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Lynch Syndrome or Hereditary Non-Polyposis Colorectal Cancer (HNPCC) Lynch Syndrome- A Genetic Disease Most colon cancers occur by chance. Some colon cancers are inherited. Lynch Syndrome is a genetic condition which increases one’s risk of getting colon and other cancers. 2-5% of patients with colon cancer have Lynch Syndrome. 2% of women with endometrial cancer have Lynch Syndrome. Genes Determine Our Characteristics The human body is made of small living units called cells. Cells in the body contain millions of genes. Genes are the basic structural and functional units of heredity. Genes determine our characteristics. For example, our genes determine our height, eye color, blood type etc Image Courtesy: National Institute of General Medical Sciences Genes Code for Proteins Genes are made of a molecule called DNA. DNA contains instructions to make proteins. A protein is named after the gene which codes for it. Image Courtesy: National Library of Medicine DNA Structure T G A C G A T G G A T A A A T C T A T A A C G T T T T G C A C C T T A C A A T T T A A G A C G C G G C G G C G C G T T G T A C A C G T C C A C G DNA is a double-helical molecule. It holds instructions to make proteins. These instructions are stored as a code or sequence which is made up of four chemical bases: Copying of DNA Cells in the body divide and grow. When a cell divides, it has to first copy its DNA carefully so that each new cell gets a copy of the DNA without any mistakes. Special genes called Mismatch Repair (MMR) genes control this process. They make DNA repair proteins. DNA repair proteins act like a spell checker and fix mistakes in the new DNA. Image Courtesy: National Institute of General Medical Sciences Mutations in DNA Mismatch Repair (MMR) Genes Mutations: Changes in the DNA that do not allow a gene to work properly. When a DNA repair gene is mutated, it results in the loss of a DNA repair protein in the body. Mistakes in the DNA are not corrected and the new cells’ errors can cause them to divide uncontrollably, thus resulting in cancer. Image Courtesy: Genetic Science Learning CenterUniversity of Utah http://learn.genetics.utah.edu Lynch Syndrome increases cancer risk in these organs • • • • • • • • • • Colon and Rectum Endometrium (Uterus lining) Ovaries Stomach Pancreas Upper urinary tract Biliary tract Small intestine Brain Skin (Sebaceous carcinoma) Image Courtesy: http://www.cdc.gov/cancer/colorectal/pdf/ Basic_FS_Eng_Color.pdf Increased Risk of Multiple Cancers in Lynch Syndrome 80.0% Lynch Syndrome increases a person’s risk of getting some cancers when compared to the general population. Early detection can be life-saving!!! Cancer Risk for General Population 70.0% Cancer Risk for Lynch Syndrome patients 60.0% 50.0% 40.0% 30.0% 20.0% 10.0% 0.0% Note the Increased Risk of Multiple Cancers In Lynch Syndrome Inheritance of Lynch Syndrome Lynch Syndrome is inherited such that one copy of the mutated gene is sufficient to cause cancer in the new generation. If a person has Lynch Syndrome, he or she will have a 1 in 2 chance to pass this condition onto each child. Lynch Syndrome can be inherited equally by men and women. Image Courtesy: Genetic Science Learning Center-University of Utah http://learn.genetics.utah.edu Potential Red Flags in a Family History for Lynch Syndrome • Multiple close relatives on the same side of the family with Lynch Syndrome-associated cancers1. • Individuals with more than one primary Lynch Syndromeassociated cancer • A family member with a Lynch Syndrome-associated cancer diagnosed before age 50 • 1. Lynch Syndrome-associated cancer: Colorectal, endometrial, stomach, ovarian, upper urinary tract, biliary tract, small intestinal cancers Testing for Lynch Syndrome Microsatellites are short DNA sequence repeats. Everyone has microsatellites. When there is damage to the DNA repair genes, these microsatellites become unstable and change size. This is called Micro Satellite Instability (MSI). This is why doctors test for MSI to see if a tumor is associated with Lynch Syndrome. Lynch Syndrome Screening Strategy Tumor Testing for Microsatellite Instability Abnormal Normal Genetic testing for mutations Probably not Lynch Syndrome. You need family history evaluation Catch Colon Cancer Early! Important! Colonoscopy helps detect colon cancer early in Lynch Syndrome patients. Doctors may advise Colonoscopy every 1-2 years, starting by age 20-25 years. Image Courtesy: http://learn.genetics.utah.edu Genetic Counseling Genetic Counselors are trained professionals who can look at your personal and family history and evaluate your cancer risk. Based on your risk, they may recommend the apt screening measures for you and your family members. They help you learn about your disease, and provide emotional support. Image Courtesy: Genetic Science Learning Center-University of Utah http://learn.genetics.utah.edu