Peter Brenneisen

Lab Head, Prof. Dr.

Heinrich-Heine-Universität Düsseldorf Medizinische Fakultät

Germany

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Prof. Dr. Peter Brenneisen is a Lab Head at Heinrich-Heine-Universität Düsseldorf Medizinische Fakultät in Germany. His research areas include the anti-cancer potential of nanoparticles and natural compounds, as well as mechanisms of selective toxicity in melanoma and other cancers. Recent publications highlight the effects of cerium oxide nanoparticles, cardamonin, and artesunate in cancer cell viability and apoptosis.

Articles (13)

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2025

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2024

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2024

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2023

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2023

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2023

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2023

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2023

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2021

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2020

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2020

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2020

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2020

Collaborators (1)

Andreas Reichert

Prof. Dr.

Heinrich-Heine-Universität Düsseldorf Medizinische Fakultät

GERMANY

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Peter Brenneisen

Research Interests

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Articles (13)

Combination of cerium oxide nanoparticles and antimalarial drug chloroquine: characterization and anti-cancer potential for triple negative breast cancer

A Combination of Cardamonin and Doxorubicin Selectively Affect Cell Viability of Melanoma Cells: An In Vitro Study

The role of GAPDH in the selective toxicity of CNP in melanoma cells

The Antimalarial Drug Artesunate Mediates Selective Cytotoxicity by Upregulating HO-1 in Melanoma Cells

The natural chalcone cardamonin selectively induces apoptosis in human neuroblastoma cells

Involvement of necroptosis in the selective toxicity of the natural compound (±) gossypol on squamous skin cancer cells in vitro

Carbon monoxide exposure activates ULK1 via AMPK phosphorylation in murine embryonic fibroblasts

Investigating the surfactant antagonism with the Open Source Reconstructed Epidermis (OS-Rep) model

The BH3 mimetic (±) gossypol induces ROS-independent apoptosis and mitochondrial dysfunction in human A375 melanoma cells in vitro

CNP mediated selective toxicity on melanoma cells is accompanied by mitochondrial dysfunction.

Ammonia inhibits energy metabolism in astrocytes in a rapid and glutamate dehydrogenase 2-dependent manner

Endogenous Carbon Monoxide Signaling Modulates Mitochondrial Function and Intracellular Glucose Utilization: Impact of the Heme Oxygenase Substrate Hemin

Effects of frequently applied carbon monoxide releasing molecules (CORMs) in typical CO-sensitive model systems – A comparative in vitro study

Collaborators (1)

Andreas Reichert

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