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. 2007 Jul-Aug;1(4 Suppl 2):S7–S12.

Table 2.

Data from five studies that have identified chromosomal gains and losses using comparative genomic hybridization techniques.*

Recurrent chromosomal losses and deletions
Aguirre et al52 Bashyam et al53 Gysin et al51 Heidenblad et al54 Nowak et al55
9p X X X X X CDKN2A, TUSC3
18q X X X X X Smad4
3p X X X X FHIT, FOXP1
4q X X X X FBXW7
6q X X X X SEC63, SASH1, LPA
8p X X X X DEFB103, DEFB105
17p X X X X TP53, MKK4
6p X X X
13q X X X GPC5
21q X X X PARD6G
9q X X TNFSF15
10q X X CDH23
12q X X DUSP6
15q X X
21p X X
22q X X
Xp X X FMR2, ARSC1
Recurrent chromosomal gains and amplifications
12p X X X X KRAS2
20q X X X CTSZ, NCOA3
8q X X X MYC
11q X X X Cyclin D
17q X X X ERBB2
7q X X X SMURF1
5p X X BASP1
7p X X EGFR
14q X X TGFB3
6p X X NOTCH4
19q X X AKT2, eIF3k
3q X X
*

Genes highlighted in boldface are known to be associated with pancreatic carcinoma.