01:06am Thursday 28 May 2020

Familial risk of colorectal cancer: the genes only tell part of the story

On the basis of a current epidemiological study, scientists at the German Cancer Research Center (DKFZ) conclude that the role of genes has been overestimated in patients with a higher familial risk of colorectal cancer. Other risk factors such as family dietary habits presumably have a greater impact that previously assumed. This will have implications for future calculations of individual risk and for the ensuing recommendations.

Colorectal cancer is the third most common cancer in the world. Researchers currently assume that the disease is 35 percent hereditary. The main risk factors include a family history of the disease. In recent years, researchers have also identified around 100 tiny gene variations that are widespread in the population (single nucleotide polymorphisms – SNPs) and that affect the risk of colorectal cancer. However, current results obtained by the DKFZ scientists led by Hermann Brenner and Korbinian Weigl suggest that these SNPs account for a considerably lower share of the higher familial risk of colorectal cancer than previously assumed.

The DKFZ researchers began by examining the standard statistical methods used to estimate this share and noticed a number of weaknesses in the calculation which, when aggregated, lead to the impact of the SNPs being considerably overestimated. “In particular, the standard methods currently used assume that the familial clustering is ultimately 100 percent hereditary,” noted Korbinian Weigl, lead author of the study. “On that basis, they then calculated the percentage that can be accounted for by the gene variants known to date.”

The team led by Brenner and Weigl evaluated data on 7,927 subjects in a case control study, including 4,447 patients with colorectal cancer and 3,480 healthy subjects in the control group. “We developed a new method of calculation that does not assume right from the start that the familial risk is completely genetic in nature,” explained study director Hermann Brenner. The researchers then used this method to evaluate the data on their probands.

The influence of the SNPs was indeed considerably lower using this method than assumed. While previous calculations estimated that the currently known gene variants account for 9.6 to 23.1 percent of the higher familial risk of colorectal cancer, the new calculations by the DKFZ researchers found an estimated influence of the SNPs of between 5.4 and 14.3 percent.

“The results correlate very well with the results of a different DKFZ study published last year,” Brenner remarked. The previous study showed that in half-siblings of colorectal cancer patients, the risk of developing cancer was the same as for “real” siblings. “That suggests that common risk factors, such as particular dietary habits, smoking, or a lack of exercise, play a considerably greater role than previously assumed.”

For the future assessment of the individual risk of colorectal cancer, that certainly does not mean that the gene variants associated with a heightened risk have become meaningless, however. “Instead, our study shows how important it is to look at both genetic and other risk factors in the family to arrive at a realistic assessment,” Weigl continued. In other words, someone who only has a few risk-associated gene variants in their DNA should not rest assured that they will not develop colorectal cancer, for example if their lifestyle increases their risk. Conversely, colorectal cancer is not inevitable in people with an unfavorable genetic disposition if their individual behavior decreases their risk. At any rate, it is always advisable to make use of the very effective screening options for colorectal cancer.

Weigl K, Chang-Claude J, Hsu L, Hoffmeister M, Brenner H. Establishing a valid approach for estimating familial risk of cancer explained by common genetic variants. International Journal of Cancer 2019, DOI: 10.1002/ijc.32664

The German Cancer Research Center (Deutsches Krebsforschungszentrum, DKFZ) with its more than 3,000 employees is the largest biomedical research institution in Germany. At DKFZ, more than 1,300 scientists investigate how cancer develops, identify cancer risk factors and endeavor to find new strategies to prevent people from getting cancer. They develop novel approaches to make tumor diagnosis more precise and treatment of cancer patients more successful. DKFZ’s Cancer Information Service (KID) provides individual answers to all questions about cancer for patients, the general public, and health care professionals. Jointly with partners from Heidelberg University Hospital, DKFZ runs the National Center for Tumor Diseases (NCT) located in Heidelberg and Dresden, and, also in Heidelberg, the Hopp Children’s Cancer Center (KiTZ). In the German Cancer Consortium (DKTK), one of six German Centers for Health Research, DKFZ maintains translational centers at seven university partnering sites. Combining excellent university hospitals with high-profile research at a Helmholtz Center at the NCT and DKTK sites is an important contribution to the endeavor of translating promising approaches from cancer research into the clinic in order to improve the chances of cancer patients. DKFZ is a member of the Helmholtz Association of National Research Centers, with ninety percent of its funding coming from the German Federal Ministry of Education and Research and the remaining ten percent from the State of Baden-Württemberg.



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