Poulikos Poulikakos, PhD
- ASSOCIATE PROFESSOR | Oncological Sciences
Research Topics:
Biochemistry, Breast Cancer, Cancer, Cell Biology, Cell Cycle, Dermatology, Drug Design and Discovery, Drug Resistance, Phosphorylation, Protein Kinases, Signal Transduction, Translational Research, Tumor Suppressor GenesDr. Poulikos I. Poulikakos is a biochemist and a cancer biologist whose research is focused on regulation of oncogenic signaling and tumor sensitivity and resistance to targeted cancer therapeutics. He completed his doctoral studies in Athens, Greece and he then moved for postdoctoral training first to Fox Chase Cancer Center in Philadelphia and subsequently to Memorial Sloan-Kettering Cancer Center New York. During the course of that work, he brought to light hitherto underappreciated aspects of kinase regulation, controlled by conformational switch and dimerization, as well as novel mechanisms of resistance to drugs targeting MAPK signaling (BRAF and MEK inhibitors) in melanoma and other cancers. He subsequently developed a mechanistic model that explains and predicts the biochemical effects of diverse inhibitors based on their structural properties, thus enabling the use of specific inhibitors tailored for clinical contexts.
The long-term goal of his research group is to improve our understanding on the role of signal transduction networks in tumor resistance to targeted therapies and in tumor immunity, to help the design of more effective cancer therapies. The research program of his laboratory is focused on several important areas. They investigate oncogenic signaling by studying the effects of blocking the network at various points (RTK, SHP2, RAF, MEK, ERK, CDK4/6) on signaling and they are developing strategies to overcome adaptive and acquired resistance to these drugs, a major limitation in current therapeutic approaches to cancer. Secondly, they investigate the effect of targeted cancer therapies on immune signaling and on tumor immunity, with the goal of developing more effective integrated therapeutic strategies. Finally, they investigate novel approaches to target oncogenic signaling more broadly, using alternative pharmacologic approaches and next generation proteasome-targeted technologies.
Visit the Poulikakos Laboratory
Education
PhD, University of Athens, School of Biology
Fox Chase Cancer Center
Memorial Sloan-Kettering Cancer Center
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Research Career Developmenet Award -
Unraveling mechanistic requirements for RAF dimerization, catalytic activation and response to kinase inhibitors -
Identification of effective therapeutic strategies against RAF-inhibitor resistant melanoma -
Molecular Determinants of Tumor Dependence on ERK Signaling -
RSK Kinase as a mediator of oncogenic ERK signaling and a novel therapeutic Target in Melanoma
Using small molecule compounds to dissect and target oncogenic signaling.
We use small molecule inhibitors to acutely disrupt oncogenic signal transduction networks. Our goal is to understand the regulation of their components and their role in tumor maintenance and resistance to targeted therapies. Current research in the lab focuses on elucidating the complex biologic and biochemical effects of components of the RAS/RAF/MEK/ERK pathway (ERK signaling) in cancer in order to design mechanism-based therapeutic strategies.
Biochemical and biological properties of RAF inhibitors
The discovery that established tumors usually remain dependent on signaling pathways activated by mutationally activated oncoproteins led to the idea that targeted inhibition of components of these pathways would be especially effective for therapy. The RAS/RAF/MEK/ERK signaling pathway (ERK signaling) regulates key cellular processes, such as cell proliferation, differentiation and survival and has been found deregulated in about a third of human cancers. Hyperactivation of ERK signaling is especially prevalent in malignant melanomas. About 50% of these tumors contain BRAF mutations (almost exclusively V600E), whereas 15%–30% contain mutations in NRAS.
Melanoma tumors expressing the mutant BRAF(V600E) almost universally depend on it for growth. This led to the aggressive development of inhibitors of ERK signaling as potential therapeutics. In general, kinase inhibitors (e.g. MEK inhibitors) inhibit their target in all cells. In contrast, RAF inhibitors affect ERK signaling in a mutation-specific manner: they inhibit ERK signaling in cells with BRAF(V600E), but paradoxically activate ERK signaling in cells with wild-type BRAF. The underlying mechanism of this phenomenon is summarized in the following model (Poulikakos PI et al., Nature, 2010): Activation of RAS promotes the dimerization of members of the RAF family. Binding of an ATP-competitive RAFinhibitor to one member of the dimer inhibits it while also causing its transition to the active state. This is associated with the allosteric transactivation of the other, unbound member of the dimer, resulting in a marked increase in RAF specific activity and induction of ERK signaling. RAF induction by inhibitor requires levels of RAS activity sufficient to support formation of RAF dimers. In BRAF(V600E) melanomas, RAS-GTP levels are inadequate and RAF inhibitors inhibit the active RAF monomers. This model predicts that RAF inhibitors will have a wide therapeutic index in patients with mutant BRAF tumors, but that they could cause toxicity by activating ERK signaling in normal cells. Clinical trials of RAF inhibitors in metastatic melanoma emphatically confirmed these predictions.
BRAF splicing variants as a novel mechanism of resistance to RAF inhibitors in melanoma
The model of RAF transactivation by RAF inhibitors predicts that any molecular lesion that enhances RAF dimerization will promote resistance to RAF inhibitors. These could include changes that cause increased activation of RAS and alterations in RAF that cause it to dimerize in a RAS-independent manner. We identified a novel mechanism of acquired resistance to RAF inhibitors in preclinical models and patients: expression of aberrant splicing variants of BRAF(V600E) that lack the RAS-binding domain and therefore dimerize in a RAS-independent manner (Poulikakos PI et al., Nature, 2011).
Major areas of research in the lab include:
1. Understand RAF kinase regulation and function in signaling and disease.
2. Elucidate mechanisms of resistance to RAF and MEK inhibitors and develop rationally-designed therapeutic strategies to overcome resistance in melanoma.
3. Investigate novel approaches to target RAS and RAF mutant tumors.
Visit the Poulikakos Lab
Physicians and scientists on the faculty of the Icahn School of Medicine at Mount Sinai often interact with pharmaceutical, device and biotechnology companies to improve patient care, develop new therapies and achieve scientific breakthroughs. In order to promote an ethical and transparent environment for conducting research, providing clinical care and teaching, Mount Sinai requires that salaried faculty inform the School of their relationships with such companies.
Below are financial relationships with industry reported by Dr. Poulikakos during 2020 and/or 2021. Please note that this information may differ from information posted on corporate sites due to timing or classification differences.
Consulting:
- Guidepoint Global, LLC.
Mount Sinai's faculty policies relating to faculty collaboration with industry are posted on our website. Patients may wish to ask their physician about the activities they perform for companies.