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Pancreas cancer genetic

other-digestive-cancer

By Li Dali, Ph.D.

If you tested your DNA with a personal genomics service like 23andMe, AncestryDNA, FamilyTreeDNA, MyHeritage or another testing company, you can learn more about your risk factors for hundreds of diseases. By clicking the button above ⬆️, you can upload your raw DNA data file and receive a personalized 250-page health report with research links that is the most comprehensive.

Up to 15% of pancreatic cancers are attributed to gene mutations that are passed down through families. Individuals with a family history of pancreatic cancer are at a significantly higher risk of developing the disease. Research has identified six different cancer syndromes that contribute to inherited pancreatic cancers.

There are numerous factors that have led to a higher likelihood of developing pancreatic cancer. These risk factors include tobacco consumption, being overweight or obese, exposure to specific chemicals in the workplace (such as benzene, petrochemicals, dyes, and pesticides), age, gender, race, family history, inherited genetic syndromes, diabetes, chronic pancreatitis, cirrhosis of the liver, stomach issues, dietary habits, lack of physical activity, and consumption of coffee and alcohol.

It is not widely known that mutations in the BRCA gene can increase the likelihood of developing pancreatic cancer. A study conducted by the Pancreas Center in 2014 revealed that around 10% of pancreatic cancer cases at their facility were linked to breast ovarian cancer syndromes caused by BRCA 1 and 2 mutations. Other studies have shown that the connection between pancreatic cancer and BRCA2 mutations could be as high as 19%. In 2015, Holter et al. conducted research on BRCA mutations in pancreatic cancer patients and recommended broader testing for BRCA mutations in these patients than what is currently recommended by guidelines.

Most cases of pancreatic cancer involve genes such as Kras, CDKN2A, TP53, and SMAD4 [3]. Understanding these key genes has provided valuable knowledge for diagnosing and treating pancreatic cancer. However, the primary driver genes for pancreatic tumors - KRAS (90%), CDKN2A (90%), TP53 (70%), and SMAD4 (55%) - undergo various mutations that lead to the development of pancreatic tumors.

Follow the link of the selected polymorphism to read a brief description of how the selected polymorphism affects Other cancers of the digestive system and see a list of existing studies.

SNP polymorphisms related to the topic Other cancers of the digestive system:

rs2274223There is a 1.9 times increased risk of stomach and oesophageal cancer.
rs505922There is a 1.2-fold increased risk of pancreatic cancer.
rs372883The BACH1 polymorphism causes a predisposition to pancreatic cancer.
rs9543325Pancreatic cancer predisposition locus.
rs3790844NR5A2 variation is associated with pancreatic cancer risk, especially among Caucasian individuals.
rs7190458BCAR1 polymorphism is associated with susceptibility to pancreatic cancer.
rs11614913A variant of the MIR196A2 gene increases the risk of gastrointestinal cancer.
rs2259816
rs9573163
rs1547374
rs2255280
rs5768709
rs12413624
rs225190
rs3016539
rs9502893
rs1585440
rs1000589
rs9874556
rs9363918
rs6464375
rs4924935
rs1886449
rs2257205
rs12615966
rs6879627
rs12456874
rs6736997
rs6971499
rs9581943
rs1561927
rs16986825
rs1169310
rs7310409
rs1183910
rs144848
rs1047972
rs12953717
rs17655
rs121909229
rs13181
rs3746444
rs11615
rs1229984
rs1048943
rs121908291
rs521102
rs9895829

About The Author
Li Dali Li Dali

Li Dali, a National Foundation for Outstanding Youth Fund recipient, is a researcher at the School of Life Sciences in East China Normal University. He earned his PhD in genetics from Hunan Normal University in 2007 and conducted collaborative research at Texas A&M University during his doctoral studies. Li Dali and his team have optimized and innovated gene editing technology, leading to the establishment of a world-class system for constructing gene editing disease models.

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