Chemotherapy remains the most widely used cancer treatment, and much attention has been paid to the mechanisms underlying chemotherapy resistance. Sofie Deschoemaeker (VIB/KU Leuven) and a research team led by Massimiliano Mazzone (VIB/KU Leuven) recently investigated the interplay between p53 and the PHD family of oxygen sensors and their potential role in the response of CRC to chemotherapy.
Blocking PHD1 prevents p53 activation upon chemotherapy
The proteins PHD1, PHD2 and PHD3 are oxygen-sensitive enzymes known to be involved during cell damage and metabolic stress, such as that induced by chemotherapeutic treatment. The transcription factor p53 is a well-known cell stress sensor that, when mutated in cancer cells, can be activated to promote DNA repair in those cells, reducing chemotherapy's effectiveness. Prof. Mazzone's team found that inhibiting PHD1, but not PHD2 or PHD3, prevented p53 activation and improved the response of CRC to multiple chemotherapeutic agents.
The study's novel insight into the molecular mechanisms underlying chemotherapy resistance adds another layer of complexity to the role of PHD1 in cancer.
Robbing cancer cells of their ability to heal
Sofie Deschoemaeker: "We demonstrated that PHD1 can affect the way colorectal cancer responds to the three most common chemotherapeutic drugs used to treat CRC today. By blocking PHD1, we rob CRC cells of their ability to harness p53 to the cell-repair yoke, even when this protein is mutated (as often occurs in CRC). That means the CRC cells are exposed to the full DNA damage caused by these genotoxic drugs, resulting in greater cell death and thus a better response to the chemotherapy and, ultimately, an improved outcome."
The research, which appeared in EMBO Molecular Medicine, opens the door to the design and validation of PHD1-specific inhibitors in colorectal cancer patients, with the aim of increasing their sensitivity to currently used chemotherapeutic treatments.
Materials provided by VIB - Flanders Interuniversity Institute for Biotechnology. Note: Content may be edited for style and length.
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