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== Description ==
 
== Description ==
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NUP214-SET is a fusion of the genes ''NUP214'' (Nucleoporin 214kDa) and ''SET'' (SET Nuclear Proto-Oncogene), located at 9q34.13 and 9q34.11, respectively. The fusion has been described as resulting from a recurrent cryptic deletion, del(9)(q34.11q34.13) and a chromosomal translocation, t(9;9)(q34;q34) [5,6].
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NUP214-SET is a fusion of the genes ''NUP214'' (Nucleoporin 214kDa) and ''SET'' (SET Nuclear Proto-Oncogene), located at 9q34.13 and 9q34.11, respectively. The fusion has been described as resulting from a recurrent cryptic deletion, del(9)(q34.11q34.13) and a chromosomal translocation, t(9;9)(q34;q34) [5,6]. In [[T-ALL| T-cell acute lymphoblastic leukemia]], the fusion has been shown to mediate elevated expression of [[HOXA| ''HOXA'']] cluster genes [7].
    
== Tumor Types ==
 
== Tumor Types ==
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[[T-ALL|T-cell Acute Lymphoblastic Leukemia]]  
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[[T-ALL|T-cell Acute Lymphoblastic Leukemia/Lymphoma]]  
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[[AML| Acute Myeloid Leukemia]]
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[[AML| Acute Myeloid Leukemia]] (single case report)
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== Prevalence ==
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== Genes Involved / Domains Affected ==
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== Diagnostic Testing ==
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== Clinical Significance ==
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== Therapeutics ==
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== Links ==
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==References==
 
<ref> Reference: Ann Clin Lab Sci. 2011 Summer;41(3):267-72.
 
<ref> Reference: Ann Clin Lab Sci. 2011 Summer;41(3):267-72.
 
T-cell acute lymphoblastic leukemia associated with complex karyotype and SET-NUP214 rearrangement: a case study and review of the literature.
 
T-cell acute lymphoblastic leukemia associated with complex karyotype and SET-NUP214 rearrangement: a case study and review of the literature.
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<ref> Characterization of the translocation breakpoint sequences of two DEK-CAN fusion genes present in t(6;9) acute myeloid leukemia and a SET-CAN fusion gene found in a case of acute undifferentiated leukemia. Genes Chromosomes Cancer. Von Lindern M, Breems D, van Baal S, Adriaansen H, Grosveld G. Genes Chromosomes Cancer. 1992;5:227–234. doi: 10.1002/gcc.2870050309. PMID: https://www.ncbi.nlm.nih.gov/pubmed/1384675</ref>
 
<ref> Characterization of the translocation breakpoint sequences of two DEK-CAN fusion genes present in t(6;9) acute myeloid leukemia and a SET-CAN fusion gene found in a case of acute undifferentiated leukemia. Genes Chromosomes Cancer. Von Lindern M, Breems D, van Baal S, Adriaansen H, Grosveld G. Genes Chromosomes Cancer. 1992;5:227–234. doi: 10.1002/gcc.2870050309. PMID: https://www.ncbi.nlm.nih.gov/pubmed/1384675</ref>
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<ref> The recurrent SET-NUP214 fusion as a new HOXA activation mechanism in pediatric T-cell acute lymphoblastic leukemia. Van Vlierberghe, van Grotel M, Tchinda J, Lee C, Beverloo HB, van der Spek PJ, Stubbs A, Cools J, Nagata K, Fornerod M, Buijs-Gladdines J, Horstmann M, van Wering ER, Soulier J, Pieters R, Meijerink JP. Blood. 2008 May 1;111(9):4668-80. doi: 10.1182/blood-2007-09-111872. Epub 2008 Feb 25. PMID: http://www.ncbi.nlm.nih.gov/pubmed/18299449 </ref>
    
Rare: <ref>B-cell Lymphoid Leukemia Test Reference: Oncol Lett. 2016 Apr;11(4):2644-2650. Epub 2016 Feb 23.
 
Rare: <ref>B-cell Lymphoid Leukemia Test Reference: Oncol Lett. 2016 Apr;11(4):2644-2650. Epub 2016 Feb 23.
 
B-cell acute lymphoblastic leukemia associated with SET-NUP214 rearrangement: A case report and review of the literature.
 
B-cell acute lymphoblastic leukemia associated with SET-NUP214 rearrangement: A case report and review of the literature.
 
Zhu HH1, Zhao XS1, Qin YZ1, Lai YY1, Jiang H1 PMID:[http://www.ncbi.nlm.nih.gov/pubmed/    27073532] </ref>
 
Zhu HH1, Zhao XS1, Qin YZ1, Lai YY1, Jiang H1 PMID:[http://www.ncbi.nlm.nih.gov/pubmed/    27073532] </ref>
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== Prevalence ==
  −
  −
Write your comments here
  −
  −
== Genes Involved / Domains Affected ==
  −
  −
Write your comments here
  −
  −
== Diagnostic Testing ==
  −
  −
Write your comments here
  −
  −
== Clinical Significance ==
  −
  −
Write your comments here
  −
  −
== Therapeutics ==
  −
  −
Write your comments here
  −
  −
== Links ==
  −
  −
==References==