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In squamous cell carcinoma, a protein ensures that unneeded proteins are no longer disposed of. A research team at the University of Würzburg has switched off this protein for the first time.
Squamous cell carcinoma is a very unusual type of cancer. They occur in many tissues – for example in the lungs, esophagus, pancreas, throat and pharynx, and on the skin. Due to the many mutations in this type of cancer, treatment is a particularly challenging task for medicine.
However, all squamous cell carcinoma have a common Achilles' heel: They are dependent on the cancer protein ∆NP63. This is a protein that only occurs in this type of tumor and regulates essential biological processes.
An international research team led by Julius-Maximilians-Universität (JMU) Würzburg in Bavaria, Germany, has now found a way to inactivate the cancer protein with the help of another protein and thus curb the growth of squamous cell carcinoma.
Traffic tickets become effective again
The helpful protein is the deubiquitylase USP28, which is particularly common in squamous cell carcinoma. It controls the amount of the cancer protein ∆NP63.
"The deubiquitylase belongs to the so-called ubiquitin-proteasome system, which can be imagined as a towing company," explains Dr. Markus Diefenbacher, group leader at the JMU Chair of Biochemistry and Molecular Biology I. His research group was in charge of the study.
"In healthy cells, this towing company marks ‚incorrectly parked‘ proteins with a kind of parking ticket, namely the protein ubiquitin. "It then towed the parkers away and disposed of them. But the protein can remove the parking ticket and thus prevent the towing. In tumour cells, there is often a loss of traffic wardens/controllers or an accumulation of USP28. Therefore, ∆NP63 in a tumour cell behaves in a similar way to an incorrectly parked car where the parking ticket is permanently removed," explains Diefenbacher.
No direct attack possible
The research team has now been able to prove the dependence of squamous cell carcinoma on the protein USP28: Using a preclinical inhibitor, it switched off ∆NP63's parking ticket remover in the tumor cells. The tumors then stopped growing.
"Many cancer proteins are constructed in such a way that it is not possible to develop a direct active substance against them with the methods currently available," explains the Würzburg researcher. Also, no direct therapeutic attack on the cancer protein ΔNP63 is possible. However, by switching off USP28, the cancer protein could be rapidly degraded in human and animal tumor cells and the tumor could be fought. At the same time, there were no side effects in healthy cells. "We have thus discovered a good new way of attacking squamous cell carcinoma," said Diefenbacher.
Searching for other inhibitors
The inhibitor used is not yet suitable for therapeutic use in humans. It still needs further research. This is done in collaboration with the research group of JMU professor Caroline Kisker at the Rudolf Virchow Centre for Experimental Biomedicine. Diefenbacher: "In cancer therapy, inhibitors are already being used that switch off the entire ubiquitin-proteasome system. Our work now shows a possibility of switching off only one component of this system and thus being able to combat the tumour cells even more specifically.“
Next, Diefenbacher's team will look for further inhibitors that can also be used against USP28. "In addition, we will also look for other proteins in squamous cell carcinoma which these tumours depend on, and investigate whether the ubiquitin-proteasome system can be used to target these proteins for therapy," says the JMU researcher.
Publication partners and sponsors
The study results are published open access in the journal EMBO Molecular Medicine. The study involves groups from JMU (Biocentre, Comprehensive Cancer Centre Mainfranken, Rudolf Virchow Centre, Faculty of Medicine) and research teams from the University Hospital Würzburg, the University of Córdoba, the Instituto Maimónides de Investigación Biomédica Córdoba (IMIBIC), the Hospital Universitario Reina Sofía in Córdoba, the Technion Haifa in Israel and the Goethe University Frankfurt.
The study was supported by the German Cancer Aid, the German Research Foundation, the German Israeli Foundation and the Interdisciplinary Centre for Clinical Research Würzburg.
Dr. Markus Diefenbacher, Biocentre, Chair of Biochemistry and Molecular Biology I, University of Würzburg, T +49 931 31-88167, markus.diefenbacher@uni-wuerzburg.de
Cristian Prieto-Garcia, Oliver Hartmann, Michaela Reissland, Fabian Braun, Thomas Fischer, Susanne Walz, Christina Schülein-Völk, Ursula Eilers, Carsten P. Ade, Marco A. Calzado, Amir Orian, Hans M. Maric, Christian Münch, Mathias Rosenfeldt, Martin Eilers, and Markus E. Diefenbacher: "Maintaining protein stability of ∆Np63 via USP28 is required by squamous cancer cells", 4 March 2020, EMBO Molecular Medicine, DOI: 10.15252/emmm.201911101
https://www.embopress.org/doi/full/10.15252/emmm.201911101 Link zur Publikation in EMBO Molecular Medicine
A lung tumor that expresses USP28 (left). On the right, however, tumors are shown in which USP28 has ...
(Images: Markus Diefenbacher)
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A lung tumor that expresses USP28 (left). On the right, however, tumors are shown in which USP28 has ...
(Images: Markus Diefenbacher)
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