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

      Science (New York, N.Y.)
      Animals, Carbon Tetrachloride, administration & dosage, Diethylnitrosamine, metabolism, Estradiol, pharmacology, Female, Hepatocytes, Interleukin-6, blood, genetics, Kupffer Cells, Liver, pathology, Liver Neoplasms, Experimental, chemically induced, immunology, physiopathology, Male, Mice, Mice, Inbred C57BL, Mice, Knockout, Myeloid Differentiation Factor 88, physiology, Necrosis, Ovariectomy, RNA, Messenger, Sex Characteristics

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          Abstract

          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.

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