Gender disparity in liver cancer due to sex differences in MyD88-dependent IL-6 production

被引:1537
作者
Naugler, Willscott E.
Sakurai, Toshiharu
Kim, Sunhwa
Maeda, Shin
Kim, KyoungHyun
Elsharkawy, Ahmed M.
Karin, Michael
机构
[1] Univ Calif San Diego, Dept Pharmacol, Lab Gene Regulat & Signal Transduct, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Ctr Canc, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Dept Med, Div Gastroenterol, San Diego, CA 93093 USA
[4] Asahi Life Fdn, Inst Adult Dis, Div Gastroenterol, Chiyoda Ku, Tokyo 1000005, Japan
[5] Univ Newcastle Upon Tyne, Liver Res Grp, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England
关键词
NF-KAPPA-B; HEPATOCELLULAR-CARCINOMA; CHEMICAL HEPATOCARCINOGENESIS; ESTROGEN-RECEPTOR; INNATE IMMUNITY; RISK-FACTORS; INFLAMMATION; MICE; REGENERATION; CIRRHOSIS;
D O I
10.1126/science.1140485
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Hepatocellular carcinoma (HCC), the most common liver cancer, occurs mainly in men. Similar gender disparity is seen in mice given a chemical carcinogen, diethylnitrosamine ( DEN). DEN administration caused greater increases in serum interleukin-6 (IL-6) concentration in males than it did in females. Furthermore, ablation of IL-6 abolished the gender differences in hepatocarcinogenesis in mice. DEN exposure promoted production of IL-6 in Kupffer cells (KCs) in a manner dependent on the Toll-like receptor adaptor protein MyD88, ablation of which also protected male mice from DEN-induced hepatocarcinogenesis. Estrogen inhibited secretion of IL-6 from KCs exposed to necrotic hepatocytes and reduced circulating concentrations of IL-6 in DEN-treated male mice. We propose that estrogen-mediated inhibition of IL-6 production by KCs reduces liver cancer risk in females, and these findings may be used to prevent HCC in males.
引用
收藏
页码:121 / 124
页数:4
相关论文
共 27 条
[1]   Serum cytokine and soluble cytokine receptor levels in patients with non-alcoholic steatohepatitis [J].
Abiru, S ;
Migita, K ;
Maeda, Y ;
Daikoku, M ;
Ito, M ;
Ohata, K ;
Nagaoka, S ;
Matsumoto, T ;
Takil, Y ;
Kusumoto, K ;
Nakamura, M ;
Komori, A ;
Yano, K ;
Yatsuhashi, H ;
Eguchi, K ;
Ishibashi, H .
LIVER INTERNATIONAL, 2006, 26 (01) :39-45
[2]   Pathogen recognition and innate immunity [J].
Akira, S ;
Uematsu, S ;
Takeuchi, O .
CELL, 2006, 124 (04) :783-801
[3]   Inflammation and cancer: back to Virchow? [J].
Balkwill, F ;
Mantovani, A .
LANCET, 2001, 357 (9255) :539-545
[4]   Primary liver cancer:: Worldwide incidence and trends [J].
Bosch, FX ;
Ribes, J ;
Díaz, M ;
Cléries, R .
GASTROENTEROLOGY, 2004, 127 (05) :S5-S16
[5]   Liver failure and defective hepatocyte regeneration in interleukin-6-deficient mice [J].
Cressman, DE ;
Greenbaum, LE ;
DeAngelis, RA ;
Ciliberto, G ;
Furth, EE ;
Poli, V ;
Taub, R .
SCIENCE, 1996, 274 (5291) :1379-1383
[6]   Effects of gender on the severity of sepsis [J].
Erikoglu, M ;
Sahin, M ;
Özer, S ;
Avunduk, MC .
SURGERY TODAY, 2005, 35 (06) :467-472
[7]   Hepatocellular carcinoma in cirrhosis: Incidence and risk factors [J].
Fattovich, G ;
Stroffolini, T ;
Zagni, I ;
Donato, F .
GASTROENTEROLOGY, 2004, 127 (05) :S35-S50
[8]   Hepatitis B injury male gender, aflatoxin, and p53 expression each contribute to hepatocarcinogenesis in transgenic mice [J].
Ghebranious, N ;
Sell, S .
HEPATOLOGY, 1998, 27 (02) :383-391
[9]   Innate immunity gone awry: Linking microbial infections to chronic inflammation and cancer [J].
Karin, M ;
Lawrence, T ;
Nizet, V .
CELL, 2006, 124 (04) :823-835
[10]   NFκB:: Linking inflammation and immunity to cancer development and progression [J].
Karin, M ;
Greten, FR .
NATURE REVIEWS IMMUNOLOGY, 2005, 5 (10) :749-759