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

DOT Name Galectin-12 (LGALS12)
Synonyms Gal-12; Galectin-related inhibitor of proliferation
Gene Name LGALS12
Related Disease
Colorectal carcinoma ( )
Obesity ( )
Promyelocytic leukaemia ( )
Acute myelogenous leukaemia ( )
UniProt ID
LEG12_HUMAN
3D Structure
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2D Sequence (FASTA)
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3D Structure (PDB)
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Pfam ID
PF00337
Sequence
MSQPSGGRAPGTRIYSWSCPTVMSPGEKLDPIPDSFILQPPVFHPVVPYVTTIFGGLHAG
KMVMLQGVVPLDAHRFQVDFQCGCSLCPRPDIAFHFNPRFHTTKPHVICNTLHGGRWQRE
ARWPHLALRRGSSFLILFLFGNEEVKVSVNGQHFLHFRYRLPLSHVDTLGIFGDILVEAV
GFLNINPFVEGSREYPAGHPFLLMSPRLEVPCSHALPQGLSPGQVIIVRGLVLQEPKHFT
VSLRDQAAHAPVTLRASFADRTLAWISRWGQKKLISAPFLFYPQRFFEVLLLFQEGGLKL
ALNGQGLGATSMNQQALEQLRELRISGSVQLYCVHS
Function Binds lactose. May participate in the apoptosis of adipocytes.
Tissue Specificity Not widely expressed. Predominantly expressed in adipose tissue.

Molecular Interaction Atlas (MIA) of This DOT

4 Disease(s) Related to This DOT
Disease Name Disease ID Evidence Level Mode of Inheritance REF
Colorectal carcinoma DIS5PYL0 Strong Altered Expression [1]
Obesity DIS47Y1K Strong Altered Expression [2]
Promyelocytic leukaemia DISYGG13 Strong Biomarker [3]
Acute myelogenous leukaemia DISCSPTN Disputed Altered Expression [3]
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Molecular Interaction Atlas (MIA) Jump to Detail Molecular Interaction Atlas of This DOT
6 Drug(s) Affected the Gene/Protein Processing of This DOT
Drug Name Drug ID Highest Status Interaction REF
Tretinoin DM49DUI Approved Tretinoin increases the expression of Galectin-12 (LGALS12). [4]
Cisplatin DMRHGI9 Approved Cisplatin increases the expression of Galectin-12 (LGALS12). [5]
Dexamethasone DMMWZET Approved Dexamethasone increases the expression of Galectin-12 (LGALS12). [6]
(+)-JQ1 DM1CZSJ Phase 1 (+)-JQ1 decreases the expression of Galectin-12 (LGALS12). [8]
Bisphenol A DM2ZLD7 Investigative Bisphenol A increases the expression of Galectin-12 (LGALS12). [9]
Sulforaphane DMQY3L0 Investigative Sulforaphane increases the expression of Galectin-12 (LGALS12). [10]
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⏷ Show the Full List of 6 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 Galectin-12 (LGALS12). [7]
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References

1 Analyzing epigenetic control of galectin expression indicates silencing of galectin-12 by promoter methylation in colorectal cancer.IUBMB Life. 2017 Dec;69(12):962-970. doi: 10.1002/iub.1690. Epub 2017 Nov 3.
2 Allyl Isothiocyanate Ameliorates Obesity by Inhibiting Galectin-12.Mol Nutr Food Res. 2018 Mar;62(6):e1700616. doi: 10.1002/mnfr.201700616. Epub 2018 Mar 12.
3 Galectin-12 inhibits granulocytic differentiation of human NB4 promyelocytic leukemia cells while promoting lipogenesis.J Leukoc Biol. 2016 Oct;100(4):657-664. doi: 10.1189/jlb.1HI0316-134R. Epub 2016 Jun 2.
4 Transcriptional and Metabolic Dissection of ATRA-Induced Granulocytic Differentiation in NB4 Acute Promyelocytic Leukemia Cells. Cells. 2020 Nov 5;9(11):2423. doi: 10.3390/cells9112423.
5 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.
6 Identification of mechanisms of action of bisphenol a-induced human preadipocyte differentiation by transcriptional profiling. Obesity (Silver Spring). 2014 Nov;22(11):2333-43.
7 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.
8 Highly active combination of BRD4 antagonist and histone deacetylase inhibitor against human acute myelogenous leukemia cells. Mol Cancer Ther. 2014 May;13(5):1142-54.
9 Bisphenol A and bisphenol S induce distinct transcriptional profiles in differentiating human primary preadipocytes. PLoS One. 2016 Sep 29;11(9):e0163318.
10 Sulforaphane-induced apoptosis in human leukemia HL-60 cells through extrinsic and intrinsic signal pathways and altering associated genes expression assayed by cDNA microarray. Environ Toxicol. 2017 Jan;32(1):311-328.