General Information of Drug Off-Target (DOT) (ID: OTLFL0DG)

DOT Name Pro-cathepsin H (CTSH)
Gene Name CTSH
UniProt ID
CATH_HUMAN
3D Structure
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2D Sequence (FASTA)
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3D Structure (PDB)
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PDB ID
6CZK; 6CZS
EC Number
3.4.22.16
Pfam ID
PF08246 ; PF00112
Sequence
MWATLPLLCAGAWLLGVPVCGAAELCVNSLEKFHFKSWMSKHRKTYSTEEYHHRLQTFAS
NWRKINAHNNGNHTFKMALNQFSDMSFAEIKHKYLWSEPQNCSATKSNYLRGTGPYPPSV
DWRKKGNFVSPVKNQGACGSCWTFSTTGALESAIAIATGKMLSLAEQQLVDCAQDFNNHG
CQGGLPSQAFEYILYNKGIMGEDTYPYQGKDGYCKFQPGKAIGFVKDVANITIYDEEAMV
EAVALYNPVSFAFEVTQDFMMYRTGIYSSTSCHKTPDKVNHAVLAVGYGEKNGIPYWIVK
NSWGPQWGMNGYFLIERGKNMCGLAACASYPIPLV
Function Important for the overall degradation of proteins in lysosomes.
KEGG Pathway
Lysosome (hsa04142 )
Apoptosis (hsa04210 )
Reactome Pathway
Surfactant metabolism (R-HSA-5683826 )
Neutrophil degranulation (R-HSA-6798695 )
MHC class II antigen presentation (R-HSA-2132295 )

Molecular Interaction Atlas (MIA) of This DOT

Molecular Interaction Atlas (MIA) Jump to Detail Molecular Interaction Atlas of This DOT
31 Drug(s) Affected the Gene/Protein Processing of This DOT
Drug Name Drug ID Highest Status Interaction REF
Valproate DMCFE9I Approved Valproate increases the expression of Pro-cathepsin H (CTSH). [1]
Ciclosporin DMAZJFX Approved Ciclosporin decreases the expression of Pro-cathepsin H (CTSH). [2]
Tretinoin DM49DUI Approved Tretinoin decreases the expression of Pro-cathepsin H (CTSH). [3]
Acetaminophen DMUIE76 Approved Acetaminophen increases the expression of Pro-cathepsin H (CTSH). [4]
Doxorubicin DMVP5YE Approved Doxorubicin decreases the expression of Pro-cathepsin H (CTSH). [5]
Cupric Sulfate DMP0NFQ Approved Cupric Sulfate decreases the expression of Pro-cathepsin H (CTSH). [6]
Cisplatin DMRHGI9 Approved Cisplatin increases the expression of Pro-cathepsin H (CTSH). [7]
Estradiol DMUNTE3 Approved Estradiol decreases the expression of Pro-cathepsin H (CTSH). [8]
Temozolomide DMKECZD Approved Temozolomide increases the expression of Pro-cathepsin H (CTSH). [9]
Arsenic trioxide DM61TA4 Approved Arsenic trioxide decreases the expression of Pro-cathepsin H (CTSH). [10]
Triclosan DMZUR4N Approved Triclosan increases the expression of Pro-cathepsin H (CTSH). [11]
Carbamazepine DMZOLBI Approved Carbamazepine affects the expression of Pro-cathepsin H (CTSH). [12]
Decitabine DMQL8XJ Approved Decitabine increases the expression of Pro-cathepsin H (CTSH). [13]
Marinol DM70IK5 Approved Marinol decreases the expression of Pro-cathepsin H (CTSH). [14]
Fluorouracil DMUM7HZ Approved Fluorouracil increases the expression of Pro-cathepsin H (CTSH). [15]
Fulvestrant DM0YZC6 Approved Fulvestrant increases the expression of Pro-cathepsin H (CTSH). [8]
Cytarabine DMZD5QR Approved Cytarabine decreases the expression of Pro-cathepsin H (CTSH). [16]
Nicotine DMWX5CO Approved Nicotine increases the expression of Pro-cathepsin H (CTSH). [17]
Sodium lauryl sulfate DMLJ634 Approved Sodium lauryl sulfate decreases the expression of Pro-cathepsin H (CTSH). [18]
Cyclophosphamide DM4O2Z7 Approved Cyclophosphamide increases the expression of Pro-cathepsin H (CTSH). [19]
Bexarotene DMOBIKY Approved Bexarotene increases the expression of Pro-cathepsin H (CTSH). [20]
SNDX-275 DMH7W9X Phase 3 SNDX-275 increases the expression of Pro-cathepsin H (CTSH). [21]
Seocalcitol DMKL9QO Phase 3 Seocalcitol decreases the expression of Pro-cathepsin H (CTSH). [22]
GSK2110183 DMZHB37 Phase 2 GSK2110183 increases the expression of Pro-cathepsin H (CTSH). [23]
Afimoxifene DMFORDT Phase 2 Afimoxifene increases the expression of Pro-cathepsin H (CTSH). [8]
PMID28460551-Compound-2 DM4DOUB Patented PMID28460551-Compound-2 decreases the expression of Pro-cathepsin H (CTSH). [25]
Bisphenol A DM2ZLD7 Investigative Bisphenol A affects the expression of Pro-cathepsin H (CTSH). [26]
Milchsaure DM462BT Investigative Milchsaure decreases the expression of Pro-cathepsin H (CTSH). [27]
Coumestrol DM40TBU Investigative Coumestrol decreases the expression of Pro-cathepsin H (CTSH). [28]
Acetaldehyde DMJFKG4 Investigative Acetaldehyde increases the expression of Pro-cathepsin H (CTSH). [29]
Bilirubin DMI0V4O Investigative Bilirubin decreases the expression of Pro-cathepsin H (CTSH). [30]
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⏷ Show the Full List of 31 Drug(s)
1 Drug(s) Affected the Post-Translational Modifications of This DOT
Drug Name Drug ID Highest Status Interaction REF
Benzo(a)pyrene DMN7J43 Phase 1 Benzo(a)pyrene increases the methylation of Pro-cathepsin H (CTSH). [24]
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References

1 Human embryonic stem cell-derived test systems for developmental neurotoxicity: a transcriptomics approach. Arch Toxicol. 2013 Jan;87(1):123-43.
2 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.
3 Systems analysis of transcriptome and proteome in retinoic acid/arsenic trioxide-induced cell differentiation/apoptosis of promyelocytic leukemia. Proc Natl Acad Sci U S A. 2005 May 24;102(21):7653-8.
4 Predictive toxicology using systemic biology and liver microfluidic "on chip" approaches: application to acetaminophen injury. Toxicol Appl Pharmacol. 2012 Mar 15;259(3):270-80.
5 Bringing in vitro analysis closer to in vivo: studying doxorubicin toxicity and associated mechanisms in 3D human microtissues with PBPK-based dose modelling. Toxicol Lett. 2018 Sep 15;294:184-192.
6 Physiological and toxicological transcriptome changes in HepG2 cells exposed to copper. Physiol Genomics. 2009 Aug 7;38(3):386-401.
7 Activation of AIFM2 enhances apoptosis of human lung cancer cells undergoing toxicological stress. Toxicol Lett. 2016 Sep 6;258:227-236.
8 Comparative gene expression profiling reveals partially overlapping but distinct genomic actions of different antiestrogens in human breast cancer cells. J Cell Biochem. 2006 Aug 1;98(5):1163-84.
9 Temozolomide induces activation of Wnt/-catenin signaling in glioma cells via PI3K/Akt pathway: implications in glioma therapy. Cell Biol Toxicol. 2020 Jun;36(3):273-278. doi: 10.1007/s10565-019-09502-7. Epub 2019 Nov 22.
10 Arsenic suppresses gene expression in promyelocytic leukemia cells partly through Sp1 oxidation. Blood. 2005 Jul 1;106(1):304-10.
11 Transcriptome and DNA methylome dynamics during triclosan-induced cardiomyocyte differentiation toxicity. Stem Cells Int. 2018 Oct 29;2018:8608327.
12 Gene Expression Regulation and Pathway Analysis After Valproic Acid and Carbamazepine Exposure in a Human Embryonic Stem Cell-Based Neurodevelopmental Toxicity Assay. Toxicol Sci. 2015 Aug;146(2):311-20. doi: 10.1093/toxsci/kfv094. Epub 2015 May 15.
13 The DNA methyltransferase inhibitors azacitidine, decitabine and zebularine exert differential effects on cancer gene expression in acute myeloid leukemia cells. Leukemia. 2009 Jun;23(6):1019-28.
14 THC exposure of human iPSC neurons impacts genes associated with neuropsychiatric disorders. Transl Psychiatry. 2018 Apr 25;8(1):89. doi: 10.1038/s41398-018-0137-3.
15 Dissecting progressive stages of 5-fluorouracil resistance in vitro using RNA expression profiling. Int J Cancer. 2004 Nov 1;112(2):200-12. doi: 10.1002/ijc.20401.
16 Cytosine arabinoside induces ectoderm and inhibits mesoderm expression in human embryonic stem cells during multilineage differentiation. Br J Pharmacol. 2011 Apr;162(8):1743-56.
17 Characterizing the genetic basis for nicotine induced cancer development: a transcriptome sequencing study. PLoS One. 2013 Jun 18;8(6):e67252.
18 CXCL14 downregulation in human keratinocytes is a potential biomarker for a novel in vitro skin sensitization test. Toxicol Appl Pharmacol. 2020 Jan 1;386:114828. doi: 10.1016/j.taap.2019.114828. Epub 2019 Nov 14.
19 Comparative gene expression analysis of a chronic myelogenous leukemia cell line resistant to cyclophosphamide using oligonucleotide arrays and response to tyrosine kinase inhibitors. Leuk Res. 2007 Nov;31(11):1511-20.
20 Identification of biomarkers modulated by the rexinoid LGD1069 (bexarotene) in human breast cells using oligonucleotide arrays. Cancer Res. 2006 Dec 15;66(24):12009-18.
21 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.
22 Expression profiling in squamous carcinoma cells reveals pleiotropic effects of vitamin D3 analog EB1089 signaling on cell proliferation, differentiation, and immune system regulation. Mol Endocrinol. 2002 Jun;16(6):1243-56.
23 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.
24 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.
25 Cell-based two-dimensional morphological assessment system to predict cancer drug-induced cardiotoxicity using human induced pluripotent stem cell-derived cardiomyocytes. Toxicol Appl Pharmacol. 2019 Nov 15;383:114761. doi: 10.1016/j.taap.2019.114761. Epub 2019 Sep 15.
26 Comprehensive analysis of transcriptomic changes induced by low and high doses of bisphenol A in HepG2 spheroids in vitro and rat liver in vivo. Environ Res. 2019 Jun;173:124-134. doi: 10.1016/j.envres.2019.03.035. Epub 2019 Mar 18.
27 Transcriptional profiling of lactic acid treated reconstructed human epidermis reveals pathways underlying stinging and itch. Toxicol In Vitro. 2019 Jun;57:164-173.
28 Pleiotropic combinatorial transcriptomes of human breast cancer cells exposed to mixtures of dietary phytoestrogens. Food Chem Toxicol. 2009 Apr;47(4):787-95.
29 Transcriptome profile analysis of saturated aliphatic aldehydes reveals carbon number-specific molecules involved in pulmonary toxicity. Chem Res Toxicol. 2014 Aug 18;27(8):1362-70.
30 Global changes in gene regulation demonstrate that unconjugated bilirubin is able to upregulate and activate select components of the endoplasmic reticulum stress response pathway. J Biochem Mol Toxicol. 2010 Mar-Apr;24(2):73-88.