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Encyclopedia > APC gene

Familial adenomatous polyposis (FAP) is an inherited condition in which numerous polyps to form in the epithelium of the large intestine. While these are benign, they may become malignant, predisposing patients to colorectal cancer. It inherits in an autosomal dominant fashion.

Contents

Signs and symptoms

From the age of 16 onward, patients develop hundreds to thousands of polyps. These may bleed, leading to admixture of blood in the stool. If the blood is not visible, it is still possible for the patient to develop anemia due to gradually developing iron deficiency. If malignancy develops (the median age in FAP patients is about 40), this may present with weight loss, altered bowel habit, or even with metastasis in the liver or elsewhere.


The genetic determinant in familial polyposis may also predispose carriers to other malignancies, e.g. of the duodenum and stomach. Other signs that may point at FAP are pigmented lesions of the retina ("congenital hypertrophy of the retinal pigment"), jaw cysts, sebaceous cysts, and osteomata (benign bone tumors). The combination of polyposis, osteomas, fibromas and sebaceous cysts is termed Gardner syndrome (with or without abnormal scarring).


Diagnosis and treatment

In patients with a strong family of colorectal cancer and symptoms suggestive of polyposis, colonoscopy is indicated, with biopsy of a number of polyps (especially of those that appear dysplastic).


Blood tests (liver enzymes) and ultrasound of the abdomen are often performed to rule out metastasis to the liver.


Genetic testing provides the ultimate diagnosis in 95%; genetic counseling is usually needed in families where FAP has been diagnosed. Testing may also aid in the diagnosis of borderline cases in families that are otherwise known to have the FAP mutation.


Pathophysiology

FAP is due to mutations in the APC gene, which is located on the fifth chromosome (5q21_q22). It is a tumour suppressor gene, acting as a "gatekeeper" to prevent development of tumours. Mutation of APC also occurs commonly in incident cases of colorectal carcinoma, emphasizing its importance in this form of cancer.


Although the polyps are inherently benign, the first step of the two-hit hypothesis has already taken place. Often, the remaining "normal" allele is mutated or deleted, accelerating generation of polyps. Further mutations (e.g. in p53 or KRAS) to APC-mutated cells are much more likely to lead to cancer than they would in non-mutated epithelial cells.


The normal function of the APC gene product is still being investigated; it is present both the cell nucleus and the membrane. Possible functions may be related to cell adherence and cytoskeleton organisation.


Genetics

FAP is inherited in an autosomal dominant manner. Approximately 75-80% of individuals with FAP have an affected parent. Offspring of an affected individual have a 50% risk of inheriting the altered APC gene. Prenatal testing is possible if a disease-causing mutation is identified in an affected family member; however, prenatal testing for typically adult-onset disorders is uncommon and requires careful genetic counseling.


Epidemiology

The incidence of the mutation is between 1 in 10,000 and 1 in 15,000 births. By age 35 years, 95% of individuals with FAP have polyps. Without colectomy, colon cancer is virtually inevitable. The mean age of colon cancer in untreated individuals is 39 years (range 34-43 years).


Treatment

Treatment for FAP will require frequent surveillance colonoscopy investigations; in a number of cases, removal of the colon is necessary to prevent (or cure) development to malignancy.


Various medications are being investigated for slowing malignant degeneration of polyps, most prominently the non-steroidal anti-inflammatory drugs (NSAIDs).


References

  • Gardner EJ. A genetic and clinical study of intestinal polyposis, a predisposing factor for carcinoma of the colon and rectum. Am J Hum Genet 1951;3:167-76. Medline abstract (http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=14902760) (PMID 14902760)

External links

  • OMIM 175100 (http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=175100)
  • Cancerindex entry on the APC gene (http://www.cancerindex.org/geneweb/APC.htm)



  Results from FactBites:
 
Familial Adenomatous Polyposis (5462 words)
APC is the gene associated with familial adenomatous polyposis in a majority of cases.
APC gene is identified in an affected family member using one of the molecular genetic tests.
APC gene, the diagnosis of FAP or one of its variants is still possible because of the less than 100% detection rate with current genetic testing methods.
Gene APC118 (651 words)
Both copies of the APC gene are mutated in 80% of sporadic colorectal tumours.
Somatic mutation of the APC gene is found in the majority of colorectal adenocarcinomas.
Loss of normal APC function is known to be an early event in both familial and sporadic colon cancer pathogenesis, occurring at the pre-adenoma stage.
  More results at FactBites »

 
 

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