Molecular Pharmacology and Chemical Biology
Understanding the fate (pharmacokinetics or PK) and action (pharmacodynamics or PD) of a drug is essential for preclinical and clinical drug development as well as the practice of precision medicine. The MPCBSR helps investigators study new therapeutics for the leading causes of cancer deaths within the cancer center’s catchment area by providing comprehensive services for
- High-quality collection, processing, and management of clinical trial specimens and evaluation of clinical PK/PD and potential drug-drug interactions (DDI)
- Preclinical molecular pharmacological studies on novel agents that are translatable to the clinic, including drug metabolism and disposition (DMD), PK/PD, on-target mechanisms, biomarkers, and combination effects
- Chemical synthesis of new compounds and drug delivery nanomaterials for drug discovery and development
The technologies and state-of-the-art instruments available at the MPCBSR support a wide variety of molecular pharmacology and chemical biology studies. Our faculty and staff members are worldwide leaders in the fields and have the expertise to offer guidance and training for scientists on the principles and technologies used in anticancer pharmacology and chemical biology.
Services
The MPCBSR provides essential and a broad spectrum of services for the assessment of new therapeutics, including high-quality collection and management of clinical trial specimens and determination of clinical PK/PD and potential drug-drug interactions (DDI), pharmacological studies on novel therapeutics in preclinical models, including DM/PK/PD, on-target mechanisms, biomarkers, and combination effects, and chemical synthesis of new compounds and drug delivery nanomaterials for improved therapy.
Clinical Specimens and PK/PD Studies
We offer timely, 24/7 collection, processing, and management of specimens for clinical PK/PD and safety studies. The MPCBSR conducts around 3,000 patient specimen collections each year. Many involve unique protocols and processing requirements. We oversee virtually all patient specimen collection for oncology clinical trials at the cancer center.
We also help investigators develop and use new assays to:
- Quantify specific drugs, metabolites and biomarkers in patient samples
- Perform PK/PD analyses and modeling
- Evaluate possible DDIs
- Interpret study data and results
Preclinical Molecular Pharmacology Studies
The MPCBSR assists UC Davis Comprehensive Cancer Center investigators in evaluating new therapeutics that are translatable to the clinic, by using clinically relevant animal models, cell lines and organoids. We have many established assays and the capability to develop new methods to:
- Assess potential DDIs
- Determine on- and off-target effects
- Evaluate synergistic, additive or antagonist effects of new drug combinations
- Investigate pharmacological actions and possible biomarkers
- Understand the DM/PK/PD properties of new agents
We also provide one-of-a-kind bioengineered RNA molecules (including miRNAs, siRNAs, aptamers and other forms of small RNAs) to study cancer biology and investigate new therapeutics, which are made in vivo and distinguished from conventional agents synthesized in vitro.
Chemical Biology Studies
The MPCBSR provides a wide variety of chemical compounds to investigators and offers chemistry support for their cancer research. Examples of services include:
- Provide pre-made and custom-made OBOC and OB2C peptide and small molecule combinatorial libraries
- Synthesize peptides and peptide derivatives including biotin or fluorescent-labeled peptides
- Design and synthesize peptide- and antibody-drug conjugates
- Provide micelle, polymer, peptide, or protein-based nanoplatforms for drug delivery
- Assist drug design, structure-activity relationship study and lead optimization
Investigators working with the MPCBSR gain access to state-of-the-art equipment and instrumentation, including:
- Four HIPA- compliant, ultra-low freezers storing up to 72,000 aliquots per freezer
- LC-MS/MS and HPLC systems
- Seahorse and IncuCyte live-cell analyzers
- FPLC systems
- Lago X in vivo animal imaging system
- Confocal microscope
- Lyophilizers
- Automated peptide synthesizers
We’re here to support your cancer research study. Fill out a request to use our services.
NOTE: A PPMS account is required. View our quick start guide for creating an account or set up an account.
For questions about molecular pharmacology and chemical biology or how our faculty can assist you, call the lab at 916-734-1566 or contact us.
Aiming Yu, Ph.D. | Director of the MPCBSR: Email
Anthony Martinez, B.S. | Technical Director (Clinical Specimens Collection, Processing and Management): Email
Ruiwu Liu, Ph.D. | Technical Director (Chemical Biology Studies): 916-734-0905, Email
Meijuan Tu, Ph.D. | Manager (Pharmacological Studies; DM/PK/PD): Email
Locations
MPCBSR Office: Oak Park Research Building, Room 2130, 2700 Stockton Blvd , Sacramento, CA 95817
FDA Drug Development Policies and Regulations
Read about FDA regulations pertaining to drug development:
Lawrence Livermore National Laboratory Biological Accelerator Mass Spectrometry
UC Davis Comprehensive Cancer Center members can access the Lawrence Livermore National Laboratory (LLNL) National User Resource for Biological Accelerator Mass Spectrometry (bioAMS). The bioAMS facility supports investigators studying the behavior of new drug candidates. For more information about cancer research services at LLNL, contact Matt Coleman.
NOTICE TO ALL NIH-FUNDED INVESTIGATORS
CCSG Acknowledgement: research reported in this publication was supported by the National Cancer Institute of the National Institutes of Health under award number P30CA093373. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
MPCBSR Acknowledgement: the authors wish to acknowledge the support of the UC Davis Comprehensive Cancer Center Molecular Pharmacology and Chemical Biology Shared Resource, supported by the National Cancer Institute of the National Institutes of Health under award number P30CA093373. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
This resource is funded by the Cancer Center Support Grant (CCSG) awarded by the National Cancer Institute (NCI P30CA093373). Publications that have utilized facility resources, services or scientific data generated by the resource should acknowledge the resource or the assistance provided by resource staff and cite the NCI CCSG. An electronic copy of the publication should also be sent to the resource directors.