Kontakt 2008, 10(2):442-448 | DOI: 10.32725/kont.2008.065
New generation of anti-cancer medicinesHealth and Social Sciences
- Výzkumný ústav potravinářský Praha, v. v. i.
New anti-cancer medicines take advantage of knowledge of molecular mechanisms of malignities for aimed intervention suppressing the pathological process. The targets of the intervention are on the one hand receptors of growth factors, their ligands and molecules from connected signal paths and, on the other hand, deacetylases of histones and further molecules of the transcription apparatus. The first group comprises antibodies against receptors and mainly "small molecules" inhibiting their function. In contrast, inhibitors of histone deacetylases are a chemically heterogeneous group of substances providing the transcription of genes of different molecules exerting anti-oncogenic action by maintaining a high level of the acetylation of target molecules. A number of substances from both groups successfully passed preclinical or also clinical tests and certain products, particularly antibodies, already principally affected the treatment of particular malignities. The purpose of the present article is to offer a review of at least most important substances from these recently occurring groups of anti-cancer medicines. A general mechanism of effects, achieved level of preclinical and clinical testing, chemistry and possibly particular molecular interactions in the malignant cells are described with each group.
Keywords: therapeutic antibodies; small inhibitor molecules; inhibitors of histone deacetylases; anti-cancer medicines; review
Received: September 2, 2008; Accepted: October 20, 2008; Prepublished online: December 17, 2008; Published: December 17, 2009 Show citation
References
- BUTLER, L. M., ZHOU, X. et al.: The histone deacetylase inhibitor SAHA arrests cancer cell growth, up-regulates thioredoxin-binding protein-2, and down-regulates thioredoxin. Proceedings of the National Academy of Sciences, 2002. Vol. 99, no 18, s. 11700-11705.
Go to original source...
Go to PubMed...
- DATE, K., MATSUMOTO, K. et al.: HGF/NK4 is a specific antagonist for pleiotrophic actions of hepatocyte growth factor. Febs Letters, 1997. Vol. 420, no 1, s. 1-6.
Go to original source...
Go to PubMed...
- DOKMANOVIC, M., MARKS, P. A.: Prospects: Histone deacetylase inhibitors. Journal of Cellular Biochemistry, 2005. Vol. 96, no 2, s. 293-304.
Go to original source...
Go to PubMed...
- DUVIC, M., VU, J.: Vorinostat in cutaneous T-cell lymphoma. Drugs of Today, 2007. Vol. 43, no 9, s. 585-599.
Go to original source...
Go to PubMed...
- GLICK, R. D., SWENDEMAN, S. L. et al.: Hybrid polar histone deacetylase inhibitor induces apoptosis and CD95/CD95 ligand expression in human neuroblastoma. Cancer Research, 1999. Vol. 59, no 17, s. 4392-4399.
Go to PubMed...
- GUI, C. Y., NGO, L. et al.: Histone deacetylase (HDAC) inhibitor activation of p21(WAF1) involves changes in promoter-associated proteins, including HDAC1. Proceedings of the National Academy of Sciences of the United States of America, 2004. Vol. 101, no 5, s. 1241-1246.
Go to original source...
Go to PubMed...
- HUANG, L. L., PARDEE, A. B.: Suberoylanilide hydroxamic acid as a potential therapeutic agent for human breast cancer treatment. Molecular Medicine, 2000. Vol. 6, no 10, s. 849-866.
Go to original source...
- CHRISTENSEN, J. G., SCHRECK, R. et al.: A selective small molecule inhibitor of c-Met kinase inhibits c-Met-dependent phenotypes in vitro and exhibits cytoreductive antitumor activity in vivo. Cancer Research, 2003. Vol. 63, no 21, s. 7345-7355.
Go to PubMed...
- INSINGA, A., MONESTIROLI, S. et al.: Inhibitors of histone deacetylases induce tumor-selective apoptosis through activation of the death receptor pathway (vol 11, pg 71, 2005). Nature Medicine, 2005. Vol. 11, no 2, s. 233-233.
Go to original source...
- JIANG, W. G., MARTIN, T. A. et al.: Hepatocyte growth factor, its receptor, and their potential value in cancer therapies. Critical Reviews in Oncology Hematology, 2005. Vol. 53, no 1, s. 35-69.
Go to original source...
Go to PubMed...
- KOCÁKOVÁ, I., DEMLOVÁ, R. et al.: Bevacizumab v kombinaci s chemoterapií FOLFOX4 v léčbě metastatického kolorektálního karcinomu. Klinická onkologie, 2006. Vol. 19, no 1.
- LACKEY, K. E.: Lessons from the drug discovery of lapatinib, a dual ErbB1/2 tyrosine kinase inhibitor. Current Topics in Medicinal Chemistry, 2006. Vol. 6, no 5, s. 435-460.
Go to original source...
Go to PubMed...
- LARKIN, J. M., EISEN, T.: Renal cell carcinoma and the use of sorafenib. Therapeutics and Clinical Risk Management, 2006. Vol. 2, no 1, s. 87-98.
Go to PubMed...
- LETOURNEAU, C., RAYMOND, E. et al.: Sunitinib: a novel tyrosine kinase inhibitor. A brief review of its therapeutic potential in the treatment of renal carcinoma and gastrointestinal stromal tumors (GIST). Therapeutics and Clinical Risk Management, 2007. Vol. 3, no 2, s. 341-348.
Go to original source...
Go to PubMed...
- MARKS, P. A., DOKMANOVIC, M.: Histone deacetylase inhibitors: discovery and development as anticancer agents. Expert Opinion on Investigational Drugs, 2005. Vol. 14, no 12, s. 1497-1511.
Go to original source...
Go to PubMed...
- MATSUMOTO, K., KATAOKA, H. et al.: Cooperative interaction between alpha and beta chains of hepatocyte growth factor on c-Met receptor confers ligand-induced receptor tyrosine phosphorylation and multiple biological responses. Journal of Biological Chemistry, 1998. Vol. 273, no 36, s. 22913-22920.
Go to original source...
Go to PubMed...
- NIMMANAPALLI, R., FUINO, L. et al.: Cotreatment with the histone deacetylase inhibitor suberoylanilide hydroxarmic acid (SAHA) enhances imatinib-induced apoptosis of Bcr-Abl-positive human acute leukemia cells. Blood, 2003. Vol. 101, no 8, s. 3236-3239.
Go to original source...
Go to PubMed...
- ORLOWSKI, R. Z.: Targeting the proteasome in cancer therapy. Apoptotic pathways as targets for novel therapies in cancer and other diseases. L. a. Gibson, Springer, 2005. s. 243-274.
Go to original source...
- PANG, R. W. C. and R. T. P. POON: From molecular biology to targeted therapies for hepatocellular carcinoma: The future is now. Oncology, 2007. Vol. 72, no, s. 30-44.
Go to original source...
- PIEKARZ, R., BATES, S.: A review of depsipeptide and other histone deacetylase inhibitors in clinical trials. Current Pharmaceutical Design, 2004. Vol. 10, no 19, s. 2289-2298.
Go to original source...
Go to PubMed...
- PIEKARZ, R. L., ROBEY, R. et al.: Inhibitor of histone deacetylation, depsipeptide (FR901228), in the treatment of peripheral and cutaneous T-cell lymphoma: a case report. Blood, 2001. Vol. 98, no 9, s. 2865-2868.
Go to original source...
Go to PubMed...
- PODAR, K., TONON, G. et al.: The small-molecule VEGF receptor inhibitor pazopanib (GW786034B) targets both tumor and endothelial cells in multiple myeloma. Proceedings of the National Academy of Sciences, 2006. Vol. 103, no 51, s. 19478-19483.
Go to original source...
Go to PubMed...
- SATTLER, M., PRIDE, Y. B. et al.: A novel small molecule met inhibitor induces apoptosis in cells transformed by the oncogenic TPR-MET tyrosine kinase. Cancer Research, 2003. Vol. 63, no 17, s. 5462-5469.
Go to PubMed...
- UEDA, H., NAKAJIMA, H. et al.: Fr901228, a Novel Antitumor Bicyclic Depsipeptide Produced by Chromobacterium Violaceum No. 968.1. Taxonomy, Fermentation, Isolation, Physicochemical and Biological Properties, and Antitumor-Activity. Journal of Antibiotics, 1994. Vol. 47, no 3, s. 301-310.
Go to original source...
Go to PubMed...
- VAN OOSTEROM, A. T., JUDSON, I. et al.: Safety and efficacy of imatinib (ST1571) in metastatic gastrointestinal stromal tumours: a phase I study. Lancet, 2001. Vol. 358, no 9291, s. 1421-1423.
Go to original source...
Go to PubMed...
- VIDAL, A., KOFF, A.: Cell-cycle inhibitors: three families united by a common cause. Gene, 2000. Vol. 247, no 1-2, s. 1-15.
Go to original source...
Go to PubMed...
- XU, W. S., PARMIGIANI, R. B. et al.: Histone deacetylase inhibitors: molecular mechanisms of action. Oncogene, 2007. Vol. 26, no 37, s. 5541.
Go to original source...
Go to PubMed...
- ZHANG, X. D., GILLESPIE, S. K. et al.: The histone deacetylase inhibitor suberic bishydroxamate regulates the expression of multiple apoptotic mediators and induces mitochondria-dependent apoptosis of melanoma cells. Mol Cancer Ther, 2004. Vol. 3, no 4, s. 425-435.
Go to original source...
Go to PubMed...