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Erschienen in: Tumor Biology 1/2011

01.02.2011 | Research Article

Circulating LTD4 in patients with hepatocellular carcinoma

verfasst von: Yan Zhou, Dongmei Guo, Huiyu Li, Shenghua Jie

Erschienen in: Tumor Biology | Ausgabe 1/2011

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Abstract

Hepatocellular carcinoma (HCC) is a type of inflammation-related cancer that usually follows chronic inflammations. Leukotriene D4 (LTD4) is a potent biologically active arachidonic acid-derived lipid mediator that is intimately involved in inflammations and cancers. Although previous researches found overexpression of LTD4 in several other cancers, the circulating LTD4 level in HCC remains unknown. The aim of this study was to examine concentrations of LTD4 and analyze its roles in HCC. The results showed that remarkably high circulating LTD4 in HCC versus healthy subjects (p < 0.001). The levels of LTD4 were neither associated with parameters expressing tumor burden, such as AFP, nor with inflammation factors AST and γ-GT. In addition, the significant increase of circulating LTD4 levels was obtained in patients with HCC accompanied by chronic hepatitis B (CHB), compared with those patients suffering HCC alone(P < 0.05). Furthermore, although the slightly lower levels of LTD4 were detected in HCC patients with non-metastasis and therapy compared with metastasis and non-therapy, no significant differences were detected. Taken together, the levels of circulating LTD4 are elevated in HCC and it may participate in the pathogenesis of HCC as an inflammatory factor from CHB disease to HCC.
Literatur
1.
Zurück zum Zitat Berasain C, Castillo J, Perugorria MJ, et al. Inflammation and liver cancer: new molecular links. Ann NY Acad Sci. 2009;1155:206–21.CrossRefPubMed Berasain C, Castillo J, Perugorria MJ, et al. Inflammation and liver cancer: new molecular links. Ann NY Acad Sci. 2009;1155:206–21.CrossRefPubMed
2.
Zurück zum Zitat Berasain C, Castillo J, Prieto J, et al. New molecular targets for hepatocellular carcinoma: the ErbB1 signaling system. Liver Int. 2007;27:174–85.CrossRefPubMed Berasain C, Castillo J, Prieto J, et al. New molecular targets for hepatocellular carcinoma: the ErbB1 signaling system. Liver Int. 2007;27:174–85.CrossRefPubMed
3.
Zurück zum Zitat De Mitri MS, Cassini R, Bernardi M. Hepatitis B virus-related hepatocarcinogenesis: molecular oncogenic potential of clear or occult infections. Eur J Cancer. 2010;46(12):2178–86.CrossRefPubMed De Mitri MS, Cassini R, Bernardi M. Hepatitis B virus-related hepatocarcinogenesis: molecular oncogenic potential of clear or occult infections. Eur J Cancer. 2010;46(12):2178–86.CrossRefPubMed
4.
Zurück zum Zitat Samuelsson B. Leukotrienes: mediators of immediate hypersensitivity reactions and inflammation. Science. 1983;220:568–75.CrossRefPubMed Samuelsson B. Leukotrienes: mediators of immediate hypersensitivity reactions and inflammation. Science. 1983;220:568–75.CrossRefPubMed
5.
Zurück zum Zitat Bautz F, Denzlinger C, Kanz L, et al. Chemotaxis and transendothelial migration of CD34+ hematopoietic progenitor cells induced by the inflammatory mediator leukotriene D4 are mediated by the 7-transmembrane receptor CysLT1. Blood. 2001;97:3433–40.CrossRefPubMed Bautz F, Denzlinger C, Kanz L, et al. Chemotaxis and transendothelial migration of CD34+ hematopoietic progenitor cells induced by the inflammatory mediator leukotriene D4 are mediated by the 7-transmembrane receptor CysLT1. Blood. 2001;97:3433–40.CrossRefPubMed
6.
7.
Zurück zum Zitat Heise CE, O’Dowd BF, Figueroa DJ, et al. Characterization of the human cysteinyl leukotriene 2 receptor. J Biol Chem. 2000;275:30531–6.CrossRefPubMed Heise CE, O’Dowd BF, Figueroa DJ, et al. Characterization of the human cysteinyl leukotriene 2 receptor. J Biol Chem. 2000;275:30531–6.CrossRefPubMed
8.
Zurück zum Zitat Funk CD. Prostaglandins and leukotrienes: advances in eicosanoidbiology. Science. 2001;294:1871–5.CrossRefPubMed Funk CD. Prostaglandins and leukotrienes: advances in eicosanoidbiology. Science. 2001;294:1871–5.CrossRefPubMed
9.
Zurück zum Zitat Panettieri RA, Tan EM, Ciocca V, et al. Effects of LTD4 on human airway smooth muscle cell proliferation, matrix expression, and contraction in vitro:differential sensitivity to cysteinyl leukotriene receptor antagonists. Am J Respir Cell Mol Biol. 1998;19:453–61.PubMed Panettieri RA, Tan EM, Ciocca V, et al. Effects of LTD4 on human airway smooth muscle cell proliferation, matrix expression, and contraction in vitro:differential sensitivity to cysteinyl leukotriene receptor antagonists. Am J Respir Cell Mol Biol. 1998;19:453–61.PubMed
10.
Zurück zum Zitat Liu CY, Yu QJ, Lv M, et al. Effect of leukotrienes on proliferation of human esophageal carcinoma cell line. Chin Pract Med. 2007;2:1–5.CrossRef Liu CY, Yu QJ, Lv M, et al. Effect of leukotrienes on proliferation of human esophageal carcinoma cell line. Chin Pract Med. 2007;2:1–5.CrossRef
11.
Zurück zum Zitat Ohd JF, Wikström K, Sjölander A. Leukotrienes induce cell-survival signaling in intestinal epithelial cells. Gastroenterology. 2000;119:1007–18.CrossRefPubMed Ohd JF, Wikström K, Sjölander A. Leukotrienes induce cell-survival signaling in intestinal epithelial cells. Gastroenterology. 2000;119:1007–18.CrossRefPubMed
12.
Zurück zum Zitat Broom OJ, Nielsen OH. The role of cysteinyl leukotrienes in chronic inflammation and neoplasia of the intestine. Ugeskr Laeger. 2009;171:243–6.PubMed Broom OJ, Nielsen OH. The role of cysteinyl leukotrienes in chronic inflammation and neoplasia of the intestine. Ugeskr Laeger. 2009;171:243–6.PubMed
13.
Zurück zum Zitat Ohd JF, Nielsen CK, Campbell J, et al. Expression of the leukotriene D4 receptor CysLT1, COX-2, and other cell survival factors in colorectal adenocarcinomas. Gastroenterology. 2003;124:57–70.CrossRefPubMed Ohd JF, Nielsen CK, Campbell J, et al. Expression of the leukotriene D4 receptor CysLT1, COX-2, and other cell survival factors in colorectal adenocarcinomas. Gastroenterology. 2003;124:57–70.CrossRefPubMed
14.
Zurück zum Zitat Leier I, Müller M, Jedlitschky G, et al. Leukotriene uptake by hepatocytes and hepatoma cells. Eur J Biochem. 1992;209:281–9.CrossRefPubMed Leier I, Müller M, Jedlitschky G, et al. Leukotriene uptake by hepatocytes and hepatoma cells. Eur J Biochem. 1992;209:281–9.CrossRefPubMed
15.
16.
Zurück zum Zitat Martínez-Clemente M, Ferré N, González-Périz A, et al. 5-lipoxygenase deficiency reduces hepatic inflammation and tumor necrosis factor alpha-induced hepatocyte damage in hyperlipidemia-prone ApoE-null mice. Hepatology. 2010;51:817–27.CrossRefPubMed Martínez-Clemente M, Ferré N, González-Périz A, et al. 5-lipoxygenase deficiency reduces hepatic inflammation and tumor necrosis factor alpha-induced hepatocyte damage in hyperlipidemia-prone ApoE-null mice. Hepatology. 2010;51:817–27.CrossRefPubMed
17.
Zurück zum Zitat Zhang JS, Wu LR, Cui HS, et al. Determination of levels of leukotrienes in patients with hepatitis B. Chin J Clin Hepatol. 2007;23:172–3. Zhang JS, Wu LR, Cui HS, et al. Determination of levels of leukotrienes in patients with hepatitis B. Chin J Clin Hepatol. 2007;23:172–3.
18.
Zurück zum Zitat Möbius C, Aust G, Wiedmann M, et al. Prognostic value of eicosanoid pathways in extrahepatic cholangiocarcinoma. Anticancer Res. 2008;28:873–8.PubMed Möbius C, Aust G, Wiedmann M, et al. Prognostic value of eicosanoid pathways in extrahepatic cholangiocarcinoma. Anticancer Res. 2008;28:873–8.PubMed
19.
Zurück zum Zitat Okada F, Kawaguchi T, Habelhah H, et al. Conversion of human colonic adenoma cells to adenocarcinoma cells through inflammation in nude mice. Lab Invest. 2000;80:1617–28.CrossRefPubMed Okada F, Kawaguchi T, Habelhah H, et al. Conversion of human colonic adenoma cells to adenocarcinoma cells through inflammation in nude mice. Lab Invest. 2000;80:1617–28.CrossRefPubMed
20.
Zurück zum Zitat Zhou GX, Ding XL. Arachidonic acid metabolic pathways and pancreatic cancer. World J Gastroenterol. 2008;16:1483–6. Zhou GX, Ding XL. Arachidonic acid metabolic pathways and pancreatic cancer. World J Gastroenterol. 2008;16:1483–6.
21.
Zurück zum Zitat Ihara A, Wada K, Yoneda M, et al. Blockade of leukotriene B4 signaling pathway induces apoptosis and suppresses cell proliferation in colon cancer. J Pharmacol Sci. 2007;103:24–32.CrossRefPubMed Ihara A, Wada K, Yoneda M, et al. Blockade of leukotriene B4 signaling pathway induces apoptosis and suppresses cell proliferation in colon cancer. J Pharmacol Sci. 2007;103:24–32.CrossRefPubMed
Metadaten
Titel
Circulating LTD4 in patients with hepatocellular carcinoma
verfasst von
Yan Zhou
Dongmei Guo
Huiyu Li
Shenghua Jie
Publikationsdatum
01.02.2011
Verlag
Springer Netherlands
Erschienen in
Tumor Biology / Ausgabe 1/2011
Print ISSN: 1010-4283
Elektronische ISSN: 1423-0380
DOI
https://doi.org/10.1007/s13277-010-0107-8

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