozen in carbon dioxide snow and kept at −70°C until needed. In addition, a blood sample for thyroid hormone determination (TSH, fT3, and fT4) was taken from each patient before the operation. The results were within the normal ranges (Table 2).
The tissue samples were thawed and then homogenized in homogenization buffer (0.1 M PE [K2HPO4/KH2PO4], 1 mM EDTA, 10 mM DTT-dithiothreitol, and 0.25 M sucrose, dH2O, pH 7.0). Protein concentration was measured by the BCA (bicinchonic acid) method using bovine albumin as the standard.
D1 activity was measured by quantification of radioactive iodide released from 3′5′[125I]-rT3, which was purified by Sephadex LH20 column chromatography just before each assay. It was washed out with 10 ml of H2O followed by elution with 2 ml of 75% ethanol in 0.5-ml fractions (this amount of 75% alcohol did not affect the reaction). We used fractions with the highest activity (50,000–60,000 CMP-counts per minutes) and added 70 μl into each reaction tube.
The samples were incubated for 30 min at 37°C in phosphate buffer (0.1 M PE and 1 mM EDTA, pH 6.9) with 1 nM unlabeled rT3 and 10 mM DTT. Each assay was performed twice and there was always one extra sample with propylthiouracyl added to show the inhibition of D1 by this agent. After incubation, the reaction was stopped by placing the samples in an ice bath. Precipitation was then caused by adding 100 μl of horse serum and 50 μl of 50% trichloroacetic acid. The samples were vortex for 1.5 min and centrifuged at 9,000 rpm for 5 min. An aliquot of the supernatant containing 125I, but not labeled iodothyronines, was counted in a gamma counter (Wzard-1470, Wallac). Final enzymatic activity was expressed as the fmol of released 125I per mg of protein per minute. The STATISTICA program was used for the statistical analysis.
Results
As this was a preliminary study only, seven tissue samples were examined. The median value of D1 enzyme activity in the tumor tissue was 32 fmol/(mg-protein min) (range: 0–132). The median value of its enzymatic activity in the healthy control samples was 549 fmol/(mg-protein min) (range: 244–1243). D1 activity was significantly lower in the hemagiomas than in the healthy liver samples (p < 0.0017; Figs. 1, 2).
Discussion
The presented data showed very low, almost undetectable, activity of D1 in 6 of the 7 investigated hemangioma tissue samples, especially in comparison with healthy liver tissue, which was thought to be responsible for ca. 70% of the peripheral activation of T4 (Macke-Nauman 1990). However, more recent data suggest that more T3 may be produced by D2 deiodination, which takes place in skeletal muscle as well as in liver tissue (Maia et al. 2005; Salvatore et al. 1996). This result could be associated with the differences in hemangioma and healthy liver tissue morphology. The largest part of the tumor develops from endothelial cells derived from epithelium, not hepatocytes. It was demonstrated that there is a high prevalence of the major physiological inactivator of thyroid hormones, D3, in the epithelium, which causes results opposite to those of D1 (Huang 2005; Huang et al. 2003; Zhang et al. 2006). The effect of D3 could appear as a very low concentration of thyroid hormones in the lesion, but there is no strong evidence concerning this occurrence. It seems reasonable to investigate rT3 and fT3 concentration in situ as next part of our studies.
It was also observed that the rapid resolution of consumptive hypothyroidism in children with multiple hepatic hemangiomas is a result of the high enzymatic activity of D3 and the production of TSH-like hormone by the tumor tissue. Children who required high doses of thyroid hormones were cured following liver transplantation, which proves the positive correlation between D3 enzyme activity in hemangiomas and hypothyroidism. Isolated incidents were also noted in adults (Ho et al. 2005; Huang et al. 2005; Konrad et al. 2003).
In conclusion, thyroid hormones play important roles not only in the regulation of cell metabolism, but also in cell growth, division, and apoptosis. The active form T3 acts through its nuclear receptors and influences the up- and down-regulation of target genes. Disturbed activity of D1 may result in changes in the local concentration of T3. Furthermore, it may impair some gene transcription. Our finding clearly demonstrates a low enzymatic activity of D1 in liver hemangioma and suggests a so far unknown role of thyroid hormones in this type of liver tumor, which makes further investigation reasonable.
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Kornasiewicz, O., Debski, M., Stepnowska, M. et al. The Enzymatic Activity of Type 1 Iodothyronine Deiodinase (D1) is Low in Liver Hemangioma: A Preliminary Study. Arch. Immunol. Ther. Exp. 58, 77–80 (2010). https://doi.org/10.1007/s00005-009-0056-3
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DOI: https://doi.org/10.1007/s00005-009-0056-3