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. 2009 Dec 21;16(3-4):102–115. doi: 10.2119/molmed.2009.00119

Table 5.

Differentially expressed genes in HCC cell lines.

Downregulated genes
AFFY_ID Gene Gene symbol mRNA NCBI accession numbera Foldb P valuec Chromosomal location Chromosomal aberration in HCCd Epigenetic regulation in HCC
203400_s_at Transferrin TF NM_001063 −8.988 0.042 3q22.1 3q22–24 (gain)
219465_at Apolipoprotein A-II APOA II NM_001643 −8.932 0.050 1q21–q23 1q21–23 (gain)
219466_s_at Apolipoprotein A-II APOA II NM_001643 −8.686 0.026 1q21–q23 1q21–23 (gain)
205892_s_at Fatty acid binding protein 1, liver FABP1 NM_001443 −7.260 0.048 2p11
209560_s_at Delta-like 1 homolog (Drosophila) DLK1 NM_003836 and NM_001032997 −6.914 0.017 14q32 Upregulation due to deregulation of methylation
224588_at X (inactive)-specific transcript XIST BX648323 −6.746 0.002 Xq13.2
214218_s_at X (inactive)-specific transcript XIST BX648323 −5.244 0.034 Xq13.2
217073_x_at Apolipoprotein A-I APOA I NM_000039 −6.390 0.027 11q23–q24 11q23.1 (AI)
209505_at Nuclear receptor subfamily 2, group F, member 1 NR2F1 NM_005654 −5.292 0.054 5q14
209459_s_at 4-Aminobutyrate aminotransferase ABAT NM_020686 and NM_000663 −5.195 0.020 16p13.2 16p13 (AI)
242375_x_at Phenylalanine hydroxylase PAH NM_000277 −5.103 0.015 12q22–q24.2 12q22–q23 (breakpoints of chromosome rearrangement)
204059_s_at Malic enzyme 1, NADP(+)-dependent, cytosolic ME1 NM_002395 −5.029 0.038 6q12
200824_at Glutathione S-transferase pi GSTP1 NM_000852 −4.999 0.045 11q13 Silenced by hypermethylation
225424_at Glycerol-3-phosphate acyltransferase, mitochondrial GPAM NM_020918 −4.771 0.008 10q25.2
206130_s_at Asialoglycoprotein receptor 2 ASGR2 NM_001181, NM_080912, NM_080913, and NM_080914 −4.510 0.044 17p 17p1–p2 (MDR); 17p13.1 (LOH of p53 locus); 17p11.2–p13.3 (AI); 17p12-pter (LOH)
205352_at Serine (or cysteine) proteinase inhibitor, clade I (neuroserpin), member 1 SERPINI1 NM_005025 −4.484 0.043 3q26.1 3q25-qter (gain)
211237_s_at Fibroblast growth factor receptor 4 FGFR4 NM_002011, NM_022963, and NM_213647 −4.228 0.050 5q35.1-qter 5q35-qter (LOH)
201917_s_at Hypothetical protein FLJ10618 (solute carrier family 25, member 36) SLC25A36 NM_018155 −3.026 0.031 3q23
201918_at Hypothetical protein FLJ10618 (solute carrier family 25, member 36) SLC25A36 NM_018155 −2.862 0.043 3q23
207819_s_at ATP-binding cassette, sub-family B (MDR/TAP), member 4 ABCB4 NM_000443, NM_018849, and NM_018850 −2.035 0.001 7q21.1 7q21–32 (gain); 7q21.3–7q22 (amplification of CYP3A locus)
213198_at Activin A receptor, type IB ACVR1B NM_004302, NM_020327, and NM_020328 −1.963 0.023 12q13
1552474_a_at Guanidinoacetate N-methyltransferase GAMT NM_000156, and NM_138924 −1.749 0.023 19p13.3 19p13.3 (AI)
219569_s_at Transmembrane protein 22 TMEM22 NM_025246 −1.487 0.007 3q22.3 3q22–24 (gain)

Upregulated genes
44120_at aarF domain containing kinase 2 ADCK1 NM_020421 1.349 0.037 14q24.3 14q24–q32 (LOH in less than 10% of HCC cases)
228737_at Chromosome 20 open reading frame 100 (TOX high mobility group box family member 2) TOX2 NM_032883 1.937 0.025 20q13.12
219587_at Tetratricopeptide repeat domain 12 TTC12 NM_017868 2.192 0.016 11q23.1 11q23.1 (AI)
212295_s_at Solute carrier family 7 (cationic amino acid transporter, y+ system), member 1 SLC7A1 NM_003045 2.323 0.034 13q12–q14 13q13–14 (LOH of Rb locus); 13q12.1–q12.3 (AI); 13q12–q13 (deletion of BRCA2 locus); 13q13.3 –q22.1 (loss)
219582_at Opioid growth factor receptor-like 1 OGFRL1 NM_024576 2.582 0.026 6q13
233540_s_at CDK5 regulatory subunit associated protein 2 CDK5RAP2 NM_018249 and NM_001011649 2.812 0.054 9q33.2 9p13–9q33 (LOH)
212607_at v-akt Murine thymoma viral oncogene homolog 3 (protein kinase B, gamma) AKT3 NM_005465 and NM_181690 2.832 0.002 1q43–q44 Amplification of AKT3 gene
208502_s_at Paired-like homeodomain transcription factor 1 PITX1 NM_002653 3.178 0.032 5q31 5q31 (amplification of SMAD5 gene)
201189_s_at Inositol 1,4,5-triphosphate receptor, type 3 ITPR3 NM_002224 3.315 0.011 6p21
217339_x_at Cancer/testis antigen 1 CTAG1 NM_139250 and NM_001327 3.650 0.020 Xq28
211966_at Collagen, type IV, α 2 COLIVa2 NM_001846 3.743 0.038 13q34 13q34 (gain)
225147_at Pleckstrin homology, Sec7 and coiled-coil domains 3 PSCD3 NM_004227 3.830 0.049 7p22.1
1552390_a_at Hypothetical protein FLJ39553 C8orf47 NM_173549 3.922 0.033 8q22.2 8q22–24 (gain)
241418_at cDNA DKFZp686B14224 (from clone DKFZp686B14224) LOC344887 BX640843 4.222 0.029 3q27.2 3q25-qter (gain)
1553830_s_at Melanoma antigen, family A, 3 MAGEA3 NM_005362 4.296 0.007 Xq28 Demethylation of MAGEA3 gene
212223_at Iduronate 2-sulfatase (Hunter syndrome) IDS NM_000202 and NM_006123 4.413 0.029 Xq28
219279_at Dedicator of cytokinesis 10 DOCK10 NM_014689 4.716 0.039 2q36.2
223642_at Zic family member 2 (odd-paired homolog, Drosophila) ZIC2 NM_007129 4.745 0.025 13q32 13q32-qter (AI); 13q31–34 (gain)
204341_at Tripartite motif-containing 16 TRIM16 NM_006470 4.933 0.008 17p11.2 17p11.2–p13.3 (AI)
208966_x_at Interferon, γ-inducible protein 16 IFI16 NM_152501, NM_198928, NM_198929, and NM_198930 5.510 0.037 1q22 1q21–q22 (gain); 1q22–q23 (gain)
209288_s_at CDC42 effector protein (Rho GTPase binding) 3 Cdc42ep3 NM_006449 5.802 0.015 2p21
200600_at Moesin MSN NM_002444 6.446 0.012 Xq11.2-q12
204955_at Sushi-repeat-containing protein, X-linked SRPX NM_006307 6.835 0.020 Xp21.1 Xp21-pter (gain)
201105_at Lectin, galactoside-binding, soluble, 1 (galectin 1) LGALS1 NM_002305 6.850 0.005 22q13.1 Hypomethylation of LGALS1 gene
225275_at EGF-like repeats and discoidin I-like domains 3 EDIL3 NM_005711 7.133 0.009 5q14
204268_at S100 calcium binding protein A2 S100A2 NM_005978 7.183 0.039 1q21 1q21–23 (gain)
209160_at Aldo-keto reductase family 1, member C3 (3-α hydroxysteroid dehydrogenase, type II) AKR1C3 NM_003739 7.595 0.024 10p15-p14
a

For the genes that have alternatively spliced variants the NCBI accession numbers of each alternatively spliced variant are shown.

b

The changes in gene expression of JHH6 versus HuH7 are shown as log2.

c

P value adjusted according to the Bonferroni method.

d

LOH, loss of heterozygosity; MDR, minimal delition region; AI, allelic imbalance.