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Erschienen in: Cancer and Metastasis Reviews 2-3/2018

10.08.2018

Triumph and tumult of matrix metalloproteinases and their crosstalk with eicosanoids in cancer

verfasst von: Kasturi Chatterjee, Sayantan Jana, Preety Choudhary, Snehasikta Swarnakar

Erschienen in: Cancer and Metastasis Reviews | Ausgabe 2-3/2018

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Abstract

Cancer development and metastasis are associated to perturbation in metabolic functions of tumor cells and surrounding inflammatory and stromal cell responses. Eicosanoids and lipid mediators, in this regard, attract potential attention during cancer development. Eicosanoids, which include prostaglandin, prostacyclin, thromboxane, and leukotriene, are synthesized from arachidonic acid when cells are stimulated by stress, cytokines, or other growth factors. However, the underlying mechanism of eicosanoids in cancer development, specially their interactions with proto-oncogene factors in tumor microenvironment, remain unexplored. On the other hand, matrix metalloproteinases (MMPs) are a group of zinc-dependent endopeptidases which are involved in degradation of different extracellular matrix (ECM) proteins. MMPs are associated with different physiological responses, including embryogenesis, vasculogenesis, and cellular remodeling, as well as different disease pathogenesis. Induced MMP responses are especially associated with cancer metastasis and secondary tumor development through proteolytic cleavage of several ECM and non-ECM proteins. Although both eicosanoids and MMPs are involved with cancer progression and metastasis, the interrelation between these two molecules are less explored. The present review discusses relevant studies that connect eicosanoids and MMPs and highlight the crosstalk between them offering novel therapeutic approach in cancer treatment.
Literatur
17.
Zurück zum Zitat Krysan, K., Reckamp, K. L., Dalwadi, H., Sharma, S., Rozengurt, E., Dohadwala, M., et al. (2005). Prostaglandin E2 activates mitogen-activated protein kinase/Erk pathway signaling and cell proliferation in non-small cell lung cancer cells in an epidermal growth factor receptor-independent manner. Cancer Research, 65(14), 6275–6281. https://doi.org/10.1158/0008-5472.Can-05-0216.PubMedCrossRef Krysan, K., Reckamp, K. L., Dalwadi, H., Sharma, S., Rozengurt, E., Dohadwala, M., et al. (2005). Prostaglandin E2 activates mitogen-activated protein kinase/Erk pathway signaling and cell proliferation in non-small cell lung cancer cells in an epidermal growth factor receptor-independent manner. Cancer Research, 65(14), 6275–6281. https://​doi.​org/​10.​1158/​0008-5472.​Can-05-0216.PubMedCrossRef
20.
Zurück zum Zitat Ihara, A., Wada, K., Yoneda, M., Fujisawa, N., Takahashi, H., & Nakajima, A. (2007). Blockade of leukotriene B4 signaling pathway induces apoptosis and suppresses cell proliferation in colon cancer. Journal of Pharmacological Sciences, 103(1), 24–32.PubMedCrossRef Ihara, A., Wada, K., Yoneda, M., Fujisawa, N., Takahashi, H., & Nakajima, A. (2007). Blockade of leukotriene B4 signaling pathway induces apoptosis and suppresses cell proliferation in colon cancer. Journal of Pharmacological Sciences, 103(1), 24–32.PubMedCrossRef
28.
Zurück zum Zitat Chang, S. H., Liu, C. H., Conway, R., Han, D. K., Nithipatikom, K., Trifan, O. C., et al. (2004). Role of prostaglandin E2-dependent angiogenic switch in cyclooxygenase 2-induced breast cancer progression. Proceedings of the National Academy of Sciences of the United States of America, 101(2), 591–596. https://doi.org/10.1073/pnas.2535911100.PubMedCrossRef Chang, S. H., Liu, C. H., Conway, R., Han, D. K., Nithipatikom, K., Trifan, O. C., et al. (2004). Role of prostaglandin E2-dependent angiogenic switch in cyclooxygenase 2-induced breast cancer progression. Proceedings of the National Academy of Sciences of the United States of America, 101(2), 591–596. https://​doi.​org/​10.​1073/​pnas.​2535911100.PubMedCrossRef
31.
Zurück zum Zitat Spinella, F., Rosano, L., Di Castro, V., Natali, P. G., & Bagnato, A. (2004). Endothelin-1-induced prostaglandin E2-EP2, EP4 signaling regulates vascular endothelial growth factor production and ovarian carcinoma cell invasion. The Journal of Biological Chemistry, 279(45), 46700–46705. https://doi.org/10.1074/jbc.M408584200.PubMedCrossRef Spinella, F., Rosano, L., Di Castro, V., Natali, P. G., & Bagnato, A. (2004). Endothelin-1-induced prostaglandin E2-EP2, EP4 signaling regulates vascular endothelial growth factor production and ovarian carcinoma cell invasion. The Journal of Biological Chemistry, 279(45), 46700–46705. https://​doi.​org/​10.​1074/​jbc.​M408584200.PubMedCrossRef
33.
36.
Zurück zum Zitat Daniel, T. O., Liu, H., Morrow, J. D., Crews, B. C., & Marnett, L. J. (1999). Thromboxane A2 is a mediator of cyclooxygenase-2-dependent endothelial migration and angiogenesis. Cancer Research, 59(18), 4574–4577.PubMed Daniel, T. O., Liu, H., Morrow, J. D., Crews, B. C., & Marnett, L. J. (1999). Thromboxane A2 is a mediator of cyclooxygenase-2-dependent endothelial migration and angiogenesis. Cancer Research, 59(18), 4574–4577.PubMed
37.
38.
Zurück zum Zitat Baratelli, F., Lin, Y., Zhu, L., Yang, S. C., Heuze-Vourc'h, N., Zeng, G., et al. (2005). Prostaglandin E2 induces FOXP3 gene expression and T regulatory cell function in human CD4+ T cells. Journal of Immunology, 175(3), 1483–1490.CrossRef Baratelli, F., Lin, Y., Zhu, L., Yang, S. C., Heuze-Vourc'h, N., Zeng, G., et al. (2005). Prostaglandin E2 induces FOXP3 gene expression and T regulatory cell function in human CD4+ T cells. Journal of Immunology, 175(3), 1483–1490.CrossRef
40.
Zurück zum Zitat Swarnakar, S., & Jana, S. (2018). Matrix metalloproteinase. In S. Choi (Ed.), Encyclopedia of Signaling Molecules (2nd ed., pp. 3162–3162). Cham: Springer International Publishing. Swarnakar, S., & Jana, S. (2018). Matrix metalloproteinase. In S. Choi (Ed.), Encyclopedia of Signaling Molecules (2nd ed., pp. 3162–3162). Cham: Springer International Publishing.
43.
Zurück zum Zitat Ha, H. Y., Moon, H. B., Nam, M. S., Lee, J. W., Ryoo, Z. Y., Lee, T. H., et al. (2001). Overexpression of membrane-type matrix metalloproteinase-1 gene induces mammary gland abnormalities and adenocarcinoma in transgenic mice. Cancer Research, 61(3), 984–990.PubMed Ha, H. Y., Moon, H. B., Nam, M. S., Lee, J. W., Ryoo, Z. Y., Lee, T. H., et al. (2001). Overexpression of membrane-type matrix metalloproteinase-1 gene induces mammary gland abnormalities and adenocarcinoma in transgenic mice. Cancer Research, 61(3), 984–990.PubMed
44.
Zurück zum Zitat Sternlicht, M. D., Lochter, A., Sympson, C. J., Huey, B., Rougier, J. P., Gray, J. W., et al. (1999). The stromal proteinase MMP3/stromelysin-1 promotes mammary carcinogenesis. Cell, 98(2), 137–146.PubMedPubMedCentralCrossRef Sternlicht, M. D., Lochter, A., Sympson, C. J., Huey, B., Rougier, J. P., Gray, J. W., et al. (1999). The stromal proteinase MMP3/stromelysin-1 promotes mammary carcinogenesis. Cell, 98(2), 137–146.PubMedPubMedCentralCrossRef
47.
Zurück zum Zitat Ichikawa, Y., Ishikawa, T., Momiyama, N., Kamiyama, M., Sakurada, H., Matsuyama, R., et al. (2006). Matrilysin (MMP-7) degrades VE-cadherin and accelerates accumulation of beta-catenin in the nucleus of human umbilical vein endothelial cells. Oncology Reports, 15(2), 311–315.PubMed Ichikawa, Y., Ishikawa, T., Momiyama, N., Kamiyama, M., Sakurada, H., Matsuyama, R., et al. (2006). Matrilysin (MMP-7) degrades VE-cadherin and accelerates accumulation of beta-catenin in the nucleus of human umbilical vein endothelial cells. Oncology Reports, 15(2), 311–315.PubMed
49.
Zurück zum Zitat Chatterjee, K., Jana, S., DasMahapatra, P., & Swarnakar, S. (2018). EGFR-mediated matrix metalloproteinase-7 up-regulation promotes epithelial-mesenchymal transition via ERK1-AP1 axis during ovarian endometriosis progression. The FASEB Journal, fj201701382RR. https://doi.org/10.1096/fj.201701382RR. Chatterjee, K., Jana, S., DasMahapatra, P., & Swarnakar, S. (2018). EGFR-mediated matrix metalloproteinase-7 up-regulation promotes epithelial-mesenchymal transition via ERK1-AP1 axis during ovarian endometriosis progression. The FASEB Journal, fj201701382RR. https://​doi.​org/​10.​1096/​fj.​201701382RR.
50.
Zurück zum Zitat Suzuki, M., Raab, G., Moses, M. A., Fernandez, C. A., & Klagsbrun, M. (1997). Matrix metalloproteinase-3 releases active heparin-binding EGF-like growth factor by cleavage at a specific juxtamembrane site. The Journal of Biological Chemistry, 272(50), 31730–31737.PubMedCrossRef Suzuki, M., Raab, G., Moses, M. A., Fernandez, C. A., & Klagsbrun, M. (1997). Matrix metalloproteinase-3 releases active heparin-binding EGF-like growth factor by cleavage at a specific juxtamembrane site. The Journal of Biological Chemistry, 272(50), 31730–31737.PubMedCrossRef
51.
Zurück zum Zitat Peschon, J. J., Slack, J. L., Reddy, P., Stocking, K. L., Sunnarborg, S. W., Lee, D. C., et al. (1998). An essential role for ectodomain shedding in mammalian development. Science, 282(5392), 1281–1284.PubMedCrossRef Peschon, J. J., Slack, J. L., Reddy, P., Stocking, K. L., Sunnarborg, S. W., Lee, D. C., et al. (1998). An essential role for ectodomain shedding in mammalian development. Science, 282(5392), 1281–1284.PubMedCrossRef
52.
Zurück zum Zitat Vargo-Gogola, T., Crawford, H. C., Fingleton, B., & Matrisian, L. M. (2002). Identification of novel matrix metalloproteinase-7 (matrilysin) cleavage sites in murine and human Fas ligand. Archives of Biochemistry and Biophysics, 408(2), 155–161.PubMedCrossRef Vargo-Gogola, T., Crawford, H. C., Fingleton, B., & Matrisian, L. M. (2002). Identification of novel matrix metalloproteinase-7 (matrilysin) cleavage sites in murine and human Fas ligand. Archives of Biochemistry and Biophysics, 408(2), 155–161.PubMedCrossRef
54.
Zurück zum Zitat Bergers, G., Brekken, R., McMahon, G., Vu, T. H., Itoh, T., Tamaki, K., et al. (2000). Matrix metalloproteinase-9 triggers the angiogenic switch during carcinogenesis. Nature Cell Biology, 2(10), 737–744.PubMedPubMedCentralCrossRef Bergers, G., Brekken, R., McMahon, G., Vu, T. H., Itoh, T., Tamaki, K., et al. (2000). Matrix metalloproteinase-9 triggers the angiogenic switch during carcinogenesis. Nature Cell Biology, 2(10), 737–744.PubMedPubMedCentralCrossRef
56.
Zurück zum Zitat Sheu, B. C., Hsu, S. M., Ho, H. N., Lien, H. C., Huang, S. C., & Lin, R. H. (2001). A novel role of metalloproteinase in cancer-mediated immunosuppression. Cancer Research, 61(1), 237–242.PubMed Sheu, B. C., Hsu, S. M., Ho, H. N., Lien, H. C., Huang, S. C., & Lin, R. H. (2001). A novel role of metalloproteinase in cancer-mediated immunosuppression. Cancer Research, 61(1), 237–242.PubMed
57.
Zurück zum Zitat Yu, Q., & Stamenkovic, I. (2000). Cell surface-localized matrix metalloproteinase-9 proteolytically activates TGF-beta and promotes tumor invasion and angiogenesis. Genes & Development, 14(2), 163–176. Yu, Q., & Stamenkovic, I. (2000). Cell surface-localized matrix metalloproteinase-9 proteolytically activates TGF-beta and promotes tumor invasion and angiogenesis. Genes & Development, 14(2), 163–176.
58.
Zurück zum Zitat Gorelik, L., & Flavell, R. A. (2001). Immune-mediated eradication of tumors through the blockade of transforming growth factor-beta signaling in T cells. Nature Medicine, 7(10), 1118–1122.PubMedCrossRef Gorelik, L., & Flavell, R. A. (2001). Immune-mediated eradication of tumors through the blockade of transforming growth factor-beta signaling in T cells. Nature Medicine, 7(10), 1118–1122.PubMedCrossRef
59.
Zurück zum Zitat O'Reilly, M. S., Holmgren, L., Shing, Y., Chen, C., Rosenthal, R. A., Moses, M., et al. (1994). Angiostatin: a novel angiogenesis inhibitor that mediates the suppression of metastases by a Lewis lung carcinoma. Cell, 79(2), 315–328.PubMedCrossRef O'Reilly, M. S., Holmgren, L., Shing, Y., Chen, C., Rosenthal, R. A., Moses, M., et al. (1994). Angiostatin: a novel angiogenesis inhibitor that mediates the suppression of metastases by a Lewis lung carcinoma. Cell, 79(2), 315–328.PubMedCrossRef
62.
Zurück zum Zitat Hamano, Y. (2003). Physiological levels of tumstatin, a fragment of collagen IV [alpha]3 chain, are generated by MMP-9 proteolysis and suppress angiogenesis via [alpha]V [beta]3 integrin. Cancer Cell, 3, 589–601.PubMedPubMedCentralCrossRef Hamano, Y. (2003). Physiological levels of tumstatin, a fragment of collagen IV [alpha]3 chain, are generated by MMP-9 proteolysis and suppress angiogenesis via [alpha]V [beta]3 integrin. Cancer Cell, 3, 589–601.PubMedPubMedCentralCrossRef
71.
Zurück zum Zitat Pavlovic, S., Du, B., Sakamoto, K., Khan, K. M., Natarajan, C., Breyer, R. M., et al. (2006). Targeting prostaglandin E2 receptors as an alternative strategy to block cyclooxygenase-2-dependent extracellular matrix-induced matrix metalloproteinase-9 expression by macrophages. The Journal of Biological Chemistry, 281(6), 3321–3328. https://doi.org/10.1074/jbc.M506846200.PubMedCrossRef Pavlovic, S., Du, B., Sakamoto, K., Khan, K. M., Natarajan, C., Breyer, R. M., et al. (2006). Targeting prostaglandin E2 receptors as an alternative strategy to block cyclooxygenase-2-dependent extracellular matrix-induced matrix metalloproteinase-9 expression by macrophages. The Journal of Biological Chemistry, 281(6), 3321–3328. https://​doi.​org/​10.​1074/​jbc.​M506846200.PubMedCrossRef
75.
Zurück zum Zitat Zahner, G., Harendza, S., Muller, E., Wolf, G., Thaiss, F., & Stahl, R. A. (1997). Prostaglandin E2 stimulates expression of matrix metalloproteinase 2 in cultured rat mesangial cells. Kidney International, 51(4), 1116–1123.PubMedCrossRef Zahner, G., Harendza, S., Muller, E., Wolf, G., Thaiss, F., & Stahl, R. A. (1997). Prostaglandin E2 stimulates expression of matrix metalloproteinase 2 in cultured rat mesangial cells. Kidney International, 51(4), 1116–1123.PubMedCrossRef
76.
Zurück zum Zitat Choi, Y. A., Lee, D. J., Lim, H. K., Jeong, J. H., Sonn, J. K., Kang, S. S., et al. (2004). Interleukin-1beta stimulates matrix metalloproteinase-2 expression via a prostaglandin E2-dependent mechanism in human chondrocytes. Experimental & Molecular Medicine, 36(3), 226–232. https://doi.org/10.1038/emm.2004.31.CrossRef Choi, Y. A., Lee, D. J., Lim, H. K., Jeong, J. H., Sonn, J. K., Kang, S. S., et al. (2004). Interleukin-1beta stimulates matrix metalloproteinase-2 expression via a prostaglandin E2-dependent mechanism in human chondrocytes. Experimental & Molecular Medicine, 36(3), 226–232. https://​doi.​org/​10.​1038/​emm.​2004.​31.CrossRef
79.
Zurück zum Zitat Hernandez-Anzaldo, S., Berry, E., Brglez, V., Leung, D., Yun, T. J., Lee, J. S., et al. (2015). Identification of a novel heart-liver axis: matrix metalloproteinase-2 negatively regulates cardiac secreted phospholipase A2 to modulate lipid metabolism and inflammation in the liver. Journal of the American Heart Association, 4(11). https://doi.org/10.1161/jaha.115.002553. Hernandez-Anzaldo, S., Berry, E., Brglez, V., Leung, D., Yun, T. J., Lee, J. S., et al. (2015). Identification of a novel heart-liver axis: matrix metalloproteinase-2 negatively regulates cardiac secreted phospholipase A2 to modulate lipid metabolism and inflammation in the liver. Journal of the American Heart Association, 4(11). https://​doi.​org/​10.​1161/​jaha.​115.​002553.
80.
Zurück zum Zitat Weinreb, R. N., Kashiwagi, K., Kashiwagi, F., Tsukahara, S., & Lindsey, J. D. (1997). Prostaglandins increase matrix metalloproteinase release from human ciliary smooth muscle cells. Investigative Ophthalmology & Visual Science, 38(13), 2772–2780. Weinreb, R. N., Kashiwagi, K., Kashiwagi, F., Tsukahara, S., & Lindsey, J. D. (1997). Prostaglandins increase matrix metalloproteinase release from human ciliary smooth muscle cells. Investigative Ophthalmology & Visual Science, 38(13), 2772–2780.
81.
Zurück zum Zitat Li, X., & Tai, H. H. (2012). Increased expression of matrix metalloproteinases mediates thromboxane A2-induced invasion in lung cancer cells. Current Cancer Drug Targets, 12(6), 703–715.PubMedCrossRef Li, X., & Tai, H. H. (2012). Increased expression of matrix metalloproteinases mediates thromboxane A2-induced invasion in lung cancer cells. Current Cancer Drug Targets, 12(6), 703–715.PubMedCrossRef
84.
Zurück zum Zitat Hennig, R., Kehl, T., Noor, S., Ding, X. Z., Rao, S. M., Bergmann, F., et al. (2007). 15-lipoxygenase-1 production is lost in pancreatic cancer and overexpression of the gene inhibits tumor cell growth. Neoplasia, 9(11), 917–926.PubMedPubMedCentralCrossRef Hennig, R., Kehl, T., Noor, S., Ding, X. Z., Rao, S. M., Bergmann, F., et al. (2007). 15-lipoxygenase-1 production is lost in pancreatic cancer and overexpression of the gene inhibits tumor cell growth. Neoplasia, 9(11), 917–926.PubMedPubMedCentralCrossRef
87.
Zurück zum Zitat Piromkraipak, P., Sangpairoj, K., Tirakotai, W., Chaithirayanon, K., Unchern, S., Supavilai, P., et al. (2018). Cysteinyl leukotriene receptor antagonists inhibit migration, invasion, and expression of MMP-2/9 in human glioblastoma. Cellular and Molecular Neurobiology, 38(2), 559–573. https://doi.org/10.1007/s10571-017-0507-z.PubMedCrossRef Piromkraipak, P., Sangpairoj, K., Tirakotai, W., Chaithirayanon, K., Unchern, S., Supavilai, P., et al. (2018). Cysteinyl leukotriene receptor antagonists inhibit migration, invasion, and expression of MMP-2/9 in human glioblastoma. Cellular and Molecular Neurobiology, 38(2), 559–573. https://​doi.​org/​10.​1007/​s10571-017-0507-z.PubMedCrossRef
91.
Zurück zum Zitat Leppert, D., Hauser, S. L., Kishiyama, J. L., An, S., Zeng, L., & Goetzl, E. J. (1995). Stimulation of matrix metalloproteinase-dependent migration of T cells by eicosanoids. The FASEB Journal, 9(14), 1473–1481.PubMedCrossRef Leppert, D., Hauser, S. L., Kishiyama, J. L., An, S., Zeng, L., & Goetzl, E. J. (1995). Stimulation of matrix metalloproteinase-dependent migration of T cells by eicosanoids. The FASEB Journal, 9(14), 1473–1481.PubMedCrossRef
94.
Zurück zum Zitat Michaelis, U. R., Fisslthaler, B., Barbosa-Sicard, E., Falck, J. R., Fleming, I., & Busse, R. (2005). Cytochrome P450 epoxygenases 2C8 and 2C9 are implicated in hypoxia-induced endothelial cell migration and angiogenesis. Journal of Cell Science, 118(Pt 23), 5489–5498. https://doi.org/10.1242/jcs.02674.PubMedCrossRef Michaelis, U. R., Fisslthaler, B., Barbosa-Sicard, E., Falck, J. R., Fleming, I., & Busse, R. (2005). Cytochrome P450 epoxygenases 2C8 and 2C9 are implicated in hypoxia-induced endothelial cell migration and angiogenesis. Journal of Cell Science, 118(Pt 23), 5489–5498. https://​doi.​org/​10.​1242/​jcs.​02674.PubMedCrossRef
Metadaten
Titel
Triumph and tumult of matrix metalloproteinases and their crosstalk with eicosanoids in cancer
verfasst von
Kasturi Chatterjee
Sayantan Jana
Preety Choudhary
Snehasikta Swarnakar
Publikationsdatum
10.08.2018
Verlag
Springer US
Erschienen in
Cancer and Metastasis Reviews / Ausgabe 2-3/2018
Print ISSN: 0167-7659
Elektronische ISSN: 1573-7233
DOI
https://doi.org/10.1007/s10555-018-9756-7

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