They’re not blue and they’re not science fiction. They are avatars, at least of the
cancer kind. From the hands of Dr.
Sandeep Pingle, MD PhD from Moore’s Cancer Center in UC San Diego, CA comes
computer representations of tumor cells.
Defined as an icon or figure representing a person, avatar is an
appropriate term to describe the computer simulation modeling the genomic
signatures of individual cancers and how they will respond to specific
therapeutic interventions.
In light of the recent discussions on how each tumor is
unique and the need for personalized medicine, this newest discovery
provides a tool for a comprehensive analysis of individual cancers. Most importantly, it can be customized
for each patient, allowing clinicians to treat patients selectively with drugs
believed to have the greatest chance of success.
Published recently in the Journal of Translational Medicine,
the generation of this virtual cell combined intensive analysis of the
literature with basic cell survival assays in response to targeted therapies. Cell lines with different genetic
backgrounds, like patients, will respond differently to specific
therapeutics. Using this
knowledge, the virtual cell can predict how cells, or individual tumors, will
respond to these different drug treatments.
To validate their model, they generated cell lines from
glioblastoma tumors. They used
their cancer avatar to predict survival and tested this against actual survival
data generated in the laboratory.
In this situation, their models saw a high degree of agreement with
greater than 75% corroboration between in
vitro cell line models and the cancer avatar. Ultimately such a model should be tested in clinical trials
with real patient data.
Where do we go from here?
You can imagine that such a model could provide enormous
benefit for clinicians, providing an effective platform for testing and
developing personalized therapeutic regimens. However, the future development of this model relies on its
accuracy. With new technologies,
including next generation sequencing, we have access to large amounts of
data including genomic, transcriptomic, metabolomic, and proteomic data, among
others. Integration of these
datasets is necessary for accurate predictions. The incorporation of extracellular factors such as the tumor
microenvironment and tumor-associated inflammation is also critical.
I’ll leave you with this thought: Are we placing too much faith in computer simulations. Cancer is, by definition, unpredictable
and ever changing. Can we
accurately model that disease?
References:
Pingle
SC, Sultana Z, Pastorino S, et al. In
silico modeling predicts drug sensitivity of patient-derived cancer
cells. J. Transl. Med. 2014.
12:128.
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