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

DOT Name Calmegin (CLGN)
Gene Name CLGN
Related Disease
Prostate cancer ( )
Prostate carcinoma ( )
Seminoma ( )
Breast cancer ( )
Breast carcinoma ( )
UniProt ID
CLGN_HUMAN
3D Structure
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2D Sequence (FASTA)
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3D Structure (PDB)
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Pfam ID
PF00262
Sequence
MHFQAFWLCLGLLFISINAEFMDDDVETEDFEENSEEIDVNESELSSEIKYKTPQPIGEV
YFAETFDSGRLAGWVLSKAKKDDMDEEISIYDGRWEIEELKENQVPGDRGLVLKSRAKHH
AISAVLAKPFIFADKPLIVQYEVNFQDGIDCGGAYIKLLADTDDLILENFYDKTSYIIMF
GPDKCGEDYKLHFIFRHKHPKTGVFEEKHAKPPDVDLKKFFTDRKTHLYTLVMNPDDTFE
VLVDQTVVNKGSLLEDVVPPIKPPKEIEDPNDKKPEEWDERAKIPDPSAVKPEDWDESEP
AQIEDSSVVKPAGWLDDEPKFIPDPNAEKPDDWNEDTDGEWEAPQILNPACRIGCGEWKP
PMIDNPKYKGVWRPPLVDNPNYQGIWSPRKIPNPDYFEDDHPFLLTSFSALGLELWSMTS
DIYFDNFIICSEKEVADHWAADGWRWKIMIANANKPGVLKQLMAAAEGHPWLWLIYLVTA
GVPIALITSFCWPRKVKKKHKDTEYKKTDICIPQTKGVLEQEEKEEKAALEKPMDLEEEK
KQNDGEMLEKEEESEPEEKSEEEIEIIEGQEESNQSNKSGSEDEMKEADESTGSGDGPIK
SVRKRRVRKD
Function
Functions during spermatogenesis as a chaperone for a range of client proteins that are important for sperm adhesion onto the egg zona pellucida and for subsequent penetration of the zona pellucida. Required for normal sperm migration from the uterus into the oviduct. Required for normal male fertility. Binds calcium ions.
Tissue Specificity Detected in testis (at protein level). Detected in testis.

Molecular Interaction Atlas (MIA) of This DOT

5 Disease(s) Related to This DOT
Disease Name Disease ID Evidence Level Mode of Inheritance REF
Prostate cancer DISF190Y Strong Genetic Variation [1]
Prostate carcinoma DISMJPLE Strong Genetic Variation [1]
Seminoma DIS3J8LJ Strong Altered Expression [2]
Breast cancer DIS7DPX1 Limited Biomarker [3]
Breast carcinoma DIS2UE88 Limited Biomarker [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
Mitomycin DMH0ZJE Approved Calmegin (CLGN) affects the response to substance of Mitomycin. [33]
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37 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 Calmegin (CLGN). [4]
Ciclosporin DMAZJFX Approved Ciclosporin increases the expression of Calmegin (CLGN). [5]
Tretinoin DM49DUI Approved Tretinoin decreases the expression of Calmegin (CLGN). [6]
Acetaminophen DMUIE76 Approved Acetaminophen increases the expression of Calmegin (CLGN). [7]
Doxorubicin DMVP5YE Approved Doxorubicin affects the expression of Calmegin (CLGN). [8]
Cupric Sulfate DMP0NFQ Approved Cupric Sulfate decreases the expression of Calmegin (CLGN). [9]
Cisplatin DMRHGI9 Approved Cisplatin increases the expression of Calmegin (CLGN). [10]
Estradiol DMUNTE3 Approved Estradiol increases the expression of Calmegin (CLGN). [11]
Quercetin DM3NC4M Approved Quercetin decreases the expression of Calmegin (CLGN). [12]
Temozolomide DMKECZD Approved Temozolomide decreases the expression of Calmegin (CLGN). [13]
Arsenic trioxide DM61TA4 Approved Arsenic trioxide decreases the expression of Calmegin (CLGN). [14]
Calcitriol DM8ZVJ7 Approved Calcitriol increases the expression of Calmegin (CLGN). [15]
Vorinostat DMWMPD4 Approved Vorinostat decreases the expression of Calmegin (CLGN). [16]
Methotrexate DM2TEOL Approved Methotrexate decreases the expression of Calmegin (CLGN). [17]
Progesterone DMUY35B Approved Progesterone decreases the expression of Calmegin (CLGN). [18]
Panobinostat DM58WKG Approved Panobinostat decreases the expression of Calmegin (CLGN). [16]
Dexamethasone DMMWZET Approved Dexamethasone decreases the expression of Calmegin (CLGN). [19]
Folic acid DMEMBJC Approved Folic acid increases the expression of Calmegin (CLGN). [20]
Azathioprine DMMZSXQ Approved Azathioprine decreases the expression of Calmegin (CLGN). [17]
Ethanol DMDRQZU Approved Ethanol increases the expression of Calmegin (CLGN). [21]
Irinotecan DMP6SC2 Approved Irinotecan increases the expression of Calmegin (CLGN). [22]
Piroxicam DMTK234 Approved Piroxicam decreases the expression of Calmegin (CLGN). [17]
Lucanthone DMZLBUO Approved Lucanthone decreases the expression of Calmegin (CLGN). [23]
Clorgyline DMCEUJD Approved Clorgyline increases the expression of Calmegin (CLGN). [24]
Bicalutamide DMZMSPF Approved Bicalutamide increases the expression of Calmegin (CLGN). [25]
Prednisolone DMQ8FR2 Approved Prednisolone decreases the expression of Calmegin (CLGN). [17]
Methylprednisolone DM4BDON Approved Methylprednisolone decreases the expression of Calmegin (CLGN). [17]
Ampicillin DMHWE7P Approved Ampicillin decreases the expression of Calmegin (CLGN). [12]
Dihydrotestosterone DM3S8XC Phase 4 Dihydrotestosterone increases the expression of Calmegin (CLGN). [26]
SNDX-275 DMH7W9X Phase 3 SNDX-275 increases the expression of Calmegin (CLGN). [27]
(+)-JQ1 DM1CZSJ Phase 1 (+)-JQ1 increases the expression of Calmegin (CLGN). [28]
Leflunomide DMR8ONJ Phase 1 Trial Leflunomide increases the expression of Calmegin (CLGN). [29]
Bisphenol A DM2ZLD7 Investigative Bisphenol A increases the expression of Calmegin (CLGN). [30]
Trichostatin A DM9C8NX Investigative Trichostatin A decreases the expression of Calmegin (CLGN). [4]
Formaldehyde DM7Q6M0 Investigative Formaldehyde increases the expression of Calmegin (CLGN). [31]
Sulforaphane DMQY3L0 Investigative Sulforaphane increases the expression of Calmegin (CLGN). [32]
OXYQUINOLINE DMZVS9Y Investigative OXYQUINOLINE decreases the expression of Calmegin (CLGN). [12]
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⏷ Show the Full List of 37 Drug(s)

References

1 Heritable methylation marks associated with breast and prostate cancer risk.Prostate. 2018 Sep;78(13):962-969. doi: 10.1002/pros.23654. Epub 2018 May 29.
2 Genomic and expression profiling of human spermatocytic seminomas: primary spermatocyte as tumorigenic precursor and DMRT1 as candidate chromosome 9 gene.Cancer Res. 2006 Jan 1;66(1):290-302. doi: 10.1158/0008-5472.CAN-05-2936.
3 Soy Foods Might Weaken the Sensitivity of Tamoxifen in Premenopausal Patients With Lumina A Subtype of Breast Cancer.Clin Breast Cancer. 2019 Apr;19(2):e337-e342. doi: 10.1016/j.clbc.2018.12.003. Epub 2018 Dec 12.
4 From transient transcriptome responses to disturbed neurodevelopment: role of histone acetylation and methylation as epigenetic switch between reversible and irreversible drug effects. Arch Toxicol. 2014 Jul;88(7):1451-68.
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 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.
7 Multiple microRNAs function as self-protective modules in acetaminophen-induced hepatotoxicity in humans. Arch Toxicol. 2018 Feb;92(2):845-858.
8 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.
9 Physiological and toxicological transcriptome changes in HepG2 cells exposed to copper. Physiol Genomics. 2009 Aug 7;38(3):386-401.
10 Low doses of cisplatin induce gene alterations, cell cycle arrest, and apoptosis in human promyelocytic leukemia cells. Biomark Insights. 2016 Aug 24;11:113-21.
11 Long-term estrogen exposure promotes carcinogen bioactivation, induces persistent changes in gene expression, and enhances the tumorigenicity of MCF-7 human breast cancer cells. Toxicol Appl Pharmacol. 2009 Nov 1;240(3):355-66.
12 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.
13 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.
14 Classification of heavy-metal toxicity by human DNA microarray analysis. Environ Sci Technol. 2007 May 15;41(10):3769-74.
15 Large-scale in silico and microarray-based identification of direct 1,25-dihydroxyvitamin D3 target genes. Mol Endocrinol. 2005 Nov;19(11):2685-95.
16 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.
17 Antirheumatic drug response signatures in human chondrocytes: potential molecular targets to stimulate cartilage regeneration. Arthritis Res Ther. 2009;11(1):R15.
18 Endometrial receptivity is affected in women with high circulating progesterone levels at the end of the follicular phase: a functional genomics analysis. Hum Reprod. 2011 Jul;26(7):1813-25.
19 Identification of mechanisms of action of bisphenol a-induced human preadipocyte differentiation by transcriptional profiling. Obesity (Silver Spring). 2014 Nov;22(11):2333-43.
20 Impact of extracellular folate levels on global gene expression. Mol Pharmacol. 2001 Dec;60(6):1288-95. doi: 10.1124/mol.60.6.1288.
21 Gene expression signatures after ethanol exposure in differentiating embryoid bodies. Toxicol In Vitro. 2018 Feb;46:66-76.
22 Clinical determinants of response to irinotecan-based therapy derived from cell line models. Clin Cancer Res. 2008 Oct 15;14(20):6647-55.
23 Lucanthone is a novel inhibitor of autophagy that induces cathepsin D-mediated apoptosis. J Biol Chem. 2011 Feb 25;286(8):6602-13.
24 Anti-oncogenic and pro-differentiation effects of clorgyline, a monoamine oxidase A inhibitor, on high grade prostate cancer cells. BMC Med Genomics. 2009 Aug 20;2:55. doi: 10.1186/1755-8794-2-55.
25 Microarray analysis of bicalutamide action on telomerase activity, p53 pathway and viability of prostate carcinoma cell lines. J Pharm Pharmacol. 2005 Jan;57(1):83-92.
26 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.
27 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.
28 Targeting MYCN in neuroblastoma by BET bromodomain inhibition. Cancer Discov. 2013 Mar;3(3):308-23.
29 Endoplasmic reticulum stress and MAPK signaling pathway activation underlie leflunomide-induced toxicity in HepG2 Cells. Toxicology. 2017 Dec 1;392:11-21.
30 Bisphenolic compounds alter gene expression in MCF-7 cells through interaction with estrogen receptor . Toxicol Appl Pharmacol. 2020 Jul 15;399:115030. doi: 10.1016/j.taap.2020.115030. Epub 2020 May 6.
31 Characterization of formaldehyde's genotoxic mode of action by gene expression analysis in TK6 cells. Arch Toxicol. 2013 Nov;87(11):1999-2012.
32 Transcriptome and DNA methylation changes modulated by sulforaphane induce cell cycle arrest, apoptosis, DNA damage, and suppression of proliferation in human liver cancer cells. Food Chem Toxicol. 2020 Feb;136:111047. doi: 10.1016/j.fct.2019.111047. Epub 2019 Dec 12.
33 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.