General Information of Drug Transporter (DT)
DT ID DTD0105 Transporter Info
Gene Name SLC16A14
Transporter Name Monocarboxylate transporter 14
Gene ID
151473
UniProt ID
Q7RTX9
Exogenous factors (drugs, dietary constituents, etc.) Modulation of This DT (EGM)

Chemical Compound

  DT Modulation1

Testosterone co-treated with Calcitriol results in decreased expression of SLC16A14 mRNA [1]

Regulation Mechanism

Transcription Factor Info

  DT Modulation1

Testosterone co-treated with Calcitriol results in decreased expression of SLC16A14 mRNA [1]

Regulation Mechanism

Transcription Factor Info

  DT Modulation1

NOG protein co-treated with Panobinostat co-treated with dorsomorphin co-treated with 4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide results in decreased expression of SLC16A14 mRNA [15]

Regulation Mechanism

Transcription Factor Info

  DT Modulation1

Estradiol co-treated with TGFB1 protein results in decreased expression of SLC16A14 mRNA [34]

Regulation Mechanism

Transcription Factor Info

  DT Modulation1

Valproic Acid affects the expression of SLC16A14 mRNA [41]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

Valproic Acid results in increased expression of SLC16A14 mRNA [40]

Regulation Mechanism

Transcription Factor Info

  DT Modulation1

Gasoline co-treated with Ethanol results in increased abundance of Particulate Matter co-treated with Polycyclic Aromatic Hydrocarbons which results in decreased expression of SLC16A14 mRNA [25]

Regulation Mechanism

Transcription Factor Info

  1-Butanol

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Gasoline co-treated with 1-Butanol results in increased abundance of Particulate Matter co-treated with Polycyclic Aromatic Hydrocarbons which results in decreased expression of SLC16A14 mRNA [25]

Regulation Mechanism

Transcription Factor Info

  1-Methyl-4-phenylpyridinium

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

1-Methyl-4-phenylpyridinium results in increased expression of SLC16A14 mRNA [13]

Regulation Mechanism

Transcription Factor Info

  2,5,2',5'-tetrachlorobiphenyl

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

2,5,2',5'-tetrachlorobiphenyl analog results in increased expression of SLC16A14 mRNA [26]

Regulation Mechanism

Transcription Factor Info

  4-(4-((5-(4,5-dimethyl-2-nitrophenyl)-2-furanyl)methylene)-4,5-dihydro-3-methyl-5-oxo-1H-pyrazol-1-yl)benzoic acid

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

4-(4-((5-(4,5-dimethyl-2-nitrophenyl)-2-furanyl)methylene)-4,5-dihydro-3-methyl-5-oxo-1H-pyrazol-1-yl)benzoic acid results in increased expression of SLC16A14 mRNA [14]

Regulation Mechanism

Transcription Factor Info

  4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide

           4 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

NOG protein co-treated with belinostat co-treated with dorsomorphin co-treated with 4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide results in decreased expression of SLC16A14 mRNA [15]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

NOG protein co-treated with entinostat co-treated with dorsomorphin co-treated with 4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide results in decreased expression of SLC16A14 mRNA [15]

Regulation Mechanism

Transcription Factor Info

  DT Modulation3

NOG protein co-treated with Panobinostat co-treated with dorsomorphin co-treated with 4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide results in decreased expression of SLC16A14 mRNA [15]

Regulation Mechanism

Transcription Factor Info

  DT Modulation4

NOG protein co-treated with trichostatin A co-treated with dorsomorphin co-treated with 4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide results in decreased expression of SLC16A14 mRNA [15]

Regulation Mechanism

Transcription Factor Info

  7,8-Dihydro-7,8-dihydroxybenzo(a)pyrene 9,10-oxide

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

7,8-Dihydro-7,8-dihydroxybenzo(a)pyrene 9,10-oxide results in decreased expression of SLC16A14 mRNA [27]

Regulation Mechanism

Transcription Factor Info

  belinostat

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

belinostat results in decreased expression of SLC16A14 mRNA [4]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

NOG protein co-treated with belinostat co-treated with dorsomorphin co-treated with 4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide results in decreased expression of SLC16A14 mRNA [15]

Regulation Mechanism

Transcription Factor Info

  bisphenol A

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

bisphenol A results in increased expression of SLC16A14 mRNA [18]

Regulation Mechanism

Transcription Factor Info

  CGP 52608

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

CGP 52608 promotes the reaction RORA protein binds to SLC16A14 gene [31]

Regulation Mechanism

Transcription Factor Info

  Copper

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

NSC 689534 binds to Copper which results in decreased expression of SLC16A14 mRNA [32]

Regulation Mechanism

Transcription Factor Info

  cupric chloride

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

cupric chloride results in decreased expression of SLC16A14 mRNA [33]

Regulation Mechanism

Transcription Factor Info

  Dichlorodiphenyl Dichloroethylene

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Dichlorodiphenyl Dichloroethylene results in increased expression of SLC16A14 mRNA [33]

Regulation Mechanism

Transcription Factor Info

  dorsomorphin

           4 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

NOG protein co-treated with belinostat co-treated with dorsomorphin co-treated with 4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide results in decreased expression of SLC16A14 mRNA [15]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

NOG protein co-treated with entinostat co-treated with dorsomorphin co-treated with 4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide results in decreased expression of SLC16A14 mRNA [15]

Regulation Mechanism

Transcription Factor Info

  DT Modulation3

NOG protein co-treated with Panobinostat co-treated with dorsomorphin co-treated with 4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide results in decreased expression of SLC16A14 mRNA [15]

Regulation Mechanism

Transcription Factor Info

  DT Modulation4

NOG protein co-treated with trichostatin A co-treated with dorsomorphin co-treated with 4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide results in decreased expression of SLC16A14 mRNA [15]

Regulation Mechanism

Transcription Factor Info

  entinostat

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

entinostat results in decreased expression of SLC16A14 mRNA [4]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

NOG protein co-treated with entinostat co-treated with dorsomorphin co-treated with 4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide results in decreased expression of SLC16A14 mRNA [15]

Regulation Mechanism

Transcription Factor Info

  Gasoline

           3 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Gasoline co-treated with 1-Butanol results in increased abundance of Particulate Matter co-treated with Polycyclic Aromatic Hydrocarbons which results in decreased expression of SLC16A14 mRNA [25]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

Gasoline co-treated with Ethanol results in increased abundance of Particulate Matter co-treated with Polycyclic Aromatic Hydrocarbons which results in decreased expression of SLC16A14 mRNA [25]

Regulation Mechanism

Transcription Factor Info

  DT Modulation3

Gasoline results in increased abundance of Particulate Matter co-treated with Polycyclic Aromatic Hydrocarbons which results in decreased expression of SLC16A14 mRNA [25]

Regulation Mechanism

Transcription Factor Info

  ICG 001

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

ICG 001 results in increased expression of SLC16A14 mRNA [14]

Regulation Mechanism

Transcription Factor Info

  Manganese

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

manganese chloride results in increased abundance of Manganese which results in increased expression of SLC16A14 mRNA [30]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

sodium arsenite results in increased abundance of Arsenic co-treated with manganese chloride results in increased abundance of Manganese results in increased expression of SLC16A14 mRNA [30]

Regulation Mechanism

Transcription Factor Info

  manganese chloride

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

manganese chloride results in increased abundance of Manganese which results in increased expression of SLC16A14 mRNA [30]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

sodium arsenite results in increased abundance of Arsenic co-treated with manganese chloride results in increased abundance of Manganese results in increased expression of SLC16A14 mRNA [30]

Regulation Mechanism

Transcription Factor Info

  methylmercuric chloride

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

methylmercuric chloride results in increased expression of SLC16A14 mRNA [12]

Regulation Mechanism

Transcription Factor Info

  Methyl Methanesulfonate

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Methyl Methanesulfonate results in decreased expression of SLC16A14 mRNA [2]

Regulation Mechanism

Transcription Factor Info

  Niclosamide

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Niclosamide results in increased expression of SLC16A14 mRNA [36]

Regulation Mechanism

Transcription Factor Info

  NSC 689534

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

NSC 689534 binds to Copper which results in decreased expression of SLC16A14 mRNA [32]

Regulation Mechanism

Transcription Factor Info

  Ozone

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Air Pollutants results in increased abundance of Ozone which affects the expression of SLC16A14 mRNA [37]

Regulation Mechanism

Transcription Factor Info

  potassium chromate(VI)

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

potassium chromate(VI) results in decreased expression of SLC16A14 mRNA [38]

Regulation Mechanism

Transcription Factor Info

  S-(1,2-dichlorovinyl)cysteine

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

S-(1,2-dichlorovinyl)cysteine affects the susceptibility to Lipopolysaccharides which results in increased expression of SLC16A14 mRNA [39]

Regulation Mechanism

Transcription Factor Info

  sodium arsenite

           4 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

sodium arsenite results in decreased expression of SLC16A14 mRNA [33]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

sodium arsenite results in increased abundance of Arsenic co-treated with manganese chloride results in increased abundance of Manganese results in increased expression of SLC16A14 mRNA [30]

Regulation Mechanism

Transcription Factor Info

  DT Modulation3

sodium arsenite results in increased abundance of Arsenic which results in increased expression of SLC16A14 mRNA [30]

Regulation Mechanism

Transcription Factor Info

  DT Modulation4

sodium arsenite results in increased expression of SLC16A14 mRNA [23]

Regulation Mechanism

Transcription Factor Info

  sulforaphane

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

sulforaphane results in increased expression of SLC16A14 mRNA [22]

Regulation Mechanism

Transcription Factor Info

  Tetrachlorodibenzodioxin

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Tetrachlorodibenzodioxin results in decreased expression of SLC16A14 mRNA [17]

Regulation Mechanism

Transcription Factor Info

  Thiram

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Thiram results in decreased expression of SLC16A14 mRNA [33]

Regulation Mechanism

Transcription Factor Info

  trichostatin A

           3 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

NOG protein co-treated with trichostatin A co-treated with dorsomorphin co-treated with 4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide results in decreased expression of SLC16A14 mRNA [15]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

trichostatin A results in decreased expression of SLC16A14 mRNA [40]

Regulation Mechanism

Transcription Factor Info

  DT Modulation3

trichostatin A results in increased expression of SLC16A14 mRNA [40]

Regulation Mechanism

Transcription Factor Info

Mycotoxins

  Aflatoxin B1

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Aflatoxin B1 results in increased methylation of SLC16A14 intron [28]

Regulation Mechanism

Transcription Factor Info

Drug Withdrawn

  Fenfluramine

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Fenfluramine results in decreased expression of SLC16A14 mRNA [35]

Regulation Mechanism

Transcription Factor Info

Approved Drug

  Calcitriol

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Calcitriol inhibits the expression of SLC16A14 [1]

  Testosterone

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Testosterone inhibits the expression of SLC16A14 [1]

  Vincristine

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Vincristine inhibits the expression of SLC16A14 [2]

  Zoledronic Acid

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Zoledronic Acid inhibits the expression of SLC16A14 [3]

  Belinostat

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Belinostat inhibits the expression of SLC16A14 [4]

  Panobinostat

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Panobinostat inhibits the expression of SLC16A14 [4]

  Cyclosporine

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Cyclosporine inhibits the expression of SLC16A14 [5]

  Leflunomide

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Leflunomide increases the expression of SLC16A14 [6]

  Sunitinib

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Sunitinib inhibits the expression of SLC16A14 [8]

  Estradiol

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Estradiol increases the expression of SLC16A14 [9]

  Temozolomide

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Temozolomide inhibits the expression of SLC16A14 [10]

  Tretinoin

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Tretinoin inhibits the expression of SLC16A14 [11]

  Valproic Acid

           3 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Valproic Acid inhibits the expression of SLC16A14 [12]

Drug Marketed but not Approved by US FDA

  Demecolcine

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Demecolcine inhibits the expression of SLC16A14 [2]

  Rotenone

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Rotenone increases the expression of SLC16A14 [7]

Drug in Phase 3 Trial

  Sulforafan

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Sulforafan increases the expression of SLC16A14 [22]

Drug in Phase 2 Trial

  MS-275

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

MS-275 inhibits the expression of SLC16A14 [4]

  Bisphenol A

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Bisphenol A increases the expression of SLC16A14 [18]

  Ethanol

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Ethanol increases the expression of SLC16A14 [20]

Drug in Phase 1 Trial

  Sodium arsenite

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Sodium arsenite increases the expression of SLC16A14 [23]

  Trichostatin A

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Trichostatin A inhibits the expression of SLC16A14 [4]

Drug in Preclinical Test

  (+)-JQ1

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

(+)-JQ1 inhibits the expression of SLC16A14 [16]

Patented Pharmaceutical Agent

  ICG-001

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

ICG-001 increases the expression of SLC16A14 [14]

Natural Product

  Particulate Matter

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Particulate Matter increases the expression of SLC16A14 [19]

  Tobacco Smoke Pollution

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Tobacco Smoke Pollution inhibits the expression of SLC16A14 [24]

Environmental toxicant

  Polychlorinated dibenzodioxin

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Polychlorinated dibenzodioxin inhibits the expression of SLC16A14 [17]

Acute Toxic Substance

  Formaldehyde

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Formaldehyde inhibits the expression of SLC16A14 [2]

  Thimerosal

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Thimerosal increases the expression of SLC16A14 [15]

Carcinogen

  Ethyl Methanesulfonate

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Ethyl Methanesulfonate inhibits the expression of SLC16A14 [2]

  Arsenic

           3 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Arsenic affects the methylation of SLC16A14 gene [29]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

sodium arsenite results in increased abundance of Arsenic co-treated with manganese chloride results in increased abundance of Manganese results in increased expression of SLC16A14 mRNA [30]

Regulation Mechanism

Transcription Factor Info

  DT Modulation3

sodium arsenite results in increased abundance of Arsenic which results in increased expression of SLC16A14 mRNA [30]

Regulation Mechanism

Transcription Factor Info

Health and Environmental Toxicant

  1-methyl-4-phenylpyridinium

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

1-methyl-4-phenylpyridinium increases the expression of SLC16A14 [13]

  Diethylhexyl Phthalate

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Diethylhexyl Phthalate inhibits the expression of SLC16A14 [21]
References
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3 Interleukin-19 as a translational indicator of renal injury. Arch Toxicol. 2015 Jan;89(1):101-6.
4 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.
5 Integrative "-Omics" Analysis in Primary Human Hepatocytes Unravels Persistent Mechanisms of Cyclosporine A-Induced Cholestasis. Chem Res Toxicol. 2016 Dec 19;29(12):2164-2174.
6 Endoplasmic reticulum stress and MAPK signaling pathway activation underlie leflunomide-induced toxicity in HepG2 Cells. Toxicology. 2017 Dec 1;392:11-21.
7 Toxicity, recovery, and resilience in a 3D dopaminergic neuronal in vitro model exposed to rotenone. Arch Toxicol. 2018 Aug;92(8):2587-2606.
8 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.
9 17 beta-Estradiol Activates HSF1 via MAPK Signaling in ER alpha-Positive Breast Cancer Cells. Cancers (Basel). 2019 Oct 11;11(10):1533.
10 Temozolomide induces activation of Wnt/beta-catenin signaling in glioma cells via PI3K/Akt pathway: implications in glioma therapy. Cell Biol Toxicol. 2020 Jun;36(3):273-278.
11 Transcriptional and Metabolic Dissection of ATRA-Induced Granulocytic Differentiation in NB4 Acute Promyelocytic Leukemia Cells. Cells. 2020 Nov 5;9(11):2423.
12 Stem Cell Transcriptome Responses and Corresponding Biomarkers That Indicate the Transition from Adaptive Responses to Cytotoxicity. Chem Res Toxicol. 2017 Apr 17;30(4):905-922.
13 Transcriptional and metabolic adaptation of human neurons to the mitochondrial toxicant MPP(+). Cell Death Dis. 2014 May 8;5(5):e1222.
14 Altering cancer transcriptomes using epigenomic inhibitors. Epigenetics Chromatin. 2015 Feb 24;8:9.
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17 Comparative analysis of TCDD-induced AhR-mediated gene expression in human, mouse and rat primary B cells. Toxicol Appl Pharmacol. 2017 Feb 1;316:95-106.
18 Bisphenol A induces DSB-ATM-p53 signaling leading to cell cycle arrest, senescence, autophagy, stress response, and estrogen release in human fetal lung fibroblasts. Arch Toxicol. 2018 Apr;92(4):1453-1469.
19 Transcriptional profiling of human bronchial epithelial cell BEAS-2B exposed to diesel and biomass ultrafine particles. BMC Genomics. 2018 Apr 27;19(1):302.
20 Cardiac Toxicity From Ethanol Exposure in Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes. Toxicol Sci. 2019 May 1;169(1):280-292.
21 Di-(2-ethylhexyl)-phthalate induces apoptosis via the PPAR Gamma/PTEN/AKT pathway in differentiated human embryonic stem cells. Food Chem Toxicol. 2019 Sep;131:110552.
22 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.
23 Dynamic alteration in miRNA and mRNA expression profiles at different stages of chronic arsenic exposure-induced carcinogenesis in a human cell culture model of skin cancer. Arch Toxicol. 2021 Jul;95(7):2351-2365.
24 Integration of transcriptome analysis with pathophysiological endpoints to evaluate cigarette smoke toxicity in an in vitro human airway tissue model. Arch Toxicol. 2021 May;95(5):1739-1761.
25 Transcriptional response to organic compounds from diverse gasoline and biogasoline fuel emissions in human lung cells. Toxicol In Vitro. 2018;48:329-341.
26 Hydroxylation markedly alters how the polychlorinated biphenyl (PCB) congener, PCB52, affects gene expression in human preadipocytes. Toxicol In Vitro. 2023;89:105568.
27 Early whole-genome transcriptional response induced by benzo[a]pyrene diol epoxide in a normal human cell line. Genomics. 2009;93(4):332-42.
28 Effect of aflatoxin B(1), benzo[a]pyrene, and methapyrilene on transcriptomic and epigenetic alterations in human liver HepaRG cells. Food Chem Toxicol. 2018;121:214-223.
29 Prenatal arsenic exposure and the epigenome: identifying sites of 5-methylcytosine alterations that predict functional changes in gene expression in newborn cord blood and subsequent birth outcomes. Toxicol Sci. 2015 Jan;143(1):97-106.
30 Using transcriptomic signatures to elucidate individual and mixture effects of inorganic arsenic and manganese in human placental trophoblast HTR-8/SVneo cells. Toxicol Sci. 2025;203(2):216-226.
31 Identification of potential target genes of ROR-alpha in THP1 and HUVEC cell lines. Exp Cell Res. 2017;353(1):6-15.
32 A copper chelate of thiosemicarbazone NSC 689534 induces oxidative/ER stress and inhibits tumor growth in vitro and in vivo. Free Radic Biol Med. 2011 Jan 1;50(1):110-21.
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