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Dilday, Tinslee ; Abt, Melissa ; Ramos-Solis, Nicole , et al. Cell Chem. Biol.,2024,31(5):989-999. DOI: 10.1016/j.chembiol.2024.01.001 PubMed ID: 38307028
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Abstract: Human epidermal growth factor receptor 2 (HER2)-targeted agents have proven to be effective, however, the development of resistance to these agents has become an obstacle in treating HER2+ breast cancer. Evidence implicates HUNK as an anti-cancer target for primary and resistant HER2+ breast cancers. In this study, a selective inhibitor of HUNK is characterized alongside a phosphorylation event in a downstream substrate of HUNK as a marker for HUNK activity in HER2+ breast cancer. Rubicon has been established as a substrate of HUNK that is phosphorylated at serine (S) 92. Findings indicate that HUNK-mediated phosphorylation of Rubicon at S92 promotes both autophagy and tumorigenesis in HER2/neu+ breast cancer. HUNK inhibition prevents Rubicon S92 phosphorylation in HER2/neu+ breast cancer models and inhibits tumorigenesis. This study characterizes a downstream phosphorylation event as a measure of HUNK activity and identifies a selective HUNK inhibitor that has meaningful efficacy toward HER2+ breast cancer.
Purchased from AmBeed: 10601-99-7 ; 67967-17-3 ; 694499-26-8 ; 148893-10-1
CAS No. : | 694499-26-8 | MDL No. : | MFCD09909924 |
Formula : | C13H18F3N3 | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | ZMWAZMYBMAAMAW-UHFFFAOYSA-N |
M.W : | 273.30 | Pubchem ID : | 46838908 |
Synonyms : |
|
Signal Word: | Warning | Class: | |
Precautionary Statements: | P280-P305+P351+P338-P310 | UN#: | |
Hazard Statements: | H302-H315-H319-H332-H335 | Packing Group: | |
GHS Pictogram: |
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
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