Difference between revisions of "Li-Fraumeni syndrome"

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'''Li-Fraumeni syndrome''' is due to germline mutations in the gene TP53 (p53),<ref>{{OMIM|191170}}</ref> an important regulator of apoptosis and the cell cycle, i.e. cell division.  It is implicated in a very large number of sporadic cancer.
'''Li-Fraumeni syndrome''', also known as '''SBLA syndrome''', is due to germline mutations in the gene TP53 (p53),<ref name=omim191170>{{OMIM|191170}}</ref> 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.
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==
==Associated cancers==
This is not an exhaustive list:
This is not an exhaustive list:
*[[Adrenocortical carcinoma]].<ref name=Ref_PBoD8_1157>{{Ref PBoD8|1157}}</ref>
*[[Adrenocortical carcinoma]].<ref name=Ref_PBoD8_1157>{{Ref PBoD8|1157}}</ref>
*[[Breast cancer]].<ref name=emed987356ov>URL: [http://emedicine.medscape.com/article/987356-overview http://emedicine.medscape.com/article/987356-overview]. Accessed on: 19 March 2011.</ref>
*[[Osteosarcoma]].<ref name=emed987356ov/>
*[[Chondrosarcoma]].<ref name=emed987356ov/>
*[[Brain tumours]].<ref name=emed987356ov/>
*Acute [[leukemia]].<ref name=emed987356ov/>
*[[Soft tissue lesions|Soft tissue sarcomas]].<ref name=emed987356ov/>
The alternate name '''SBLA syndrome''' is a ''mnemonic'':<ref name=omim151623>{{OMIM|151623}}</ref>
*[[Sarcoma|'''S'''arcomas]].
*[[Invasive breast cancer|'''B'''reast cancer]].
*[[brain tumours|'''B'''rain tumours]].
*[[leukemia|'''L'''eukemia]].
*'''L'''aryngeal carcinoma.
*[[Lung cancer|'''L'''ung cancer]].
*[[Adrenal cortical carcinoma|'''A'''drenal cortical carcinoma]].
==Li-Fraumeni variant==
A germline mutation in CHEK2<ref name=omim604373>{{OMIM|604373}}</ref> is considered to be a '''Li-Fraumeni variant''', as it interacts with TP53 and BRCA1.
CHEK2 mutations are most strongly associated with [[breast cancer]] and [[colon cancer]]; thus, it is also known as ''hereditary breast & colorectal cancer'' (HBCC).<ref name=omim604373/>  In addition to breast and colon cancers, it has also been associated with prostate, kidney and thyroid cancer.<ref name=Ref_PCPBoD8_545>{{Ref PCPBoD8|545}}</ref>
''CHEK2'' associated cancers in a list:
*Breast.
*Colon.
*Thyroid.
*Kidney.
*Prostate.


==See also==
==See also==
*[[Basics]].
*[[Basics]].
*[[Immunohistochemistry]].
*[[Immunohistochemistry]].
*[[p53]].


==References==
==References==
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[[Category:Syndromes]]
[[Category:Syndromes]]
[[Category:Diagnosis]]
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