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Samuels Lab

@samuels-lab.bsky.social
32 followers 22 following 11 posts

We aim to shed new light on the complex networks formed in #melanoma, and learn how we can utilize this information to treat melanoma patients @Weizmann Institute of Science

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Samuels Lab @samuels-lab.bsky.social · 29/04/2025
Proud of @yardenasamuels.bsky.social for her fascinating plenary session at the @theaacr.bsky.social annual meeting in Chicago! A great thank you to the program committee chairs, Drs. Matthew Vander Heiden and Lillian Siu for this opportunity. @mvhlab.bsky.social @lilliansiu.bsky.social #AACR25
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Cancer Cell @cp-cancercell.bsky.social · 27/03/2025
Online Now: Translation dysregulation in cancer as a source for targetable antigens
dlvr.it
Translation dysregulation in cancer as a source for targetable antigens
Weller et al. substantiate the role of translation dysregulation in mediating anti-tumor immunity by demonstrating that TYW2 loss in melanoma cells induces aberrant peptide MHC presentation, increasing both tumor immunogenicity and sensitivity to ICB therapy. TYW2 expression levels in patients with melanoma predict clinical outcomes, highlighting translation regulatory factors as immunotherapy targets.
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ACIR @acir-org.bsky.social · 02/04/2025
Translation dysregulation may serve as a new source for identifying cancer-associated antigens, and may also help to predict responses to checkpoint blockade bit.ly/3E4OMY8 #CheckpointBlockade #CancerImmunotherapy @wellerchen.bsky.social @Samuels-lab.bsky.social  @yardenasamuels.bsky.social
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Samuels Lab @samuels-lab.bsky.social · 03/04/2025
In a study published in @cp-cancercell.bsky.social researchers from our lab manipulated cancer cells into making themselves visible to the immune system, creating a new approach that gives hope to patients with previously untreatable disease>> bit.ly/cancer-expos...
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Samuels Lab @samuels-lab.bsky.social · 30/03/2025
✨ We are thankful to the @CancerCell editorial team and the reviewers for their constructive comments, and I am grateful to have such a wonderful team. (7/7)
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Samuels Lab @samuels-lab.bsky.social · 30/03/2025
🏥 Patient data completed the picture: Primary melanoma tumors with low TYW2 showed enhanced responses to ICB, even in patients with low TMB (@Tiangen). Translation fidelity defects may help predict immunotherapy responders, opening new paths for precision cancer treatment. (6/7)
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Samuels Lab @samuels-lab.bsky.social · 30/03/2025
Together with Yaron Carmi, we identified FS peptides that triggered robust T cell responses. Moreover, these peptides elicited de novo T cell responses specifically in TYW2-KO tumor-bearing mice! (5/7)
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Samuels Lab @samuels-lab.bsky.social · 30/03/2025
🐭 In mice, TYW2 loss increased tumor immunogenicity, specifically in immunocompetent mice. scRNA-seq revealed that TYW2-KO tumors were enriched for exhausted T cells. Indeed, TYW2-KO tumor-bearing mice were sensitive to immune checkpoint blockade (ICB) therapy. (4/7)
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Samuels Lab @samuels-lab.bsky.social · 30/03/2025
Furthermore, in vitro T cell stimulation assays (@Johannaolweus & team) demonstrated that these aberrant peptides are potent immune triggers! Could translation errors fuel anti-tumor immunity? (3/7)
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Samuels Lab @samuels-lab.bsky.social · 30/03/2025
🧬 Loss of TYW2, a tRNA modifier, disrupts translation fidelity—causing ribosomes to pause at Phe codons and increasing frameshift (FS) events. This generates out-of-frame peptides, which are presented by MHC class I molecules. (2/7)
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Samuels Lab @samuels-lab.bsky.social · 30/03/2025
Thrilled to share our latest work in Cancer Cell! 🚨 Led by Chen Weller, Osnat Bartok, with amazing collaborators Chris Mcginnis, Ansuman Satpathy, Andreas Schlosser, Eytan Ruppin & more, we reveal that impaired translation fidelity enhances anti-tumor immunity!🧵(1/7)
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Yardena Samuels @yardenasamuels.bsky.social · 10/03/2025
Proud of my PhD student Nofar Gumpert giving an excellent talk at the #MICC conference un Athens!!!
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Samuels Lab @samuels-lab.bsky.social · 09/03/2025
All this is thanks to the hard work and wonderful collaboration with Sapir Cohen Shvefel, Joy Pai, the Sathpathy lab, the Ruppin lab, Mitch Levesque, @yardenasamuels.bsky.social and colleagues. #CancerResearch #Immunotherapy #ITH
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Samuels Lab @samuels-lab.bsky.social · 09/03/2025
Thrilled to share that our new paper on Macrophage Migration Inhibitory Factor (MIF) as a key regulator of immune evasion in melanoma, is now published in Cancer Discovery! Find the full study here: aacrjournals.org/cancerdiscov...
aacrjournals.org
Temporal Genomic Analysis of Homogeneous Tumor Models Reveals Key Regulators of Immune Evasion in Melanoma
Analysis of homogeneous rejected and non-rejected melanoma tumors uncovers critical immune evasion mechanisms, identifies MIF as a key regulator, and stresses the key role of tumor-associated macropha...
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