Diethylnitrosamine (BioDeep_00000002955)

Main id: BioDeep_00000396956

 

PANOMIX_OTCML-2023


代谢物信息卡片


N-Nitrosodiethylamine (NDEA)

化学式: C4H10N2O (102.0793)
中文名称: N-二乙基亚硝胺, N-亚硝基二乙胺
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CCN(CC)N=O
InChI: InChI=1S/C4H10N2O/c1-3-6(4-2)5-7/h3-4H2,1-2H3

描述信息

CONFIDENCE standard compound; EAWAG_UCHEM_ID 3452
D009676 - Noxae > D000477 - Alkylating Agents
N-Nitrosodiethylamine (Diethylnitrosamine) is a potent hepatocarcinogenic dialkylnitrosoamine. N-Nitrosodiethylamine is mainly present in tobacco smoke, water, cheddar cheese, cured, fried meals and many alcoholic beverages. N-Nitrosodiethylamine is responsible for the changes in the nuclear enzymes associated with DNA repair/replication. N-Nitrosodiethylamine results in various tumors in all animal species. The main target organs are the nasal cavity, trachea, lung, esophagus and liver.

同义名列表

7 个代谢物同义名

N-Nitrosodiethylamine (NDEA); N-Nitrosodiethylamine; Diethylnitrosamine; NDEA; DEN; N-Nitrosodiethylamine; N-nitrosodiethylamine



数据库引用编号

19 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(0)

PlantCyc(0)

代谢反应

0 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(0)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

1 个相关的物种来源信息

在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有:

  • PubMed: 来源于PubMed文献库中的文献信息,我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表,这个列表按照代谢物同时出现的文献数量降序排序,取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
  • NCBI Taxonomy: 通过文献数据挖掘,得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序,取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
  • Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
  • Chemical Reaction: 在化学反应过程中,存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。

点击图上的相关代谢物的名称,可以跳转到相关代谢物的信息页面。

亚细胞结构定位 关联基因列表
Cytoplasm 12 EGFR, HIF1A, MAPK14, MTOR, NOS2, NQO1, ODC1, PIK3CA, PTGS2, STAT3, TLR4, VEGFA
Peripheral membrane protein 2 MTOR, PTGS2
Endosome membrane 2 EGFR, TLR4
Endoplasmic reticulum membrane 5 EGFR, HSP90B1, MTOR, PTGS2, TGFA
Nucleus 10 EGFR, HIF1A, HSP90B1, MAPK14, MET, MTOR, NOS2, NQO1, STAT3, VEGFA
cytosol 10 HIF1A, HSP90B1, KRT19, MAPK14, MTOR, NOS2, NQO1, ODC1, PIK3CA, STAT3
dendrite 2 MTOR, NQO1
nuclear body 2 HIF1A, MET
phagocytic vesicle 1 MTOR
nucleoplasm 6 HIF1A, MAPK14, MET, MTOR, NOS2, STAT3
RNA polymerase II transcription regulator complex 2 HIF1A, STAT3
Cell membrane 3 CD8A, EGFR, TLR4
Cytoplasmic side 1 MTOR
lamellipodium 1 PIK3CA
ruffle membrane 1 EGFR
Early endosome membrane 1 EGFR
Golgi apparatus membrane 1 MTOR
Synapse 1 NQO1
cell junction 1 EGFR
cell surface 5 EGFR, MET, TGFA, TLR4, VEGFA
glutamatergic synapse 2 EGFR, MAPK14
Golgi apparatus 1 VEGFA
Golgi membrane 3 EGFR, INS, MTOR
lysosomal membrane 2 EGF, MTOR
neuronal cell body 1 NQO1
postsynapse 1 MET
sarcolemma 1 KRT19
smooth endoplasmic reticulum 1 HSP90B1
Cytoplasm, cytosol 2 NOS2, NQO1
Lysosome 1 MTOR
endosome 1 EGFR
plasma membrane 11 CD8A, EGF, EGFR, IFNLR1, KRT19, MET, NOS2, PIK3CA, STAT3, TGFA, TLR4
Membrane 10 EGF, EGFR, HSP90B1, IFNLR1, MET, MTOR, NQO1, TGFA, TLR4, VEGFA
apical plasma membrane 1 EGFR
basolateral plasma membrane 2 EGFR, TGFA
caveola 1 PTGS2
extracellular exosome 3 EGF, HSP90B1, KRT19
Lysosome membrane 1 MTOR
endoplasmic reticulum 3 HSP90B1, PTGS2, VEGFA
extracellular space 5 EGF, EGFR, INS, TGFA, VEGFA
perinuclear region of cytoplasm 6 EGFR, HSP90B1, NOS2, PIK3CA, TGFA, TLR4
adherens junction 1 VEGFA
apicolateral plasma membrane 1 KRT19
intercalated disc 1 PIK3CA
mitochondrion 1 MAPK14
protein-containing complex 4 EGFR, HIF1A, HSP90B1, PTGS2
Microsome membrane 2 MTOR, PTGS2
TORC1 complex 1 MTOR
TORC2 complex 1 MTOR
Single-pass type I membrane protein 4 CD8A, EGFR, IFNLR1, TLR4
Secreted 2 INS, VEGFA
extracellular region 8 CD8A, EGF, HSP90B1, INS, MAPK14, MET, TGFA, VEGFA
Mitochondrion outer membrane 1 MTOR
Single-pass membrane protein 1 MET
mitochondrial outer membrane 1 MTOR
[Isoform 2]: Secreted 1 CD8A
transcription regulator complex 1 STAT3
motile cilium 1 HIF1A
nuclear membrane 1 EGFR
external side of plasma membrane 2 CD8A, TLR4
Secreted, extracellular space, extracellular matrix 1 VEGFA
Z disc 1 KRT19
cytoplasmic vesicle 1 TGFA
axon cytoplasm 1 HIF1A
midbody 1 HSP90B1
Cytoplasm, P-body 1 NOS2
P-body 1 NOS2
Early endosome 1 TLR4
Cytoplasm, perinuclear region 1 NOS2
Membrane raft 1 EGFR
focal adhesion 2 EGFR, HSP90B1
extracellular matrix 1 VEGFA
Peroxisome 1 NOS2
intracellular vesicle 1 EGFR
peroxisomal matrix 1 NOS2
Nucleus, PML body 1 MTOR
PML body 1 MTOR
collagen-containing extracellular matrix 1 HSP90B1
secretory granule 1 VEGFA
intermediate filament 1 KRT19
nuclear speck 2 HIF1A, MAPK14
Nucleus inner membrane 1 PTGS2
Nucleus outer membrane 1 PTGS2
nuclear inner membrane 1 PTGS2
nuclear outer membrane 1 PTGS2
Cell projection, ruffle 1 TLR4
ruffle 1 TLR4
receptor complex 4 CD8A, EGFR, MET, TLR4
neuron projection 1 PTGS2
chromatin 2 HIF1A, STAT3
phagocytic cup 1 TLR4
cell periphery 1 KRT19
cytoskeleton 1 KRT19
Secreted, extracellular space 1 TGFA
spindle pole 1 MAPK14
nuclear envelope 1 MTOR
Endomembrane system 1 MTOR
endosome lumen 1 INS
Melanosome 1 HSP90B1
Nucleus speckle 1 HIF1A
euchromatin 1 HIF1A
sperm plasma membrane 1 HSP90B1
basal plasma membrane 2 EGFR, MET
synaptic membrane 1 EGFR
lipopolysaccharide receptor complex 1 TLR4
plasma membrane raft 1 CD8A
ficolin-1-rich granule lumen 1 MAPK14
secretory granule lumen 2 INS, MAPK14
Golgi lumen 1 INS
endoplasmic reticulum lumen 3 HSP90B1, INS, PTGS2
platelet alpha granule lumen 2 EGF, VEGFA
phosphatidylinositol 3-kinase complex 1 PIK3CA
phosphatidylinositol 3-kinase complex, class IA 1 PIK3CA
transport vesicle 1 INS
Endoplasmic reticulum-Golgi intermediate compartment membrane 2 INS, TGFA
ER to Golgi transport vesicle membrane 1 TGFA
clathrin-coated endocytic vesicle membrane 3 EGF, EGFR, TGFA
Sarcoplasmic reticulum lumen 1 HSP90B1
costamere 1 KRT19
[Isoform 1]: Cell membrane 1 CD8A
Cytoplasmic vesicle, phagosome 1 MTOR
terminal web 1 KRT19
multivesicular body, internal vesicle lumen 1 EGFR
Shc-EGFR complex 1 EGFR
endocytic vesicle lumen 1 HSP90B1
T cell receptor complex 1 CD8A
cortical cytoskeleton 1 NOS2
endoplasmic reticulum chaperone complex 1 HSP90B1
[N-VEGF]: Cytoplasm 1 VEGFA
[VEGFA]: Secreted 1 VEGFA
[Isoform L-VEGF189]: Endoplasmic reticulum 1 VEGFA
[Isoform VEGF121]: Secreted 1 VEGFA
[Isoform VEGF165]: Secreted 1 VEGFA
VEGF-A complex 1 VEGFA
phosphatidylinositol 3-kinase complex, class IB 1 PIK3CA
interleukin-28 receptor complex 1 IFNLR1


文献列表

  • Mohamed S Abdel-Bakky, Hamdoon A Mohammed, Nesreen I Mahmoud, Elham Amin, Mansour Alsharidah, Osamah Al Rugaie, Mohamed G Ewees. Targeting the PI3K/pAKT/mTOR/NF-κB/FOXO3a signaling pathway for suppressing the development of hepatocellular carcinoma in rats: Role of the natural remedic Suaeda vermiculata forssk. Environmental toxicology. 2024 Jun; 39(6):3666-3678. doi: 10.1002/tox.24217. [PMID: 38506534]
  • Xuerao Lan, Haiyan Huang, Jianjun Liu, Jing Zhao, Guowei Li, Mingyang Zuo, Xiumei Xing, Xiaohu Ren. Compromised very-low density lipoprotein induced polyunsaturated triglyceride accumulation in N-nitrosodiethylamine-induced hepatic steatosis. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 2024 Apr; 186(?):114519. doi: 10.1016/j.fct.2024.114519. [PMID: 38369053]
  • Obeid Shanab, Laila Mostafa, Ahmed Abdeen, Rania Atia, Ahmed Y Nassar, Mohammed Youssef, Samah F Ibrahim, Zainab M Maher, Florin Imbrea, Liana Fericean, Khaled Ghareeb, Tabinda Hasan, Heba I Ghamry, Reem T Atawia, Omar Sadeq, Afaf Abdelkader. Modulatory mechanisms of copperII-albumin complex toward N-nitrosodiethylamine-induced neurotoxicity in mice via regulating oxidative damage, inflammatory, and apoptotic signaling pathways. Ecotoxicology and environmental safety. 2024 Jan; 270(?):115841. doi: 10.1016/j.ecoenv.2023.115841. [PMID: 38113799]
  • Peter Waziri, Richard Auta, Mustapha U Imam, Ben A Chindo, Zakari Ladan, Zainab Mohammed, Samson Wayah, Ja'afar Mohammed, Mohammed I Tahir, Abdurrahman E Ahmad, Yusuf Alhassan, Daniel Tyoapine, Abel S Agbaji. In Vivo Anti-Hepatocellular Carcinoma Effects of the Chloroform Root Extract of Clausena excavata Burm. Journal of evidence-based integrative medicine. 2024 Jan; 29(?):2515690X241251558. doi: 10.1177/2515690x241251558. [PMID: 38689490]
  • Esraa S Habiba, Sahar A Harby, Norhan S El-Sayed, Eman M Omar, Basant A Bakr, Maria Augustyniak, Lamia M El-Samad, Mohamed A Hassan. Sericin and melatonin mitigate diethylnitrosamine-instigated testicular impairment in mice: Implications of oxidative stress, spermatogenesis, steroidogenesis, and modulation of Nrf2/WT1/SF-1 signaling pathways. Life sciences. 2023 Oct; 334(?):122220. doi: 10.1016/j.lfs.2023.122220. [PMID: 37898455]
  • Miaoqing Ye, Chunyan Liu, Jiaojiao Liu, Fenping Lu, Jingdong Xue, Fenping Li, Yinghui Tang. Scoparone inhibits the development of hepatocellular carcinoma by modulating the p38 MAPK/Akt/NF-κB signaling in nonalcoholic fatty liver disease mice. Environmental toxicology. 2023 Jul; ?(?):. doi: 10.1002/tox.23851. [PMID: 37436232]
  • Jaime Sánchez-Meza, Marina Campos-Valdez, José Alfredo Domínguez-Rosales, Juliana Marisol Godínez-Rubí, Sarai Citlalic Rodríguez-Reyes, Erika Martínez-López, Guillermo M Zúñiga-González, Laura Verónica Sánchez-Orozco. Chronic Administration of Diethylnitrosamine and 2-Acetylaminofluorene Induces Hepatocellular Carcinoma in Wistar Rats. International journal of molecular sciences. 2023 May; 24(9):. doi: 10.3390/ijms24098387. [PMID: 37176094]
  • Asmaa I Owis, Noheir H Sherif, Asmaa A Hassan, El-Moataz Bellah El-Naggar, Iman H El-Khashab, El-Sayed El-Ghaly. Tropaeolum majus L. and low dose gamma radiation suppress liver carcinoma development via EGFR-HER2 signaling pathway. Natural product research. 2023 Mar; 37(6):1030-1035. doi: 10.1080/14786419.2022.2098958. [PMID: 35834717]
  • Fauzia Jamal, Ghufran Ahmed, Mohammad Farazuddin, Ishrat Altaf, Saba Farheen, Qamar Zia, Asim Azhar, Hira Ahmad, Aijaz Ahmed Khan, Satyanarayana Somavarapu, Anshu Agrawal, Mohammad Owais. Potential of siRNA-Bearing Subtilosomes in the Treatment of Diethylnitrosamine-Induced Hepatocellular Carcinoma. Molecules (Basel, Switzerland). 2023 Feb; 28(5):. doi: 10.3390/molecules28052191. [PMID: 36903437]
  • Fatma Sayed Abdel-Aal Farag, Hend Mohamed Anwar, Tarek Aboushousha, Hala Sh Mohammed, Lotfi Diab Mousa Ismail. Ameliorative Effects of Thunbergia erecta L. Leaves Against the Initiation of Hepatocarcinogenesis Induced by Diethylnitrosamine in the Rat Model. Applied biochemistry and biotechnology. 2023 Jan; ?(?):. doi: 10.1007/s12010-022-04292-x. [PMID: 36708488]
  • Hany Khalil, Alaa H Nada, Hoda Mahrous, Amr Hassan, Patricia Rijo, Ibrahim A Ibrahim, Dalia D Mohamed, Fawziah A Al-Salmi, Doaa D Mohamed, Ahmed I Abd Elmaksoud. Amelioration effect of 18β-Glycyrrhetinic acid on methylation inhibitors in hepatocarcinogenesis -induced by diethylnitrosamine. Frontiers in immunology. 2023; 14(?):1206990. doi: 10.3389/fimmu.2023.1206990. [PMID: 38322013]
  • Mohammed S Abdel-Hamid, Ahmed M Mansour, Memy H Hassan, Rasha Abdelhady, Bakheet E M Elsadek, El-Sayed M El-Sayed, Salama A Salama. Estrogen Attenuates Diethylnitrosamine-Induced Hepatocellular Carcinoma in Female Rats via Modulation of Estrogen Receptor/FASN/CD36/IL-6 Axis. Biological & pharmaceutical bulletin. 2023; 46(11):1558-1568. doi: 10.1248/bpb.b23-00342. [PMID: 37914358]
  • Fan Yang, Xiaoqiang Shi, Weidong Yang, Chao Gao, Zhenyu Cui, Wentao Wang. Pueraria montana (Kudzu vine) Ameliorate the Inflammation and Oxidative Stress against Fe-NTA Induced Renal Cancer. Journal of oleo science. 2022 Sep; 71(10):1481-1492. doi: 10.5650/jos.ess22151. [PMID: 36089399]
  • Haiyang Shen, Qian Li, Youtao Yu. Chemoprotective Effect of Decalactone on Hepatic Cancer via Diminishing the Inflammatory Response and Oxidative Stress. Journal of oleo science. 2022 Sep; 71(9):1327-1335. doi: 10.5650/jos.ess22033. [PMID: 35965085]
  • Suphunwadee Sawong, Dumrongsak Pekthong, Pennapha Suknoppakit, Thanwarat Winitchaikul, Worasak Kaewkong, Julintorn Somran, Chaidan Intapa, Supawadee Parhira, Piyarat Srisawang. Calotropis gigantea stem bark extracts inhibit liver cancer induced by diethylnitrosamine. Scientific reports. 2022 07; 12(1):12151. doi: 10.1038/s41598-022-16321-0. [PMID: 35840761]
  • Charatda Punvittayagul, Theerapat Luangsuphabool, Rawiwan Wongpoomchai. Protocatechuic acid as a potent anticarcinogenic compound in purple rice bran against diethylnitrosamine-initiated rat hepatocarcinogenesis. Scientific reports. 2022 06; 12(1):10548. doi: 10.1038/s41598-022-14888-2. [PMID: 35732709]
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  • Yuan Lu, Yanli Wang, Yan He, Jie Pan, Yang Jin, Lin Zheng, Yong Huang, Yongjun Li, Wen Liu. Aidi injection altered the activity of CYP2D4, CYP1A2, CYP2C19, CYP3A2, CYP2E1 and CYP2C11 in normal and diethylnitrosamine-induced hepatocellular carcinoma in rats. Journal of ethnopharmacology. 2022 Mar; 286(?):114930. doi: 10.1016/j.jep.2021.114930. [PMID: 34952190]
  • Chao Liu, Han Yu, Xia Li, Yanju Gong, Peijie Wu, Quan-Sheng Feng. Anti-hepatocellular carcinoma efficacy of Fuzheng Xiaozheng prescription and its interventional mechanism studies. Journal of ethnopharmacology. 2022 Mar; 285(?):114913. doi: 10.1016/j.jep.2021.114913. [PMID: 34910953]
  • Magda I Mohamad, Islam A Desoky, Kamelia Ahmed Zaki, Doaa R Sadek, Samar Kamal Kassim, Dalia Abdel-Wahab Mohamed. Pterostilbene ameliorates the disrupted Adars expression and improves liver fibrosis in DEN-induced liver injury in Wistar rats: A novel potential effect. Gene. 2022 Mar; 813(?):146124. doi: 10.1016/j.gene.2021.146124. [PMID: 34921950]
  • Ting Zhang, Hong-Wei Gu, Jin-Xing Gao, Yu-Sang Li, He-Bin Tang. Ethanol supernatant extracts of Gynura procumbens could treat nanodiethylnitrosamine-induced mouse liver cancer by interfering with inflammatory factors for the tumor microenvironment. Journal of ethnopharmacology. 2022 Mar; 285(?):114917. doi: 10.1016/j.jep.2021.114917. [PMID: 34919988]
  • Xia Li, Han Yu, Yanju Gong, Peijie Wu, Quansheng Feng, Chao Liu. Fuzheng Xiaozheng prescription relieves rat hepatocellular carcinoma through improving anti-inflammation capacity and regulating lipid related metabolisms. Journal of ethnopharmacology. 2022 Feb; 284(?):114801. doi: 10.1016/j.jep.2021.114801. [PMID: 34748868]
  • P Amudha, M Jayalakshmi, R Vidya, B N Poojitha. Chemopreventive and Therapeutic Efficacy of Enhalus acoroides against Diethylnitrosamine Induced Hepatocellular Carcinoma in Wistar Albino Rats. Applied biochemistry and biotechnology. 2022 Feb; ?(?):. doi: 10.1007/s12010-022-03832-9. [PMID: 35106713]
  • Hee Jeong Chun, Yeon Joo Shim, Young Hye Kwon. Cholic acid supplementation accelerates the progression of nonalcoholic fatty liver disease to the procarcinogenic state in mice fed a high-fat and high-cholesterol diet. The Journal of nutritional biochemistry. 2022 02; 100(?):108869. doi: 10.1016/j.jnutbio.2021.108869. [PMID: 34563665]
  • Ke-Xin Wang, Guan-Hua Du, Xue-Mei Qin, Li Gao. 1H-NMR-based metabolomics reveals the biomarker panel and molecular mechanism of hepatocellular carcinoma progression. Analytical and bioanalytical chemistry. 2022 Feb; 414(4):1525-1537. doi: 10.1007/s00216-021-03768-9. [PMID: 35024914]
  • Satoshi Kidoguchi, Kento Kitada, Kazuki Nakajima, Daisuke Nakano, Hiroyuki Ohsaki, Wararat Kittikulsuth, Hideki Kobara, Tsutomu Masaki, Takashi Yokoo, Kazuo Takahashi, Jens Titze, Akira Nishiyama. Hepatocellular carcinoma induces body mass loss in parallel with osmolyte and water retention in rats. Life sciences. 2022 Jan; 289(?):120192. doi: 10.1016/j.lfs.2021.120192. [PMID: 34871664]
  • Gaber Ali, Hany Omar, Fatema Hersi, Amira Abo-Youssef, Osama Ahmed, Wafaa Mohamed. The Protective Role of Etoricoxib Against Diethylnitrosamine/2-acetylaminofluorene- Induced Hepatocarcinogenesis in Wistar Rats: The Impact of NF-κB/COX-2/PGE2 Signaling. Current molecular pharmacology. 2022; 15(1):252-262. doi: 10.2174/1874467214666210708103752. [PMID: 34238176]
  • Renata L Goto, Mariana B Tablas, Gabriel B Prata, Sara G Espírito Santo, Ana Angélica H Fernandes, Bruno Cogliati, Luis F Barbisan, Guilherme R Romualdo. Vitamin D3 supplementation alleviates chemically-induced cirrhosis-associated hepatocarcinogenesis. The Journal of steroid biochemistry and molecular biology. 2022 01; 215(?):106022. doi: 10.1016/j.jsbmb.2021.106022. [PMID: 34774723]
  • Khairy M A Zoheir, Mohamed A Abdelhafez, Ahmed M Darwish, Karima F Mahrous. New Approach about the Signaling Crosstalk between IQGAPs/ NF- κB/IL-8 and PDCD5/p53/TRAIL Pathways that Modulate Malignant Transformation in Hepatocellular Carcinoma. Asian Pacific journal of cancer prevention : APJCP. 2022 Jan; 23(1):271-279. doi: 10.31557/apjcp.2022.23.1.271. [PMID: 35092397]
  • Nabil Mohie Abdel-Hamid, Sara Gamal Abd Allah, Mohamed K Hassan, Amal A M Ahmed, Nahla H Anber, Ibrahim Adel Faried. Possible Protective Potency of Argun Nut (Medemia argun - An Ancient Egyptian Palm) against Hepatocellular Carcinoma in Rats. Nutrition and cancer. 2022; 74(2):527-538. doi: 10.1080/01635581.2021.1883683. [PMID: 33570439]
  • R Vidya, K Kalaivani, P Amudha. Therapeutic Potential of Cucumis melo (L.) Fruit Extract and Its Silver Nanopartciles Against DEN-Induced Hepatocellular Cancer in Rats. Applied biochemistry and biotechnology. 2022 Jan; 194(1):368-381. doi: 10.1007/s12010-021-03765-9. [PMID: 34792748]
  • Vichununt Kerdput, Kritsakorn Kanjanapongkul, Arunporn Itharat, Ratchadaporn Pramong, Wouter H Lamers, Theodorus B M Hakvoort, Aldo Jongejan, Wisuit Pradidarcheep. Molecular Changes Following Induction of Hepatocellular Carcinoma by Diethylnitrosamine and Thioacetamide, and Subsequent Treatment with Dioscorea membranacea Extract. International journal of medical sciences. 2022; 19(12):1806-1815. doi: 10.7150/ijms.72987. [PMID: 36313224]
  • Ashish Kumar, Manisha Naithani, Nitesh Kumar, Neha Singh, Shruti Agrawal, Ambika Sharma, Surabhi Thapliyal, Jagjit Singh, Shailendra Handu. Piperlongumine inhibits diethylnitrosamine induced hepatocellular carcinoma in rats. Human & experimental toxicology. 2022 Jan; 41(?):9603271211073593. doi: 10.1177/09603271211073593. [PMID: 35113675]
  • Osama M Ahmed, Adel A Ahmed, Hanaa I Fahim, Mohamed Y Zaky. Quercetin and naringenin abate diethylnitrosamine/acetylaminofluorene-induced hepatocarcinogenesis in Wistar rats: the roles of oxidative stress, inflammation and cell apoptosis. Drug and chemical toxicology. 2022 Jan; 45(1):262-273. doi: 10.1080/01480545.2019.1683187. [PMID: 31665932]
  • Ryo Ichikawa, Sosuke Masuda, Junta Nakahara, Mio Kobayashi, Risako Yamashita, Suzuka Uomoto, Ohshima Kanami, Erika Hara, Yuko Ito, Makoto Shibutani, Toshinori Yoshida. Inhibition of autophagy with expression of NADPH oxidase subunit p22phox in preneoplastic lesions in a high-fat diet and streptozotocin-related hepatocarcinogenesis rat model. The Journal of toxicological sciences. 2022; 47(7):289-300. doi: 10.2131/jts.47.289. [PMID: 35786680]
  • Hongwu Huang, Zhenzhen Liu, Xiaoru Qi, Nailong Gao, Jianguo Chang, Miaomiao Yang, Sha Na, Yanyan Liu, Rui Song, Lu Li, Guangliang Chen, Hui Zhou. Rhubarb granule promotes diethylnitrosamine-induced liver tumorigenesis by activating the oxidative branch of pentose phosphate pathway via G6PD in rats. Journal of ethnopharmacology. 2021 Dec; 281(?):114479. doi: 10.1016/j.jep.2021.114479. [PMID: 34343647]
  • María José Rodríguez, Matías Sabaj, Gerardo Tolosa, Francisca Herrera Vielma, María José Zúñiga, Daniel R González, Jessica Zúñiga-Hernández. Maresin-1 Prevents Liver Fibrosis by Targeting Nrf2 and NF-κB, Reducing Oxidative Stress and Inflammation. Cells. 2021 12; 10(12):. doi: 10.3390/cells10123406. [PMID: 34943914]
  • Nahed Abdel-Aziz, Sawsan M El-Sonbaty, Marwa G A Hegazy. Ameliorative potential of manganese nanoparticles with low-level ionizing radiation against experimentally induced hepatocarcinogenesis. Environmental science and pollution research international. 2021 Dec; 28(46):65474-65486. doi: 10.1007/s11356-021-15571-1. [PMID: 34322790]
  • Shanshan Li, Yang Li, Hongjian Sun, Yang Jiang, Keming Pan, Yue Su, Nan Bu. Mulberry fruit polysaccharides alleviate diethylnitrosamine/phenobarbital-induced hepatocarcinogenesis in vivo: the roles of cell apoptosis and inflammation. Bioengineered. 2021 12; 12(2):11599-11611. doi: 10.1080/21655979.2021.1993716. [PMID: 34866538]
  • Gopalakrishnan Balaraman, Jagan Sundaram, Ashok Mari, Palanisamy Krishnan, Sharmila Salam, Nirmala Subramaniam, Immaduddin Sirajduddin, Devaki Thiruvengadam. Farnesol alleviates diethyl nitrosamine induced inflammation and protects experimental rat hepatocellular carcinoma. Environmental toxicology. 2021 Dec; 36(12):2467-2474. doi: 10.1002/tox.23359. [PMID: 34473392]
  • Sang R Lee, Su Hee Jeong, Jun H Heo, Seong Lae Jo, Je-Won Ko, Hyo-Jung Kwun, Eui-Ju Hong. Dietary Intake of 17α-Ethinylestradiol Promotes HCC Progression in Humanized Male Mice Expressing Sex Hormone-Binding Globulin. International journal of molecular sciences. 2021 Nov; 22(22):. doi: 10.3390/ijms222212557. [PMID: 34830439]
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