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

DOT Name Serpin B5 (SERPINB5)
Synonyms Maspin; Peptidase inhibitor 5; PI-5
Gene Name SERPINB5
UniProt ID
SPB5_HUMAN
3D Structure
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2D Sequence (FASTA)
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3D Structure (PDB)
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PDB ID
1WZ9; 1XQG; 1XQJ; 1XU8
Pfam ID
PF00079
Sequence
MDALQLANSAFAVDLFKQLCEKEPLGNVLFSPICLSTSLSLAQVGAKGDTANEIGQVLHF
ENVKDVPFGFQTVTSDVNKLSSFYSLKLIKRLYVDKSLNLSTEFISSTKRPYAKELETVD
FKDKLEETKGQINNSIKDLTDGHFENILADNSVNDQTKILVVNAAYFVGKWMKKFSESET
KECPFRVNKTDTKPVQMMNMEATFCMGNIDSINCKIIELPFQNKHLSMFILLPKDVEDES
TGLEKIEKQLNSESLSQWTNPSTMANAKVKLSIPKFKVEKMIDPKACLENLGLKHIFSED
TSDFSGMSETKGVALSNVIHKVCLEITEDGGDSIEVPGARILQHKDELNADHPFIYIIRH
NKTRNIIFFGKFCSP
Function
Tumor suppressor. It blocks the growth, invasion, and metastatic properties of mammary tumors. As it does not undergo the S (stressed) to R (relaxed) conformational transition characteristic of active serpins, it exhibits no serine protease inhibitory activity.
Tissue Specificity Normal mammary epithelial cells.
KEGG Pathway
p53 sig.ling pathway (hsa04115 )
MicroR.s in cancer (hsa05206 )

Molecular Interaction Atlas (MIA) of This DOT

Molecular Interaction Atlas (MIA) Jump to Detail Molecular Interaction Atlas of This DOT
This DOT Affected the Drug Response of 2 Drug(s)
Drug Name Drug ID Highest Status Interaction REF
Arsenic trioxide DM61TA4 Approved Serpin B5 (SERPINB5) decreases the response to substance of Arsenic trioxide. [24]
Deoxycholic acid DM3GYAL Approved Serpin B5 (SERPINB5) decreases the response to substance of Deoxycholic acid. [25]
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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 increases the methylation of Serpin B5 (SERPINB5). [1]
Decitabine DMQL8XJ Approved Decitabine decreases the methylation of Serpin B5 (SERPINB5). [8]
Bisphenol A DM2ZLD7 Investigative Bisphenol A increases the methylation of Serpin B5 (SERPINB5). [19]
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22 Drug(s) Affected the Gene/Protein Processing of This DOT
Drug Name Drug ID Highest Status Interaction REF
Cisplatin DMRHGI9 Approved Cisplatin increases the expression of Serpin B5 (SERPINB5). [2]
Estradiol DMUNTE3 Approved Estradiol increases the expression of Serpin B5 (SERPINB5). [3]
Arsenic DMTL2Y1 Approved Arsenic increases the expression of Serpin B5 (SERPINB5). [4]
Hydrogen peroxide DM1NG5W Approved Hydrogen peroxide increases the expression of Serpin B5 (SERPINB5). [5]
Calcitriol DM8ZVJ7 Approved Calcitriol increases the expression of Serpin B5 (SERPINB5). [6]
Methotrexate DM2TEOL Approved Methotrexate increases the expression of Serpin B5 (SERPINB5). [7]
Menadione DMSJDTY Approved Menadione increases the expression of Serpin B5 (SERPINB5). [5]
Fluorouracil DMUM7HZ Approved Fluorouracil increases the expression of Serpin B5 (SERPINB5). [9]
Aspirin DM672AH Approved Aspirin increases the expression of Serpin B5 (SERPINB5). [10]
Cidofovir DMA13GD Approved Cidofovir increases the expression of Serpin B5 (SERPINB5). [11]
Adefovir dipivoxil DMMAWY1 Approved Adefovir dipivoxil increases the expression of Serpin B5 (SERPINB5). [11]
2-deoxyglucose DMIAHVU Approved 2-deoxyglucose increases the expression of Serpin B5 (SERPINB5). [12]
Resveratrol DM3RWXL Phase 3 Resveratrol increases the expression of Serpin B5 (SERPINB5). [13]
Epigallocatechin gallate DMCGWBJ Phase 3 Epigallocatechin gallate increases the expression of Serpin B5 (SERPINB5). [14]
Curcumin DMQPH29 Phase 3 Curcumin increases the expression of Serpin B5 (SERPINB5). [15]
Tanespimycin DMNLQHK Phase 2 Tanespimycin increases the expression of Serpin B5 (SERPINB5). [16]
Benzo(a)pyrene DMN7J43 Phase 1 Benzo(a)pyrene increases the expression of Serpin B5 (SERPINB5). [17]
(+)-JQ1 DM1CZSJ Phase 1 (+)-JQ1 decreases the expression of Serpin B5 (SERPINB5). [18]
Formaldehyde DM7Q6M0 Investigative Formaldehyde decreases the expression of Serpin B5 (SERPINB5). [20]
chloropicrin DMSGBQA Investigative chloropicrin affects the expression of Serpin B5 (SERPINB5). [21]
[3H]methyltrienolone DMTSGOW Investigative [3H]methyltrienolone decreases the expression of Serpin B5 (SERPINB5). [22]
4-hydroxy-2-nonenal DM2LJFZ Investigative 4-hydroxy-2-nonenal decreases the expression of Serpin B5 (SERPINB5). [23]
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⏷ Show the Full List of 22 Drug(s)

References

1 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.
2 The thioxotriazole copper(II) complex A0 induces endoplasmic reticulum stress and paraptotic death in human cancer cells. J Biol Chem. 2009 Sep 4;284(36):24306-19.
3 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.
4 Genome-wide analysis of BEAS-2B cells exposed to trivalent arsenicals and dimethylthioarsinic acid. Toxicology. 2010 Jan 31;268(1-2):31-9.
5 Gene expression after treatment with hydrogen peroxide, menadione, or t-butyl hydroperoxide in breast cancer cells. Cancer Res. 2002 Nov 1;62(21):6246-54.
6 Identification of vitamin D3 target genes in human breast cancer tissue. J Steroid Biochem Mol Biol. 2016 Nov;164:90-97.
7 Functional gene expression profile underlying methotrexate-induced senescence in human colon cancer cells. Tumour Biol. 2011 Oct;32(5):965-76.
8 Effects of 5-Aza-CdR on cell proliferation of breast cancer cell line MDA-MB-435S and expression of maspin gene. J Huazhong Univ Sci Technolog Med Sci. 2007 Oct;27(5):543-6. doi: 10.1007/s11596-007-0517-z.
9 Apoptosis, cell cycle progression and gene expression in TP53-depleted HCT116 colon cancer cells in response to short-term 5-fluorouracil treatment. Int J Oncol. 2007 Dec;31(6):1491-500.
10 Restoration by aspirin of impaired plasma maspin level in human breast cancer. Acta Oncol. 2006;45(2):184-7. doi: 10.1080/02841860500516584.
11 Transcriptomics hit the target: monitoring of ligand-activated and stress response pathways for chemical testing. Toxicol In Vitro. 2015 Dec 25;30(1 Pt A):7-18.
12 IKK inibition by a glucosamine derivative enhances Maspin expression in osteosarcoma cell line. Chem Biol Interact. 2017 Jan 25;262:19-28. doi: 10.1016/j.cbi.2016.12.005. Epub 2016 Dec 6.
13 Resveratrol reduces prostate cancer growth and metastasis by inhibiting the Akt/MicroRNA-21 pathway. PLoS One. 2012;7(12):e51655. doi: 10.1371/journal.pone.0051655. Epub 2012 Dec 13.
14 Mechanisms of DNA methyltransferase-inhibitor interactions: Procyanidin B2 shows new promise for therapeutic intervention of cancer. Chem Biol Interact. 2015 May 25;233:122-38. doi: 10.1016/j.cbi.2015.03.022. Epub 2015 Mar 31.
15 [Up-regulates the expression of maspin gene in prostate cancer cell line LNCaP]. Yao Xue Xue Bao. 2006 Dec;41(12):1152-6.
16 Candidate therapeutic agents for hepatocellular cancer can be identified from phenotype-associated gene expression signatures. Cancer. 2009 Aug 15;115(16):3738-48. doi: 10.1002/cncr.24417.
17 Identification of a transcriptomic signature of food-relevant genotoxins in human HepaRG hepatocarcinoma cells. Food Chem Toxicol. 2020 Jun;140:111297. doi: 10.1016/j.fct.2020.111297. Epub 2020 Mar 28.
18 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.
19 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.
20 Regulation of chromatin assembly and cell transformation by formaldehyde exposure in human cells. Environ Health Perspect. 2017 Sep 21;125(9):097019.
21 Transcriptomic analysis of human primary bronchial epithelial cells after chloropicrin treatment. Chem Res Toxicol. 2015 Oct 19;28(10):1926-35.
22 Evaluation of an in vitro model of androgen ablation and identification of the androgen responsive proteome in LNCaP cells. Proteomics. 2007 Jan;7(1):47-63.
23 Microarray analysis of H2O2-, HNE-, or tBH-treated ARPE-19 cells. Free Radic Biol Med. 2002 Nov 15;33(10):1419-32.
24 The NRF2-mediated oxidative stress response pathway is associated with tumor cell resistance to arsenic trioxide across the NCI-60 panel. BMC Med Genomics. 2010 Aug 13;3:37. doi: 10.1186/1755-8794-3-37.
25 Development and molecular characterization of HCT-116 cell lines resistant to the tumor promoter and multiple stress-inducer, deoxycholate. Carcinogenesis. 2002 Dec;23(12):2063-80. doi: 10.1093/carcin/23.12.2063.