General Information of Drug Off-Target (DOT) (ID: OTEC13I5)

DOT Name Fructose-bisphosphate aldolase C (ALDOC)
Synonyms EC 4.1.2.13; Brain-type aldolase
Gene Name ALDOC
Related Disease
Hepatocellular carcinoma ( )
Liver cancer ( )
Schizophrenia ( )
Neuroblastoma ( )
UniProt ID
ALDOC_HUMAN
3D Structure
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2D Sequence (FASTA)
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3D Structure (PDB)
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PDB ID
1XFB
EC Number
4.1.2.13
Pfam ID
PF00274
Sequence
MPHSYPALSAEQKKELSDIALRIVAPGKGILAADESVGSMAKRLSQIGVENTEENRRLYR
QVLFSADDRVKKCIGGVIFFHETLYQKDDNGVPFVRTIQDKGIVVGIKVDKGVVPLAGTD
GETTTQGLDGLSERCAQYKKDGADFAKWRCVLKISERTPSALAILENANVLARYASICQQ
NGIVPIVEPEILPDGDHDLKRCQYVTEKVLAAVYKALSDHHVYLEGTLLKPNMVTPGHAC
PIKYTPEEIAMATVTALRRTVPPAVPGVTFLSGGQSEEEASFNLNAINRCPLPRPWALTF
SYGRALQASALNAWRGQRDNAGAATEEFIKRAEVNGLAAQGKYEGSGEDGGAAAQSLYIA
NHAY
KEGG Pathway
Glycolysis / Gluconeogenesis (hsa00010 )
Pentose phosphate pathway (hsa00030 )
Fructose and mannose metabolism (hsa00051 )
Metabolic pathways (hsa01100 )
Carbon metabolism (hsa01200 )
Biosynthesis of amino acids (hsa01230 )
HIF-1 sig.ling pathway (hsa04066 )
Reactome Pathway
Glycolysis (R-HSA-70171 )
Gluconeogenesis (R-HSA-70263 )
Neutrophil degranulation (R-HSA-6798695 )
BioCyc Pathway
MetaCyc:HS03200-MONOMER

Molecular Interaction Atlas (MIA) of This DOT

4 Disease(s) Related to This DOT
Disease Name Disease ID Evidence Level Mode of Inheritance REF
Hepatocellular carcinoma DIS0J828 Strong Biomarker [1]
Liver cancer DISDE4BI Strong Biomarker [1]
Schizophrenia DISSRV2N Strong Altered Expression [2]
Neuroblastoma DISVZBI4 moderate Altered Expression [3]
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Molecular Interaction Atlas (MIA) Jump to Detail Molecular Interaction Atlas of This DOT
This DOT Affected the Drug Response of 1 Drug(s)
Drug Name Drug ID Highest Status Interaction REF
Etoposide DMNH3PG Approved Fructose-bisphosphate aldolase C (ALDOC) affects the response to substance of Etoposide. [35]
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3 Drug(s) Affected the Post-Translational Modifications of This DOT
Drug Name Drug ID Highest Status Interaction REF
Valproate DMCFE9I Approved Valproate decreases the methylation of Fructose-bisphosphate aldolase C (ALDOC). [4]
Benzo(a)pyrene DMN7J43 Phase 1 Benzo(a)pyrene increases the methylation of Fructose-bisphosphate aldolase C (ALDOC). [28]
PMID28870136-Compound-52 DMFDERP Patented PMID28870136-Compound-52 affects the phosphorylation of Fructose-bisphosphate aldolase C (ALDOC). [30]
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29 Drug(s) Affected the Gene/Protein Processing of This DOT
Drug Name Drug ID Highest Status Interaction REF
Ciclosporin DMAZJFX Approved Ciclosporin decreases the expression of Fructose-bisphosphate aldolase C (ALDOC). [5]
Tretinoin DM49DUI Approved Tretinoin decreases the expression of Fructose-bisphosphate aldolase C (ALDOC). [6]
Acetaminophen DMUIE76 Approved Acetaminophen decreases the expression of Fructose-bisphosphate aldolase C (ALDOC). [7]
Doxorubicin DMVP5YE Approved Doxorubicin decreases the expression of Fructose-bisphosphate aldolase C (ALDOC). [8]
Cisplatin DMRHGI9 Approved Cisplatin decreases the expression of Fructose-bisphosphate aldolase C (ALDOC). [9]
Estradiol DMUNTE3 Approved Estradiol decreases the expression of Fructose-bisphosphate aldolase C (ALDOC). [5]
Ivermectin DMDBX5F Approved Ivermectin decreases the expression of Fructose-bisphosphate aldolase C (ALDOC). [10]
Quercetin DM3NC4M Approved Quercetin decreases the expression of Fructose-bisphosphate aldolase C (ALDOC). [11]
Arsenic trioxide DM61TA4 Approved Arsenic trioxide decreases the expression of Fructose-bisphosphate aldolase C (ALDOC). [12]
Vorinostat DMWMPD4 Approved Vorinostat decreases the expression of Fructose-bisphosphate aldolase C (ALDOC). [13]
Triclosan DMZUR4N Approved Triclosan decreases the expression of Fructose-bisphosphate aldolase C (ALDOC). [14]
Decitabine DMQL8XJ Approved Decitabine increases the expression of Fructose-bisphosphate aldolase C (ALDOC). [15]
Niclosamide DMJAGXQ Approved Niclosamide decreases the expression of Fructose-bisphosphate aldolase C (ALDOC). [16]
Cannabidiol DM0659E Approved Cannabidiol decreases the expression of Fructose-bisphosphate aldolase C (ALDOC). [17]
Ethanol DMDRQZU Approved Ethanol decreases the expression of Fructose-bisphosphate aldolase C (ALDOC). [18]
Obeticholic acid DM3Q1SM Approved Obeticholic acid increases the expression of Fructose-bisphosphate aldolase C (ALDOC). [19]
Mifepristone DMGZQEF Approved Mifepristone decreases the expression of Fructose-bisphosphate aldolase C (ALDOC). [20]
Fluoxetine DM3PD2C Approved Fluoxetine increases the expression of Fructose-bisphosphate aldolase C (ALDOC). [21]
Imatinib DM7RJXL Approved Imatinib decreases the expression of Fructose-bisphosphate aldolase C (ALDOC). [22]
Resveratrol DM3RWXL Phase 3 Resveratrol increases the expression of Fructose-bisphosphate aldolase C (ALDOC). [23]
Epigallocatechin gallate DMCGWBJ Phase 3 Epigallocatechin gallate increases the expression of Fructose-bisphosphate aldolase C (ALDOC). [24]
Curcumin DMQPH29 Phase 3 Curcumin decreases the expression of Fructose-bisphosphate aldolase C (ALDOC). [25]
Fenretinide DMRD5SP Phase 3 Fenretinide increases the expression of Fructose-bisphosphate aldolase C (ALDOC). [26]
GSK2110183 DMZHB37 Phase 2 GSK2110183 increases the expression of Fructose-bisphosphate aldolase C (ALDOC). [27]
(+)-JQ1 DM1CZSJ Phase 1 (+)-JQ1 increases the expression of Fructose-bisphosphate aldolase C (ALDOC). [29]
PMID28870136-Compound-48 DMPIM9L Patented PMID28870136-Compound-48 decreases the expression of Fructose-bisphosphate aldolase C (ALDOC). [31]
THAPSIGARGIN DMDMQIE Preclinical THAPSIGARGIN decreases the expression of Fructose-bisphosphate aldolase C (ALDOC). [32]
Bisphenol A DM2ZLD7 Investigative Bisphenol A increases the expression of Fructose-bisphosphate aldolase C (ALDOC). [33]
PP-242 DM2348V Investigative PP-242 decreases the expression of Fructose-bisphosphate aldolase C (ALDOC). [34]
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⏷ Show the Full List of 29 Drug(s)

References

1 Molecular cloning and expression of rat aldolase C messenger RNA during development and hepatocarcinogenesis.Eur J Biochem. 1987 Mar 16;163(3):513-8. doi: 10.1111/j.1432-1033.1987.tb10898.x.
2 Alterations in oligodendrocyte proteins, calcium homeostasis and new potential markers in schizophrenia anterior temporal lobe are revealed by shotgun proteome analysis.J Neural Transm (Vienna). 2009 Mar;116(3):275-89. doi: 10.1007/s00702-008-0156-y. Epub 2008 Nov 26.
3 The transcription of the human fructose-bisphosphate aldolase C gene is activated by nerve-growth-factor-induced B factor in human neuroblastoma cells.Biochem J. 1997 Apr 1;323 ( Pt 1)(Pt 1):245-50. doi: 10.1042/bj3230245.
4 Integrative omics data analyses of repeated dose toxicity of valproic acid in vitro reveal new mechanisms of steatosis induction. Toxicology. 2018 Jan 15;393:160-170.
5 Comparison of HepG2 and HepaRG by whole-genome gene expression analysis for the purpose of chemical hazard identification. Toxicol Sci. 2010 May;115(1):66-79.
6 Phenotypic characterization of retinoic acid differentiated SH-SY5Y cells by transcriptional profiling. PLoS One. 2013 May 28;8(5):e63862.
7 Multiple microRNAs function as self-protective modules in acetaminophen-induced hepatotoxicity in humans. Arch Toxicol. 2018 Feb;92(2):845-858.
8 RNA sequence analysis of inducible pluripotent stem cell-derived cardiomyocytes reveals altered expression of DNA damage and cell cycle genes in response to doxorubicin. Toxicol Appl Pharmacol. 2018 Oct 1;356:44-53.
9 Characterisation of cisplatin-induced transcriptomics responses in primary mouse hepatocytes, HepG2 cells and mouse embryonic stem cells shows conservation of regulating transcription factor networks. Mutagenesis. 2014 Jan;29(1):17-26.
10 Quantitative proteomics reveals a broad-spectrum antiviral property of ivermectin, benefiting for COVID-19 treatment. J Cell Physiol. 2021 Apr;236(4):2959-2975. doi: 10.1002/jcp.30055. Epub 2020 Sep 22.
11 Comparison of phenotypic and transcriptomic effects of false-positive genotoxins, true genotoxins and non-genotoxins using HepG2 cells. Mutagenesis. 2011 Sep;26(5):593-604.
12 Changes in gene expression profiles of multiple myeloma cells induced by arsenic trioxide (ATO): possible mechanisms to explain ATO resistance in vivo. Br J Haematol. 2005 Mar;128(5):636-44.
13 Definition of transcriptome-based indices for quantitative characterization of chemically disturbed stem cell development: introduction of the STOP-Toxukn and STOP-Toxukk tests. Arch Toxicol. 2017 Feb;91(2):839-864.
14 Transcriptome and DNA methylome dynamics during triclosan-induced cardiomyocyte differentiation toxicity. Stem Cells Int. 2018 Oct 29;2018:8608327.
15 Gene induction and apoptosis in human hepatocellular carci-noma cells SMMC-7721 exposed to 5-aza-2'-deoxycytidine. Chin Med J (Engl). 2007 Sep 20;120(18):1626-31.
16 Growth inhibition of ovarian tumor-initiating cells by niclosamide. Mol Cancer Ther. 2012 Aug;11(8):1703-12.
17 Cannabidiol Displays Proteomic Similarities to Antipsychotics in Cuprizone-Exposed Human Oligodendrocytic Cell Line MO3.13. Front Mol Neurosci. 2021 May 28;14:673144. doi: 10.3389/fnmol.2021.673144. eCollection 2021.
18 Chronic ethanol exposure increases goosecoid (GSC) expression in human embryonic carcinoma cell differentiation. J Appl Toxicol. 2014 Jan;34(1):66-75.
19 Pharmacotoxicology of clinically-relevant concentrations of obeticholic acid in an organotypic human hepatocyte system. Toxicol In Vitro. 2017 Mar;39:93-103.
20 Mifepristone induced progesterone withdrawal reveals novel regulatory pathways in human endometrium. Mol Hum Reprod. 2007 Sep;13(9):641-54.
21 Screening autism-associated environmental factors in differentiating human neural progenitors with fractional factorial design-based transcriptomics. Sci Rep. 2023 Jun 29;13(1):10519. doi: 10.1038/s41598-023-37488-0.
22 A systems biology understanding of the synergistic effects of arsenic sulfide and Imatinib in BCR/ABL-associated leukemia. Proc Natl Acad Sci U S A. 2009 Mar 3;106(9):3378-83.
23 Resveratrol-induced cell growth inhibition and apoptosis is associated with modulation of phosphoglycerate mutase B in human prostate cancer cells: two-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresis and mass spectrometry evaluation. Cancer Detect Prev. 2004;28(6):443-52. doi: 10.1016/j.cdp.2004.08.009.
24 Comparative proteomics reveals concordant and discordant biochemical effects of caffeine versus epigallocatechin-3-gallate in human endothelial cells. Toxicol Appl Pharmacol. 2019 Sep 1;378:114621. doi: 10.1016/j.taap.2019.114621. Epub 2019 Jun 10.
25 Gene-expression profiling during curcumin-induced apoptosis reveals downregulation of CXCR4. Exp Hematol. 2007 Jan;35(1):84-95.
26 Regulation of lipocalin-2 gene by the cancer chemopreventive retinoid 4-HPR. Int J Cancer. 2006 Oct 1;119(7):1599-606.
27 Novel ATP-competitive Akt inhibitor afuresertib suppresses the proliferation of malignant pleural mesothelioma cells. Cancer Med. 2017 Nov;6(11):2646-2659. doi: 10.1002/cam4.1179. Epub 2017 Sep 27.
28 Air pollution and DNA methylation alterations in lung cancer: A systematic and comparative study. Oncotarget. 2017 Jan 3;8(1):1369-1391. doi: 10.18632/oncotarget.13622.
29 Inhibition of BRD4 attenuates tumor cell self-renewal and suppresses stem cell signaling in MYC driven medulloblastoma. Oncotarget. 2014 May 15;5(9):2355-71.
30 Quantitative phosphoproteomics reveal cellular responses from caffeine, coumarin and quercetin in treated HepG2 cells. Toxicol Appl Pharmacol. 2022 Aug 15;449:116110. doi: 10.1016/j.taap.2022.116110. Epub 2022 Jun 7.
31 Global expression profiling of theophylline response genes in macrophages: evidence of airway anti-inflammatory regulation. Respir Res. 2005 Aug 8;6(1):89. doi: 10.1186/1465-9921-6-89.
32 Endoplasmic reticulum stress impairs insulin signaling through mitochondrial damage in SH-SY5Y cells. Neurosignals. 2012;20(4):265-80.
33 Bisphenol A induces DSB-ATM-p53 signaling leading to cell cycle arrest, senescence, autophagy, stress response, and estrogen release in human fetal lung fibroblasts. Arch Toxicol. 2018 Apr;92(4):1453-1469.
34 Marine biogenics in sea spray aerosols interact with the mTOR signaling pathway. Sci Rep. 2019 Jan 24;9(1):675.
35 Gene expression profiling of 30 cancer cell lines predicts resistance towards 11 anticancer drugs at clinically achieved concentrations. Int J Cancer. 2006 Apr 1;118(7):1699-712. doi: 10.1002/ijc.21570.