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* myc - regulation of gene expression - sarcomas and carcinomas
* myc - regulation of gene expression - sarcomas and carcinomas
* src - Tyr-specific protein kinase - sarcomas
* src - Tyr-specific protein kinase - sarcomas
<noinclude>
=== External links ===
[http://www.news-medical.net/health/What-are-Proto-Oncogenes.aspx What are Proto-Oncogenes]
[http://www.nature.com/scitable/topicpage/proto-oncogenes-to-oncogenes-to-cancer-883 Proto-Oncogenes to Oncogenes to Cancer]
=== Bibliography ===
{{Cite
| type = book
| surname1 = ALBERTS, B – BRAY, D – JOHNSON, A
| title = Základy buněčné biologie
| edition = 2.vydání
| year = 2005
| isbn = 80-902906-2-0
}}
{{Cite
| type = book
| surname1 = KUMAR, Vinay – ABBAS, Abul K – FAUSTO, Nelson, et al
| title = Robbins basic pathology
| edition = 8
| year = 2008
| isbn = 978-1-4160-2973-1
}}
</noinclude>




[[Category:Genetics]]
[[Category:Genetics]]
[[Category:Biology]]
[[Category:Biology]]

Revision as of 18:11, 23 July 2011

Protooncogenes are genes that are commonly found in the body and are responsible for proliferation. If the mutation occurs, there is an increase in protein expression or hyperactivity. As a result of excessive cell division. This mutated form is called oncogene.


Another mechanism of tumor proliferation is a mutation of antiproliferative tumor-suppressor genes. They always occur in the genome in two copies, and their damage is the intervention of both copies. Protooncogenes, however, differs in that area - mutation of one copy of the protooncogene to oncogene is enough of a speech (the dominant character).


Protooncogenes can encode a wide variety of proteins with multiple functions (cell differentiation genes, signaling molecules, surface receptors, regulatory genes ,...). If there is damage signaling pathways such as protein, may alter the reactivity of cells to the action of growth factors. The following significant cell division. This may be caused by several mechanisms:

  • protein begins to be formed in cells in which they normally do not form
  • protein is made up of appropriate cells, but in excessive amounts
  • protein is formed in a form that can not be regulated by normal mechanisms


New research links appeared relationship between the activation of protooncogenes to oncogenes through microRNAs. MicroRNAs are parts of RNA which have size of 21-25 nucleotides. You can control the expression of these genes with their down-regulation. In the future they could possibly be used to block the activity of oncogenes.


Currently, 40 species known protooncogenes. That in 16 of them were proven direct correlation with tumor proliferation, such as:

  • Her-2 / neu: breast cancer
  • K-ras: tumors of the esophagus, colon, pancreas
  • beta-Catenin: Pancreatic cancer
  • Cyclin E: liver tumors
  • mutant B-Raf: melanomas


Examples of (proto) oncogenes

Among oncogenes include forms derived growth factor PDGF, receptors for growth hormones or proteins, intracellular signaling pathways. All these cells are characterized by similar behavior - responding as if they constantly receive instructions for signaling division. The cells are so completely beyond regulatory control.


Among oncogenes include the viral src gene. Viruses that cause cancer are called transformation viruses (often it is a retrovirus). Normally, the src protein kinase regulates gene controlling cell division. Individual structures of oncogene and protooncogene differ in several amino acids.


Viral oncogenes - normal function protooncogene - tumors caused by mutations:

  • abl oncogene - Tyr-specific protein kinase - pre-B-lymphocytic leukemia
  • crest-B - epidermal growth factor (EGF) - erytroleukémie
  • fos, jun - gene regulation - osteosarcomas, fibrosarcomas
  • myc - regulation of gene expression - sarcomas and carcinomas
  • src - Tyr-specific protein kinase - sarcomas


External links

What are Proto-Oncogenes

Proto-Oncogenes to Oncogenes to Cancer

Bibliography

ALBERTS, B – BRAY, D – JOHNSON, A,. Základy buněčné biologie. 2.vydání edition. 2005. ISBN 80-902906-2-0.

KUMAR, VINAY – ABBAS, ABUL K – FAUSTO, NELSON, ET AL,. Robbins basic pathology. 8. edition. 2008. ISBN 978-1-4160-2973-1.