Disrupting cancer cell cycle with two commercially available inhibitors causes tumor cell death2021-02-12
With two commercially available inhibitors, the cell cycle of the cancer cells in the childhood tumor neuroblastoma can be disrupted at a key point causing tumor cell death.
Neuroblastomas are malignant solid tumors that occur mainly in early childhood. They arise from degenerated immature cells of the sympathetic nervous system.
One prognostic marker to assess the malignancy of the tumor is the MYCN oncogene. High-risk neuroblastoma patients often have amplification of MYCN, i.e. very high levels of this protein, which drives uncontrolled tumor growth. Conversely, inhibiting MYCN or its function could be a promising therapeutic opportunity.
An important step towards this direction was taken by an international research project led by scientists from Julius-Maximilians-Universität Würzburg (JMU) in Bavaria, Germany, which was recently published in the journal Nature Cancer.
News about the role of MYCN in the cell cycle
The co-lead author of the publication is Dr Gabriele Büchel from the Chair of Biochemistry and Molecular Biology at the JMU Biocentre. The principle investigator explains: "Until now, it was known that MYCN controls the function of RNA polymerase. This reads the DNA in the cell nucleus and converts it into mRNA. Through our research, we were able to show that MYCN also plays a specific role during the S phase of the cell cycle, when DNA is also duplicated."
In this phase, therefore, two processes take place simultaneously: the reading and replication of DNA. Figuratively speaking, according to Gabriele Büchel, "two trains are on the same track".
Goal: Promote transcription-replication conflicts
Together with the doctoral student Isabelle Roeschert, she found out that MYCN prevents collisions of the two trains – so-called transcription-replication conflicts.
This signaling effect requires the two enzymes Aurora-A and ATR, both of which can be inhibited with existing pharmaceuticals. In this way, targeted "train collisions" can be induced to damage the tumor cell. Or in medical terms: the combination of both drugs leads to DNA damage and cell death – highly specifically in tumors, while other tissues remain unaffected.
"In mouse models of neuroblastoma, we were able to achieve tumor growth regression using this strategy. Some of the experimental animals could be even cured with the combinational treatment", Gabriele Büchel clarifies the effect of this "therapy".
Clinical trials already on the horizon
According to her, patients could also benefit from the knowledge gained in the near future. "The substances we use are all already commercially available. Aurora A and ATR inhibitors as well as the combinations we use are currently being tested in a number of practical models which are closer tot he clinic. If they are successful there, clinical trials could start soon," Büchel announces.
In addition to the JMU working group, research teams from the Charité in Berlin, the Universities of Göttingen and Zurich and the Institute of Cancer Research in London were involved in the study. It was funded by the German Cancer Aid and the European Research Council.
Julius-Maximilians-Universität Würzburg, JMU
Roeschert, I., et al. (2021) Combined inhibition of Aurora-A and ATR kinases results in regression of MYCN-amplified neuroblastoma. Nature Cancer. doi.org/10.1038/s43018-020-00171-8.
Posted in: Cell Biology
Tags: Biochemistry, Cancer, Cell, Cell Cycle, Cell Death, Cell Nucleus, DNA, DNA Damage, Drugs, Malignant, Molecular Biology, Nervous System, Neuroblastoma, Oncogene, Pharmaceuticals, Polymerase, Protein, Research, Research Project, RNA, Transcription
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