University of California, Riverside

MolMed



Oncology


Targeted Delivery of Drugs to Cancer Cells: Changing the Face of Chemotherapy

ChemotherapyProfessor of Biomedical Sciences Maurizio Pellecchia of the UCR School of Medicine, in collaboration with the Cedars-Sinai Medical Center, is developing innovative strategies to target specifically cancer cells for the selective delivery of chemotherapy. These strategies are based on the EphA2 receptor that is expressed mainly on the surface of cancer cells where it promotes cell proliferation, tumor angiogenesis, cancer cell migration and metastases. The collaborative groups are investigating the approach against prostate cancer, melanoma, and pancreatic cancers.

Targeting Apoptosis via Chemical Design

Hydrophobic groove near the BH3 peptideIn tumor cells, deregulation of programmed cell death, also known as apoptosis, provide cancer cells a growth advantage, and confers resistance to chemo- and immuno-therapy and radiation. Two classes of proteins, namely anti-apoptotic Bcl-2 proteins, and IAPs, are responsible for defective apoptosis in cancer cells. Professor of Biomedical Sciences Maurizio Pellecchia of the UCR School of Medicine is developing novel agents targeting several members of these two classes of proteins using innovative approaches. In collaboration with researchers at UC San Diego, these agents are being sought to revert resistance to chemotherapy in Chronic Lymphocytic Leukemia (CLL), while a collaborative study with the City of Hope aims at developing the agents against Acute Myelogenous Leukemia. The agents are also effective in disease models of several solid tumors such as prostate, lung, and breast cancers and potentially other tumors, and collaborative studies are ongoing with the Cedars-Sinai Medical Center in these tumors.

Targeting a Specific Metastasis-Promoting Form of the Prolactin Receptor in Breast, Ovarian and Prostate Cancer

Ameae WalkerProfessor Ameae Walker and colleagues have designed novel splice modulating oligonucleotides (SMOs) that decrease expression of the proliferation-promoting and metastasis-promoting form of the prolactin receptor without affecting expression of other forms of the prolactin receptor. This extreme specificity is the next step in highly targeted therapeutics designed to reduce the possibility of untoward side effects. Approximately 95% of breast, ovarian and prostate cancers express prolactin receptors and all cancer stem cells examined so far are positive for the prolactin receptor. This compares favorably with the 70% of breast cancers that express estrogen receptors and suggests utility of the SMOs in triple negative breast cancers, chemotherapy resistant ovarian cancer and castration resistant prostate cancer. Published work to date has shown that the administered SMOs were extremely effective at reducing lung and liver metastases in two highly aggressive metastatic models of breast cancer: BT474 human xenografts, used for testing Herceptin, and a 4T1 syngeneic mouse model, which allowed testing in an animal with an intact immune system. An international patent has been filed and has completed one round of review.

The SUMO and Ubiquitin Pathway as Targets for Anti-Cancer Therapeutics

SUMO–SIM complex structure, with the SUMO-1 structure in cyan and the PIAS2-like peptide in greenThe lab of Professor Jefferson Perry uses macromolecular crystallography and in-solution small angle x-ray scattering technologies to study the molecular mechanisms of signal transduction pathways controlling genome stability. In particular, the lab is studying the roles of components of the SUMO and ubiquitin pathways, in addition to kinase accessory proteins, which have critical roles in human health and disease. Current research projects include translational aspects, where the Perry laboratory uses fragment-based ligand discovery and computer-aided drug discovery methods as part of the rational-based drug discovery process. The lab is focusing on various targets that likely cause resistance to therapy in breast cancer, acute myeloid leukemia, chronic myeloid leukemia or multiple myeloma, as part of collaborations with labs at UCR, UC San Diego, The Scripps Research Institute and the City of Hope.

Novel Strategies to Combat Glioblastoma Multiforme (GBM)

Novel strategies to combat Glioblastoma The lab of Associate Professor Emma Wilson collaborates extensively with lecturer Jack Eichler of the chemistry department to teach undergraduates about glioma and develop novel drug therapies from design and synthesis through to in vitro and in vivo testing. Glioblastoma multiforme is a devastating cancer that even with all available therapies gives a life expectancy of ~ 18 months. This collaboration has discovered several novel metal based compounds and associated ligands that have significant anti-glioma efficacy against murine and human glioma cell lines and one in particular that demonstrates significant in vivo efficacy. Further work is being conducted to understand the mechanism of action of these compounds.

Selective Proteasome Inhibitors Against Multiple Myeloma and Solid Tumors

proteasome inhibitorsThe laboratory of Distinguished Professor Michael Pirrung in the UCR Department of Chemistry has developed a family of natural product-based proteasome inhibitors, the syrbactins. Proteasome inhibitors are approved drugs for treating multiple myeloma. In collaboration with structural biophysics groups, the interactions of these compounds with one of the seven unique catalytic sites of human proteasomes have been elucidated. One syrbactin, TIR-199, has passed several hurdles in the National Cancer Institute’s Developmental Therapeutics Program. It is about to enter tumor xenograft and other preclinical studies, and its commercialization is being pursued via a spin-off company, Hibiscus Bioscience, founded by Pirrung and his collaborator, Professor Andre S. Bachmann, Ph.D. of Michigan State University's College of Human Medicine. Among proteasome inhibitors the syrbactins are unique in that they are cyclic and have a defined conformation, which affects their selectivity for proteasome catalytic subunits. Using this property, compounds have been discovered that target catalytic sites otherwise difficult to address, such as the trypsin-like subunit of the immunoproteasome.

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