The Application of GHRH Antagonist as a Treatment for Resistant APL

GHRH is a hypothalamic peptide shown to stimulate the proliferation of malignant cells in humans. We have previously shown that the use of GHRH antagonist MIA-602 successfully suppressed the growth of many human cancer cell lines, spanning more than 20 types of cancers. In this study, we demonstrate...

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Veröffentlicht in:Cancers 2023-06, Vol.15 (12), p.3104
Hauptverfasser: Chale, Ravinder S, Almeida, Stephanie M, Rodriguez, Mario, Jozic, Ivan, Gaumond, Simonetta I, Schally, Andrew V, Jimenez, Joaquin J
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Sprache:eng
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Zusammenfassung:GHRH is a hypothalamic peptide shown to stimulate the proliferation of malignant cells in humans. We have previously shown that the use of GHRH antagonist MIA-602 successfully suppressed the growth of many human cancer cell lines, spanning more than 20 types of cancers. In this study, we demonstrate the presence of GHRH-R in the NB4, NB4-RAA, and K-562 model cell lines. Furthermore, we demonstrate the inhibited proliferation of all three cell lines in vitro after incubation with MIA-602. The treatment of xenografts of human APL cell lines with MIA-602 led to a significant reduction in tumor growth. Additionally, combination therapy with both doxorubicin (DOX) and MIA-602 showed a marked synergistic effect in reducing the proliferation of the K-562 AML cell line. These findings suggest that MIA-602 could be utilized to address resistance to all- retinoic acid (ATRA) and arsenic trioxide (ATO) therapies, as well as in augmenting anthracycline-based regimens.
ISSN:2072-6694
2072-6694
DOI:10.3390/cancers15123104