AUTHOR=Gupta Prakamya , Rai Ashutosh , Mukherjee Kanchan Kumar , Sachdeva Naresh , Radotra Bishan Das , Punia Raj Pal Singh , Vashista Rakesh Kumar , Hota Debasish , Srinivasan Anand , Dhandapani Sivashanmugam , Gupta Sunil Kumar , Bhansali Anil , Dutta Pinaki 

TITLE=Imatinib Inhibits GH Secretion From Somatotropinomas

JOURNAL=Frontiers in Endocrinology

VOLUME=9

YEAR=2018

URL=https://www.frontiersin.org/journals/endocrinology/articles/10.3389/fendo.2018.00453

DOI=10.3389/fendo.2018.00453

ISSN=1664-2392

ABSTRACT=<p><bold>Background:</bold> Imatinib, a tyrosine kinase inhibitor, causes growth failure in children with chronic myeloid leukemia probably by targeting the growth hormone (GH)/insulin like growth factor-1 (IGF-1) axis. We aim to explore the imatinib targets expression in pituitary adenomas and study the effect of imatinib on GH secretion in somatotropinoma cells and GH3 cell line.</p><p><bold>Materials and Methods:</bold> The expression pattern of imatinib's targets (c-kit, VEGF, and PDGFR-α/β) was studied using immunohistochemistry and immunoblotting 157 giant (≥4 cm) pituitary adenomas (121 non-functioning pituitary adenomas, 32 somatotropinomas, and four prolactinomas) and compared to normal pituitary (<italic>n</italic> = 4) obtained at autopsy. The effect imatinib on GH secretion, cell viability, immunohistochemistry, electron microscopy, and apoptosis was studied in primary culture of human somatotropinomas (<italic>n</italic> = 20) and in rat somato-mammotroph GH3 cell-line. A receptor tyrosine kinase array was applied to human samples to identify altered pathways.</p><p><bold>Results:</bold> Somatotropinomas showed significantly higher immunopositivity for c-kit and platelet-derived growth factor receptor-β (PDGFR-β; <italic>P</italic> &lt; 0.009 and <italic>P</italic> &lt; 0.001, respectively), while staining for platelet-derived growth factor receptor-α (PDGFR-α) and vascular endothelial growth factor (VEGF) revealed a weaker expression (<italic>P</italic> &lt; 0.001) compared to normal pituitary. Imatinib inhibited GH secretion from both primary culture (<italic>P</italic> &lt; 0.01) and GH3 cells (<italic>P</italic> &lt; 0.001), while it did not affect cell viability and apoptosis. The receptor tyrosine kinase array showed that imatinib inhibits GH signaling via PDGFR-β pathway.</p><p><bold>Conclusion:</bold> Imatinib inhibits GH secretion in somatotropinoma cells without affecting cell viability and may be used as an adjunct therapy for treating GH secreting pituitary adenomas.</p>