Sandra Incerpi
Osnat Ashur-Fabian
Paul J. Davis
Jens Z. Pedersen- 1Department of Sciences, University Roma Tre, Rome, Italy
- 2Translational Oncology Laboratory, Meir Medical Center, Kfar-Saba, Israel
- 3Department of Human Molecular Genetics and Biochemistry, Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel
- 4Department of Medicine, Albany Medical College, Albany, NY, United States
- 5Pharmaceutical Research Institute, Albany College of Pharmacy and Health Sciences, Albany, NY, United States
- 6Department of Biology, University Tor Vergata, Rome, Italy
Editorial on the Research Topic
Crosstalk between thyroid hormones, analogs and ligands of integrin αvβ3 in health and disease. Who is talking now?
The classical molecular mechanism of thyroid hormone action is genomic, involving nuclear thyroid hormone receptors (TRs) complexed with 3,5,3’-triiodo-L-thyronine (T3) and transcription of specific genes (1). A nongenomic pathway is now understood to exist and is particularly important to tumor cells (1, 2). The pathway begins at a cell surface thyroid hormone analogue receptor on plasma membrane integrin αvβ3; the principal hormone at physiological concentrations at this receptor is L-thyroxine (T4), the thyroid gland product that is the prohormone for T3. Downstream of the cell surface receptor, the hormone-integrin complex initiates intracellular signal transduction pathway sequences that culminate in differential expression of multiple genes relevant to cancer cell proliferation and tumor-linked angiogenesis (2). Certain of these signaling pathways can remarkably lead to TR activation in the nucleus. This issue of Frontiers in Endocrinology includes a set of papers focused on actions of T4 that are nongenomic in mechanism.
T3 is the principal ligand of nuclear TRs in all types of tissues, whereas T4, as noted above, is the major functional ligand for the cell surface αvβ3 integrin receptor for thyroid hormone analogues. The integrin is overexpressed and activated on cancer cells and rapidly-dividing endothelial cells. The specific cellular signal transduction pathways linked to the T4 receptor include mitogen-activated protein kinase (MAPK) and signal transducer and activator of transcription-1α (STAT-1 α) that lead to nuclear compartment co-activator and co-repressor proteins that regulate expression of specific genes related to tumor cell proliferation and tumor cell defense mechanisms. Among the proteins that move to the nuclear compartment as a result of the integrin-based actions of T4 include TRβ1, estrogen receptor- α (ER α) and tumor suppressor protein p53. The nuclear thyroid hormone receptor TRβ acts as an inhibitor of cancer cell proliferation and as a tumor suppressor.
TRα, instead, can be oncogenic as reported also in the first paper of the issue by Lasa and Contreras-Jurado, where the authors show the role of thyroid hormones in the inflammatory process leading to tumorigenesis and other pathological processes such as infectious disease up to Covid -19. The inflammatory process is described in details both in the short–term and in the chronic situation, as well as in the crosstalk between thyroid hormones and infection and thyroid hormones and cancer. A crosstalk between thyroid hormones and the immune system is widely recognized, thyroid hormones may behave as anti-inflammarory agents (3–6).
In the second paper, Ariyani et al. show that the TR-dependent signaling pathway via integrin αvβ3 plays a role in cerebellar development, neuritogenesis and dendritogenesis. The knockdown of integrin αv or integrin β3 or the double knock down of integrin αvβ3 significantly reduces dendritic arborization in Purkinje cells. The effect of thyroid hormones is mediated, in part, by activation of PI3-K and ERK1/2 (MAPK). The experiments were carried out mainly in primary culture of cerebellar Purkinje cells from mice and in cells in culture of neuroblastoma, Neuro –2A cells, with similar results, suggesting that neuritogenesis process is similar in primary culture and neuroblastoma cells.
The effects of thyroid hormones on tumor progression and metastasis is inhibited by tetraiodothyroacetic acid (tetrac) and nanoderivatives, tetrac is a metabolite of thyroid homone that binds the integrin αvβ3 at the RGD binding site or in close proximity to it (7, 8).
The paper of Tobi et al., shows by in-silico docking the affinity of more than 20 thyroid hormone metabolites with a variety of structural features sulfated, deiodinated, deaminated or decarboxylated, including the biologically active hormones T3 and T4, with integrin αvβ3. All the tested molecules show a negative energy suggesting good affinity with the RGD site, at the integrin, with differences. The RGD peptide was used both in linear or cyclic conformation, and it was found that iodination at the 3,5 and 3’ positions shows an increased affinity with respect to other iodination positions of other metabolites, but also the binding capability could be improved.
The Incerpi et al. paper is based on data on thyroid hormones, T3 and 3,5-diiodothyronine (3,5-T2) on the Na/K-ATPase in chick embryo hepatocytes. The metabolite 3,5-T2 shows a significant effect in the inhibition of the Na-pump, higher than T3, whereas T4 is without effect. The Na-pump is an ubiquitous enzyme present both in plant and in animal cells, whose inhibition by T3 and 3,5-T2 is mediated by PKA, PKC and PI3-K in the early stages of development. This inhibition gives rise to a protected or an anti-inflammatory environment, with high intracellular Na+ and Ca2+ ions, similar to the activation of the anti-inflammatory response elicited by the α7 acetylcholine receptor (α7nAChR) at the level of the vagus nerve (9). 3,5-T2 is a metabolite with strong effects on mitochondrial activity (resting metabolic rate) that is more efficient than T3, 3,5-T2 is also a vasodilator.
At the end of the story, we may find the answer to the question raised in the title of the Issue:
‘Crosstalk between thyroid hormones, analogs and ligands of integrin αvβ3 in health and disease. Who is talking now?’ The endogenous TH metabolites and their nanoderivatives may represent a therapeutic tool able to interact with integrin-modulated intracellular pathways in infective diseases and cancer. But we should also take into account the crossttalk between nongenomic and genomic signaling of thyroid hormones and steroid hormones and their analogues that appear to play a pivotal role in the physiopathology of cancer and in cancer management.
Author contributions
PJD and SI wrote the first draft of the editorial. All the authors read, revised and approved the manuscript in the final form.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
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References
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2. Davis PJ, Mousa SA, Lin H-Y. Nongenomic actions of thyroid hormone: the integrin component. Physiol Rev (2021) 101:319–52. doi: 10.1152/physrev.00038.2019
3. Klein JR. The immune system as a regulator of thyroid hormone activity. Exp Biol Med (Maywood) (2006) 231:229–36. doi: 10.1177/153537020623100301
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6. Candelotti E, De Luca R, Megna R, Maiolo M, De Vito P, Gionfra F, et al. Inhibition by thyroid hormones of cell migration activated by IGF-1 and MCP-1 in THP-1 monocytes: Focus on signal transduction events proximal to integrin αvβ3. Front Cell Dev Biol (2021) 9:651492. doi: 10.3389/fcell.2021.651492
7. Cheng T-M, Chang W-J, Chu H-Y, De Luca R, Pedersen JZ, Incerpi S. Nano-strategies targeting the integrin αvβ3 network for cancer therapy. Cells (2021) 10:1684. doi: 10.3390/cells10071684
8. Glinsky GV, Godugu K, Sudha T, Rajabi M, Chittur SV, Hercbergs AA, et al. Effects of anticancer agent p-bi-TAT on gene expression link the integrin thyroid hormone receptor to expression of stemness and energy metabolism genes in cancer cells. Metabolites (2022) 12:325. doi: 10.3390/metabol;12040325
Keywords: integrin αvβ3, signal transduction, thyroid hormone receptor, nongenomic mechanism, cancer, COVID-19, Na/K-ATPase, tetraiodothyroacetic acid (tetrac)
Citation: Incerpi S, Ashur-Fabian O, Davis PJ and Pedersen JZ (2023) Editorial: Crosstalk between thyroid hormones, analogs and ligands of integrin αvβ3 in health and disease. Who is talking now? Front. Endocrinol. 13:1119952. doi: 10.3389/fendo.2022.1119952
Received: 09 December 2022; Accepted: 19 December 2022;
Published: 05 January 2023.
Edited and Reviewed by:
Claire Perks, University of Bristol, United KingdomCopyright © 2023 Incerpi, Ashur-Fabian, Davis and Pedersen. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Sandra Incerpi, c2FuZHJhLmluY2VycGlAZ21haWwuY29t