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Erschienen in: Cellular Oncology 6/2012

01.12.2012 | Original Papers

High expression of heme oxygenase-1 is associated with tumor invasiveness and poor clinical outcome in non-small cell lung cancer patients

verfasst von: Jong-Rung Tsai, Hui-Min Wang, Po-Len Liu, Yung-Hsiang Chen, Ming-Chan Yang, Shah-Hwa Chou, Yu-Jen Cheng, Wei-Hsian Yin, Jhi-Jhu Hwang, Inn-Wen Chong

Erschienen in: Cellular Oncology | Ausgabe 6/2012

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Abstract

Background

Heme oxygenase-1 (HO-1), a rate-limiting enzyme in heme catabolism, is known to play a role in the protection of cells against oxidative stress, inflammation, anomalous proliferation and apoptosis. As yet, the role of HO-1 expression in non-small cell lung cancer (NSCLC) development and metastasis remains unclear and insufficient data are available regarding its impact on the prognosis of NSCLC patients.

Methods

Seventy NSCLC patients who underwent surgical resection were included in this HO-1 expression study and, concomitantly, clinical parameters were collected. Two lung adenocarcinoma cell lines (A549 and H441) were used to assess both invasive and migratory parameters in vitro.

Results

NSCLC patients with a high HO-1 expression ratio (tumor tissue/normal tissue) (> 1) exhibited a significantly poorer prognosis and a higher metastatic rate compared to those with a low HO-1 expression ratio (p < 0.05). The invasive and migratory abilities of A549 and H441 cells significantly increased after exogenous HO-1 over-expression and significantly decreased after siRNA-mediated HO-1 expression silencing. HO-1 up- and down-regulation also positively correlated with the expression of metastasis-associated proteins EGFR, CD147 and MMP-9. In addition, we found that HO-1 expression can be inhibited by PI3K and AKT inhibitors, but not by MAPK inhibitors.

Conclusions

HO-1 is a poor prognostic NSCLC predictor and its over-expression may increase the metastatic potential of NSCLC. Based on our findings and those of others, HO-1 may be considered as a novel NSCLC therapeutic target.
Literatur
1.
Zurück zum Zitat M.D. Maines, Heme oxygenase: Function, multiplicity, regulatory mechanisms, and clinical applications. FASEB J. 2, 2557–2568 (1988)PubMed M.D. Maines, Heme oxygenase: Function, multiplicity, regulatory mechanisms, and clinical applications. FASEB J. 2, 2557–2568 (1988)PubMed
2.
Zurück zum Zitat J.C. Becker, H. Fukui, Y. Imai, A. Sekikawa, T. Kimura, H. Yamagishi et al., Colonic expression of heme oxygenase-1 is associated with a better long-term survival in patients with colorectal cancer. Scand. J. Gastroenterol. 42, 852–858 (2007)PubMedCrossRef J.C. Becker, H. Fukui, Y. Imai, A. Sekikawa, T. Kimura, H. Yamagishi et al., Colonic expression of heme oxygenase-1 is associated with a better long-term survival in patients with colorectal cancer. Scand. J. Gastroenterol. 42, 852–858 (2007)PubMedCrossRef
3.
Zurück zum Zitat M.D. Maines, The heme oxygenase system: A regulator of second messenger gases. Annu. Rev. Pharmacol. Toxicol. 37, 517–554 (1997)PubMedCrossRef M.D. Maines, The heme oxygenase system: A regulator of second messenger gases. Annu. Rev. Pharmacol. Toxicol. 37, 517–554 (1997)PubMedCrossRef
4.
Zurück zum Zitat W. Durante, Heme oxygenase-1 in growth control and its clinical application to vascular disease. J. Cell. Physiol. 195, 373–382 (2003)PubMedCrossRef W. Durante, Heme oxygenase-1 in growth control and its clinical application to vascular disease. J. Cell. Physiol. 195, 373–382 (2003)PubMedCrossRef
5.
Zurück zum Zitat D. Morse, A.M. Choi, Heme oxygenase-1: The “emerging molecule” has arrived. American journal of respiratory cell and molecular biology 27, 8–16 (2002)PubMed D. Morse, A.M. Choi, Heme oxygenase-1: The “emerging molecule” has arrived. American journal of respiratory cell and molecular biology 27, 8–16 (2002)PubMed
6.
Zurück zum Zitat S.S. Lee, S.F. Yang, C.H. Tsai, M.C. Chou, M.Y. Chou, Y.C. Chang, Upregulation of heme oxygenase-1 expression in areca-quid-chewing-associated oral squamous cell carcinoma. Journal of the Formosan Medical Association Taiwan yi zhi. 107, 355–363 (2008)PubMedCrossRef S.S. Lee, S.F. Yang, C.H. Tsai, M.C. Chou, M.Y. Chou, Y.C. Chang, Upregulation of heme oxygenase-1 expression in areca-quid-chewing-associated oral squamous cell carcinoma. Journal of the Formosan Medical Association Taiwan yi zhi. 107, 355–363 (2008)PubMedCrossRef
7.
Zurück zum Zitat S. Ishikawa, S. Tamaki, M. Ohata, K. Arihara, M. Itoh, Heme induces DNA damage and hyperproliferation of colonic epithelial cells via hydrogen peroxide produced by heme oxygenase: A possible mechanism of heme-induced colon cancer. Mol. Nutr. Food. Res. 54, 1182–1191 (2010)PubMed S. Ishikawa, S. Tamaki, M. Ohata, K. Arihara, M. Itoh, Heme induces DNA damage and hyperproliferation of colonic epithelial cells via hydrogen peroxide produced by heme oxygenase: A possible mechanism of heme-induced colon cancer. Mol. Nutr. Food. Res. 54, 1182–1191 (2010)PubMed
8.
Zurück zum Zitat T. Ishikawa, N. Yoshida, H. Higashihara, M. Inoue, K. Uchiyama, T. Takagi et al., Different effects of constitutive nitric oxide synthase and heme oxygenase on pulmonary or liver metastasis of colon cancer in mice. Clinical & experimental metastasis. 20, 445–450 (2003)CrossRef T. Ishikawa, N. Yoshida, H. Higashihara, M. Inoue, K. Uchiyama, T. Takagi et al., Different effects of constitutive nitric oxide synthase and heme oxygenase on pulmonary or liver metastasis of colon cancer in mice. Clinical & experimental metastasis. 20, 445–450 (2003)CrossRef
9.
Zurück zum Zitat G. Gueron, A. De Siervi, M. Ferrando, M. Salierno, P. De Luca, B. Elguero et al., Critical role of endogenous heme oxygenase 1 as a tuner of the invasive potential of prostate cancer cells. Mol. Cancer Res. 7, 1745–1755 (2009)PubMedCrossRef G. Gueron, A. De Siervi, M. Ferrando, M. Salierno, P. De Luca, B. Elguero et al., Critical role of endogenous heme oxygenase 1 as a tuner of the invasive potential of prostate cancer cells. Mol. Cancer Res. 7, 1745–1755 (2009)PubMedCrossRef
10.
Zurück zum Zitat M.A. Alaoui-Jamali, T.A. Bismar, A. Gupta, W.A. Szarek, J. Su, W. Song et al., A novel experimental heme oxygenase-1-targeted therapy for hormone-refractory prostate cancer. Cancer Res. 69, 8017–8024 (2009)PubMedCrossRef M.A. Alaoui-Jamali, T.A. Bismar, A. Gupta, W.A. Szarek, J. Su, W. Song et al., A novel experimental heme oxygenase-1-targeted therapy for hormone-refractory prostate cancer. Cancer Res. 69, 8017–8024 (2009)PubMedCrossRef
11.
Zurück zum Zitat H.R. Kim, S. Kim, E.J. Kim, J.H. Park, S.H. Yang, E.T. Jeong et al., Suppression of Nrf2-driven heme oxygenase-1 enhances the chemosensitivity of lung cancer A549 cells toward cisplatin. Lung Cancer 60, 47–56 (2008)PubMedCrossRef H.R. Kim, S. Kim, E.J. Kim, J.H. Park, S.H. Yang, E.T. Jeong et al., Suppression of Nrf2-driven heme oxygenase-1 enhances the chemosensitivity of lung cancer A549 cells toward cisplatin. Lung Cancer 60, 47–56 (2008)PubMedCrossRef
12.
Zurück zum Zitat K. Hirai, T. Sasahira, H. Ohmori, K. Fujii, H. Kuniyasu, Inhibition of heme oxygenase-1 by zinc protoporphyrin IX reduces tumor growth of LL/2 lung cancer in C57BL mice. Int. J. Cancer 120, 500–505 (2007)PubMedCrossRef K. Hirai, T. Sasahira, H. Ohmori, K. Fujii, H. Kuniyasu, Inhibition of heme oxygenase-1 by zinc protoporphyrin IX reduces tumor growth of LL/2 lung cancer in C57BL mice. Int. J. Cancer 120, 500–505 (2007)PubMedCrossRef
13.
Zurück zum Zitat P. Boschetto, E. Zeni, L. Mazzetti, D. Miotto, N. Lo Cascio, P. Maestrelli et al., Decreased heme-oxygenase (HO)-1 in the macrophages of non-small cell lung cancer. Lung Cancer 59, 192–197 (2008)PubMedCrossRef P. Boschetto, E. Zeni, L. Mazzetti, D. Miotto, N. Lo Cascio, P. Maestrelli et al., Decreased heme-oxygenase (HO)-1 in the macrophages of non-small cell lung cancer. Lung Cancer 59, 192–197 (2008)PubMedCrossRef
14.
Zurück zum Zitat M.S. Degese, J.E. Mendizabal, N.A. Gandini, J.S. Gutkind, A. Molinolo, S.M. Hewitt et al., Expression of heme oxygenase-1 in non-small cell lung cancer (NSCLC) and its correlation with clinical data. Lung Cancer 77, 168–175 (2012)PubMedCrossRef M.S. Degese, J.E. Mendizabal, N.A. Gandini, J.S. Gutkind, A. Molinolo, S.M. Hewitt et al., Expression of heme oxygenase-1 in non-small cell lung cancer (NSCLC) and its correlation with clinical data. Lung Cancer 77, 168–175 (2012)PubMedCrossRef
15.
Zurück zum Zitat A. Jozkowicz, H. Was, J. Dulak, Heme oxygenase-1 in tumors: Is it a false friend? Antioxid. Redox. Signal. 9, 2099–2117 (2007)PubMedCrossRef A. Jozkowicz, H. Was, J. Dulak, Heme oxygenase-1 in tumors: Is it a false friend? Antioxid. Redox. Signal. 9, 2099–2117 (2007)PubMedCrossRef
16.
Zurück zum Zitat R.S. Herbst, Review of epidermal growth factor receptor biology. Int. J. Radiat. Oncol. Biol. Phys. 59, 21–26 (2004)PubMedCrossRef R.S. Herbst, Review of epidermal growth factor receptor biology. Int. J. Radiat. Oncol. Biol. Phys. 59, 21–26 (2004)PubMedCrossRef
17.
Zurück zum Zitat H. Sasaki, H. Yukiue, K. Mizuno, A. Sekimura, A. Konishi, M. Yano et al., Elevated serum epidermal growth factor receptor level is correlated with lymph node metastasis in lung cancer. International journal of clinical oncology/Japan Society of Clinical Oncology. 8, 79–82 (2003)PubMedCrossRef H. Sasaki, H. Yukiue, K. Mizuno, A. Sekimura, A. Konishi, M. Yano et al., Elevated serum epidermal growth factor receptor level is correlated with lymph node metastasis in lung cancer. International journal of clinical oncology/Japan Society of Clinical Oncology. 8, 79–82 (2003)PubMedCrossRef
18.
Zurück zum Zitat T. Kanekura, X. Chen, CD147/basigin promotes progression of malignant melanoma and other cancers. J. Dermatol. Sci. 57, 149–154 (2010)PubMedCrossRef T. Kanekura, X. Chen, CD147/basigin promotes progression of malignant melanoma and other cancers. J. Dermatol. Sci. 57, 149–154 (2010)PubMedCrossRef
19.
Zurück zum Zitat J. Xu, H.Y. Xu, Q. Zhang, F. Song, J.L. Jiang, X.M. Yang et al., HAb18G/CD147 functions in invasion and metastasis of hepatocellular carcinoma. Mol. Cancer Res. 5, 605–614 (2007)PubMedCrossRef J. Xu, H.Y. Xu, Q. Zhang, F. Song, J.L. Jiang, X.M. Yang et al., HAb18G/CD147 functions in invasion and metastasis of hepatocellular carcinoma. Mol. Cancer Res. 5, 605–614 (2007)PubMedCrossRef
20.
Zurück zum Zitat H. Voigt, C.S. Vetter-Kauczok, D. Schrama, U.B. Hofmann, J.C. Becker, R. Houben, CD147 impacts angiogenesis and metastasis formation. Cancer investigation. 27, 329–333 (2009)PubMedCrossRef H. Voigt, C.S. Vetter-Kauczok, D. Schrama, U.B. Hofmann, J.C. Becker, R. Houben, CD147 impacts angiogenesis and metastasis formation. Cancer investigation. 27, 329–333 (2009)PubMedCrossRef
21.
Zurück zum Zitat H. Was, J. Dulak, A. Jozkowicz, Heme oxygenase-1 in tumor biology and therapy. Current drug targets. 11, 1551–1570 (2010)PubMedCrossRef H. Was, J. Dulak, A. Jozkowicz, Heme oxygenase-1 in tumor biology and therapy. Current drug targets. 11, 1551–1570 (2010)PubMedCrossRef
22.
Zurück zum Zitat H. Was, T. Cichon, R. Smolarczyk, D. Rudnicka, M. Stopa, C. Chevalier et al., Overexpression of heme oxygenase-1 in murine melanoma: Increased proliferation and viability of tumor cells, decreased survival of mice. Am. J. Pathol. 169, 2181–2198 (2006)PubMedCrossRef H. Was, T. Cichon, R. Smolarczyk, D. Rudnicka, M. Stopa, C. Chevalier et al., Overexpression of heme oxygenase-1 in murine melanoma: Increased proliferation and viability of tumor cells, decreased survival of mice. Am. J. Pathol. 169, 2181–2198 (2006)PubMedCrossRef
23.
Zurück zum Zitat M.H. Tsuji, T. Yanagawa, S. Iwasa, K. Tabuchi, K. Onizawa, S. Bannai et al., Heme oxygenase-1 expression in oral squamous cell carcinoma as involved in lymph node metastasis. Cancer Lett. 138, 53–59 (1999)PubMedCrossRef M.H. Tsuji, T. Yanagawa, S. Iwasa, K. Tabuchi, K. Onizawa, S. Bannai et al., Heme oxygenase-1 expression in oral squamous cell carcinoma as involved in lymph node metastasis. Cancer Lett. 138, 53–59 (1999)PubMedCrossRef
24.
Zurück zum Zitat M. Sunamura, D.G. Duda, M.H. Ghattas, L. Lozonschi, F. Motoi, J. Yamauchi et al., Heme oxygenase-1 accelerates tumor angiogenesis of human pancreatic cancer. Angiogenesis 6, 15–24 (2003)PubMedCrossRef M. Sunamura, D.G. Duda, M.H. Ghattas, L. Lozonschi, F. Motoi, J. Yamauchi et al., Heme oxygenase-1 accelerates tumor angiogenesis of human pancreatic cancer. Angiogenesis 6, 15–24 (2003)PubMedCrossRef
25.
Zurück zum Zitat P. Boschetto, E. Zeni, L. Mazzetti, D. Miotto, N.L. Cascio, P. Maestrelli et al., Decreased heme-oxygenase (HO)-1 in the macrophages of non-small cell lung cancer. Lung Cancer 59, 192–197 (2008)PubMedCrossRef P. Boschetto, E. Zeni, L. Mazzetti, D. Miotto, N.L. Cascio, P. Maestrelli et al., Decreased heme-oxygenase (HO)-1 in the macrophages of non-small cell lung cancer. Lung Cancer 59, 192–197 (2008)PubMedCrossRef
26.
Zurück zum Zitat C.K. Andreadi, L.M. Howells, P.A. Atherfold, M.M. Manson, Involvement of Nrf2, p38, B-Raf, and nuclear factor-kappaB, but not phosphatidylinositol 3-kinase, in induction of hemeoxygenase-1 by dietary polyphenols. Mol. Pharmacol. 69, 1033–1040 (2006)PubMed C.K. Andreadi, L.M. Howells, P.A. Atherfold, M.M. Manson, Involvement of Nrf2, p38, B-Raf, and nuclear factor-kappaB, but not phosphatidylinositol 3-kinase, in induction of hemeoxygenase-1 by dietary polyphenols. Mol. Pharmacol. 69, 1033–1040 (2006)PubMed
27.
Zurück zum Zitat S. Kocanova, E. Buytaert, J.Y. Matroule, J. Piette, J. Golab, P. de Witte et al., Induction of heme-oxygenase 1 requires the p38MAPK and PI3K pathways and suppresses apoptotic cell death following hypericin-mediated photodynamic therapy. Apoptosis 12, 731–741 (2007)PubMedCrossRef S. Kocanova, E. Buytaert, J.Y. Matroule, J. Piette, J. Golab, P. de Witte et al., Induction of heme-oxygenase 1 requires the p38MAPK and PI3K pathways and suppresses apoptotic cell death following hypericin-mediated photodynamic therapy. Apoptosis 12, 731–741 (2007)PubMedCrossRef
28.
Zurück zum Zitat E.J. Joung, M.H. Li, H.G. Lee, N. Somparn, Y.S. Jung, H.K. Na et al., Capsaicin induces heme oxygenase-1 expression in HepG2 cells via activation of PI3K-Nrf2 signaling: NAD(P)H:quinone oxidoreductase as a potential target. Antioxid. Redox. Signal. 9, 2087–2098 (2007)PubMedCrossRef E.J. Joung, M.H. Li, H.G. Lee, N. Somparn, Y.S. Jung, H.K. Na et al., Capsaicin induces heme oxygenase-1 expression in HepG2 cells via activation of PI3K-Nrf2 signaling: NAD(P)H:quinone oxidoreductase as a potential target. Antioxid. Redox. Signal. 9, 2087–2098 (2007)PubMedCrossRef
29.
Zurück zum Zitat C.F. Mountain, Revisions in the International System for Staging Lung Cancer. Chest 111, 1710–1717 (1997)PubMedCrossRef C.F. Mountain, Revisions in the International System for Staging Lung Cancer. Chest 111, 1710–1717 (1997)PubMedCrossRef
30.
Zurück zum Zitat V.K. Sarhadi, H. Wikman, K. Salmenkivi, E. Kuosma, T. Sioris, J. Salo et al., Increased expression of high mobility group A proteins in lung cancer. J. Pathol. 209, 206–212 (2006)PubMedCrossRef V.K. Sarhadi, H. Wikman, K. Salmenkivi, E. Kuosma, T. Sioris, J. Salo et al., Increased expression of high mobility group A proteins in lung cancer. J. Pathol. 209, 206–212 (2006)PubMedCrossRef
31.
Zurück zum Zitat H. Wikman, E. Kettunen, J.K. Seppanen, A. Karjalainen, J. Hollmen, S. Anttila et al., Identification of differentially expressed genes in pulmonary adenocarcinoma by using cDNA array. Oncogene 21, 5804–5813 (2002)PubMedCrossRef H. Wikman, E. Kettunen, J.K. Seppanen, A. Karjalainen, J. Hollmen, S. Anttila et al., Identification of differentially expressed genes in pulmonary adenocarcinoma by using cDNA array. Oncogene 21, 5804–5813 (2002)PubMedCrossRef
32.
Zurück zum Zitat T.C. Wu, Y.H. Chen, H.B. Leu, Y.L. Chen, F.Y. Lin, S.J. Lin et al., Carvedilol, a pharmacological antioxidant, inhibits neointimal matrix metalloproteinase-2 and −9 in experimental atherosclerosis. Free Radic. Biol. Med. 43, 1508–1522 (2007)PubMedCrossRef T.C. Wu, Y.H. Chen, H.B. Leu, Y.L. Chen, F.Y. Lin, S.J. Lin et al., Carvedilol, a pharmacological antioxidant, inhibits neointimal matrix metalloproteinase-2 and −9 in experimental atherosclerosis. Free Radic. Biol. Med. 43, 1508–1522 (2007)PubMedCrossRef
33.
Zurück zum Zitat S.J. Lin, I.T. Lee, Y.H. Chen, F.Y. Lin, L.M. Sheu, H.H. Ku et al., Salvianolic acid B attenuates MMP-2 and MMP-9 expression in vivo in apolipoprotein-E-deficient mouse aorta and in vitro in LPS-treated human aortic smooth muscle cells. J. Cell. Biochem. 100, 372–384 (2007)PubMedCrossRef S.J. Lin, I.T. Lee, Y.H. Chen, F.Y. Lin, L.M. Sheu, H.H. Ku et al., Salvianolic acid B attenuates MMP-2 and MMP-9 expression in vivo in apolipoprotein-E-deficient mouse aorta and in vitro in LPS-treated human aortic smooth muscle cells. J. Cell. Biochem. 100, 372–384 (2007)PubMedCrossRef
34.
Zurück zum Zitat H.M. Wang, C.C. Chiu, P.F. Wu, C.Y. Chen, Subamolide E from Cinnamomum subavenium induces sub-G1 cell-cycle arrest and caspase-dependent apoptosis and reduces the migration ability of human melanoma cells. J. Agric. Food Chem. 59, 8187–8192 (2011)PubMedCrossRef H.M. Wang, C.C. Chiu, P.F. Wu, C.Y. Chen, Subamolide E from Cinnamomum subavenium induces sub-G1 cell-cycle arrest and caspase-dependent apoptosis and reduces the migration ability of human melanoma cells. J. Agric. Food Chem. 59, 8187–8192 (2011)PubMedCrossRef
35.
Zurück zum Zitat F. Shiraishi, L.M. Curtis, L. Truong, K. Poss, G.A. Visner, K. Madsen, H.S. Nick, A. Agarwal, Heme oxygenase-1 gene ablation or expression modulates cisplatin-induced renal tubular apoptosis. Am J Physiol Renal Physiol 278, F726–F736 (2000)PubMed F. Shiraishi, L.M. Curtis, L. Truong, K. Poss, G.A. Visner, K. Madsen, H.S. Nick, A. Agarwal, Heme oxygenase-1 gene ablation or expression modulates cisplatin-induced renal tubular apoptosis. Am J Physiol Renal Physiol 278, F726–F736 (2000)PubMed
36.
Zurück zum Zitat A. Albini, R. Benelli, The chemoinvasion assay: A method to assess tumor and endothelial cell invasion and its modulation. Nat. Protoc. 2(504–11) (2007) A. Albini, R. Benelli, The chemoinvasion assay: A method to assess tumor and endothelial cell invasion and its modulation. Nat. Protoc. 2(504–11) (2007)
37.
Zurück zum Zitat S. Tang, K.G. Morgan, C. Parker, J.A. Ware, Requirement for protein kinase C theta for cell cycle progression and formation of actin stress fibers and filopodia in vascular endothelial cells. J. Biol. Chem. 272, 28704–28711 (1997)PubMedCrossRef S. Tang, K.G. Morgan, C. Parker, J.A. Ware, Requirement for protein kinase C theta for cell cycle progression and formation of actin stress fibers and filopodia in vascular endothelial cells. J. Biol. Chem. 272, 28704–28711 (1997)PubMedCrossRef
38.
Zurück zum Zitat G. Wang, E. Reed, Q.Q. Li, Molecular basis of cellular response to cisplatin chemotherapy in non-small cell lung cancer (Review). Oncol. Rep. 12, 955–965 (2004)PubMed G. Wang, E. Reed, Q.Q. Li, Molecular basis of cellular response to cisplatin chemotherapy in non-small cell lung cancer (Review). Oncol. Rep. 12, 955–965 (2004)PubMed
39.
Zurück zum Zitat N. Grabinski, K. Bartkowiak, K. Grupp, B. Brandt, K. Pantel, M. Jucker, Distinct functional roles of Akt isoforms for proliferation, survival, migration and EGF-mediated signalling in lung cancer derived disseminated tumor cells. Cell. Signal. 23, 1952–1960 (2011)PubMedCrossRef N. Grabinski, K. Bartkowiak, K. Grupp, B. Brandt, K. Pantel, M. Jucker, Distinct functional roles of Akt isoforms for proliferation, survival, migration and EGF-mediated signalling in lung cancer derived disseminated tumor cells. Cell. Signal. 23, 1952–1960 (2011)PubMedCrossRef
40.
Zurück zum Zitat L. Mansi, E. Viel, E. Curtit, J. Medioni, C. Le Tourneau, Targeting the RAS signalling pathway in cancer therapy. Nat. Rev. Cancer 3, 11–22 (2003)CrossRef L. Mansi, E. Viel, E. Curtit, J. Medioni, C. Le Tourneau, Targeting the RAS signalling pathway in cancer therapy. Nat. Rev. Cancer 3, 11–22 (2003)CrossRef
41.
Zurück zum Zitat R. Tenhunen, H.S. Marver, R. Schmid, The enzymatic conversion of heme to bilirubin by microsomal heme oxygenase. Proc. Natl. Acad. Sci. U. S. A. 61, 748–755 (1968)PubMedCrossRef R. Tenhunen, H.S. Marver, R. Schmid, The enzymatic conversion of heme to bilirubin by microsomal heme oxygenase. Proc. Natl. Acad. Sci. U. S. A. 61, 748–755 (1968)PubMedCrossRef
42.
Zurück zum Zitat K. Doi, T. Akaike, S. Fujii, S. Tanaka, N. Ikebe, T. Beppu et al., Induction of haem oxygenase-1 nitric oxide and ischaemia in experimental solid tumours and implications for tumour growth. Br. J. Cancer 80, 1945–1954 (1999)PubMedCrossRef K. Doi, T. Akaike, S. Fujii, S. Tanaka, N. Ikebe, T. Beppu et al., Induction of haem oxygenase-1 nitric oxide and ischaemia in experimental solid tumours and implications for tumour growth. Br. J. Cancer 80, 1945–1954 (1999)PubMedCrossRef
43.
Zurück zum Zitat E. Hara, K. Takahashi, T. Tominaga, T. Kumabe, T. Kayama, H. Suzuki et al., Expression of heme oxygenase and inducible nitric oxide synthase mRNA in human brain tumors. Biochem. Biophys. Res. Commun. 224, 153–158 (1996)PubMedCrossRef E. Hara, K. Takahashi, T. Tominaga, T. Kumabe, T. Kayama, H. Suzuki et al., Expression of heme oxygenase and inducible nitric oxide synthase mRNA in human brain tumors. Biochem. Biophys. Res. Commun. 224, 153–158 (1996)PubMedCrossRef
44.
Zurück zum Zitat M.Y. Li, J. Yip, M.K. Hsin, T.S. Mok, Y. Wu, M.J. Underwood et al., Haem oxygenase-1 plays a central role in NNK-mediated lung carcinogenesis. Eur. Respir. J. 32, 911–923 (2008)PubMedCrossRef M.Y. Li, J. Yip, M.K. Hsin, T.S. Mok, Y. Wu, M.J. Underwood et al., Haem oxygenase-1 plays a central role in NNK-mediated lung carcinogenesis. Eur. Respir. J. 32, 911–923 (2008)PubMedCrossRef
45.
Zurück zum Zitat H. Kuroda, M. Takeno, S. Murakami, N. Miyazawa, T. Kaneko, Y. Ishigatsubo, Inhibition of heme oxygenase-1 with an epidermal growth factor receptor inhibitor and cisplatin decreases proliferation of lung cancer A549 cells. Lung Cancer 67, 31–36 (2010)PubMedCrossRef H. Kuroda, M. Takeno, S. Murakami, N. Miyazawa, T. Kaneko, Y. Ishigatsubo, Inhibition of heme oxygenase-1 with an epidermal growth factor receptor inhibitor and cisplatin decreases proliferation of lung cancer A549 cells. Lung Cancer 67, 31–36 (2010)PubMedCrossRef
46.
Zurück zum Zitat P.L. Liu, J.R. Tsai, A.L. Charles, J.J. Hwang, S.H. Chou, Y.H. Ping et al., Resveratrol inhibits human lung adenocarcinoma cell metastasis by suppressing heme oxygenase 1-mediated nuclear factor-kappaB pathway and subsequently downregulating expression of matrix metalloproteinases. Mol. Nutr. Food Res. 54(2), S196–S204 (2010)PubMedCrossRef P.L. Liu, J.R. Tsai, A.L. Charles, J.J. Hwang, S.H. Chou, Y.H. Ping et al., Resveratrol inhibits human lung adenocarcinoma cell metastasis by suppressing heme oxygenase 1-mediated nuclear factor-kappaB pathway and subsequently downregulating expression of matrix metalloproteinases. Mol. Nutr. Food Res. 54(2), S196–S204 (2010)PubMedCrossRef
47.
Zurück zum Zitat T. Yanagawa, K. Omura, H. Harada, K. Nakaso, S. Iwasa, Y. Koyama et al., Heme oxygenase-1 expression predicts cervical lymph node metastasis of tongue squamous cell carcinomas. Oral oncology. 40, 21–27 (2004)PubMedCrossRef T. Yanagawa, K. Omura, H. Harada, K. Nakaso, S. Iwasa, Y. Koyama et al., Heme oxygenase-1 expression predicts cervical lymph node metastasis of tongue squamous cell carcinomas. Oral oncology. 40, 21–27 (2004)PubMedCrossRef
48.
Zurück zum Zitat G. De Palma, P. Mozzoni, O. Acampa, E. Internullo, P. Carbognani, M. Rusca et al., Expression levels of some antioxidant and epidermal growth factor receptor genes in patients with early-stage non-small cell lung cancer. Journal of nucleic acids (2010). G. De Palma, P. Mozzoni, O. Acampa, E. Internullo, P. Carbognani, M. Rusca et al., Expression levels of some antioxidant and epidermal growth factor receptor genes in patients with early-stage non-small cell lung cancer. Journal of nucleic acids (2010).
49.
Zurück zum Zitat M. Mareel, I. Madani, Tumour-associated host cells participating at invasion and metastasis: Targets for therapy? Acta. chirurgica. Belgica. 106, 635–640 (2006)PubMed M. Mareel, I. Madani, Tumour-associated host cells participating at invasion and metastasis: Targets for therapy? Acta. chirurgica. Belgica. 106, 635–640 (2006)PubMed
50.
Zurück zum Zitat A. Prawan, J.K. Kundu, Y.J. Surh, Molecular basis of heme oxygenase-1 induction: Implications for chemoprevention and chemoprotection. Antioxid. Redox. Signal. 7, 1688–1703 (2005)PubMedCrossRef A. Prawan, J.K. Kundu, Y.J. Surh, Molecular basis of heme oxygenase-1 induction: Implications for chemoprevention and chemoprotection. Antioxid. Redox. Signal. 7, 1688–1703 (2005)PubMedCrossRef
51.
Zurück zum Zitat J. Alam, C. Wicks, D. Stewart, P. Gong, C. Touchard, S. Otterbein et al., Mechanism of heme oxygenase-1 gene activation by cadmium in MCF-7 mammary epithelial cells. Role of p38 kinase and Nrf2 transcription factor. J. Biol. Chem. 275, 27694–27702 (2000)PubMed J. Alam, C. Wicks, D. Stewart, P. Gong, C. Touchard, S. Otterbein et al., Mechanism of heme oxygenase-1 gene activation by cadmium in MCF-7 mammary epithelial cells. Role of p38 kinase and Nrf2 transcription factor. J. Biol. Chem. 275, 27694–27702 (2000)PubMed
52.
Zurück zum Zitat E.H. Kim, D.H. Kim, H.K. Na, Y.J. Surh, Effects of cyclopentenone prostaglandins on the expression of heme oxygenase-1 in MCF-7 cells. Ann. N. Y. Acad. Sci. 1030, 493–500 (2004)PubMedCrossRef E.H. Kim, D.H. Kim, H.K. Na, Y.J. Surh, Effects of cyclopentenone prostaglandins on the expression of heme oxygenase-1 in MCF-7 cells. Ann. N. Y. Acad. Sci. 1030, 493–500 (2004)PubMedCrossRef
Metadaten
Titel
High expression of heme oxygenase-1 is associated with tumor invasiveness and poor clinical outcome in non-small cell lung cancer patients
verfasst von
Jong-Rung Tsai
Hui-Min Wang
Po-Len Liu
Yung-Hsiang Chen
Ming-Chan Yang
Shah-Hwa Chou
Yu-Jen Cheng
Wei-Hsian Yin
Jhi-Jhu Hwang
Inn-Wen Chong
Publikationsdatum
01.12.2012
Verlag
Springer Netherlands
Erschienen in
Cellular Oncology / Ausgabe 6/2012
Print ISSN: 2211-3428
Elektronische ISSN: 2211-3436
DOI
https://doi.org/10.1007/s13402-012-0105-5

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