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Tuesday, January 12 2021 - 11:30
AsiaNet
DarwinHealth Scientists Publish Foundational Research Identifying Regulatory Mechanisms Controlling Cancer Cell States and Drug Response
NEW YORK, Jan. 12, 2021 /PRNewswire-AsiaNet/ --

DarwinHealth, Inc., a New York-based biotechnology and cancer drug discovery 
company announces the January 11, 2021 online publication in Cell of a landmark 
paper, "A Modular Master Regulator Landscape Controls Cancer Transcriptional 
Identity,"(1,2) in which scientists from Columbia University and DarwinHealth 
apply the VIPER (Virtual Inference of Protein activity by Enriched Regulon) 
analysis algorithm to identify recurrent regulatory networks -- "tumor 
checkpoints" -- operative across the pancancer subtype continuum.

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This research paper, with lead author Dr. Evan Paull, from the Department of 
Systems Biology at Columbia University, in conjunction with DarwinHealth 
Co-Founder, Professor Andrea Califano and Chief Scientific Officer, Dr. Mariano 
Alvarez and other investigators, presents results and analyses, using a novel 
Multi-Omics Master-Regulator Analysis framework (MOMA), that validates the 
foundational paradigm informing DarwinHealth technologies. 

The study, funded by the U.S. National Institutes of Health and the Instituto 
de Salud Carlos III/Ministerio de Asuntos Economicos y Transformacion Digital 
(Spain), demonstrates that different genetic alterations in individual patients 
within the same tumor subtype induce aberrant activation of the same Master 
Regulator proteins, which maintain the subtype's transcriptional identity. 
Moreover, it shows that Master Regulators operate within small, hyperconnected 
modules (Master Regulator Blocks [MRBs]) that mechanistically control key 
cancer hallmarks necessary for the survival of the cancer cell. 

The results reported in Cell provide one of the most comprehensive 
confirmations to date of the value of proprietary, network-based approaches for 
the identification of therapeutic targets in cancer using VIPER technology. The 
latter has been exclusively licensed, for commercial use, to DarwinHealth by 
Columbia University. The Cell publication concludes that, "Taken together, 
these data suggest that MRBs may provide complementary 'molecular recipes' for 
implementing the same cancer hallmarks in different tumor contexts." 

"These data support the Oncotecture Hypothesis, which suggests that a much 
larger and finer grain mutational repertoire than previously suspected may be 
responsible for inducing aberrant MR activity and implementing transcriptional 
tumor identities," explains Dr. Califano. "The results presented by this 
multi-disciplinary team also confirm that Tumor Checkpoint-based Master 
Regulators implement regulatory bottlenecks in cancer that are responsible for 
canalizing the effect of multiple functional mutations." He adds that, 
"Importantly, the Tumor Checkpoints that define each subtype can thus be 
deconstructed into highly specific combinations of a handful of activated and 
inactivated Master Regulator-Blocks -- specifically, 24 identified in this 
study. The MRBs can potentially regulate complementary genetic programs 
required to implement and maintain a tumor cell's transcriptional identity, 
which undergirds key aspects of cancer cell behavior and determines 
susceptibility to specific drugs and therapeutic interventions." 

The study provides a data-driven roadmap for identifying potential therapeutic 
targets that may benefit a large subset of cancer patients within each one of 
112 tumor subtypes, independent of their mutational state, characterized by the 
analysis. Accordingly, the authors note that, "Consistent with the notion that 
transcriptional cell states have emerged as more accurate predictors of 
drug-sensitivity compared to genetics, this suggests that MR-based analyses may 
produce a more tractable landscape of potential therapeutic targets than what 
could be achieved by genetic-based approaches."

These research findings and planned follow-up studies are likely to change the 
trajectory of classification schemes for cancer and evolving approaches to 
precision-based drug discovery in a number of important ways. The methodologies 
and results reported in Cell introduce to the cancer research and clinical 
community an entirely new approach for taxonomizing cancer subtypes -- 
essentially, categorizing them according to the composition of downstream 
regulatory bottlenecks with unique compositions of MRBs representing targetable 
tumor dependencies, independent of canonical mutational signatures. In fact, 
ongoing studies suggest these MR-based, tumor checkpoints are more reliable 
off-on switches for cancer cell governance than mutations themselves. 
Accordingly, this novel, data-driven taxonomization of molecular species (i.e., 
MR proteins comprising tumor checkpoints) responsible for cancer cell behavior 
-- and susceptibility to therapeutic targeting -- represents a paradigmatic 
shift opening up multiple avenues of inquiry and applications that have 
translational impact at the front lines of clinical care for cancer patients. 

Dr. Gideon Bosker, DarwinHealth CEO, notes, "The new molecular classification 
reported in Cell sets the stage for identifying and testing drugs that can 
induce a state of 'regulatory network contraception,' that is, disable or 
disrupt formation of checkpoint-governed programs that maintain and perpetuate 
the cancer cell state."

Importantly, the identification of Master Regulators has been made possible by 
the VIPER technology, developed by Califano and Alvarez at Columbia and 
licensed exclusively to DarwinHealth. VIPER allows precise measurement of 
protein activity from inexpensive and easily-accessible gene expression 
profiles -- as measured by mRNA sequencing. Much like thermostats maintain a 
constant room temperature, the VIPER-inferred Master Regulators coalesce into 
complex auto-regulated modules -- the tumor checkpoints -- that are necessary 
and sufficient to maintain a consistently programmed malignant state of the 
cancer cell over time. 

"The coordinated activity of Master Regulator proteins comprising the tumor 
checkpoint activates key hallmark programs needed by the cancer cell," explains 
Dr. Alvarez, DarwinHealth CSO. "Among them are those controlling unchecked 
proliferation, migration, and metastatic progression -- while suppressing other 
hallmark functions controlling programmed cell death (or apoptosis) and immune 
system detection; as well as others, which would otherwise prevent tumor 
formation. Essentially, by channeling genetic and mutational information into a 
discrete downstream regulatory nexus, the Master Regulators in a tumor 
checkpoint initiate and maintain the biological and behavioral hallmarks of a 
cancer cell."  

"At DarwinHealth, we use the full spectrum of proprietary, patented VIPER-based 
technologies developed by our scientists and co-founders to accurately and 
reproducibly quantify the activity of Master Regulators," explained Dr. Bosker. 
"From an actionable and real world precision oncology perspective, we have 
developed specific VIPER-based diagnostic tests, including DarwinOncoTreat and 
DarwinOncoTarget, to pinpoint drugs that can invert the activity of an entire 
tumor checkpoint or of specific master regulators. These algorithms have 
received New York and California CLIA certification and are being used 
clinically, including in several ongoing clinical trials." The first clinical 
trial based on this technology, which employed the combination of the HDAC6 
inhibitor ricolinostat and NAB-paclitaxel, has shown virtually 100% accuracy in 
the prediction of responders and non-responders as reported in a recent 
manuscript currently under review and available on MedRxiv (medRxiv 
2020.04.23.20066928).

DarwinHealth's oncotecture-based, "digging deeper than genes" discovery 
framework and associated technologies described in the Cell paper will continue 
to exploit a complementary combination of experimental and computation-based, 
inferential methods to identify novel cancer targets, effective drugs and 
biomarkers on a fully mechanistic, rather than empirical basis, in line with 
the strategies reported Cell.

In addition, the company's drug and novel cancer target discovery programs, 
including the DarwinOncoMarker, Compound-2-Clinic (C2C), and novel cancer 
target initiative (NCTI) platforms allow its scientific teams, working either 
independently or in collaboration with biopharmaceutical partners, to target 
cancer at its most vulnerable and stable spots; more specifically, at the 
regulatory interfaces implemented by tumor checkpoints. 

These DarwinHealth technologies and methods, already widely published in 
leading scientific and medical journals, are currently being evaluated in 
numerous clinical trials across the globe. By using Master Regulator-based 
analyses and leveraging their capacity for dissecting more actionable 
therapeutic targets -- and by extension, discovering more effective drugs -- 
than could be achieved by genetic-based approaches alone, these validated 
approaches are expected to address the precision deficit shortfalls associated 
with more traditional, mutation-centric approaches to precision oncology, many 
of which have failed to fully deliver on their initial promise.  

About DarwinHealth

DarwinHealth: Precision Therapeutics for Cancer Medicine is a "frontiers of 
cancer," biotechnology-focused company, co-founded by CEO Gideon Bosker, MD, 
and Professor Andrea Califano, Clyde and Helen Wu Professor of Chemical Systems 
Biology and Chair, Department of Systems Biology at Columbia University. The 
company's technology was developed by the Califano lab over the past 15 years 
and is exclusively licensed from Columbia University. 

DarwinHealth utilizes proprietary, systems biology algorithms to match 
virtually every cancer patient with the drugs and drug combinations that are 
most likely to produce a successful treatment outcome. "Conversely, these same 
algorithms also can prioritize investigational drugs and compound combinations 
of unknown potential against a full spectrum of human malignancies, as well as 
novel cancer targets," explained Dr. Bosker, "which make them invaluable for 
pharmaceutical companies seeking to both optimize their compound pipelines and 
discover mechanistically actionable, novel cancer targets and compound-tumor 
alignments."

DarwinHealth's mission statement is to deploy novel technologies rooted in 
systems biology to improve clinical outcomes of cancer treatment. Its core 
technology, the VIPER algorithm, can identify tightly knit modules of master 
regulator proteins that represent a new class of actionable therapeutic targets 
in cancer. The methodology is applied along two complementary axes: First, 
DarwinHealth's technologies support the systematic identification and 
validation of druggable targets at a more foundational, deep state of the 
cancer cell's regulatory logic so we and our scientific partners can exploit 
next generation actionability based on fundamental and more universal tumor 
dependencies and mechanisms. Second, from a drug development and discovery 
perspective, the same technologies are capable of identifying potentially 
druggable novel targets based on master regulators, and upstream modulators of 
those targets. This is where the DarwinHealth oncotectural approach, with its 
emphasis on elucidating and targeting tumor checkpoints, provides its most 
important solutions and repositioning roadmaps for advancing precision-focused 
cancer drug discovery and therapeutics. 

The proprietary, precision medicine-based methods employed by DarwinHealth are 
supported by a deep body of scientific literature authored by its scientific 
leadership, including DarwinHealth CSO, Mariano Alvarez, PhD, who co-developed 
the company's critical computational infrastructure. These proprietary 
strategies leverage the ability to reverse-engineer and analyze the genome-wide 
regulatory and signaling logic of the cancer cell, by integrating data from in 
silico, in vitro, and in vivo assays. This provides a fully integrated drug 
characterization and discovery platform designed to elucidate, accelerate, and 
validate precise developmental trajectories for pharmaceutical assets, so their 
full clinical and commercial potential can be realized. For more information, 
please visit: www.DarwinHealth.com.

(1)Cell 184, 1–18, January 21, 2021 (print version)
(2)Cell (online pub, January 11, 2021), 
https://www.sciencedirect.com/science/article/pii/S0092867420316172?dgcid=author

SOURCE DarwinHealth

CONTACT: Gideon Bosker, MD, CEO, DarwinHealth, Inc., Email: 
GBosker@DarwinHealth.com, Phone: (1) 503-880-2207
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