by Inka Väth, University Hospital of Bonn

Graphical abstract. Credit: The American Journal of Human Genetics (2024). DOI: 10.1016/j.ajhg.2024.09.002

The genetic confirmation of a suspected diagnosis of hereditary colorectal cancer is of great importance for the medical care of affected families. However, many of the variants identified in the known genes cannot yet be reliably classified in terms of their causal role in tumor formation.

Under the leadership of the University Hospital Bonn (UKB) and the University of Bonn, an international team of researchers has reassessed the medical relevance of a significant number of unclear variants and thus significantly reduced their number. The results of the study have now been published in The American Journal of Human Genetics.

Families with hereditary tumor diseases have a high risk of developing certain cancers such as colon cancer or breast cancer. For many common hereditary tumor syndromes, there are now very effective, intensive and early cancer screening programs and other preventive measures. Timely detection and reliable diagnosis of a hereditary predisposition is therefore extremely important for the families affected.

Due to increasingly comprehensive genetic testing, however, more and more genetic variants are being found in the responsible genes whose causal significance for the development of tumors is still unclear. These are referred to as variants of uncertain significance (VUS). As a result, more than 50% of the variants for some genes listed in public international databases (in particular ClinVar) are now VUS.

"These cannot be used for diagnosis or for testing healthy people at risk; on the other hand, they often create great uncertainty, as carriers of a VUS may have an increased tumor risk," says co-senior author Dr. Isabel Spier from the Institute of Human Genetics.

Many gene variants have no relevance for tumor formation

Researchers at the UKB's Center for Hereditary Tumor Syndromes have been working for years on identifying new genetic causes of hereditary tumor diseases. To solve the problems associated with the interpretation of VUS, special classification criteria were developed under the leadership of the Institute of Human Genetics to improve the assessment of variants in the APC gene. Hereditary genetic changes in this gene are responsible for familial adenomatous polyposis (FAP), one of the most common causes of hereditary colorectal cancer or hereditary polyp diseases of the gastrointestinal tract.

As part of the Hereditary Colorectal Cancer / Polyposis Variant Curation Expert Panel (VCEP), Prof. Stefan Aretz's research group is working with an international and multidisciplinary team of experts based on a collaboration between the International Society for Gastrointestinal Hereditary Tumors (InSiGHT) and the Clinical Genome Resource (ClinGen).

"The gene-specific classification criteria we developed have now allowed us to reclassify a significant proportion of VUS of the APC gene into a medically relevant category," says Prof. Aretz, who is also a member of the Transdisciplinary Research Area (TRA) "Life & Health" at the University of Bonn.

The research team evaluated all of the more than 10,000 APC germline variants listed in the public databases ClinVar and LOVD. Among the variants with an initial classification as benign or pathogenic, about 95% remained in their original category. In contrast, 41% of the VUS deposited in ClinVar and 61% of those in LOVD were reclassified into clinically significant classes, the vast majority of them as benign.

It was also shown that extensive data mining, i.e. the comprehensive search for all genetic and clinical information available worldwide on a genetic variant, contributes very effectively to a better classification. Overall, the total number of VUS was reduced by 37%.

"Since we were able to evaluate a large proportion of VUS as harmless norm variants, all carriers of these variants worldwide are relieved," says co-senior author Prof. Aretz, who would like to emphasize the close collaboration with first author Dr. Xiaoyu Yin from Melbourne in Australia during her six-month stay as a guest scientist at the UKB.

The study also demonstrates the feasibility of variant classification in large data sets, which could also serve as a generalizable model for the interpretation of variants of other genes in the future.

More information: Xiaoyu Yin et al, Large-scale application of ClinGen-InSiGHT APC-specific ACMG/AMP variant classification criteria leads to substantial reduction in VUS, The American Journal of Human Genetics (2024). DOI: 10.1016/j.ajhg.2024.09.002

Journal information: American Journal of Human Genetics 

Provided by University Hospital of Bonn