Cookie Settings

We use cookies to optimize our website. These include cookies that are necessary for the operation of the site, as well as those that are only used for anonymous statistic. You can decide for yourself which categories you want to allow. Further information can be found in our data privacy protection .

Essential

These cookies are necessary to run the core functionalities of this website and cannot be disabled.

Name Webedition CMS
Purpose This cookie is required by the CMS (Content Management System) Webedition for the system to function correctly. Typically, this cookie is deleted when the browser is closed.
Name econda
Purpose Session cookie emos_jcsid for the web analysis software econda. This runs in the “anonymized measurement” mode. There is no personal reference. As soon as the user leaves the site, tracking is ended and all data in the browser are automatically deleted.
Statistics

These cookies help us understand how visitors interact with our website by collecting and analyzing information anonymously. Depending on the tool, one or more cookies are set by the provider.

Name econda
Purpose Statistics
External media

Content from external media platforms is blocked by default. If cookies from external media are accepted, access to this content no longer requires manual consent.

Name YouTube
Purpose Show YouTube content
Name Twitter
Purpose activate Twitter Feeds

Wilms tumors: Genetic triggers uncovered

No. 07c | 10/02/2015

For childhood kidney tumors, scientists from Würzburg and Heidelberg have identified a series of previously unknown genetic causes. A lack of microRNA prevents kidney precursor cells from maturation. Instead they remain in an embryonic state in which rapid growth is one of their fundamental tasks.

Wilm's Tumor (Nephroblastoma)
© Ed Uthman, Wikimedia Commons

Wilms tumors, also known as nephroblastomas, are among the more common solid tumors in children. They tend to appear before the age of six and are categorized as embryonal tumors. The starting point in their development are kidney precursor cells in the embryo, which evidently do not mature as they should. Consequently, the tumor contains somewhat differing tissue structures, which is why the man who lent his name to them, Max Wilms, referred to “mixed tumors of the kidney” in his description in 1899.

In the search for the molecular causes of Wilms tumors and, in particular, the genetic culprits behind their high-risk variants, a group of scientists has now made a breakthrough. This collaboration involved teams led by Professor Manfred Gessler, chairman of the Department of Developmental Biochemistry at the University of Würzburg’s Biocenter, and teams led by Marcel Kool and Stefan Pfister at the German Cancer Research Center in Heidelberg as well as partners both within Germany and abroad. They present their findings in the current issue of the journal Cancer Cell.

Genetic defects slow down the molecular machinery

“Previously, three genes were known to be possible triggers of Wilms tumors. We have now managed to identify a whole series of other causes,” explains Manfred Gessler. These include the genes DROSHA and DGCR8. If these are defective, this leads to a partial deactivation of the molecular machinery responsible for creating so-called microRNAs. MicroRNAs, for their part, are able to regulate the function of a large number of messenger RNA molecules and thus completely reprogram cells.

“With embryonic stem cells we already know that without microRNAs they are not capable of transforming themselves into cells of different tissues,” says Gessler. The same seems to be true of Wilms tumors: in their case, individual kidney precursor cells evidently do not manage to mature fully. Instead they remain in an embryonic state in which rapid growth is one of their fundamental tasks so that the kidney grows.

A genetic defect triggers various cancers

Alongside the microRNAs, two transcription factors also attracted the attention of the teams. The proteins referred to as SIX1 and SIX2 control the activity of other genes. Animal models had already made it clear that they are absolutely vital to the formation of the kidneys; they are also particularly active in Wilms tumors. “Our findings now reveal for the first time that both genes for these transcription factors are altered in Wilms tumors by mutations and, as a result, the cells remain in an embryonic growth mode in this case, too,” explains Gessler.

Third finding of the study: Tumor genes that are known to trigger other cancers may also be responsible for Wilms tumors. The scientists were able to show that a particular gene involved in the development of neuroblastomas – tumors that arise from degenerated immature cells of the sympathetic nervous system – is also activated in Wilms tumors. “This gives real hope that treatments that are successful for a neuroblastoma will also be effective for Wilms tumors,” says Gessler.

In addition, some of the Wilms tumors demonstrated a deactivation of the most familiar tumor suppressor gene TP53, which led to dramatic genome changes accompanied by the fracture and uncontrolled loss or multiplication of chromosomal fragments. The prognosis for such degenerated tumors is particularly unfavorable.

Approaches for personalized treatment

The scientists involved believe that the new findings relating to the various triggers of Wilms tumors may help to improve treatment. Currently around 90 percent of children with the disease survive if they receive a combination of chemotherapy, surgery, and then further chemotherapy. The trick here is to identify patients with so-called high-risk tumors early and to treat them more intensively than cases with a low discernible risk of relapse. This technique should minimize the stress on the children and any possible consequential harm.

A histologic examination, routinely conducted these days, and the clinical picture provide important indicators here. But these are still not enough. “Clarifying the molecular causes offers hope of improving the classification of tumors and of being able to use increasingly targeted treatments within the framework of personalized medicine,” says Manfred Gessler.

However, with some of these genetic changes that have now been discovered it remains unclear how they contribute to tumor development. The aim of future work will mainly be to filter out from the abundance of candidates those that are best suited to predicting the progression of the disease, and to develop approaches for tailor-made treatments based on new knowledge relating to molecular networks.

Ideal combination of different areas of expertise

For the study of Wilms tumors, the various disciplines of the teams involved complemented one another perfectly: The Würzburg team contributed years of experience in the analysis of Wilms tumors and one of the world’s largest collections of these tumors, which is housed at the Biocenter. The German Cancer Research Center (DKFZ) team provided extensive capacities and experience in high-throughput sequencing and genome analysis. The changes they discovered were then checked in Würzburg against hundreds of other tumors and their function examined.

Future work will require close collaboration with numerous pediatric clinics and pathologists as part of the German Wilms Tumor Study and with European partners, as this is the only way that it will be possible to collect and analyze sufficient material and data for such tumors successfully.

This work was supported by the Wilhelm-Sander-Stiftung foundation, the German Research Foundation, the Federal Ministry of Education and Research, and the HIPO initiative of the German Cancer Research Center (DKFZ-HIPO).

Mutations in the SIX1/2 Pathway and the DROSHA/DGCR8 miRNA Microprocessor Complex Underlie High-Risk Blastemal Type Wilms Tumors. Jenny Wegert, Naveed Ishaque, Romina Vardapour, Christina Geörg, Zuguang Gu, Matthias Bieg, Barbara Ziegler, Sabrina Bausenwein, Nasenien Nourkami, Nicole Ludwig, Andreas Keller, Clemens Grimm, Susanne Kneitz, Richard D. Williams, Tas Chagtai, Kathy Pritchard-Jones, Peter van Sluis, Richard Volckmann, Jan Koster, Rogier Versteeg, Tomas Acha, Maureen J. O’Sullivan, Peter Karl Bode, Felix Niggli, Godelieve A. Tytgat, Harm van Tinteren, Marry M. van den Heuvel-Eibrink, Eckart Meese, Christian Vokuhl, Ivo Leuschner, Norbert Graf, Roland Eils, Stefan M. Pfister, Marcel Kool, Manfred Gessler. Cancer Cell, http://dx.doi.org/10.1016/j.ccell.2015.01.002 

With more than 3,000 employees, the German Cancer Research Center (Deutsches Krebsforschungszentrum, DKFZ) is Germany’s largest biomedical research institute. DKFZ scientists identify cancer risk factors, investigate how cancer progresses and develop new cancer prevention strategies. They are also developing new methods to diagnose tumors more precisely and treat cancer patients more successfully. The DKFZ's Cancer Information Service (KID) provides patients, interested citizens and experts with individual answers to questions relating to cancer.

To transfer promising approaches from cancer research to the clinic and thus improve the prognosis of cancer patients, the DKFZ cooperates with excellent research institutions and university hospitals throughout Germany:

  • National Center for Tumor Diseases (NCT, 6 sites)
  • German Cancer Consortium (DKTK, 8 sites)
  • Hopp Children's Cancer Center (KiTZ) Heidelberg
  • Helmholtz Institute for Translational Oncology (HI-TRON Mainz) - A Helmholtz Institute of the DKFZ
  • DKFZ-Hector Cancer Institute at the University Medical Center Mannheim
  • National Cancer Prevention Center (jointly with German Cancer Aid)
The DKFZ is 90 percent financed by the Federal Ministry of Education and Research and 10 percent by the state of Baden-Württemberg. The DKFZ is a member of the Helmholtz Association of German Research Centers.

RSS-Feed

Subscribe to our RSS-Feed.

to top
powered by webEdition CMS