Curcumae Ameliorates Diethylnitrosamine-Induced Hepatocellular Carcinoma via Alteration of Oxidative Stress, Inflammation and Gut Microbiota
Nonalcoholic fatty liver disease (NAFLD) increased the risk factor of hepatocellular carcinoma (HCC). NAFLD induces the hepatic-related cancer deaths mostly in middle-aged men. NAFLD enhanced the inflammatory reaction and oxidative stress in the hepatic tissue. Curcumae exhibited the anti-inflammato...
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Published in | Journal of inflammation research Vol. 14; pp. 5551 - 5566 |
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Abstract | Nonalcoholic fatty liver disease (NAFLD) increased the risk factor of hepatocellular carcinoma (HCC). NAFLD induces the hepatic-related cancer deaths mostly in middle-aged men. NAFLD enhanced the inflammatory reaction and oxidative stress in the hepatic tissue. Curcumae exhibited the anti-inflammatory and antioxidant effects. In this study, we made an attempt to scrutinize the protective effect of curcumae on obesity-induced HCC via alteration of inflammation, oxidative stress and gut microbiota.
The rats used in this experiment were Wistar rats, 100 mg/kg intraperitoneal injection of diethylnitrosamine (hepatic carcinogen) was used at 2 weeks. After 6 weeks of the experimental study, the rats were randomly divided into high-fat diet (HFD) with or without curcumae-treated group rats and received the treatment for 22 weeks. Hepatic, non-hepatic, cardiac, antioxidant, pro-inflammatory and inflammatory were estimated at the end of the study. The stools of the experimental rats were collected for estimating the gut microbiota.
Curcumae-treated group rats exposed reduction of the hepatic nodules in hepatic tissue. Curcumae significantly (P<0.001) diminished the level of hepatic parameters and antioxidant parameters in the serum. Curcumae significantly (P<0.001) suppressed the pro-inflammatory cytokines level, viz. interleukin-1β (IL-1β), interleukin-6 (IL-6), tumor necrosis factor-α (TNF-α), interleukin-2 (IL-2), interleukin-7 (IL-7) and augmented the level of interleukin-10 (IL-10) in the serum and hepatic tissue. Curcumae significantly (P<0.001) suppressed inflammatory mediators including cyclooxygenase (COX-2), prostaglandin E2 (PGE2) and nuclear factor kappa B (NF-κB) in the serum and hepatic tissue. Furthermore, curcumae increased the gut microbial diversity and richness and decreased the relative abundance of genus
and
, respectively.
Curcumae prevents HFD-induced inflammation during the hepatic carcinoma by modulating the oxidative stress, inflammatory reaction and gut microbiota. |
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AbstractList | Background: Nonalcoholic fatty liver disease (NAFLD) increased the risk factor of hepatocellular carcinoma (HCC). NAFLD induces the hepatic-related cancer deaths mostly in middle-aged men. NAFLD enhanced the inflammatory reaction and oxidative stress in the hepatic tissue. Curcumae exhibited the anti-inflammatory and antioxidant effects. In this study, we made an attempt to scrutinize the protective effect of curcumae on obesity-induced HCC via alteration of inflammation, oxidative stress and gut microbiota. Methods: The rats used in this experiment were Wistar rats, 100 mg/kg intraperitoneal injection of diethylnitrosamine (hepatic carcinogen) was used at 2 weeks. After 6 weeks of the experimental study, the rats were randomly divided into high-fat diet (HFD) with or without curcumae-treated group rats and received the treatment for 22 weeks. Hepatic, non-hepatic, cardiac, antioxidant, pro-inflammatory and inflammatory were estimated at the end of the study. The stools of the experimental rats were collected for estimating the gut microbiota. Results: Curcumae-treated group rats exposed reduction of the hepatic nodules in hepatic tissue. Curcumae significantly (p < 0.001) diminished the level of hepatic parameters and antioxidant parameters in the serum. Curcumae significantly (p < 0.001) suppressed the proinflammatory cytokines level, viz. interleukin-1[beta] (IL-1[beta]), interleukin-6 (IL-6), tumor necrosis factor-[alpha] (TNF-[alpha]), interleukin-2 (IL-2), interleukin-7 (IL-7) and augmented the level of interleukin-10 (IL-10) in the serum and hepatic tissue. Curcumae significantly (p < 0.001) suppressed inflammatory mediators including cyclooxygenase (COX-2), prostaglandin E2 (PGE2) and nuclear factor kappa B (NF-[kappa]B) in the serum and hepatic tissue. Furthermore, curcumae increased the gut microbial diversity and richness and decreased the relative abundance of genus Mucispirillum and Clostridium, respectively. Conclusion: Curcumae prevents HFD-induced inflammation during the hepatic carcinoma by modulating the oxidative stress, inflammatory reaction and gut microbiota. Keywords: curcumae, hepatic cellular carcinoma, gut microbiota, inflammation, antioxidant Nonalcoholic fatty liver disease (NAFLD) increased the risk factor of hepatocellular carcinoma (HCC). NAFLD induces the hepatic-related cancer deaths mostly in middle-aged men. NAFLD enhanced the inflammatory reaction and oxidative stress in the hepatic tissue. Curcumae exhibited the anti-inflammatory and antioxidant effects. In this study, we made an attempt to scrutinize the protective effect of curcumae on obesity-induced HCC via alteration of inflammation, oxidative stress and gut microbiota. The rats used in this experiment were Wistar rats, 100 mg/kg intraperitoneal injection of diethylnitrosamine (hepatic carcinogen) was used at 2 weeks. After 6 weeks of the experimental study, the rats were randomly divided into high-fat diet (HFD) with or without curcumae-treated group rats and received the treatment for 22 weeks. Hepatic, non-hepatic, cardiac, antioxidant, pro-inflammatory and inflammatory were estimated at the end of the study. The stools of the experimental rats were collected for estimating the gut microbiota. Curcumae-treated group rats exposed reduction of the hepatic nodules in hepatic tissue. Curcumae significantly (P<0.001) diminished the level of hepatic parameters and antioxidant parameters in the serum. Curcumae significantly (P<0.001) suppressed the pro-inflammatory cytokines level, viz. interleukin-1β (IL-1β), interleukin-6 (IL-6), tumor necrosis factor-α (TNF-α), interleukin-2 (IL-2), interleukin-7 (IL-7) and augmented the level of interleukin-10 (IL-10) in the serum and hepatic tissue. Curcumae significantly (P<0.001) suppressed inflammatory mediators including cyclooxygenase (COX-2), prostaglandin E2 (PGE2) and nuclear factor kappa B (NF-κB) in the serum and hepatic tissue. Furthermore, curcumae increased the gut microbial diversity and richness and decreased the relative abundance of genus and , respectively. Curcumae prevents HFD-induced inflammation during the hepatic carcinoma by modulating the oxidative stress, inflammatory reaction and gut microbiota. Yunyan Zhang,1 Xuelian Li,2 Xinghua Li3 1Department of Laboratory Medicine, The First People’s Hospital of Lianyungang City, Lianyungang City, Jiangsu, 222002, People’s Republic of China; 2Department of Laboratory Medicine, The Fourth People’s Hospital of Lianyungang City, Lianyungang City, Jiangsu, 222002, People’s Republic of China; 3Department of Blood Transfusion, The First People’s Hospital of Lianyungang City, Lianyungang City, Jiangsu, 222002, People’s Republic of ChinaCorrespondence: Xinghua LiDepartment of Blood Transfusion, The First People’s Hospital of Lianyungang City, Lianyungang City, Jiangsu, 222002, People’s Republic of ChinaEmail qwemn0147@sina.comBackground: Nonalcoholic fatty liver disease (NAFLD) increased the risk factor of hepatocellular carcinoma (HCC). NAFLD induces the hepatic-related cancer deaths mostly in middle-aged men. NAFLD enhanced the inflammatory reaction and oxidative stress in the hepatic tissue. Curcumae exhibited the anti-inflammatory and antioxidant effects. In this study, we made an attempt to scrutinize the protective effect of curcumae on obesity-induced HCC via alteration of inflammation, oxidative stress and gut microbiota.Methods: The rats used in this experiment were Wistar rats, 100 mg/kg intraperitoneal injection of diethylnitrosamine (hepatic carcinogen) was used at 2 weeks. After 6 weeks of the experimental study, the rats were randomly divided into high-fat diet (HFD) with or without curcumae-treated group rats and received the treatment for 22 weeks. Hepatic, non-hepatic, cardiac, antioxidant, pro-inflammatory and inflammatory were estimated at the end of the study. The stools of the experimental rats were collected for estimating the gut microbiota.Results: Curcumae-treated group rats exposed reduction of the hepatic nodules in hepatic tissue. Curcumae significantly (P< 0.001) diminished the level of hepatic parameters and antioxidant parameters in the serum. Curcumae significantly (P< 0.001) suppressed the pro-inflammatory cytokines level, viz. interleukin-1β (IL-1β), interleukin-6 (IL-6), tumor necrosis factor-α (TNF-α), interleukin-2 (IL-2), interleukin-7 (IL-7) and augmented the level of interleukin-10 (IL-10) in the serum and hepatic tissue. Curcumae significantly (P< 0.001) suppressed inflammatory mediators including cyclooxygenase (COX-2), prostaglandin E2 (PGE2) and nuclear factor kappa B (NF-κB) in the serum and hepatic tissue. Furthermore, curcumae increased the gut microbial diversity and richness and decreased the relative abundance of genus Mucispirillum and Clostridium, respectively.Conclusion: Curcumae prevents HFD-induced inflammation during the hepatic carcinoma by modulating the oxidative stress, inflammatory reaction and gut microbiota.Keywords: curcumae, hepatic cellular carcinoma, gut microbiota, inflammation, antioxidant Background: Nonalcoholic fatty liver disease (NAFLD) increased the risk factor of hepatocellular carcinoma (HCC). NAFLD induces the hepatic-related cancer deaths mostly in middle-aged men. NAFLD enhanced the inflammatory reaction and oxidative stress in the hepatic tissue. Curcumae exhibited the anti-inflammatory and antioxidant effects. In this study, we made an attempt to scrutinize the protective effect of curcumae on obesity-induced HCC via alteration of inflammation, oxidative stress and gut microbiota. Methods: The rats used in this experiment were Wistar rats, 100 mg/kg intraperitoneal injection of diethylnitrosamine (hepatic carcinogen) was used at 2 weeks. After 6 weeks of the experimental study, the rats were randomly divided into high-fat diet (HFD) with or without curcumae-treated group rats and received the treatment for 22 weeks. Hepatic, non-hepatic, cardiac, antioxidant, pro-inflammatory and inflammatory were estimated at the end of the study. The stools of the experimental rats were collected for estimating the gut microbiota. Results: Curcumae-treated group rats exposed reduction of the hepatic nodules in hepatic tissue. Curcumae significantly (P< 0.001) diminished the level of hepatic parameters and antioxidant parameters in the serum. Curcumae significantly (P< 0.001) suppressed the pro-inflammatory cytokines level, viz. interleukin-1β (IL-1β), interleukin-6 (IL-6), tumor necrosis factor-α (TNF-α), interleukin-2 (IL-2), interleukin-7 (IL-7) and augmented the level of interleukin-10 (IL-10) in the serum and hepatic tissue. Curcumae significantly (P< 0.001) suppressed inflammatory mediators including cyclooxygenase (COX-2), prostaglandin E2 (PGE2) and nuclear factor kappa B (NF-κB) in the serum and hepatic tissue. Furthermore, curcumae increased the gut microbial diversity and richness and decreased the relative abundance of genus Mucispirillum and Clostridium, respectively. Conclusion: Curcumae prevents HFD-induced inflammation during the hepatic carcinoma by modulating the oxidative stress, inflammatory reaction and gut microbiota. |
Audience | Academic |
Author | Li, Xinghua Zhang, Yunyan Li, Xuelian |
Author_xml | – sequence: 1 givenname: Yunyan surname: Zhang fullname: Zhang, Yunyan organization: Department of Laboratory Medicine, The First People's Hospital of Lianyungang City, Lianyungang City, Jiangsu, 222002, People's Republic of China – sequence: 2 givenname: Xuelian surname: Li fullname: Li, Xuelian organization: Department of Laboratory Medicine, The Fourth People's Hospital of Lianyungang City, Lianyungang City, Jiangsu, 222002, People's Republic of China – sequence: 3 givenname: Xinghua orcidid: 0000-0001-7863-4183 surname: Li fullname: Li, Xinghua organization: Department of Blood Transfusion, The First People's Hospital of Lianyungang City, Lianyungang City, Jiangsu, 222002, People's Republic of China |
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Cites_doi | 10.1080/01635581.2015.1087040 10.1186/1475-2867-13-27 10.3389/fphar.2018.01374 10.3923/ijp.2019.549.559 10.1016/j.fct.2020.111699 10.1016/j.ejca.2013.09.020 10.1080/01635581.2012.661513 10.1080/01635581.2011.523806 10.1007/s11010-011-1043-7 10.2147/IJN.S136629 10.1186/1472-6882-13-273 10.1080/13102818.2014.901678 10.1016/j.biopha.2017.07.047 10.1080/10717544.2019.1606865 10.1016/j.biopha.2020.111156 10.3892/ol.2013.1651 10.1016/j.biopha.2021.111335 10.3892/etm.2011.406 10.3390/cancers5041332 10.3892/mmr.2012.772 10.1186/1756-9966-30-49 10.3390/molecules17044672 10.1158/1940-6207.CAPR-18-0188 10.1038/sj.onc.1205248 10.1158/1940-6207.CAPR-09-0171 10.1080/17425247.2021.1860939 10.1016/j.abb.2017.05.006 10.4161/oxim.3.4.12714 10.1016/j.biomag.2013.01.006 10.1016/j.fct.2008.11.004 10.4172/2157-2518.1000102 10.1186/1749-8546-7-13 10.1002/ddr.21451 10.3390/ijms14011940 10.7314/APJCP.2013.14.1.261 10.1186/1476-4598-9-215 10.1016/j.jchromb.2020.122501 10.2147/IJN.S277545 10.12691/ajcp-1-2-1 10.1016/j.cbi.2011.12.004 10.1007/s10787-017-0350-3 10.1039/C7RA12775H |
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Keywords | curcumae antioxidant inflammation gut microbiota hepatic cellular carcinoma |
Language | English |
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References | Tekkes (ref27) 2014; 32 Singh (ref15) 2014; 50 Xia (ref1) 2018; 11 ref10 Kumar (ref24) 2017; 12 Xiao (ref31) 2014; 7 Chen (ref43) 2012; 17 Marnewick (ref46) 2009; 47 Gupta (ref39) 2011; 63 Jin (ref8) 2019; 80 Kalaiselvan (ref34) 2013; 1 Singh (ref23) 2018; 8 Zhang (ref40) 2013; 14 Duan (ref28) 2014; 14 Rahman (ref7) 2021; 1163 Shen (ref32) 2014; 34 Verma (ref22) 2018; 26 Granado-serrano (ref12) 2012; 64 Anoopraj (ref36) 2014; 7 Abdel-hamid (ref51) 2013; 1 Kumar (ref9) 2013; 13 Kakehashi (ref13) 2013; 5 Horiguchi (ref35) 2002; 21 Su (ref26) 2019; 15 Jayakumar (ref42) 2012; 360 Abdel (ref47) 2011; 30 Shi (ref18) 2012; 7 Rahman (ref37) 2019; 26 Shirakami (ref11) 2011; 33 Liu (ref17) 2014; 28 Thangavel (ref30) 2013; 3 Liu (ref19) 2018; 9 Lu (ref29) 2012; 5 Naqvi (ref4) 2021; 134 Bishayee (ref50) 2010; 3 Bishayee (ref45) 2010; 01 Dai (ref52) 2013; 14 Alharbi (ref6) 1872; 16 Chen (ref38) 2012; 7 Hou (ref16) 2020; 40 Sayed-Ahmed (ref49) 2010; 3 Dai (ref14) 2013; 13 Fang (ref48) 2010; 9 Bhatia (ref21) 2015; 67 Kumar (ref33) 2017; 94 Akbari (ref20) 2020; 145 Afzal (ref44) 2017; 623–624 Gayathri (ref25) 2009; 10 Ming (ref2) 2019; 36 Kumar (ref3) 2021; 18 Rahman (ref5) 2020; 15 Ghosh (ref41) 2012; 195 |
References_xml | – volume: 67 start-page: 1270 year: 2015 ident: ref21 publication-title: Nutr Cancer doi: 10.1080/01635581.2015.1087040 contributor: fullname: Bhatia – volume: 13 start-page: 1 year: 2013 ident: ref14 publication-title: Cancer Cell Int doi: 10.1186/1475-2867-13-27 contributor: fullname: Dai – volume: 9 year: 2018 ident: ref19 publication-title: Front Pharmacol doi: 10.3389/fphar.2018.01374 contributor: fullname: Liu – volume: 1 start-page: 2 year: 2013 ident: ref34 publication-title: Int Res J Medical Sci contributor: fullname: Kalaiselvan – volume: 15 start-page: 549 year: 2019 ident: ref26 publication-title: Int J Pharmacol doi: 10.3923/ijp.2019.549.559 contributor: fullname: Su – volume: 145 start-page: 111699 year: 2020 ident: ref20 publication-title: Food Chem Toxicol doi: 10.1016/j.fct.2020.111699 contributor: fullname: Akbari – volume: 50 start-page: 247 year: 2014 ident: ref15 publication-title: Eur J Cancer doi: 10.1016/j.ejca.2013.09.020 contributor: fullname: Singh – volume: 64 start-page: 1 year: 2012 ident: ref12 publication-title: Nutr Cancer doi: 10.1080/01635581.2012.661513 contributor: fullname: Granado-serrano – volume: 63 start-page: 234 year: 2011 ident: ref39 publication-title: Nutr Cancer doi: 10.1080/01635581.2011.523806 contributor: fullname: Gupta – volume: 360 start-page: 51 year: 2012 ident: ref42 publication-title: Mol Cell Biochem doi: 10.1007/s11010-011-1043-7 contributor: fullname: Jayakumar – volume: 16 start-page: 359 year: 1872 ident: ref6 publication-title: J Pharm Innov contributor: fullname: Alharbi – volume: 10 start-page: 933 year: 2009 ident: ref25 publication-title: Asian Pac J Cancer Prev contributor: fullname: Gayathri – volume: 12 start-page: 6747 year: 2017 ident: ref24 publication-title: Int J Nanomedicine doi: 10.2147/IJN.S136629 contributor: fullname: Kumar – volume: 13 start-page: 273 year: 2013 ident: ref9 publication-title: BMC Complement Altern Med doi: 10.1186/1472-6882-13-273 contributor: fullname: Kumar – volume: 28 start-page: 140 year: 2014 ident: ref17 publication-title: Biotechnol Biotechnol Equip doi: 10.1080/13102818.2014.901678 contributor: fullname: Liu – volume: 94 start-page: 834 year: 2017 ident: ref33 publication-title: Biomed Pharmacother doi: 10.1016/j.biopha.2017.07.047 contributor: fullname: Kumar – volume: 26 start-page: 782 year: 2019 ident: ref37 publication-title: Drug Deliv doi: 10.1080/10717544.2019.1606865 contributor: fullname: Rahman – volume: 134 start-page: 111156 year: 2021 ident: ref4 publication-title: Biomed Pharmacother doi: 10.1016/j.biopha.2020.111156 contributor: fullname: Naqvi – volume: 7 start-page: 23 year: 2014 ident: ref31 publication-title: Oncology Lett doi: 10.3892/ol.2013.1651 contributor: fullname: Xiao – volume: 36 start-page: 788 year: 2019 ident: ref2 publication-title: Royal Soc Chem contributor: fullname: Ming – ident: ref10 doi: 10.1016/j.biopha.2021.111335 – volume: 7 start-page: 285 year: 2012 ident: ref38 publication-title: Exp Ther Med doi: 10.3892/etm.2011.406 contributor: fullname: Chen – volume: 33 start-page: 1 year: 2011 ident: ref11 publication-title: Carcinogenesis contributor: fullname: Shirakami – volume: 5 start-page: 1332 year: 2013 ident: ref13 publication-title: Cancers doi: 10.3390/cancers5041332 contributor: fullname: Kakehashi – volume: 5 start-page: 637 year: 2012 ident: ref29 publication-title: Mol Med Rep doi: 10.3892/mmr.2012.772 contributor: fullname: Lu – volume: 30 start-page: 49 year: 2011 ident: ref47 publication-title: J Exp Clin Cancer Res doi: 10.1186/1756-9966-30-49 contributor: fullname: Abdel – volume: 17 start-page: 4672 year: 2012 ident: ref43 publication-title: Molecules doi: 10.3390/molecules17044672 contributor: fullname: Chen – volume: 14 start-page: 1 year: 2014 ident: ref28 publication-title: BMC Gastroenterol contributor: fullname: Duan – volume: 11 start-page: 797 year: 2018 ident: ref1 publication-title: Cancer Prev Res doi: 10.1158/1940-6207.CAPR-18-0188 contributor: fullname: Xia – volume: 21 start-page: 1791 year: 2002 ident: ref35 publication-title: Oncogene doi: 10.1038/sj.onc.1205248 contributor: fullname: Horiguchi – volume: 3 start-page: 753 year: 2010 ident: ref50 publication-title: Cancer Prev Res doi: 10.1158/1940-6207.CAPR-09-0171 contributor: fullname: Bishayee – volume: 18 start-page: 1 year: 2021 ident: ref3 publication-title: Expert Opin Drug Deliv doi: 10.1080/17425247.2021.1860939 contributor: fullname: Kumar – volume: 623–624 start-page: 58 year: 2017 ident: ref44 publication-title: Arch Biochem Biophys doi: 10.1016/j.abb.2017.05.006 contributor: fullname: Afzal – volume: 3 start-page: 254 year: 2010 ident: ref49 publication-title: Oxid Med Cell Longev doi: 10.4161/oxim.3.4.12714 contributor: fullname: Sayed-Ahmed – volume: 3 start-page: 59 year: 2013 ident: ref30 publication-title: Biomed Aging Pathol doi: 10.1016/j.biomag.2013.01.006 contributor: fullname: Thangavel – volume: 47 start-page: 220 year: 2009 ident: ref46 publication-title: Food Chem Toxicol doi: 10.1016/j.fct.2008.11.004 contributor: fullname: Marnewick – volume: 01 year: 2010 ident: ref45 publication-title: J Carcinogen Mutagen doi: 10.4172/2157-2518.1000102 contributor: fullname: Bishayee – volume: 7 year: 2012 ident: ref18 publication-title: Chin Med doi: 10.1186/1749-8546-7-13 contributor: fullname: Shi – volume: 34 start-page: 683 year: 2014 ident: ref32 publication-title: Anticancer Res contributor: fullname: Shen – volume: 80 start-page: 209 year: 2019 ident: ref8 publication-title: Drug Dev Res doi: 10.1002/ddr.21451 contributor: fullname: Jin – volume: 14 start-page: 1940 year: 2013 ident: ref40 publication-title: Int J Mol Sci doi: 10.3390/ijms14011940 contributor: fullname: Zhang – volume: 14 start-page: 261 year: 2013 ident: ref52 publication-title: Asian Pac J Cancer Prev doi: 10.7314/APJCP.2013.14.1.261 contributor: fullname: Dai – volume: 9 start-page: 1 year: 2010 ident: ref48 publication-title: Mol Cancer doi: 10.1186/1476-4598-9-215 contributor: fullname: Fang – volume: 7 start-page: 439 year: 2014 ident: ref36 publication-title: Glob Health contributor: fullname: Anoopraj – volume: 32 start-page: 1405 year: 2014 ident: ref27 publication-title: Toxicol Industr Health contributor: fullname: Tekkes – volume: 1163 start-page: 122501 year: 2021 ident: ref7 publication-title: J Chromatogr B doi: 10.1016/j.jchromb.2020.122501 contributor: fullname: Rahman – volume: 15 start-page: 9283 year: 2020 ident: ref5 publication-title: Int J Nanomed doi: 10.2147/IJN.S277545 contributor: fullname: Rahman – volume: 1 start-page: 14 year: 2013 ident: ref51 publication-title: Am J Cancer Prev doi: 10.12691/ajcp-1-2-1 contributor: fullname: Abdel-hamid – volume: 40 start-page: 782 year: 2020 ident: ref16 publication-title: J Tradit Chin Med contributor: fullname: Hou – volume: 195 start-page: 206 year: 2012 ident: ref41 publication-title: Chem Biol Interact doi: 10.1016/j.cbi.2011.12.004 contributor: fullname: Ghosh – volume: 26 start-page: 133 year: 2018 ident: ref22 publication-title: Inflammopharmacology doi: 10.1007/s10787-017-0350-3 contributor: fullname: Verma – volume: 8 start-page: 6940 year: 2018 ident: ref23 publication-title: RSC Adv doi: 10.1039/C7RA12775H contributor: fullname: Singh |
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Snippet | Nonalcoholic fatty liver disease (NAFLD) increased the risk factor of hepatocellular carcinoma (HCC). NAFLD induces the hepatic-related cancer deaths mostly in... Background: Nonalcoholic fatty liver disease (NAFLD) increased the risk factor of hepatocellular carcinoma (HCC). NAFLD induces the hepatic-related cancer... Yunyan Zhang,1 Xuelian Li,2 Xinghua Li3 1Department of Laboratory Medicine, The First People’s Hospital of Lianyungang City, Lianyungang City, Jiangsu, 222002,... |
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SubjectTerms | Animal experimentation antioxidant Antioxidants Bioengineering Carcinogens Chemotherapy curcumae Cyclooxygenase-2 Cytochrome Cytokines Diethylnitrosamine Disease Enzymes Fatty liver gut microbiota hepatic cellular carcinoma Hepatocellular carcinoma Hepatoma High fat diet IL-1β Inflammation Interleukin 10 Interleukin 2 Interleukin 6 Interleukin 7 Interleukins Intestinal microflora Liver cancer Liver cirrhosis Liver diseases Manufacturers Medical prognosis Microbiota Microbiota (Symbiotic organisms) Mortality NF-κB protein Original Research Oxidative stress Phosphatase Prostaglandin E2 Prostaglandins E Risk factors Tumor necrosis factor-α Variance analysis |
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Title | Curcumae Ameliorates Diethylnitrosamine-Induced Hepatocellular Carcinoma via Alteration of Oxidative Stress, Inflammation and Gut Microbiota |
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