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 .


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.

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

Supposedly "silent" mutation with serious consequences

No. 09c | 24/02/2021 | by Koh

So-called silent mutations have no effect on the composition of a protein. They are therefore not considered to promote cancer. However, scientists from the German Consortium for Translational Cancer Research (DKTK), partner site Essen, now describe in a case of kidney cancer an overlooked silent mutation with a major impact on prognosis.
In the DKTK, the German Cancer Research Center (DKFZ) in Heidelberg, as the core center, joins forces in the long term with university partner sites in Germany that have a special reputation in oncology.

In clear-cell renal cancer, researchers from DKTK Essen found a silent mutation with a major impact on prognosis.
© Wikipedia

Synonymous or "silent" mutations affect the DNA without causing an amino acid exchange and thus without causing a protein change. Therefore, they are often not taken into account in large genomic studies to search for cancer-causing mutations:

But scientists have now discovered more and more evidence that silent mutations are by no means necessarily without consequences: for example, a silent mutation can affect the stability and structure of the mRNA. Samuel Peña-Llopis from the DKTK partner site at the West German Cancer Center in the University Hospital Essen now describes an example of this.

In the tumor genome database "The Cancer Genome Atlas" (TCGA), the researchers came across the case of a patient with clear-cell renal cancer. A mutation profile was described in the tumor genome that predicted a rather favorable prognosis and a patient survival of 117 months. And yet, this patient had already died 56 months after cancer diagnosis. Upon closer examination, the DKTK researchers found a synonymous mutation in BAP1, a tumor suppressor and an important cancer driver in many tumors.

When a gene is read, only certain regions of the DNA sequence, known as exons, are incorporated into the mature mRNA, which ultimately serves as the building instructions for the protein. The team led by Peña-Llopis has now discovered that the silent BAP1 mutation causes exon no. 11 to be skipped when the individual exons are joined together. This throws the protein blueprint out of sync, resulting in a truncated BAP1 protein that is rapidly degraded. "The complete inactivation of BAP1 as a consequence of this pathogenic synonymous mutation causes higher tumor aggressiveness and decreases almost fourfold the expected patient survival", says Peña-Llopis, who previously classified this tumor type based solely on inactivating mutations in BAP1 and another tumor suppressor. Peña-Llopis thus recommends paying attention to even the supposedly silent mutations in tumor genome analyses, "especially those used for personalized medicine by providing specific treatments to patients depending on the genomic alterations identified".

Jennifer Niersch, Silvia Vega-Rubin-de-Celis, Anna Bazarna, Svenja Mergener, Verena Jendrossek, Jens T. Siveke, Samuel Peña-Llopis: A BAP1 synonymous mutation results in exon skipping, loss of function and worse patient prognosis
iScience 2021,


The German Cancer Research Center (Deutsches Krebsforschungszentrum, DKFZ) with its more than 3,000 employees is the largest biomedical research institution in Germany. More than 1,300 scientists at the DKFZ investigate how cancer develops, identify cancer risk factors and search for new strategies to prevent people from developing cancer. They are 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 all questions on cancer.

Jointly with partners from the university hospitals, the DKFZ operates the National Center for Tumor Diseases (NCT) in Heidelberg and Dresden, and the Hopp Children's Cancer Center KiTZ in Heidelberg. In the German Consortium for Translational Cancer Research (DKTK), one of the six German Centers for Health Research, the DKFZ maintains translational centers at seven university partner locations. NCT and DKTK sites combine excellent university medicine with the high-profile research of the DKFZ. They contribute to the endeavor of transferring promising approaches from cancer research to the clinic and thus improving the chances of cancer patients.

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.


Subscribe to our RSS-Feed.

to top
powered by webEdition CMS