Difference between revisions of "Li-Fraumeni syndrome"

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hereditary breast & colorectal cancer (HBCC).<ref name=omim604373/>  In addition to breast and colon cancers, it has also been associated with prostate and thyroid cancer.<ref>{{Ref PCPBoD8|545}}</ref>
hereditary breast & colorectal cancer (HBCC).<ref name=omim604373/>  In addition to breast and colon cancers, it has also been associated with prostate and thyroid cancer.<ref>{{Ref PCPBoD8|545}}</ref>


Memory device for ''CHEK2'' - two common cancers above and below the diaphragm:
''CHEK2'' associated cancers in a list:
*Breast.
*Breast.
*Colon.
*Thyroid.
*Thyroid.
*Colon.
*Kidney.
*Kidney.
*Prostate.


==See also==
==See also==

Revision as of 17:51, 24 September 2011

Li-Fraumeni syndrome is due to germline mutations in the gene TP53 (p53),[1] an important regulator of apoptosis and the cell cycle, i.e. cell division. It is implicated in a very large number of sporadic cancer.

Individuals with Li-Fraumeni syndrome are predisposed to cancer. TP53 is considered to be a tumour suppressor and like most tumour suppressors, inheritance is autosomal dominant.

Associated cancers

This is not an exhaustive list:

Li-Fraumeni variant

A germline mutation in CHEK2[4] is considered to a Li-Fraumeni variant, as it interacts with TP53 and BRCA1.

CHEK2 mutation are most strongly associated with breast cancer and colon cancer; thus, it is also known as hereditary breast & colorectal cancer (HBCC).[4] In addition to breast and colon cancers, it has also been associated with prostate and thyroid cancer.[5]

CHEK2 associated cancers in a list:

  • Breast.
  • Colon.
  • Thyroid.
  • Kidney.
  • Prostate.

See also

References

  1. Online 'Mendelian Inheritance in Man' (OMIM) 191170
  2. Kumar, Vinay; Abbas, Abul K.; Fausto, Nelson; Aster, Jon (2009). Robbins and Cotran pathologic basis of disease (8th ed.). Elsevier Saunders. pp. 1157. ISBN 978-1416031215.
  3. 3.0 3.1 3.2 3.3 3.4 3.5 URL: http://emedicine.medscape.com/article/987356-overview. Accessed on: 19 March 2011.
  4. 4.0 4.1 Online 'Mendelian Inheritance in Man' (OMIM) 604373
  5. Mitchell, Richard; Kumar, Vinay; Fausto, Nelson; Abbas, Abul K.; Aster, Jon (2011). Pocket Companion to Robbins & Cotran Pathologic Basis of Disease (8th ed.). Elsevier Saunders. pp. 545. ISBN 978-1416054542.