General Information of Drug Off-Target (DOT) (ID: OT4SW0HI)

DOT Name Cysteine and glycine-rich protein 2 (CSRP2)
Synonyms Cysteine-rich protein 2; CRP2; LIM domain only protein 5; LMO-5; Smooth muscle cell LIM protein; SmLIM
Gene Name CSRP2
Related Disease
Advanced cancer ( )
Gastric cancer ( )
Stomach cancer ( )
Breast cancer ( )
Breast carcinoma ( )
UniProt ID
CSRP2_HUMAN
3D Structure
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2D Sequence (FASTA)
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3D Structure (PDB)
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Pfam ID
PF00412
Sequence
MPVWGGGNKCGACGRTVYHAEEVQCDGRSFHRCCFLCMVCRKNLDSTTVAIHDEEIYCKS
CYGKKYGPKGYGYGQGAGTLNMDRGERLGIKPESVQPHRPTTNPNTSKFAQKYGGAEKCS
RCGDSVYAAEKIIGAGKPWHKNCFRCAKCGKSLESTTLTEKEGEIYCKGCYAKNFGPKGF
GYGQGAGALVHAQ
Function
Drastically down-regulated in response to PDGF-BB or cell injury, that promote smooth muscle cell proliferation and dedifferentiation. Seems to play a role in the development of the embryonic vascular system.
Tissue Specificity Highly expressed in the aorta, but not in heart and skeletal muscle.
KEGG Pathway
Cytoskeleton in muscle cells (hsa04820 )

Molecular Interaction Atlas (MIA) of This DOT

5 Disease(s) Related to This DOT
Disease Name Disease ID Evidence Level Mode of Inheritance REF
Advanced cancer DISAT1Z9 Strong Altered Expression [1]
Gastric cancer DISXGOUK Strong Altered Expression [1]
Stomach cancer DISKIJSX Strong Altered Expression [1]
Breast cancer DIS7DPX1 Limited Biomarker [2]
Breast carcinoma DIS2UE88 Limited Biomarker [2]
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Molecular Interaction Atlas (MIA) Jump to Detail Molecular Interaction Atlas of This DOT
27 Drug(s) Affected the Gene/Protein Processing of This DOT
Drug Name Drug ID Highest Status Interaction REF
Valproate DMCFE9I Approved Valproate decreases the expression of Cysteine and glycine-rich protein 2 (CSRP2). [3]
Ciclosporin DMAZJFX Approved Ciclosporin decreases the expression of Cysteine and glycine-rich protein 2 (CSRP2). [4]
Tretinoin DM49DUI Approved Tretinoin decreases the expression of Cysteine and glycine-rich protein 2 (CSRP2). [5]
Acetaminophen DMUIE76 Approved Acetaminophen increases the expression of Cysteine and glycine-rich protein 2 (CSRP2). [6]
Doxorubicin DMVP5YE Approved Doxorubicin increases the expression of Cysteine and glycine-rich protein 2 (CSRP2). [7]
Cupric Sulfate DMP0NFQ Approved Cupric Sulfate increases the expression of Cysteine and glycine-rich protein 2 (CSRP2). [8]
Estradiol DMUNTE3 Approved Estradiol decreases the expression of Cysteine and glycine-rich protein 2 (CSRP2). [9]
Ivermectin DMDBX5F Approved Ivermectin decreases the expression of Cysteine and glycine-rich protein 2 (CSRP2). [10]
Quercetin DM3NC4M Approved Quercetin increases the expression of Cysteine and glycine-rich protein 2 (CSRP2). [11]
Temozolomide DMKECZD Approved Temozolomide increases the expression of Cysteine and glycine-rich protein 2 (CSRP2). [12]
Arsenic trioxide DM61TA4 Approved Arsenic trioxide decreases the expression of Cysteine and glycine-rich protein 2 (CSRP2). [13]
Hydrogen peroxide DM1NG5W Approved Hydrogen peroxide affects the expression of Cysteine and glycine-rich protein 2 (CSRP2). [14]
Zoledronate DMIXC7G Approved Zoledronate decreases the expression of Cysteine and glycine-rich protein 2 (CSRP2). [15]
Phenobarbital DMXZOCG Approved Phenobarbital affects the expression of Cysteine and glycine-rich protein 2 (CSRP2). [16]
Progesterone DMUY35B Approved Progesterone decreases the expression of Cysteine and glycine-rich protein 2 (CSRP2). [17]
Hydroquinone DM6AVR4 Approved Hydroquinone decreases the expression of Cysteine and glycine-rich protein 2 (CSRP2). [18]
Cocaine DMSOX7I Approved Cocaine decreases the expression of Cysteine and glycine-rich protein 2 (CSRP2). [19]
Gemcitabine DMSE3I7 Approved Gemcitabine increases the expression of Cysteine and glycine-rich protein 2 (CSRP2). [20]
Urethane DM7NSI0 Phase 4 Urethane increases the expression of Cysteine and glycine-rich protein 2 (CSRP2). [21]
Dihydrotestosterone DM3S8XC Phase 4 Dihydrotestosterone increases the expression of Cysteine and glycine-rich protein 2 (CSRP2). [22]
Benzo(a)pyrene DMN7J43 Phase 1 Benzo(a)pyrene decreases the expression of Cysteine and glycine-rich protein 2 (CSRP2). [23]
Leflunomide DMR8ONJ Phase 1 Trial Leflunomide decreases the expression of Cysteine and glycine-rich protein 2 (CSRP2). [24]
PMID28460551-Compound-2 DM4DOUB Patented PMID28460551-Compound-2 decreases the expression of Cysteine and glycine-rich protein 2 (CSRP2). [26]
THAPSIGARGIN DMDMQIE Preclinical THAPSIGARGIN decreases the expression of Cysteine and glycine-rich protein 2 (CSRP2). [27]
Trichostatin A DM9C8NX Investigative Trichostatin A decreases the expression of Cysteine and glycine-rich protein 2 (CSRP2). [29]
Milchsaure DM462BT Investigative Milchsaure increases the expression of Cysteine and glycine-rich protein 2 (CSRP2). [30]
chloropicrin DMSGBQA Investigative chloropicrin increases the expression of Cysteine and glycine-rich protein 2 (CSRP2). [31]
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⏷ Show the Full List of 27 Drug(s)
2 Drug(s) Affected the Post-Translational Modifications of This DOT
Drug Name Drug ID Highest Status Interaction REF
TAK-243 DM4GKV2 Phase 1 TAK-243 increases the sumoylation of Cysteine and glycine-rich protein 2 (CSRP2). [25]
Bisphenol A DM2ZLD7 Investigative Bisphenol A decreases the methylation of Cysteine and glycine-rich protein 2 (CSRP2). [28]
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References

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2 Hypoxia promotes breast cancer cell invasion through HIF-1-mediated up-regulation of the invadopodial actin bundling protein CSRP2.Sci Rep. 2018 Jul 5;8(1):10191. doi: 10.1038/s41598-018-28637-x.
3 Human embryonic stem cell-derived test systems for developmental neurotoxicity: a transcriptomics approach. Arch Toxicol. 2013 Jan;87(1):123-43.
4 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.
5 Development of a neural teratogenicity test based on human embryonic stem cells: response to retinoic acid exposure. Toxicol Sci. 2011 Dec;124(2):370-7.
6 Gene expression analysis of precision-cut human liver slices indicates stable expression of ADME-Tox related genes. Toxicol Appl Pharmacol. 2011 May 15;253(1):57-69.
7 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.
8 Physiological and toxicological transcriptome changes in HepG2 cells exposed to copper. Physiol Genomics. 2009 Aug 7;38(3):386-401.
9 Gene expression profiling of human peri-implantation endometria between natural and stimulated cycles. Fertil Steril. 2008 Dec;90(6):2152-64.
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 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.
13 Global effects of inorganic arsenic on gene expression profile in human macrophages. Mol Immunol. 2009 Feb;46(4):649-56.
14 Global gene expression analysis reveals differences in cellular responses to hydroxyl- and superoxide anion radical-induced oxidative stress in caco-2 cells. Toxicol Sci. 2010 Apr;114(2):193-203. doi: 10.1093/toxsci/kfp309. Epub 2009 Dec 31.
15 Interleukin-19 as a translational indicator of renal injury. Arch Toxicol. 2015 Jan;89(1):101-6.
16 Reproducible chemical-induced changes in gene expression profiles in human hepatoma HepaRG cells under various experimental conditions. Toxicol In Vitro. 2009 Apr;23(3):466-75. doi: 10.1016/j.tiv.2008.12.018. Epub 2008 Dec 30.
17 Effects of progesterone treatment on expression of genes involved in uterine quiescence. Reprod Sci. 2011 Aug;18(8):781-97.
18 Keratinocyte-derived IL-36gama plays a role in hydroquinone-induced chemical leukoderma through inhibition of melanogenesis in human epidermal melanocytes. Arch Toxicol. 2019 Aug;93(8):2307-2320.
19 Gene expression in human hippocampus from cocaine abusers identifies genes which regulate extracellular matrix remodeling. PLoS One. 2007 Nov 14;2(11):e1187. doi: 10.1371/journal.pone.0001187.
20 Gene expression profiling of breast cancer cells in response to gemcitabine: NF-kappaB pathway activation as a potential mechanism of resistance. Breast Cancer Res Treat. 2007 Apr;102(2):157-72.
21 Ethyl carbamate induces cell death through its effects on multiple metabolic pathways. Chem Biol Interact. 2017 Nov 1;277:21-32.
22 LSD1 activates a lethal prostate cancer gene network independently of its demethylase function. Proc Natl Acad Sci U S A. 2018 May 1;115(18):E4179-E4188.
23 Transcriptional signature of human macrophages exposed to the environmental contaminant benzo(a)pyrene. Toxicol Sci. 2010 Apr;114(2):247-59.
24 Endoplasmic reticulum stress and MAPK signaling pathway activation underlie leflunomide-induced toxicity in HepG2 Cells. Toxicology. 2017 Dec 1;392:11-21.
25 Inhibiting ubiquitination causes an accumulation of SUMOylated newly synthesized nuclear proteins at PML bodies. J Biol Chem. 2019 Oct 18;294(42):15218-15234. doi: 10.1074/jbc.RA119.009147. Epub 2019 Jul 8.
26 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.
27 Endoplasmic reticulum stress impairs insulin signaling through mitochondrial damage in SH-SY5Y cells. Neurosignals. 2012;20(4):265-80.
28 DNA methylome-wide alterations associated with estrogen receptor-dependent effects of bisphenols in breast cancer. Clin Epigenetics. 2019 Oct 10;11(1):138. doi: 10.1186/s13148-019-0725-y.
29 A transcriptome-based classifier to identify developmental toxicants by stem cell testing: design, validation and optimization for histone deacetylase inhibitors. Arch Toxicol. 2015 Sep;89(9):1599-618.
30 Transcriptional profiling of lactic acid treated reconstructed human epidermis reveals pathways underlying stinging and itch. Toxicol In Vitro. 2019 Jun;57:164-173.
31 Transcriptomic analysis of human primary bronchial epithelial cells after chloropicrin treatment. Chem Res Toxicol. 2015 Oct 19;28(10):1926-35.