systems.crump.ucla.edu Open in urlscan Pro
128.97.26.68  Public Scan

Submitted URL: http://systems.crump.ucla.edu/
Effective URL: https://systems.crump.ucla.edu/
Submission: On November 16 via api from US — Scanned from DE

Form analysis 1 forms found in the DOM

GET https://systems.crump.ucla.edu/

<form method="get" class="searchform" action="https://systems.crump.ucla.edu/" role="search">
  <label for="s" class="assistive-text">Search</label>
  <input type="text" class="field" name="s" value="" id="s" placeholder="Search …">
  <input type="submit" class="submit" name="submit" id="searchsubmit" value="Search">
</form>

Text Content

The Graeber Lab




PRIMARY MENU

Skip to content
 * HOME
 * PROJECTS
 * MEMBERS
 * PUBLICATIONS
 * SOFTWARE
 * LAB MEETING
 * METABOLOMICS CENTER
 * CONTACT US

Search
 * HOME
 * PROJECTS
 * MEMBERS
 * PUBLICATIONS
 * SOFTWARE
 * LAB MEETING
 * METABOLOMICS CENTER
 * CONTACT US

Previous Next
123456

Systems biology of disease, cancer and immune signaling and metabolism
Our group is working to understand cancer signaling and metabolism from a
systems view. We focus on developing genome-, proteome- and metabolome-wide
assays, and applying these assays to measuring and computationally modeling
aberrant function in cancer cells. Through collaboration with clinical
scientists, we work directly with patient samples and aim to translate our
discoveries to clinical applications. We collect high dimensionality data using
mass spectrometry-based phosphoproteomic and metabolomic profiling. To
integratively analyze this data, we develop computational approaches aimed at
overlaying the raw data with known signaling and metabolic network structures. A
point of emphasis is how cellular signaling and metabolism is rewired when
cancers become resistant to molecularly targeted therapies (e.g. the mutant BRAF
kinase inhibitor used in melanoma). Our results have pointed us to the
contributions of feedback loops in maintaining cancer signaling and metabolism
homeostasis, and we are exploring therapeutic approaches to perturbing these
loops synergistically to disrupt cellular equilibrium and induce death in cancer
cells. In modeling cancer, one of our goals is to identify minimal sets of
informative components that best reflect the state of the cell and serve as
molecular targets for diagnostics, imaging, and patient tailored treatment. As
with all of systems biology, our research relies on an interdisciplinary
approach that merges biology, chemistry, mathematics and computation /
bioinformatics.

We have a multidisciplinary lab with connections to the clinic, and emphasizing
collecting large datasets in a well-designed fashion so that we can pull out
informative patterns using computer algorithms. We primarily study the
complexity of mis-wired cancer cells, and the elegance of systems programs
enacted by immune cells to accomplish their specialized functions. We have
expanding projects in the lab related to genomic instability in cancer, the
associated DNA repair deficiencies, disrupting cancer trans-differentiation as a
therapy escape route, and in cancer metabolism. We attempt to keep projects like
these, and others on tumor immunology closely linked to current medical
questions through collaborations with clinical scientists.


AFFILIATIONS

Department of Molecular and Medical Pharmacology
Crump Institute for Molecular Imaging
UCLA Metabolomics Center
 * HOME
 * PROJECTS
 * MEMBERS
 * PUBLICATIONS
 * SOFTWARE
 * LAB MEETING
 * METABOLOMICS CENTER
 * CONTACT US

Copyright © 2017 The Graeber Lab All Rights Reserved.
Adventurous Theme by Catch Themes