Bannayan-Riley-Ruvalcaba syndrome More than 30 mutations in the PTEN gene have been found to cause Bannayan-Riley-Ruvalcaba syndrome. Common features of this condition include a large head size (macrocephaly), multiple noncancerous tumors and tumor-like growths called hamartomas, and dark freckles on the penis in males. Bannayan-Riley-Ruvalcaba syndrome is one of several related conditions that are often considered together as PTEN hamartoma tumor syndrome (described below). Some of the mutations that cause Bannayan-Riley-Ruvalcaba syndrome change single DNA building blocks (base pairs) in the PTEN gene or insert or delete a small number of base pairs. Other mutations result in an abnormally short enzyme or reduce the amount of enzyme that is produced. In about 10 percent of cases, Bannayan-Riley-Ruvalcaba syndrome results from the deletion of a large amount of genetic material that includes part or all of the PTEN gene. All of these genetic changes prevent the PTEN enzyme from regulating cell proliferation effectively, which can lead to uncontrolled cell growth and the formation of hamartomas and other types of tumors. It is unclear how PTEN gene mutations cause macrocephaly and the other features of Bannayan-Riley-Ruvalcaba syndrome. breast cancer Inherited mutations in the PTEN gene increase the risk of developing breast cancer . In many cases, this increased risk occurs as part of Cowden syndrome (described above). Inherited mutations in the PTEN gene are thought to account for only a small fraction of all breast cancer cases. Noninherited (somatic) PTEN gene mutations occur in some breast cancers in women without a family history of the disease. Somatic mutations are not inherited and do not occur as part of a familial cancer syndrome. They are acquired during a person's lifetime and occur only in certain cells in the breast. These mutations impair the tumor suppressor function of the PTEN enzyme, allowing cells to grow and divide without control or order. This uncontrolled cell growth contributes to the formation of a cancerous tumor. Studies suggest that a loss of functional PTEN enzyme is also related to poor responsiveness to a drug called trastuzumab (Herceptin), which is used to treat breast cancer . Cowden syndrome Researchers have identified more than 300 mutations in the PTEN gene that can cause Cowden syndrome or a similar disorder called Cowden-like syndrome. These conditions are characterized by the growth of multiple hamartomas and an increased risk of developing certain cancers, particularly breast cancer, thyroid cancer, and cancer of the uterine lining (endometrial cancer). Cowden syndrome and Cowden-like syndrome are considered to be part of PTEN hamartoma tumor syndrome (described below). Mutations that cause Cowden syndrome and Cowden-like syndrome include changes in a small number of base pairs and, in some cases, deletions of a larger amount of genetic material from the PTEN gene. These mutations lead to the production of a PTEN enzyme that does not function properly or does not work at all. The altered enzyme is unable to restrain cell division or signal abnormal cells to die, which contributes to the development of hamartomas and cancerous tumors. head and neck squamous cell carcinoma Genetics Home Reference provides information about head and neck squamous cell carcinoma. lung cancer Genetics Home Reference provides information about lung cancer. prostate cancer Genetics Home Reference provides information about prostate cancer. other cancers Somatic mutations in the PTEN gene are among the most common genetic changes found in human cancers. The cancers associated with somatic mutations are not inherited and do not occur as part of a cancer syndrome. Somatic mutations in the PTEN gene have been reported in many types of cancer, and studies suggest that PTEN may be the most frequently mutated gene in prostate cancer and endometrial cancer. PTEN gene mutations are also commonly found in brain tumors called glioblastomas and astrocytomas, and in an aggressive form of skin cancer called melanoma. Mutations in the PTEN gene reduce or eliminate the tumor suppressor function of the PTEN enzyme. The loss of this enzyme's function likely permits certain cells to divide uncontrollably, contributing to the growth of cancerous tumors. In some cases, the presence of PTEN gene mutations is associated with more advanced stages of tumor growth. other disorders Several related conditions caused by mutations in the PTEN gene, including Bannayan-Riley-Ruvalcaba syndrome and Cowden syndrome, are often considered together as PTEN hamartoma tumor syndrome. The mutations that cause these conditions are present in cells throughout the body and are often inherited from a parent. Some of the mutations that cause PTEN hamartoma tumor syndrome lead to a defective version of the PTEN enzyme that cannot perform its function as a tumor suppressor. Other mutations prevent the PTEN gene from producing any enzyme at all. Without functional PTEN enzyme, cell division is not controlled effectively and damaged cells continue to divide inappropriately, leading to the development of hamartomas and other tumors. In some published case reports, mutations in the PTEN gene have been associated with Proteus syndrome, a rare condition characterized by asymmetric overgrowth of the bones, skin, and other tissues. However, many researchers now believe that individuals with PTEN gene mutations and asymmetric overgrowth do not meet the strict guidelines for a diagnosis of Proteus syndrome. Instead, these individuals have a condition that is considered part of PTEN hamartoma tumor syndrome. One name that has been proposed for the condition is segmental overgrowth, lipomatosis, arteriovenous malformations, and epidermal nevus (SOLAMEN) syndrome; another is type 2 segmental Cowden syndrome. However, some scientific articles still refer to PTEN-related Proteus syndrome. PTEN gene mutations have been identified in several people who have both macrocephaly and the characteristic features of autism, a developmental disorder that affects communication and social interaction. Many of these mutations change single protein building blocks (amino acids) in the PTEN enzyme or lead to the production of an abnormally short version of the enzyme. It is unknown how changes in the PTEN gene are related to the risk of developing autism. Some of these mutations have also been reported in families with PTEN hamartoma tumor syndrome, and it is unclear how these mutations can cause different disorders.

     The PTEN gene provides instructions for making an enzyme that is found in almost all tissues in the body. The enzyme acts as a tumor suppressor, which means that it helps regulate cell division by keeping cells from growing and dividing too rapidly or in an uncontrolled way. The PTEN enzyme modifies other proteins and fats (lipids) by removing phosphate groups, each of which consists of three oxygen atoms and one phosphorus atom. Enzymes with this function are called phosphatases. The PTEN enzyme is part of a chemical pathway that signals cells to stop dividing and triggers cells to self-destruct through a process called apoptosis. Evidence suggests that this enzyme also helps control cell movement (migration), the sticking (adhesion) of cells to surrounding tissues, and the formation of new blood vessels (angiogenesis). Additionally, it likely plays a role in maintaining the stability of a cell's genetic information. All of these functions help prevent uncontrolled cell growth that can lead to the formation of tumors.

The following transcription factors affect gene expression:

• NF-kappaB
• PPAR-gamma1
• PPAR-gamma2
• p53
• Egr-1
• AP-1
• c-Jun
• NF-kappaB1

Tissue specificity:

Expressed at a relatively high level in all adult tissues, including heart, brain, placenta, lung, liver, muscle, kidney and pancreas.

Induction:

Down-regulated by TGFB1.

Molecular Function:

• Magnesium Ion Binding
• Phosphatidylinositol-3-Phosphatase Activity
• Phosphoprotein Phosphatase Activity
• Protein Serine/Threonine Phosphatase Activity
• Protein Tyrosine Phosphatase Activity
• Protein Tyrosine/Serine/Threonine Phosphatase Activity
• Lipid Binding
• Anaphase-Promoting Complex Binding
• Phosphatidylinositol-3,4,5-Trisphosphate 3-Phosphatase Activity
• Enzyme Binding
• Pdz Domain Binding
• Identical Protein Binding
• Inositol-1,3,4,5-Tetrakisphosphate 3-Phosphatase Activity
• Phosphatidylinositol-3,4-Bisphosphate 3-Phosphatase Activity

Biological Processes:

• Regulation Of Cyclin-Dependent Protein Serine/Threonine Kinase Activity
• Angiogenesis
• Negative Regulation Of Protein Phosphorylation
• Regulation Of B Cell Apoptotic Process
• Protein Dephosphorylation
• Phosphatidylinositol Biosynthetic Process
• Apoptotic Process
• Neuron-Neuron Synaptic Transmission
• Synapse Assembly
• Central Nervous System Development
• Heart Development
• Aging
• Response To Nutrient
• Learning Or Memory
• Memory
• Locomotory Behavior
• Cell Proliferation
• Positive Regulation Of Cell Proliferation
• Negative Regulation Of Cell Proliferation
• Response To Glucose
• Response To Zinc Ion
• Regulation Of Neuron Projection Development
• Negative Regulation Of Phosphatidylinositol 3-Kinase Signaling
• Dentate Gyrus Development
• Central Nervous System Neuron Axonogenesis
• Negative Regulation Of Cell Migration
• Adult Behavior
• Regulation Of Protein Stability
• Negative Regulation Of Myelination
• Negative Regulation Of Cyclin-Dependent Protein Serine/Threonine Kinase Activity Involved In G1/S Transition Of Mitotic Cell Cycle
• Regulation Of Synaptic Transmission, Gabaergic
• Central Nervous System Myelin Maintenance
• Response To Estradiol
• Regulation Of Cellular Component Size
• Regulation Of Myeloid Cell Apoptotic Process
• Response To Atp
• Multicellular Organismal Response To Stress
• Social Behavior
• Maternal Behavior
• Negative Regulation Of Apoptotic Process
• Protein Kinase B Signaling
• Endothelial Cell Migration
• Inositol Phosphate Metabolic Process
• Response To Ethanol
• Locomotor Rhythm
• Negative Regulation Of Cell Size
• Negative Regulation Of Organ Growth
• Response To Arsenic-Containing Substance
• Inositol Phosphate Dephosphorylation
• Phosphatidylinositol Dephosphorylation
• Platelet-Derived Growth Factor Receptor Signaling Pathway
• Phosphatidylinositol-Mediated Signaling
• Regulation Of Axon Regeneration
• Negative Regulation Of Axon Regeneration
• Cardiac Muscle Tissue Development
• Forebrain Morphogenesis
• Brain Morphogenesis
• Negative Regulation Of Epithelial Cell Proliferation
• Negative Regulation Of Phagocytosis
• Negative Regulation Of Axonogenesis
• Protein Stabilization
• T Cell Receptor Signaling Pathway
• Positive Regulation Of Sequence-Specific Dna Binding Transcription Factor Activity
• Negative Regulation Of Focal Adhesion Assembly
• Negative Regulation Of Protein Kinase B Signaling
• Rhythmic Synaptic Transmission
• Negative Regulation Of Cardiac Muscle Cell Proliferation
• Canonical Wnt Signaling Pathway
• Synapse Maturation
• Prepulse Inhibition
• Male Mating Behavior
• Long-Term Synaptic Potentiation
• Long Term Synaptic Depression
• Prostate Gland Growth
• Dendritic Spine Morphogenesis
• Negative Regulation Of Dendritic Spine Morphogenesis
• Negative Regulation Of Erk1 And Erk2 Cascade
• Positive Regulation Of Erk1 And Erk2 Cascade
• Cellular Response To Hypoxia
• Negative Regulation Of Ribosome Biogenesis
• Negative Regulation Of Cell Aging
• Negative Regulation Of Excitatory Postsynaptic Potential
• Presynaptic Membrane Assembly
• Postsynaptic Density Assembly
• Positive Regulation Of Trail-Activated Apoptotic Signaling Pathway
• Positive Regulation Of Ubiquitin Protein Ligase Activity
• Positive Regulation Of Protein Ubiquitination Involved In Ubiquitin-Dependent Protein Catabolic Process
• Negative Regulation Of G1/S Transition Of Mitotic Cell Cycle
• Positive Regulation Of Excitatory Postsynaptic Potential
• Negative Regulation Of Synaptic Vesicle Clustering