Copyright
©The Author(s) 2017.
World J Gastroenterol. Jun 14, 2017; 23(22): 3978-3998
Published online Jun 14, 2017. doi: 10.3748/wjg.v23.i22.3978
Published online Jun 14, 2017. doi: 10.3748/wjg.v23.i22.3978
Major Independent Etiological factors | Dependent Etiological factors |
Age[6] | Tobacco consumption[15] |
Sex[6], BMI[16] | Mustard oil[17] Argemone oil (AO) and butter yellow (BY)[18] |
Family history[7,19] | Early age at first pregnancy[20] |
Cholelithiasis[6,22-24] | Use of Oral contraceptives[15,25,26] |
Chronic cholecystitis, porcelain gallbladder[27,28] | Red Chili pepper[29,30] |
Chronic infection by Salmonella species, S. paratyphi or S. typhican[6,10,31-34] | Occupational exposure, Benzene[17,35] |
Helocobacter pylori[36,37] | Secondary bile acids[13,38-40] |
High parity[20,21,24,26] | Xanthogranulomatous cholecystitis[41] |
Anomalous pancreatobiliary duct junction[42,43] | Heavy metals[44,45] |
Porcelain gallbladder[46] | Genetic factors[48] |
Gallbladder polyp[47] | |
Obesity[49] | Free radical oxidation products[50] |
Studied gene | Type of study | Methods used | Studied population | Ref. |
KRAS | Mutation at codon-12 (8%) | PCR-RFLP | India | [64] |
Mutation at codon-12 (29%-30%) | PCR-RFLP | Chile | [76,77] | |
Mutation at codon-12 (0%-59%) | PCR-RFLP, Direct sequencing | Japan | [60,78,79] | |
Mutation at codon-12 (50%-80%) | ELMA, SAB, PCR-SSCP, Direct sequencing | Japan | [63,80] | |
INK4A (p16) | Mutation, deletion | PCR-RFLP, direct sequencing, IHC | Japan, Chile | [54,79,81,82] |
D310 mtDNA | Mutation (Displacement loop) | PCR-based assay, direct sequencing | Chile | [83] |
TP53 | Mutation, overexpression, LOH | PCR-RFLP, direct sequencing, IHC | Greece, Japan, Chile | [84-86] |
Platform | Number of samples | Study population | Research planned | Key findings | Ref. |
Sequenom Mass ARRAY technology | 49 FFPE | India | 390 mutations in 30 genes | PIK3CA (4%), KRAS (2%), CTNNB1 (4%), TP53 (18%) | [95] |
Mass spectroscopy-based | 57 FFPE | MD Anderson Centre | 159 mutations in 33 genes | 14 hotspot mutations in 9 cases including (KRAS, NRAS, PIK3CA, IDH1, ALK, MET) | [94] |
26 mutations in 15cases | |||||
Next-generation sequencing (NGS) | 15 FFPE | NGS of 182 cancer-related genes | (P53, STK11, RICTOR,TSC2, FGF3-TACC fusion, FGF10 amplification) | [94] | |
Preponderance of mutations involving the PI3 kinase pathway | |||||
Whole Exome and transcriptome Sequencing | 29 Fresh Frozen | Japan | 64 non silent mutations signatures | EGFR, ERBB3, PTEN, ARID2, MLL2, | [96] |
MLL3, APOBEC, TERT | |||||
APOBEC-associated mutation signature were observed in GBC | |||||
Exome sequencing and targeted gene sequencing | 57 Fresh Frozen | China | Whole exome sequencing | TP53 (47.1%), KRAS (7.8%) and | [93] |
ERBB3 (11.8%) | |||||
ERBB pathway genes mostly mutated |
Biological sample used | Platform/studies key findings | Ref. |
17 gallbladder tissue specimens (6 advanced GBC , 6 early GBC cancers and 5 normal control | Oligonucleotide Microarray platform | [97] |
Unregulated genes: 2270 | ||
Downregulated genes: 2412 | ||
5-Normal biliary epithelial scrapings, 11- surgically resected biliary carcinomas, 9-biliary cancer cell lines | Oligonucleotide Microarray platform | [98] |
Unregulated genes : 282 genes | ||
Downregulated genes: 513 | ||
37 biliary tract carcinomas | cDNA array platform | [99] |
(15 bile duct, 11 gallbladder, 11 of ampulla of Vater) | 118 genes were identified with a prognostic value | |
12 advanced gallbladder carcinoma tissue 3 samples of normal control gallbladder epithelium | Oligonucleotide Array platform | [100] |
Upregulated: (TOPO II-alpha, cyclin B2, CDC28, ubiquitin-conjugating enzyme E2C), and one metabolism-related: (gamma-glutamyl hydrolase) | [101] | |
34 biliary tract cancers including | Oligonucleotide Array platform | |
13 intrahepatic (IHC), 12extrahepatic (EHC), 9 (GBC) | 1281 genes with deregulated expression pattern |
Studied single genes | Expression pattern | Studied population | Ref. |
TP53 | Expression (20%-70%) | India, Slovenia, Greece, Taiwan, Japan, Chile | [75,84-86,102-106] |
p16 | Overexpression | South Korea | [107] |
FHIT | Expression loss (45%-75%) | Japan, Chile | [108,109] |
ERBB2 | Overexpression (25%-64%) | India, Japan, China, South Korea | [66,103,110,111] |
Expressed in 9.4%cases of well differentiated and stage II to stage IV tumors | India | [90] | |
RB | 20% cases allelic loss | Japan | [54,112] |
4%-14%- loss of expression | |||
CDKN1A | Reduced expression 49% cases | Japan | [113] |
Cyclin D1, Cyclin E | Overexpression (41%-49%) | Japan | [114,115] |
COX2 | Over-expressed | Slovenia, Japan, Chile | [104,116,117] |
BCL2 | Over-expressed | Japan | [118] |
CKIT | Expression 45% | Japan | [119] |
SOX-4 | Overexpression | China | [120] |
Chemokine (C-X-C motif) ligand 12 | Increased expression | South Korea | [121] |
CXCR4, CXCR7 | Increased expression | China | [122] |
hedgehog pathway components (Shh, Ptch1 and Gli1) | Shh: 81.7% of cases expressed | China | [123] |
Ptch1: 75.3% of cases | |||
Gli1: 70.0% of cases | |||
CD56, CD99 | Altered expression | South Korea | [124] |
CD97, CD55 | CD97: 69.6% of cases expressed | China | [125] |
CD55: 65.2% of cases | |||
HMGA2 and CD9 | HMGA2 positive expression | China | [126] |
CD9 negative expression | |||
cholecystokinin type-A | 44.1% of cases expressed | India | [127] |
vascular endothelial growth factor-A | 53.6% of cases expressed | China | [128] |
VEGF-C, VEGF-D | VEGF-C: 64.0% of cases | China | [129] |
VEGF-D: 62.0% of cases | |||
Tumor endothelial marker 8 protein | Increased expression | India | [130] |
L1 cell adhesion molecule | Increased expression | South Korea | [131] |
Tissue factor pathway inhibitor-2 | Down-regulated | China | [132] |
HIF-1α | Increased expression | China | [133] |
VHL | Reduces expression | ||
ERCC1(excision repair cross-complementing 1) | High expression in best differentiated tumors | Chile | [134] |
NF-E2-related factor 2 (Nrf2) | Increased expression | China | [135] |
CD34 , CA15-3 | Highly expressed in stroma and in epithelium | Italy | [136] |
ADAM-17 | Overexpression | China | [137] |
Cdx2 | Aberrant expression | Japan | [138] |
TLR4 | Expressed in glandular and luminal epithelium | China | [139] |
MiRNA | Loss of Dicer and Drosha expression | China | [140] |
Inducible Nitric Oxide Synthase iNOS | Expressed | China | [141] |
Prostate stem cell antigen (PSCA) | Down-regulated | Japan, China | [142] |
OCT-4 | Down-regulated | China | [143] |
hTERT/Telomerase | Expressed in 56.66% cases | India | [144] |
Aquaporins (AQPs) | Positive expression | Japan | [145] |
Ornithine decarboxylase (ODC) and glutamate decarboxylase 65 (GAD65) | Overexpression | China | [146] |
Alpha-methylacyl coenzyme A (racemase) AMACR | Overexpression | Taiwan | [147] |
Sonic Hh (Shh) | Elevated expression | Japan | [148] |
TGF-β induced miR-182 | Overexpression | China | [149] |
SLP-2 | Overexpression | China | [150] |
TMPRSS4 | Higher expression | China | [151] |
zinc finger X-chromosomal protein | Suppressed | China | [152] |
multidrug resistance-associated protein 2 (MRP2) | Overexpression | South Korea | [153] |
HuR | Overexpression | Taiwan | [154] |
miR-155 | Overexpression | Japan | [155] |
LAPTM4B-35 | Overexpressed(76%) | China | [156] |
p27, P21 | p21 (75% cases) and p27 (25% cases) | Jordan | [157] |
Thymidylate synthase (TS) | Low expression | Japan | [158] |
CD146 | Elevated expression | China | [159] |
AEG-1 | Highly expressed (63.4%) | China | [160] |
CCKAR | Expression increased (76.6%) | India | [127] |
Nemo-like kinase (NLK) | Overexpression of NLK | China | [161] |
C-erbB2 | Overexpression (9.4%) | India | [90] |
Phospho-mTOR expression | Positive expression (64.1%) | Chile | [162] |
human telomerase reverse transcriptase (hTERT) | Expression increased | India | [163] |
Phosphoglycerate kinase 1 (PGK1) | Decreased expression (54.7%) | China | [164] |
Notch 1 and Notch 3 | Positive expression | China | [165] |
CCK-A | Decreased expression | India | [166] |
3-phosphoinositide-dependent protein kinase 1 (PDK1) | Positively expressed | China | [167] |
Zinc finger X-chromosomal protein (ZFX) | Overexpression | China | [151] |
miR-138 | Over expression | China | [168] |
HSP gp96 | Expression (90.7%) | China | [169] |
Long non-coding RNA-LET | Overexpression | China | [170] |
Survivin | higher expression (2.9- fold) | India | [171] |
Long non-coding RNA CCAT1 | Overexpressed | China | [172] |
TEM8 | Expression increased | India | [130] |
Fhit,MIh1, P53 | Reduced expression of Fhit and Mlh1 protein and Overexpression of P53 | Japan | [108] |
NDRG2, CD24 | NDRG2 down-regulation, CD24 up-regulation | China | [173] |
IL-6 | Overexpressed | China | [174] |
SLP-2 | Overexpression | China | [150] |
BCL6, p19(ARF) | BCL6 overexpression , p19 (ARF) Low Expression | Taiwan | [175] |
VEGF-A | High expression of VEGF-A | Chile | [176] |
MALAT1 | Upregulation of MALAT1 | China | [177] |
miR-182 | Upregulation of miR-182 | China | [149] |
miR-155 | High expression level of miR-155 | Japan | [155] |
p53, S100A4, p27, p16, RB, Smad4, FHIT, E-cadherin and PML | p53 and S100A4 overexpressed, | South Korea | [178] |
Loss of p27, p16, RB, Smad4, FHIT, E-cadherin and PML expression | |||
PEG10, TSG101 | PEG10 and TSG101 overexpressed | China | [179] |
CK7, CK20 | CK7 (69.05%), CK20 (28.57%) expressed | Greece | [180] |
Studied reported in respective population | LOH/MSI | Ref. |
Chilean | LOH reported in : 3p, 6q, 7q, 8p, 9p, 9q, 11q, 12q, 17p, 18q, 19p, 22q, and Xq | [57] |
Japan | LOH reported in : 2p, 4p, 4q, 8q,9q, 10p,14p,14q,16p, 19p, 21p and Xp [Maximum deletion- 2p24, 14q22 and 21q22] | [68] |
Chilean, Japan | p53, 9p.8p, DCC, KRAS, p16, 16q24, 3p,9q, 22q and p161NK4 | [54,66,109,112,185] |
Greece | BAT-26 | [186] |
Chile, Japan | MSI reported (20%-33%) | [187,188] |
India | E-cadherin (CDH1) 2p, 2q, 6q, 7q,17p | [189] |
India | Fragile histidine triad (FHIT) MSI-H 17.5% LOH :27.5% | [190] |
Japan | High incidences of LOH at 1p36 (19/36:53%), 9p21 (12/32:38%), 13q14 (20/36: 56%), 16q24 (31/54: 61%), and 17p13 (15/36: 42%) | [191] |
Chile | FHIT gene locus (3p14.2) | [109] |
India | LOH at 8 loci, that is 3p12, 3p14.2, 5q21, 9p21, 9q, 13q, 17p13, and 18q for tumor suppressor genes (DUTT1, FHIT, APC, p16, FCMD, RB1, p53, and DCC genes) | [192] |
India | genomic instability at 2p, 2q, 6q, 7q, and 17p loci | [189] |
Chile | DUTT1 (3p12), FHIT (3p14.2), BLU, RASSF1A, SEMA3B and hMLH1 (3p21.3) | [193] |
Gene | Full name | Function | Meth Freq | Population | Ref. |
CDH1 | Cadherin 1, type 1, | Tissue invasion (cell-cell adhesion) | 11%-65% | Japan, Chile | [194-200] |
E-cadherin (epithelial) | |||||
FHIT | Fragile histidine triad gene | Regulation of DNA Replication, and apoptosis | 30%-57% | Chile | [81,193-195,199] |
APC | Adenomatous polyposis coli | Tumor suppressor gene (Cell migration, adhesion and apoptosis) | 26%-35% | Chile, United States | [81,194,195,198,199] |
hMLH1 | Human homologs of | Mismatch repair | 0%-14% | Chile, United States | [81,193-195,199] |
MutL gene of bacteria | |||||
p16 | Cyclin-dependent kinase | Cell cycle regulation | 15%-60% | Chile, United States, Germany | [81,82,195,197-199,201,202] |
inhibitor 2A | |||||
p15 | Cyclin-dependent kinase inhibitor 2B | Cell cycle regulation | 22%-44% | Chile | [81,198] |
DAPK1 | Death-associated protein kinase 1 | Serine-threonine kinase | 8%-61% | Japan, Chile | [81,197,198] |
DLC1 | Deleted in liver cancer 1 | GTPase-activating protein | 39% | Chile | [81] |
RASSF1 | RAS association domain family protein 1A | Signal transduction | 0%-36% | Japan, Chile South Korea | [81,193,197,198,203] |
MGMT | O-6-methylguanine-DNAmethyltransferase | Methyltransferase | 13%-30% | Chile, United States | [81,195] |
CDH13 | CDH13 Cadherin 13, H-cadherin(heart) | Tissue invasion (cell-cell adhesion) | 44%-70% | Chile | [81,198] |
TIMP3 | Metallopeptidase inhibitor 3 | Degradation of extracellular matrix | 0%-39% | Chile | [81,198] |
GSTP1 | Glutathione S-transferase pi 1 | Conjugation of hydrophobic and electrophilic compounds | 13% | Chile | [198] |
RARβ2 | Retinoic acid receptor, beta | Encodes retinoic acid receptor beta | 4%-44% | Chile, United States | [81,198] |
REPRIMO | TP53 dependent G2 arrest mediator candidate | Cell cycle regulation (p53 mediator) | 62% | Chile | [204] |
SHP1 | Protein tyrosine phosphatase, | Regulate cell growth, | 80% | Chile | [198] |
non-receptor type 6 | differentiation, mitotic cycle | ||||
3-OST-2 | Heparan sulfate (glucosamine) | Osulfotransferase | 72% | Chile | [198] |
3-O-sulfotransferase 2 | |||||
RUNX3 | Runt-related transcription factor 3 | TGF-beta signal pathway | 22%-32% | Chile | [197,198] |
RIZ1 | PR domain containing 2, with ZNF domain | Histone/protein methyltransferase | 26% | Chile | [198] |
HPP1 | Transmembrane protein with EGF-like and two follistatin-like domains 2 | TGF-beta signal pathway | 20% | [198] | |
P73 | Tumor protein p73 | Induction of apoptosis and cell cycle regulation | 14%-28% | Chile, United States | [81,198] |
SOCS-1 | Suppressor of cytokine signaling 1 | JAK-STAT pathway | 12% | Chile | [198] |
DCR2 | Tumor necrosis factor receptor superfamily, member 10d | TNF-receptor superfamily | 6% | Chile | [198] |
SEMA3B | Sema domain, immunoglobulin domain (Ig), short basic domain, secreted,(semaphorin) 3B | Induction of apoptosis | 92% | Chile | [193] |
DUTT1 | Human homolog of | Cell migration and metastasis | 22% | Chile | [193] |
Drosophila Roundabout | |||||
(ROBO1) | |||||
BLU | Zinc finger, MYND-type containing 10 | Cell cycle regulation | 26% | Chile | [193] |
p14 | Ribonuclease P/MRP 14 kDa subunit | Cell cycle regulation | 40% | Germany | [201] |
MASPIN | Mammary serine protease inhibitor | Tumor suppressor gene | 70% | India | [205] |
THBS1 | Thrombospondin 1 | Platelet aggregation, angiogenesis, and tumorigenesis | 52% | ||
HLTF | Helicase-like transcription factor | Regulate transcription | 16% | ||
MYC | V-Myc Avian Myelocytomatosis Viral Oncogene Homolog transcription factor | Cell cycle progression, apoptosis and cellular transformation | 80% | Brazil | [206] |
APC | Adenomatous polyposis coli | Tumor suppressor gene | 71%-95% | Chile | [207] |
CDKN2A | Cyclin-dependent kinase inhibitor 2A | Cell cycle | |||
ESR1 | Estrogen receptor 1 | Transcription factor | |||
PGP9.5 | Protein gene product 9.5 | Neural and/or nerve sheath differentiation | |||
SSBP2 | Single-stranded DNA-binding protein 2 | Microsatellite instability | |||
PGP9.5 | Protein gene product 9.5 | Neural and/or nerve sheath differentiation | 27.2% | South Korea | [208] |
MLH1, CDKN2A | MutL homolog 1 | Mismatch repair | 5% | Chile | [194] |
Cyclin-dependent kinase inhibitor 2A | Cell cycle | 35% | |||
FHIT | Fragile histidine triad protein | Purine metabolism | 21% | ||
APC | Adenomatous polyposis coli | Tumor suppressor genes | 25% | ||
CDH1 | Cadherin-1 | Cell cycle | 66% |
Pathway involved | Gene | Polymorphism | Population | Ref. |
DNA repair pathway genes | XPC | (rs2228000) Ala499Val | China | [236] |
(rs2228001) Lys939Gln | China | |||
ERCC2 | (rs1799793) Asp312Asn | North Indian | [232] | |
(rs13181) Lys751Gln | North Indian | |||
MSH2 | (rs2303426) IVS1+9G>C | |||
(rs2303425) -118T>C | ||||
OGG1 | (rs2072668) 748-15C>G | |||
TP53 | (rs1042522) Pro72Arg | Chilean, Hungary, Japanese | [237-239] | |
XRCC1 | (rs1799782) Arg194Trp | North Indian Shanghai, China | [222,231] | |
(rs25487) Arg399Gln | ||||
APEX1 | (rs3136820) Asp148Glu | Shanghai, China | [222] | |
RAD23B | (rs1805335) IVS5-15A>G | [223] | ||
(rs1805329) EX7+65C>T | ||||
FEN1 | FEN1-69G>A and haplotypes | China | [240] | |
Hormonal pathway genes | CCKAR | (rs1800857) IVS1-5T>C | North Indian | [227] |
CCK and CCKAR | (rs2071011G>C, rs915889C/T, rs3822222C/T, rs1800855T/A | Shanghai, China, | [241] | |
ESR1 | (rs2234693) IVS1-397T>C | Shanghai, China, North India | [241-243] | |
(rs3841686) IVS5-34->T | ||||
(rs2228480) Ex8+229G>A | ||||
(rs1801132) Ex4-122G>C | ||||
(rs9340799) IVS1-351A>G | ||||
ESR2 | (rs1256049) Val328Val | Shanghai, China | ||
PGR | Ins/Del | North India | ||
AR | (CAG)n | Shanghai, China | [244] | |
(rs4633) His62His | Shanghai, China | [224] | ||
COMT | (rs4818) Leu136Leu | |||
CYP1A1 | (rs2606345) IVS1+606G>T | |||
CYP1B1 | (rs10012)Arg48Gly | |||
(rs1065778) IVS4-76A>G | Shanghai, China | [224] | ||
CYP19A1 | (rs700518) Val80Val | |||
(rs2304463) IVS7-106T>G | ||||
(rs700519) Arg264Cys | ||||
(rs1065779) IVS9-53G>T | ||||
(rs4646) Ex11+410G>T | ||||
HSD3B2 | (rs1819698) Ex4-133C>T | Shanghai, China | [224] | |
(rs1361530) Ex4-88C>G | ||||
HSD17B3 | (rs2066479) Gly289Arg | |||
HSD17B1 | (rs2830) Ex1-486G>A | |||
SHBG | (rs6259) Ex8+6G>A | |||
SRD5A2 | (rs523349) Ex1-17G>C | |||
RXR-a | (rs1536475) IVS6+70A>G | Shanghai, China | [245] | |
(rs1805343) IVS1-27A>G | ||||
RXR-b | (rs2744537) G392T | |||
(rs2076310) C51T | ||||
INS | (rs689) A-6T | Shanghai, China | [245] | |
PPARD | (rs2016520) Ex4+15C>T | Shanghai, China | ||
PPARG | (rs3856806) His477His | Shanghai, China | ||
Inflammatory pathway genes | CR1 | (rs2274567) His1208Arg | North Indian | [230] |
( rs12144461) Intron 27, HindIII | ||||
IL1RN | 86-bp VNTR | North Indian | [220] | |
(rs689466) -1195G>A | [233] | |||
PTGS2 | (rs20417) -765G>C | |||
(rs5275) +8473T>C | North Indian Shanghai, China | [233,246] | ||
IL1B | (rs16944) -1060T>C | Shanghai, China north Indian | [220,247] | |
IL10 | rs1800871)- 7334T>C | Shanghai | [247] | |
(rs1800872) -6653A>C | Shanghai | |||
IL-8 | (rs10805066) IL8 -13985C>G | China | [248] | |
EGF | (rs4444903) +61A>G | North Indian | [221] | |
TGFb1 | (rs1800469)-509C>T | Shanghai, north Indian | [219,221,247] | |
TNF-α | (rs1800629) -308G>A | |||
IL6 | (rs1800795) 236C>G) | |||
IL8 | (rs10805066) -13985C>G | China | [248] | |
MMP-2 | (rs2285053) -735 C>T | North Indian | [249] | |
(rs9340799) -1306 C>T | ||||
MMP-7 | (rs11568818) -181 A>G | |||
(rs2250889) P574R | ||||
MMP9 | (rs 17576) R279Q | |||
(rs 17577) R668Q | ||||
TIMP2 | (rs8179090) -418 G>C | |||
Metabolic pathway genes | MTHFR | (rs1801133) Ala222Val | Indian | [228] |
APOB | (rs17240441) 35_43del9 | Indian | [217] | |
NAT2 | (rs1799929) NAT2*5A | Indian | [216] | |
(rs1799930) NAT2*6B | ||||
rs1799931, NAT2*7A | ||||
GSTT1 | Null polymorphism | Indian | [215] | |
GSTP1 | (rs1695) Ile105Val | |||
CYP17 | (rs743572) Ex1+27T>C | Shanghai Indian (265) | [250,251] | |
GSTM1 | Null polymorphism | Indian, Chilean Hungary Japanese | [215,237,238] | |
CYP1A1 | (rs4646903) CYP1A1*2A | Indian, Chilean Hungary Japanese | [218,237,239] | |
(rs1048943) Ile462Val (*2C) | China, Chilean, Hungary Japanese | [224,237-239] | ||
Cyp1a1 cyp1b1 | CYP1A1-MspI, CYP1A1-Ile462Val, and CYP1B1-Val432Leu | India | [252] | |
(rs5930) EX10+55G>A | Shanghai | [253] | ||
LDLR | (rs6413504) IVS17_42A>G | Shanghai | ||
(rs14158) EX18+88G>A | ||||
LPL | (rs263) IVS5-540C>T | |||
ALOX5 | (rs2029253) IVS3+100G>A | |||
ApoB | rs693) Thr2515Thr | Indian Chilean | [30,217] | |
ABCG8 | (rs11887534) Asp19His | North Indian Shanghai China | [229,254] | |
CETP | (rs708272) TaqIB | Chilean Shanghai China | [30,254] | |
(rs1800775) -629C>A | Shanghai China | [254] | ||
LRPAP1 | (rs11267919)752_177_752_176 I 37 | North Indian Shanghai China | [214,254] | |
CYP7A1 | (rs3808607) -204 A>C | North Indian | [255] | |
CYP7A1 | (rs3824260) -469 T>C | North Indian | ||
CYP17 | (rs743572)A/G | North Indian | [250,251] | |
ApoB | (rs676210) Pro2739Leu | Shanghai | [253] | |
(rs673548) IVS23-79T>C | ||||
rs520354) IVS6+360C > T | ||||
(rs1367117) Thr98Ile | ||||
(rs440446) IVS1+69C>G | ||||
CYP2C19 | (rs4244285) CYP2C19*2, | Japanese | [256] | |
(rs4986893) CYP2C19*3 | ||||
ADRB3 | (rs4994)A/G | North Indian | [257] | |
Apoptosis pathway | CASP8 | (rs3834129) -652 6N ins/del | North Indian | [258] |
(rs1045485) Asp302His | ||||
(rs3769818 A) IVS12-19 G>A | ||||
Nuclear Receptors | Lxr-alpha, Beta | LXR-α (rs7120118) and LXR-β (rs35463555 and rs2695121) | North Indian | [259] |
Cancer Stem cell gene | CD44 | CD44 (rs13347) C>T, CD44 (rs353639)A>C, CD44 (rs187116) G>A, CD44 (rs187115) T>C | North Indian | [260] |
NANOG, ALCAM, EpCAM, SOX-2, OCT-4, NANOG | NANOG (rs11055786)T>C, | North Indian | [261] | |
ALCAM (rs1157)G>A | ||||
EpCAM (rs1126497)T>C, | ||||
SOX-2(rs11915160)A>C | ||||
OCT-4 (rs3130932)T>G, | ||||
NANOG (rs11055786)T>C | ||||
Prostate stem cell antigen | PSCA | (rs2294008) T/C and rs2978974) | India, Japan | [262,263] |
miRNA | hsa-miR-146a | (rs2910164) G>C | North Indian | [264] |
hsa-mir-196a2 | (rs11614913) C>T | |||
hsa-mir-499 | (rs3746444)T>C | |||
miR-27,miR-570,miR-181 | miR-27a (rs895819)A>G, | North Indian population | [265] | |
miR-570(rs4143815)G>C, | ||||
miR-181a(rs12537)C>T | ||||
GWAS-associated genes | DCC | (rs7504990)C>T | Japan | [234] |
( rs2229080) C>G | North Indian | [235] | ||
(rs4078288) A>G | ||||
(rs7504990) C>T | ||||
(rs714) A>G | ||||
Wnt signaling pathway | SFRP4, DKK2, DKK3, APC, AXIN-2, Β-CATENIN, GLI-1 | SFRP4 (rs1802073) G>T, | North Indian | [266] |
DKK2 (rs17037102) C>T | ||||
DKK3 (rs3206824) C>T, | ||||
APC (rs4595552)A/T | ||||
APC ( rs11954856) G>T, | ||||
AXIN-2 (rs4791171)C>T | ||||
β-CATENIN (rs4135385) A>G, | ||||
GLI-1(rs222826) C>G | ||||
Other genes | KRAS | codon 25 Gln25His | Eastern India | [267] |
ACE I/D | (rs4646994) 289 bp del | North Indian | [268] | |
DNMT3B | (rs1569686) -579 G>T | North Indian | [269] | |
TLR2 | -196-174del | North Indian | [270] | |
TLR4 | (rs4986791) Thr399Ile | North Indian | ||
Adrenergic receptors (ADRA) | ADRA2A C-1291G, ADRβ3 T190C or Trp64Arg, and ADRβ1 C1165G or Arg389Gly | North Indian | [271] | |
Death Receptors and their ligands (DR4) | DR4 (rs20575, rs20576 and rs6557634), FAS (rs2234767) FASL (rs763110) | North Indian | ||
PlCE1 | (rs2274223) A>G and. (rs7922612) T>C | North Indian | [272] | |
Vitamin D receptor (VDR) | FokI C>T | China | [273] |
- Citation: Sharma A, Sharma KL, Gupta A, Yadav A, Kumar A. Gallbladder cancer epidemiology, pathogenesis and molecular genetics: Recent update. World J Gastroenterol 2017; 23(22): 3978-3998
- URL: https://www.wjgnet.com/1007-9327/full/v23/i22/3978.htm
- DOI: https://dx.doi.org/10.3748/wjg.v23.i22.3978