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Anti-tumor chemotherapy utilizing peptide-based approaches - apoptotic pathways, kinases, and proteasome as targets
Manitoba Institute of Cell Biology, CancerCare Manitoba, University of Manitoba, Winnipeg, MB R3E 0V9, Canada.
Manitoba Institute of Cell Biology, CancerCare Manitoba, University of Manitoba, Winnipeg, MB R3E 0V9, Canada.
Manitoba Institute of Cell Biology, CancerCare Manitoba, University of Manitoba, Winnipeg, MB R3E 0V9, Canada.
Manitoba Institute of Cell Biology, CancerCare Manitoba, University of Manitoba, Winnipeg, MB R3E 0V9, Canada.
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2005 (Engelska)Ingår i: Archivum Immunologiae et Therapiae Experimentalis, ISSN 0004-069X, E-ISSN 1661-4917, Vol. 53, nr 1, s. 47-60Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

The pharmacological sciences are taking advantage of recent discoveries that have defined the molecular pathways governing apoptosis. These signaling cascades are frequently inactivated or distorted by mutations in cancer cells. Peptides derived from critical interaction, phosphorylation, or cleavage sites are the preferred leads (starting points) for the development of new drugs. In this review we summarize recent peptide-based approaches that target MDM2, p53, NF-kappaB, ErbB2, MAPK, as well as Smac/DIABLO, IAP BIR domains, and Bcl-2 interaction domains, with a specific focus on the BH3 domain. Separate parts of the review deal with proteasome inhibitors, integrin-derived peptides, and molecules that are being tested for tumor-selective delivery of anticancer drugs ("magic bullet" approach). The proteasome inhibitors and integrin-derived peptides show a variety of effects, targeting not only tumor growth, but also angiogenesis, metastasizing potential, and other cancer cell functions. The last part of this review describes approaches that use specific properties (surface receptors, increased enzymatic activities) of cancer cells in order to target them specifically. These new generations of anticancer drugs provide the foundations for therapies with fewer side effects and higher efficacy.

Ort, förlag, år, upplaga, sidor
2005. Vol. 53, nr 1, s. 47-60
Nyckelord [en]
angiostatin, anti-angiogenic, bcl-2 family proteins, Bortezomib, c-terminal peptide, cell lung-cancer, cytochrome-c, e-cadherin expression, egfr, Endostatin, growth-factor receptor, hmr1826, in-vivo, inhibitor ps-341, integrins, Mdm2, p53, tumor-cells, tyrosine-phosphatase 1b, Velcade
Nationell ämneskategori
Cancer och onkologi Biokemi och molekylärbiologi
Identifikatorer
URN: urn:nbn:se:liu:diva-87000ISI: 000227017600005PubMedID: 5761376OAI: oai:DiVA.org:liu-87000DiVA, id: diva2:584197
Tillgänglig från: 2013-01-08 Skapad: 2013-01-08 Senast uppdaterad: 2017-12-06

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