IsoPlexis eBook - 16
I S O P L E X I S ' U N I Q U E , P R E D I C T I V E B I O LO G Y
Overcoming the Limitations of Genomics
Using Single-Cell Proteomics
A
s mentioned earlier, GBM is a highly lethal
by single-cell proteomics and metabolomics was
cancer that mutates quickly, but rather
successful and led researchers to understand that
than a single genetic alteration, the
the two pathways they identified are independently
genomic analyses show that most tumors are driven
druggable.2
by derangements in multiple intracellular pathways.
Cancer is best addressed as a multi-dimensional
Writing in a Cancer Cell commentary, Lam and
disease beyond the initial confines of genetic pertur-
Yaffe said that this panoply of genomic alterations
bations that drive oncogenesis. Understanding how
enhances the tumor's ability to rapidly and dynam-
different systems behave within a tumor can lead to
ically rewire its signaling circuitry and to reactivate
novel therapeutic combinations that demonstrate
key regulatory nodes following treatment with single
temporal synergy by intentionally targeting dynamic
pathway blocking agents, leading to therapeutic
rewiring of signaling pathways to increase sensitivity
resistance.1
rather than drive resistance.
The authors stress that there is a likelihood to
miss this rewiring if genomics is the sole single-cell
analysis and indicate a need to break the current
"glass ceiling" of solely relying on genomic dataset
analyses to advance cancer therapeutics. They
emphatically point out that intracellular signaling
networks, or functional proteomics, need to be
investigated further in order to provide insight into
how to combat adaptive resistance.
Understanding how different systems
behave within a tumor can lead to
novel therapeutic combinations
that demonstrate temporal
synergy by intentionally targeting
dynamic rewiring of signaling
pathways to increase sensitivity
rather than drive resistance.
This is evident in the previous section, discussing
the case by Su et al., where IsoPlexis' Single-Cell Intra-
Again, IsoPlexis' unique single-cell proteomics
cellular Proteomics and Metabolomics were essential
technology was key to this discovery. Researchers
in identifying how cells progress from drug-tolerant
Wei et al. used the information they learned
to drug-resistant. Identifying this allowed researchers
from running single-cell analyses to test several
to test combinatorial therapies to prevent this
combination therapies against tumor growth. The
resistance. The combination therapy predicted
combination therapies predicted by single-cell
16 |
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IsoPlexis eBook
Table of Contents for the Digital Edition of IsoPlexis eBook
Contents
IsoPlexis eBook - 1
IsoPlexis eBook - 2
IsoPlexis eBook - Contents
IsoPlexis eBook - 4
IsoPlexis eBook - 5
IsoPlexis eBook - 6
IsoPlexis eBook - 7
IsoPlexis eBook - 8
IsoPlexis eBook - 9
IsoPlexis eBook - 10
IsoPlexis eBook - 11
IsoPlexis eBook - 12
IsoPlexis eBook - 13
IsoPlexis eBook - 14
IsoPlexis eBook - 15
IsoPlexis eBook - 16
IsoPlexis eBook - 17
IsoPlexis eBook - 18
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