Hass HG, Nehls O, Jobst J, Frilling A, Vogel U, Kaiser S. Identification of osteopontin as the most consistently over-expressed gene in intrahepatic cholangiocarcinoma: Detection by oligonucleotide microarray and real-time PCR analysis. World J Gastroenterol 2008; 14(16): 2501-2510 [PMID: 18442196 DOI: 10.3748/wjg.14.2501]
Corresponding Author of This Article
Holger G Hass, Department of Oncology, Hematology and Palliative Care, Marien Hospital, Boeheim-Street 37, Stuttgart 70199, Germany. holgerhass@vinzenz.de
Article-Type of This Article
Clinical Research
Open-Access Policy of This Article
This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
World J Gastroenterol. Apr 28, 2008; 14(16): 2501-2510 Published online Apr 28, 2008. doi: 10.3748/wjg.14.2501
Table 1 Patient demographics and histopathological data
Patient No.
Sex
Age
Histology
Stage
Grading
1
F
57
Adenocarcinoma
pT3pNxpM0
G3
2
F
65
Adenocarcinoma
pT3pN0pM0
G2
3
F
68
Adenocarcinoma
pT2pNxpM0
G2
4
M
74
Adenocarcinoma
pT3pN1pM0
G3
5
F
62
Adenocarcinoma
pT3pN0pM0
G2
6
F
47
Adenocarcinoma
pT3pNxpM0
G2
7
M
73
Adenocarcinoma
pT3pN0pM0
G2
8
F
71
Adenocarcinoma
pT2pNxpM0
G2
9
M
52
Adenocarcinoma
pT3pN2pM0
G2
10
M
65
Adenocarcinoma
pT3pNxpM0
G1
Table 2 Statistical results obtained using a supervised neuronal training method for discrimination between CCC and non-malignant liver tissue
Condition
True value
Prediction
P value
Pat. No. 1, non-malignant
Normal liver tissue
Non-malignant
0.00023
Pat. No. 2, non-malignant
Normal liver tissue
Non-malignant
0.00023
Pat. No. 3, non-malignant
Normal liver tissue
Non-malignant
0.00023
Pat. No. 4, non-malignant
Normal liver tissue
Non-malignant
0.00023
Pat. No. 5, non-malignant
Normal liver tissue
Non-malignant
0.00023
Pat. No. 6, non-malignant
Normal liver tissue
Non-malignant
0.00023
Pat. No. 7, non-malignant
Normal liver tissue
Non-malignant
0.00023
Pat. No. 8, non-malignant
Normal liver tissue
Non-malignant
0.00023
Pat. No. 1, CCC
CCC
Malignant
0.00103
Pat. No. 2, CCC
CCC
Malignant
0.00103
Pat. No. 3, CCC
CCC
Malignant
0.00103
Pat. No. 4, CCC
CCC
Malignant
0.00103
Pat. No. 5, CCC
CCC
Malignant
0.00103
Pat. No. 6, CCC
CCC
Malignant
0.00103
Pat. No. 7, CCC
CCC
Malignant
0.16100
Pat. No. 8, CCC
CCC
Malignant
0.00103
Pat. No. 9, CCC
CCC
Malignant
0.00103
Pat. No. 10, CCC
CCC
Malignant
0.00103
Table 3 Most significantly dysregulated genes (> 4-fold change in 100% of all cases) in intrahepatic cholangiocarcinoma - relation to known cellular functions and metabolic pathways (using the GenMAPP® software)
Fructose biphosphate aldolase A (Lung cancer antigen)
16.3
PPCC_HUMAN
Q16822
PCK1
100
Phosphoenolpyruvate carboxykinase, cytosolic
16.7
Q9H277
Q9H277
Q9H227
100
Cytosolic beta-glucosidase
7.6
Electron transport
ACDB_HUMAN
P45954
ACADSB
100
Acyl-CoA dehydrogenase, branched chain specific
14.1
CPA6_HUMAN
X13929
CYP2A6
100
Cytochrome P450 2A6
11.9
CP12_HUMAN
P05177
CYP1A2
100
Cytochrome P450 1A2
10.0
Protein metabolism/proteolysis
BAE2_HUMAN
Q9Y5Z0
BACE2
100
Beta secretase 2 precursor
10.5
Q9UJ28
Q9UJ28
GALNT7
100
UDP-GalNAc: N-acetylgalactosaminyltransferase 7
5.4
CATC_HUMAN
P53634
CTSC
100
Dipeptidyl-peptidase I precursor
4.7
GLMT_HUMAN
Q14749
GNMT
100
Glycine N-methyltransferase
49.5
Transport
CHLR_HUMAN
P17516
AKR1C4
100
Chlordecone reductase
22.0
APF_HUMAN
Q13790
APOF
100
Apolipoprotein F precursor
15.5
Lipid binding/metabolism
Q9Y2P5
Q9Y2P5
Q9Y2P5
100
Very-long-chain AcylCoA synthetase homolog 2
23.7
VLCS_HUMAN
O14975
FACVL1
100
Very-long-chain AcylCoA synthetase
16.6
MMSA_HUMAN
Q02252
MMSDH
100
Methylmalonate-semialdehyde dehydrogenase
8.1
Table 4 Expression levels of dysregulated genes in intrahepatic cholangiocarcinoma in relation to tumor differentiation according histopathological criteria (grading 1 to 3)
Hs. POU domain, class 1, transcription factor 1 (Pit1)
Citation: Hass HG, Nehls O, Jobst J, Frilling A, Vogel U, Kaiser S. Identification of osteopontin as the most consistently over-expressed gene in intrahepatic cholangiocarcinoma: Detection by oligonucleotide microarray and real-time PCR analysis. World J Gastroenterol 2008; 14(16): 2501-2510