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. 2015 Dec 4;6(40):42429–42444. doi: 10.18632/oncotarget.6464

Table 1. Important and selected copy number alterations in LPS cell lines relevant to transformation.

Cell Line(s) Alteration Chromosome Selected Gene(s)
SW872 HD 10q23.31 PTEN
T1000, T778 AMP 4p15.2 PPARGC1A
LPS141 HD 9p23 PTPRD
MLS402 HD 3p14.2 FHIT
MLS402 UPD 13q14.2-14.3 RB1, SETDB2, RCBTB1, DLEU2, MIR15-A, MIR16-1,
T778, FU-DDLS-1, LP6, MLS402 AMP 5p15.33 TERT
FU-DDLS-1, MLS402, LPS141, AMP 5p15.2 CTNND2
MLS402 AMP 11q22 YAP1, BIRC2, BIRC3
MLS402 AMP 14q22.2 CDKN3
LiSa-2 AMP 19q13 PAK4, AKT2
LiSa-2 HD 13q RB1, SETDB2, RCBTB1, DLEU2, MIR15-A, MIR16-1,
LiSa-2 HD 3p24 RBMS3
GOT-3 HD 9q33.1 DEC1
LPS141, GOT-3 HD 16q23 WWOX
GOT-3 AMP Xp22.31 PNPLA4
LPS1, LPS2, LPS3, SA4, HD 9p21.3 CDKN2A, CDKN2B
SA4 HD 10p14 GATA3
SA4 HD 10p11.21 PARD3
SA4 HD 15q15.3 TP53BP1
LiSa-2 HD 16q12.2 RBL2, CYLD, SALL1, SIAH
FU-DDLS-1, LPS1, LPS2, LPS3, LP6 AMP 1p32.1 JUN

HD: homozygous deletion; AMP: amplification; UPD: uniparental disomy