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DRUG:

MIA-602

i
Other names: MIA-602
Associations
Trials
Company:
University of Miami
Drug class:
GHRH antagonist
Associations
Trials
9ms
Growth Hormone-Releasing Hormone (GHRH) Antagonist Peptides Combined with PI3K Isoform Inhibitors Enhance Cell Death in Prostate Cancer. (PubMed, Cancers (Basel))
The ability of the MIA-602/690 + PI3K inhibitor combination to alter multiple signaling pathways may weaken the activation of adaptive mechanisms resulting from each drug and improve efficacy.
Journal
|
PIK3CA (Phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha) • PTEN (Phosphatase and tensin homolog) • AR (Androgen receptor) • PIK3CB (Phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) • CCNA2 (Cyclin A2) • E2F1 (E2F transcription factor 1)
|
PIK3CA mutation • PTEN mutation
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MIA-602
10ms
Growth Hormone-Releasing Hormone Antagonists Increase Radiosensitivity in Non-Small Cell Lung Cancer Cells. (PubMed, Int J Mol Sci)
Finally, both MIA-602 and MIA-690 enhanced radiosensitivity in primary human NSCLC cells. These findings highlight the potential of GHRH antagonists as radiosensitizers in NSCLC treatment.
Journal • IO biomarker
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BCL2 (B-cell CLL/lymphoma 2) • CDH1 (Cadherin 1) • IGF1 (Insulin-like growth factor 1) • CASP3 (Caspase 3)
|
MIA-602
over2years
The Application of GHRH Antagonist as a Treatment for Resistant APL. (PubMed, Cancers (Basel))
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-trans retinoic acid (ATRA) and arsenic trioxide (ATO) therapies, as well as in augmenting anthracycline-based regimens.
Journal
|
doxorubicin hydrochloride • arsenic trioxide • MIA-602