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Olivier Elemento

Researcher at Cornell University

Publications -  596
Citations -  38936

Olivier Elemento is an academic researcher from Cornell University. The author has contributed to research in topics: Medicine & Biology. The author has an hindex of 82, co-authored 471 publications receiving 27739 citations. Previous affiliations of Olivier Elemento include Princeton University & Max Planck Society.

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A Pharmacologically Reversible Epigenomic Signature of Relapse and Chemotherapy Resistance in Anaplastic Large Cell Lymphoma

TL;DR: This study provides the first comprehensive characterization of methylome in ALCL and examines whether a treatment with the 5-azacytidine (5-Aza) could reverse the hypermethylation profile of ALCL PDTX.
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Abstract 5497: Cabozantinib eradicatesde novocastrate-resistant PTEN/p53 deficient murine prostate cancer via activation of neutrophil-mediated anti-tumor innate immunity

TL;DR: It is shown that cabozaninib eradicates poorly differentiated invasive cancer that develop in the context of prostate-specific PTEN and p53 loss, respectively, within 48 hours of cabozantinib treatment, and suggest the possibility of combination therapies of Cabozant inib with T-cell checkpoint blockade or vaccine-based approaches, to augment immunologic responses in advanced cancers.
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Histone 3 Methyltransferases Alter Melanoma Initiation and Progression Through Discrete Mechanisms

TL;DR: These data demonstrate how histone 3 lysine-to-methionine mutations can be used to uncover critical roles for methyltransferases and identify FOXD1 as a top target of PRC2 that is silenced in melanocytes and found that aberrant overexpression ofFOXD1 accelerated melanoma onset.
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Mp48-18 germline dna repair single nucleotide polymorphisms in urothelial cancer patients.

TL;DR: ERBB2 is a frequent mutation at different stages of UC, and in higher stage disease, clonal selection of the S310F/Y hot-spot mutation may occur and requires further study.
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Novel Long Non Coding RNA Blackmamba Is Associated to ALK- anaplastic Large Cell Lymphoma

TL;DR: Having proven that JAK/STAT signaling pathway plays a key role in both ALK+ and ALK - ALCL, the expression of BlackMamba could be modulated after treatment with JAK1/2 (ruxolitinib) TKi is tested and found the physical interaction with the histone-lysine N-methyltransferase enzyme EZH2 by RIP in the FedP cells.