Colon Cancer Essay -- Biology Biological Medical Essays

colon crabby person unhealthiness Name Colon crab louse Chromosome Number 2 Locus style 2p16 In the summer of 1993 researchers observed a component, known as MSH2, is lack at bottom colon cells. The MSH2 genes chief(prenominal) function is to detect and correct wee mutations that occur during cell division. The contract of colon crab louse arises when this gene does non provide this protection to colon cells. This lack of protection causes multiple mutations within the colon cells until they become cancerous. scarce about 6% of all colorectal cancer is said to be communicable. Sporadic, or non hereditary colorectal cancer, makes up the other 94%. heritable colorectal cancer is made up of two syndromes- HNPCC (Hereditary Non Polyposis Colorectal Cancer) and FAP (familial Adenomatous Polyposis). HNPCC is estimated to be 5% of the total hereditary colorectal cancer. HNPCC is a autosomal superior disease, meaning that children make up a 50% chance of in heriting the transmittable trait from one of the pargonnts being autosomally governing. The pargonnts who are autosomal dominant have a defect in their mis- correspond genes which identify and repair incarnate mutations in DNA during cell division. quaternion genes have been identified as carrying this mutation hMSH2, hMHL1, hPMS1, and hPMS2. ( h standing for hereditary) FAP constitutes whole about 0.5 % of all hereditary colorectal cancer. It is also an autosomal dominant disease. Patients with FAP have a vitamin C% risk of getting colorectal cancer, moreover it can be avoided. FAP is caused by a mutation in the armored personnel carrier gene on chromosome 5. The armoured personnel carrier gene is able to be sight by a melodic phrase test. A study done in 1994 revealed that since the time the APC gene was identified 100 different mutations lede to st... ...er, making it the third hint cancer caused death rate. The main intention of doctors who deal with pati ents with colorectal cancer is not to cure, but actually to avoid mortality. With recent advancements research are finding new links to the set up of colorectal cancer genetically and physically. Works CitedCaspari, Reiner. 3/12/94. Familial Adenomatous Polyposis Mutations at Codon 1309 and Early onslaught of Colon Cancer. Lancet. Vol 343, pg. 629. Key, Sandra W. and Marble, Michelle, 11/23/98, hire Finds Gene Marker Could anticipate Colon Cancer. Cancer Weekly Plus, pg. 14, 2/3p. Goldinger, Michael. Colorectal Cancer- An Overview. The Colorectal Cancer Home page. Hochhauser, Daniel. 4/19/97, Colon Cancer Genotypes Change in Two Ways. Lancet, Vol. 349, pg. 1151. Newsweek, 12/13/93. determination the Colon Cancer Gene. Vol. 122, pg. 72. Colon Cancer Essay -- Biology biological Medical EssaysColon Cancer Disease Name Colon Cancer Chromosome Number 2 Locus Designation 2p16 In the summer of 1993 researchers discovered a gene, known as MSH2, is lacki ng within colon cells. The MSH2 genes main function is to detect and correct small mutations that occur during cell division. The cause of colon cancer arises when this gene does not provide this protection to colon cells. This lack of protection causes multiple mutations within the colon cells until they become cancerous. Only about 6% of all colorectal cancer is said to be hereditary. Sporadic, or non hereditary colorectal cancer, makes up the other 94%. Hereditary colorectal cancer is made up of two syndromes- HNPCC (Hereditary Non Polyposis Colorectal Cancer) and FAP (Familial Adenomatous Polyposis). HNPCC is estimated to be 5% of the total hereditary colorectal cancer. HNPCC is a autosomal dominant disease, meaning that children have a 50% chance of inheriting the genetic trait from one of the parents being autosomally dominant. The parents who are autosomal dominant have a defect in their mis- match genes which identify and repair somatic mutations in DNA during cel l division. Four genes have been identified as carrying this mutation hMSH2, hMHL1, hPMS1, and hPMS2. ( h standing for hereditary) FAP constitutes only about 0.5 % of all hereditary colorectal cancer. It is also an autosomal dominant disease. Patients with FAP have a 100% risk of getting colorectal cancer, but it can be avoided. FAP is caused by a mutation in the APC gene on chromosome 5. The APC gene is able to be detected by a blood test. A study done in 1994 revealed that since the time the APC gene was identified 100 different mutations leading to st... ...er, making it the third leading cancer caused death rate. The main objective of doctors who deal with patients with colorectal cancer is not to cure, but actually to reduce mortality. With recent advancements research are finding new links to the effects of colorectal cancer genetically and physically. Works CitedCaspari, Reiner. 3/12/94. Familial Adenomatous Polyposis Mutations at Codon 1309 and Early Onset of Colon Cancer. Lancet. Vol 343, pg. 629. Key, Sandra W. and Marble, Michelle, 11/23/98, Study Finds Gene Marker Could Predict Colon Cancer. Cancer Weekly Plus, pg. 14, 2/3p. Goldinger, Michael. Colorectal Cancer- An Overview. The Colorectal Cancer Home page. Hochhauser, Daniel. 4/19/97, Colon Cancer Genotypes Change in Two Ways. Lancet, Vol. 349, pg. 1151. Newsweek, 12/13/93. Finding the Colon Cancer Gene. Vol. 122, pg. 72.