4.4 Review

Reprogramming of mitochondrial proline metabolism promotes liver tumorigenesis

Journal

AMINO ACIDS
Volume 53, Issue 12, Pages 1807-1815

Publisher

SPRINGER WIEN
DOI: 10.1007/s00726-021-02961-5

Keywords

Cancer; Enzyme; Proline; Hepatocellular carcinoma; Metabolism

Funding

  1. A*STAR Biomedical Research Council

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Dysregulated cellular energetics is a recognized hallmark of cancer, with metabolic reprogramming playing a crucial role in sustaining cancer cell proliferation. The proline metabolism pathway is implicated in promoting tumorigenesis in various cancer types, including liver cancer. Research on the impact of proline metabolism on liver cancer and other cancers, as well as the related mechanisms, is a priority in current therapeutic studies.
Dysregulated cellular energetics has recently been recognized as a hallmark of cancer and garnered attention as a potential targeting strategy for cancer therapeutics. Cancer cells reprogram metabolic activities to meet bio-energetic, biosynthetic and redox requirements needed to sustain indefinite proliferation. In many cases, metabolic reprogramming is the result of complex interactions between genetic alterations in well-known oncogenes and tumor suppressors and epigenetic changes. While the metabolism of the two most abundant nutrients, glucose and glutamine, is reprogrammed in a wide range of cancers, accumulating evidence demonstrates that additional metabolic pathways are also critical for cell survival and growth. Proline metabolism is one such metabolic pathway that promotes tumorigenesis in multiple cancer types, including liver cancer, which is the fourth main cause of cancer mortality in the world. Despite the recent spate of approved treatments, including targeted therapy and combined immunotherapies, there has been no significant gain in clinical benefits in the majority of liver cancer patients. Thus, exploring novel therapeutic strategies and identifying new molecular targets remains a top priority for liver cancer. Two of the enzymes in the proline biosynthetic pathway, pyrroline-5-carboxylate reductase (PYCR1) and Aldehyde Dehydrogenase 18 Family Member A1 (ALDH18A1), are upregulated in liver cancer of both human and animal models, while proline catabolic enzymes, such as proline dehydrogenase (PRODH) are downregulated. Here we review the latest evidence linking proline metabolism to liver and other cancers and potential mechanisms of action for the proline pathway in cancer development.

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