Which genetic disease is linked to a mutation of the tumor suppressor gene?

What is a mutated tumor suppressor gene called?

When a tumor suppressor gene is mutated, uncontrolled cell growth may occur. This may contribute to the development of cancer. Also called antioncogene.

What do mutated tumor suppressor genes cause?

Tumor suppressor genes

When a tumor suppressor gene is mutated, this can lead to tumor formation or growth. Properties of tumor suppressor genes include: Both copies of a specific tumor suppressor gene pair need to be mutated to cause a change in cell growth and tumor formation to happen.

What is an example of a tumor suppressor gene?

Examples of tumor suppressor genes are the BRCA1/BRCA2 genes, otherwise known as the “breast cancer genes.” People who have a mutation in one of these genes have an increased risk of developing breast cancer (among other cancers).

What is the most common tumor suppressor gene defect?

The nuclear phosphoprotein gene TP53 has also been recognized as an important tumor suppressor gene, perhaps the most commonly altered gene in all human cancers. Inactivating mutations of the TP53 gene also cause the TP53 protein to lose its ability to regulate the cell cycle.

Are tumor suppressor genes inherited?

They cause certain types of cancer to run in families. But most tumor suppressor gene mutations are acquired, not inherited.

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What is p53 mutation?

Mutations (changes) in the p53 gene may cause cancer cells to grow and spread in the body. These changes have been found in a genetic condition called Li-Fraumeni syndrome and in many types of cancer. The p53 gene is a type of tumor suppressor gene. Also called TP53 gene and tumor protein p53 gene.

What are examples of oncogenes?

Examples of proto-oncogenes

  • Ras. The first proto-oncogene to be shown to turn into an oncogene is called Ras. …
  • HER2. Another well-known proto-oncogene is HER2. …
  • Myc. The Myc gene is associated with a type of cancer called Burkitt’s lymphoma. …
  • Cyclin D. Cyclin D is another proto-oncogene.

What is Li Fraumeni syndrome?

Li-Fraumeni syndrome (LFS) is an inherited familial predisposition to a wide range of certain, often rare, cancers. This is due to a change (mutation) in a tumor suppressor gene known as TP53.

What happens if APC gene is mutated?

People with mutations in the APC gene have familial adenomatous polyposis (FAP) or attenuated FAP (AFAP). You have an increased chance to develop multiple gastrointestinal polyps, colorectal cancer, and possibly other cancers. There are risk management options to detect cancer early or lower the risk to develop cancer.