ChemoproteomicProfiling of a Carbon-Stabilized Gold(III)Macrocycle Reveals Cellular Engagement with HMOX2

In this work, we discovered a novel organometallic gold(III) macrocycle, <b>Au-Mac1,</b> that demonstrates anticancer potency in a panel of triple-negative breast cancer cells (TNBC), and based on this complex, a biotinylated-Au-Mac1 probe was designed for target identification via chemoproteomics, which uncovered the engagement of HMOX2 of the heme-energy metabolism pathway. Using orthogonal chemical biology and molecular biology approaches, including immunoblotting, flow cytometry, and cellular thermal shift assays, it was confirmed that <b>Au-Mac1</b> engages HMOX2 in cells. Downstream effects of <b>Au-Mac1</b> on the depletion of mitochondrial membrane proteins and bioenergetics point to the potential role of HMOX2 in cancer. Importantly, <b>Au-Mac1</b> inhibits in vivo tumor growth of metastatic breast tumor-bearing mice. We believe that this approach is clinically relevant in network-oriented drug discovery. To the best of our knowledge, <b>Au-Mac1</b> is the first gold complex that targets HMOX2 to elicit an anticancer effect.

Publication Details

Journal
Figshare
Published
2025-02-21
DOI
https://doi.org/10.1021/acs.jmedchem.4c02952.s001
Primary Topic
Metal complexes synthesis and properties
Type
article
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article

ChemoproteomicProfiling of a Carbon-Stabilized Gold(III)Macrocycle Reveals Cellular Engagement with HMOX2

Figshare
Metal complexes synthesis and properties
article

ChemoproteomicProfiling of a Carbon-Stabilized Gold(III)Macrocycle Reveals Cellular Engagement with HMOX2

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Abstract

In this work, we discovered a novel organometallic gold(III) macrocycle, <b>Au-Mac1,</b> that demonstrates anticancer potency in a panel of triple-negative breast cancer cells (TNBC), and based on this complex, a biotinylated-Au-Mac1 probe was designed for target identification via chemoproteomics, which uncovered the engagement of HMOX2 of the heme-energy metabolism pathway. Using orthogonal chemical biology and molecular biology approaches, including immunoblotting, flow cytometry, and cellular thermal shift assays, it was confirmed that <b>Au-Mac1</b> engages HMOX2 in cells. Downstream effects of <b>Au-Mac1</b> on the depletion of mitochondrial membrane proteins and bioenergetics point to the potential role of HMOX2 in cancer. Importantly, <b>Au-Mac1</b> inhibits in vivo tumor growth of metastatic breast tumor-bearing mice. We believe that this approach is clinically relevant in network-oriented drug discovery. To the best of our knowledge, <b>Au-Mac1</b> is the first gold complex that targets HMOX2 to elicit an anticancer effect.

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Metal complexes synthesis and properties
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