4.1 Article

Inhibitory Effects of Antagonists of Growth Hormone-Releasing Hormone (GHRH) in Thyroid Cancer

Journal

HORMONES & CANCER
Volume 8, Issue 5-6, Pages 314-324

Publisher

SPRINGER
DOI: 10.1007/s12672-017-0307-4

Keywords

Thyroid cancer; Growth hormone-releasing hormone; GHRH antagonists; Hypothalamic hormone; mRNA for GHRH; mRNA for GHRH receptors

Funding

  1. Portuguese Foundation for Science and Technology [SFRH/BPD/85249/2012]
  2. FCT
  3. Fundo Europeu de Desenvolvimento Regional (FEDER) funds through the COMPETE 2020-Operacional Programme for Competitiveness and Internationalization (POCI), Portugal 2020
  4. Portuguese funds through Fundacao para a Ciencia e a Tecnologia (FCT)/Ministerio da Ciencia, Tecnologia e Inovacao in the framework of the project Institute for Research and Innovation in Health Sciences [POCI-01-0145-FEDER-007274]
  5. Norte 2020-Programa Operacional Regional do Norte [NORTE-01-0145-FEDER-000029]
  6. Medical Research Service of the Department of Veterans Affairs and Department of Medicine, Division of Hematology-Oncology and Sylvester Comprehensive Cancer Center, University of Miami, School of Medicine

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Growth hormone-releasing hormone (GHRH) is a peptide hormone secreted by the hypothalamus that regulates the synthesis and secretion of growth hormone (GH) in the pituitary. The extra-hypothalamic GHRH and its cognate receptors (GHRHR and splice variants) play a mitogenic role by stimulating cell proliferation and preventing apoptotic cell death. It is well established that GHRH antagonists inhibit the growth, tumorigenicity, and metastasis of various human malignancies. In this work, we studied the effect of two new GHRH antagonists, MIA602 and MIA690, on thyroid cancer. We studied the effect of MIA602 and MIA690 on thyroid cancer in vitro, using human thyroid cancer cell lines, and in vivo, using chicken embryo chorioallantoic membrane (CAM) assays. We found that mRNA for GHRH and GHRH receptor is expressed in thyroid cell lines and in samples of thyroid tumors. Immunohistochemistry confirmed the expression of GHRHR protein in specimens of thyroid tumor. We observed that GHRH antagonists inhibited the growth and increased apoptosis of thyroid cancer cells. In vivo, the antagonists inhibited growth and angiogenesis of engrafted thyroid tumors. Our results suggest that GHRH expression may play a role in growth of thyroid cancer and that GHRH antagonists can be a therapeutic option for thyroid cancer patients.

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