Proteomics

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Inhibition of the mitochondrial disulfide relay system impairs liver cancer cell proliferation


ABSTRACT: Augmenter of liver regeneration (ALR) is a critical multi-isoform protein with its longer isoform, located in the mitochondrial intermembrane space, being part of the mitochondrial disulfide relay system (DRS). Upregulation of ALR was observed in multiple forms of cancer, among them hepatocellular carcinoma (HCC). To shed light into the ALR role in the DRS in HCC, we thus pharmacologically inhibited ALR, resulting in profound mitochondrial impairment and cancer cell proliferation deficits. These effects were mostly reversed by supplementation with bioavailable hemin b, linking the DRS, and specifically ALR function, to mitochondrial iron homeostasis. Since tumor cells are known for their increased iron demand and since increased iron levels in cancer are associated with poor clinical outcome, these results help to further advance the intricate relation between iron and mitochondria in liver cancer.

INSTRUMENT(S): Q Exactive HF

ORGANISM(S): Rattus Rattus (black Rat)

TISSUE(S): Cell Culture

SUBMITTER: Ann-Christine König  

LAB HEAD: Hans Zischka

PROVIDER: PXD026695 | Pride | 2022-02-17

REPOSITORIES: Pride

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Publications

Mitochondrial Impairment by MitoBloCK-6 Inhibits Liver Cancer Cell Proliferation.

Kabiri Yaschar Y   Fuhrmann Anna A   Becker Anna A   Jedermann Luisa L   Eberhagen Carola C   König Ann-Christine AC   Silva Tiago Barros TB   Borges Fernanda F   Hauck Stefanie M SM   Michalke Bernhard B   Knolle Percy P   Zischka Hans H  

Frontiers in cell and developmental biology 20210920


Augmenter of liver regeneration (ALR) is a critical multi-isoform protein with its longer isoform, located in the mitochondrial intermembrane space, being part of the mitochondrial disulfide relay system (DRS). Upregulation of <i>ALR</i> was observed in multiple forms of cancer, among them hepatocellular carcinoma (HCC). To shed light into ALR function in HCC, we used MitoBloCK-6 to pharmacologically inhibit ALR, resulting in profound mitochondrial impairment and cancer cell proliferation defici  ...[more]

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