General Information of Drug Combination (ID: DCXANDV)

Drug Combination Name
ABIRATERONE Plicamycin
Indication
Disease Entry Status REF
Malignant melanoma Investigative [1]
Component Drugs ABIRATERONE   DM8V75C Plicamycin   DM7C8YV
Small molecular drug Small molecular drug
2D MOL 2D MOL
3D MOL 3D MOL is unavailable
High-throughput Screening Result Testing Cell Line: LOX IMVI
Zero Interaction Potency (ZIP) Score: 24.77
Bliss Independence Score: 26.27
Loewe Additivity Score: 28.99
LHighest Single Agent (HSA) Score: 30.36

Molecular Interaction Atlas of This Drug Combination

Molecular Interaction Atlas (MIA)
Indication(s) of ABIRATERONE
Disease Entry ICD 11 Status REF
Prostate cancer 2C82.0 Approved [2]
ABIRATERONE Interacts with 1 DTT Molecule(s)
DTT Name DTT ID UniProt ID Mode of Action REF
Steroid 17-alpha-monooxygenase (S17AH) TTRA5BZ CP17A_HUMAN Modulator [6]
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ABIRATERONE Interacts with 4 DOT Molecule(s)
DOT Name DOT ID UniProt ID Mode of Action REF
Steroid 17-alpha-hydroxylase/17,20 lyase (CYP17A1) OTZKVLVJ CP17A_HUMAN Decreases Activity [7]
Tissue factor (F3) OT3MSU3B TF_HUMAN Increases Expression [8]
Membrane cofactor protein (CD46) OTQ8NWJD MCP_HUMAN Increases Expression [9]
Androgen receptor (AR) OTUBKAZZ ANDR_HUMAN Decreases Response To Substance [10]
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Indication(s) of Plicamycin
Disease Entry ICD 11 Status REF
Hypercalcaemia 5B91.0 Approved [3]
Testicular cancer 2C80 Approved [3]
Solid tumour/cancer 2A00-2F9Z Withdrawn from market [4]
Lung cancer 2C25.0 Investigative [5]
Ovarian cancer 2C73 Investigative [5]
Plicamycin Interacts with 1 DTT Molecule(s)
DTT Name DTT ID UniProt ID Mode of Action REF
RNA synthesis (hRNA synth) TTX2AYW NOUNIPROTAC Modulator [12]
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Plicamycin Interacts with 16 DOT Molecule(s)
DOT Name DOT ID UniProt ID Mode of Action REF
17-beta-hydroxysteroid dehydrogenase type 2 (HSD17B2) OT3K7HY5 DHB2_HUMAN Decreases Expression [13]
Cytochrome P450 1A1 (CYP1A1) OTE4EFH8 CP1A1_HUMAN Decreases Expression [14]
Aryl hydrocarbon receptor (AHR) OTFE4EYE AHR_HUMAN Decreases Expression [14]
Cytochrome P450 1B1 (CYP1B1) OTYXFLSD CP1B1_HUMAN Decreases Expression [14]
Baculoviral IAP repeat-containing protein 5 (BIRC5) OTILXZYL BIRC5_HUMAN Decreases Expression [15]
Cellular tumor antigen p53 (TP53) OTIE1VH3 P53_HUMAN Increases Activity [15]
Epoxide hydrolase 1 (EPHX1) OTBKWQER HYEP_HUMAN Decreases Expression [16]
Transcription factor Sp1 (SP1) OTISPT4X SP1_HUMAN Decreases Expression [11]
Proto-oncogene tyrosine-protein kinase Src (SRC) OTETYX40 SRC_HUMAN Decreases Expression [17]
Tissue factor (F3) OT3MSU3B TF_HUMAN Decreases Expression [18]
Tyrosine-protein kinase receptor UFO (AXL) OTKA2SUX UFO_HUMAN Decreases Expression [19]
Transcription factor Sp3 (SP3) OTYDQZ1T SP3_HUMAN Decreases Expression [11]
Induced myeloid leukemia cell differentiation protein Mcl-1 (MCL1) OT2YYI1A MCL1_HUMAN Decreases Expression [20]
Epidermal growth factor receptor kinase substrate 8 (EPS8) OTZ6ES6V EPS8_HUMAN Decreases Expression [17]
TNFAIP3-interacting protein 1 (TNIP1) OTRAOTEW TNIP1_HUMAN Decreases Expression [21]
Sphingomyelin phosphodiesterase 3 (SMPD3) OTHQBETH NSMA2_HUMAN Decreases Expression [22]
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⏷ Show the Full List of 16 DOT(s)

Test Results of This Drug Combination in Other Disease Systems

Indication DrugCom ID Cell Line Status REF
Adult acute myeloid leukemia DCM3SEG HL-60(TB) Investigative [23]
Adult T acute lymphoblastic leukemia DCLRX99 MOLT-4 Investigative [23]
Astrocytoma DCSSNM4 U251 Investigative [23]
Astrocytoma DCW9DMG SNB-19 Investigative [23]
Childhood T acute lymphoblastic leukemia DCG14QT CCRF-CEM Investigative [23]
Chronic myelogenous leukemia DCY8SRU K-562 Investigative [23]
Clear cell renal cell carcinoma DCHM91D 786-0 Investigative [23]
Clear cell renal cell carcinoma DCM9G39 A498 Investigative [23]
Clear cell renal cell carcinoma DCX3VDW TK-10 Investigative [23]
Clear cell renal cell carcinoma DC15MP5 CAKI-1 Investigative [23]
Glioblastoma DCK9BT7 SNB-75 Investigative [23]
Glioma DCWHA60 SF-295 Investigative [23]
Glioma DCUFL1V SF-539 Investigative [23]
Papillary renal cell carcinoma DCC78EE ACHN Investigative [23]
Plasma cell myeloma DCEWB22 RPMI-8226 Investigative [23]
Renal cell carcinoma DC4YK5L UO-31 Investigative [23]
Renal cell carcinoma DCUYOOI SN12C Investigative [23]
Breast adenocarcinoma DC3A52F MDA-MB-468 Investigative [24]
Carcinoma DCC0NXQ MCF7 Investigative [24]
Colon adenocarcinoma DC20TBS COLO 205 Investigative [24]
Colon carcinoma DCJIWN6 KM12 Investigative [24]
Invasive ductal carcinoma DCBCYQ1 BT-549 Investigative [24]
Invasive ductal carcinoma DCKC3D6 T-47D Investigative [24]
Invasive ductal carcinoma DCK3LOJ HS 578T Investigative [24]
Adenocarcinoma DCP4C65 DU-145 Investigative [1]
Adenocarcinoma DC08NY5 OVCAR3 Investigative [1]
Adenocarcinoma DCDKMVK HCT116 Investigative [1]
Amelanotic melanoma DCKR6JF M14 Investigative [1]
Amelanotic melanoma DCI5JL6 MDA-MB-435 Investigative [1]
Cutaneous melanoma DCXSE44 SK-MEL-28 Investigative [1]
Cutaneous melanoma DC8I3XG SK-MEL-5 Investigative [1]
High grade ovarian serous adenocarcinoma DCJ2GEH OVCAR-8 Investigative [1]
High grade ovarian serous adenocarcinoma DC0TMU8 OVCAR-4 Investigative [1]
High grade ovarian serous adenocarcinoma DCNIN8Z OVCAR-5 Investigative [1]
Large cell lung carcinoma DC4ID0K NCI-H460 Investigative [1]
Lung adenocarcinoma DCYA9D8 MDA-MB-231 Investigative [1]
Lung adenocarcinoma DC2QCZE NCI-H522 Investigative [1]
Malignant melanoma DCO7KCZ UACC62 Investigative [1]
Melanoma DCO8MWI UACC-257 Investigative [1]
Melanoma DCTAERX SK-MEL-2 Investigative [1]
Minimally invasive lung adenocarcinoma DC2TZ3Q NCI-H322M Investigative [1]
Mixed endometrioid and clear cell carcinoma DCOORA0 IGROV1 Investigative [1]
Ovarian serous cystadenocarcinoma DC088NU SK-OV-3 Investigative [1]
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⏷ Show the Full List of 43 DrugCom(s)

References

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3 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health & Human Services. 2015
4 URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Ligand id: 8394).
5 The Pluripotency Factor Musashi-2 Is a Novel Target for Lung Cancer Therapy.Ann Am Thorac Soc. 2018 Apr;15(Supplement_2):S124.
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7 A fission yeast-based test system for the determination of IC50 values of anti-prostate tumor drugs acting on CYP21. J Enzyme Inhib Med Chem. 2006 Oct;21(5):547-56.
8 Elucidating mechanisms of toxicity using phenotypic data from primary human cell systems--a chemical biology approach for thrombosis-related side effects. Int J Mol Sci. 2015 Jan 5;16(1):1008-29. doi: 10.3390/ijms16011008.
9 Targeting CD46 for both adenocarcinoma and neuroendocrine prostate cancer. JCI Insight. 2018 Sep 6;3(17):e121497. doi: 10.1172/jci.insight.121497. eCollection 2018 Sep 6.
10 Targeting chromatin binding regulation of constitutively active AR variants to overcome prostate cancer resistance to endocrine-based therapies. Nucleic Acids Res. 2015 Jul 13;43(12):5880-97. doi: 10.1093/nar/gkv262. Epub 2015 Apr 23.
11 The activity of a novel mithramycin analog is related to its binding to DNA, cellular accumulation, and inhibition of Sp1-driven gene transcription. Chem Biol Interact. 2014 Aug 5;219:123-32. doi: 10.1016/j.cbi.2014.05.019. Epub 2014 Jun 4.
12 Role of magnesium ion in mithramycin-DNA interaction: binding of mithramycin-Mg2+ complexes with DNA. Biochemistry. 1995 Jan 31;34(4):1376-85.
13 SP1 and SP3 mediate progesterone-dependent induction of the 17beta hydroxysteroid dehydrogenase type 2 gene in human endometrium. Biol Reprod. 2006 Oct;75(4):605-14.
14 Metformin suppresses CYP1A1 and CYP1B1 expression in breast cancer cells by down-regulating aryl hydrocarbon receptor expression. Toxicol Appl Pharmacol. 2014 Oct 1;280(1):138-48.
15 Molecular mechanisms of transactivation and doxorubicin-mediated repression of survivin gene in cancer cells. J Biol Chem. 2007 Jan 26;282(4):2615-25. doi: 10.1074/jbc.M606203200. Epub 2006 Nov 22.
16 Sp1 and Sp3 transcription factors regulate the basal expression of human microsomal epoxide hydrolase (EPHX1) through interaction with the E1b far upstream promoter. Gene. 2014 Feb 15;536(1):135-44. doi: 10.1016/j.gene.2013.11.053. Epub 2013 Dec 4.
17 Mithramycin inhibits human epithelial carcinoma cell proliferation and migration involving downregulation of Eps8 expression. Chem Biol Interact. 2010 Jan 5;183(1):181-6. doi: 10.1016/j.cbi.2009.09.018.
18 Asbestos induces tissue factor in Beas-2B human lung bronchial epithelial cells in vitro. Lung. 2004;182(4):251-64. doi: 10.1007/s00408-004-2507-2.
19 The human receptor tyrosine kinase Axl gene--promoter characterization and regulation of constitutive expression by Sp1, Sp3 and CpG methylation. Biosci Rep. 2008 Jun;28(3):161-76. doi: 10.1042/BSR20080046.
20 CREB/Sp1-mediated MCL1 expression and NFB-mediated ABCB1 expression modulate the cytotoxicity of daunorubicin in chronic myeloid leukemia cells. Toxicol Appl Pharmacol. 2022 Jan 15;435:115847. doi: 10.1016/j.taap.2021.115847. Epub 2021 Dec 25.
21 Sp sites contribute to basal and inducible expression of the human TNIP1 (TNF-inducible protein 3-interacting protein 1) promoter. Biochem J. 2013 Jun 15;452(3):519-29. doi: 10.1042/BJ20121666.
22 Transcriptional regulation of neutral sphingomyelinase 2 gene expression of a human breast cancer cell line, MCF-7, induced by the anti-cancer drug, daunorubicin. Biochim Biophys Acta. 2009 Nov-Dec;1789(11-12):681-90. doi: 10.1016/j.bbagrm.2009.08.006. Epub 2009 Aug 19.
23 Recurrent recessive mutation in deoxyguanosine kinase causes idiopathic noncirrhotic portal hypertension.Hepatology. 2016 Jun;63(6):1977-86. doi: 10.1002/hep.28499. Epub 2016 Mar 31.
24 Biologically active neutrophil chemokine pattern in tonsillitis.Clin Exp Immunol. 2004 Mar;135(3):511-8. doi: 10.1111/j.1365-2249.2003.02390.x.