Correction: Liquori et al. Acute Promyelocytic Leukemia: A Constellation of Molecular Events around a Single PML-RARA Fusion Gene. Cancers 2020, 12, 624
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and
1
Accredited Research Group in Hematology and Hemotherapy, Instituto de Investigación Sanitaria La Fe, 46026 Valencia, Spain
2
Department of Hematology, Hospital Universitario y Politécnico La Fe, 46026 Valencia, Spain
3
Centro de Investigación Biomédica en Red de Cáncer (CIBERONC), 28029 Madrid, Spain
*
Author to whom correspondence should be addressed.
79 nt with no homology to sequences in the GenBank or EMBL databases
Intron 2
ctctagCCA
[104]
Intron 4
TAGgtatgt
Intron 2
ctctagCCA
[103]
NUMA1 (NUMA)-RARA
t(11;17)(q13;q21)
Sensitive
ND
1
Intron 23
CAGgtgagg
Intron 2
ctctagCCA
[89]
STAT5B-RARA
der(17)
Poorly responsive
Poorly responsive
11 [105]
Intron 15
CTCgtgagt
Intron 2
ctctagCCA
[90,105]
PRKAR1A-RARA
t(17;17)(q21;q24) or del(17)(q21;q24)
Sensitive
Sensitive
1
Intron 2
AAGgtaaaa
Intron 2
ctctagCCA
[91]
FIP1L1-RARA
t(4;17)(q12;q21)
Sensitive in 1 case
ND
2
Intron 15
ATGgtaagt
Intron 2
ctctagCCA
[92]
Intron 13
CGGgtaaat
Intron 2
ctctagCCA
[106]
BCOR-RARA
t(X;17)(p11;q21)
Sensitive in 2 cases
Insensitive in 1 case
2
Intron 12
CAGgtatga
Intron 2
ctctagCCA
[93]
Exon 12
CAGgtagaa
Intron 2
ctctagCCA
[107]
NABP1 (OBFC2A)-RARA
t(2;17)(q32;q21)
Sensitive in vitro
ND
1
Intron 5
TGGgtaaga
Intron 2
ctctagCCA
[94]
TBL1XR1 (TBLR1)-RARA
t(3;17)(q26;q21)
Insensitive
ND
4 [108]
Intron 5
CAAgtgagc
Intron 2
ctctagCCA
[95]
Intron 5
CAAgtgagc
*
Intron 2
ctctagCCA
[108]
GTF2I-RARA
t(7;17)(q11;q21)
Sensitive
Sensitive
1
Intron 6
TAGgtaagt
Intron 2
ctctagCCA
[96]
IRF2BP2-RARA
t(1;17)(q42;q21)
Sensitive
Sensitive
5 [109]
Exon 2
TGTcccctg
Intron 2
ctctagCCA
[97,109]
Exon 1
AAGgtgcgg
Intron 2
ctctagCCA
[110]
Intron 1
CAGgtaggg
Intron 2
ctctagCCA
[111]
Exon 1
CAGgcaggt
Intron 2
ctctagCCA
[111,112]
FNDC3B-RARA
t(3;17)(q26;q21)
Sensitive
ND
1
Intron 24
AAGgtgtgt
Intron 2
ctctagCCA
[98]
The genes involved in APL molecular variants are reported according to the HUGO Gene Nomenclature Committee (https://www.genenames.org/, accessed on 8 March 2020). Previous symbols are reported in brackets. * According to molecular analysis, RARA on chromosome 17 had a 12-kbp deletion, of which a small region was inserted into chromosome X and the major part was inserted within the TBL1XR1 gene between exons 5 and 6 on chromosome 3 [108].
The authors would like to apologize for any inconvenience caused to the readers by these changes. The original manuscript has been updated.
Funding
This research received no external funding.
Conflicts of Interest
The authors declare no conflict of interest.
Reference
Liquori, A.; Ibañez, M.; Sargas, C.; Sanz, M.Á.; Barragán, E.; Cervera, J. Acute Promyelocytic Leukemia: A Constellation of Molecular Events around a Single PML-RARA Fusion Gene. Cancers2020, 12, 624. [Google Scholar] [CrossRef] [Scilit] [PubMed]
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