Sylvain Baulande

ORCID: 0000-0003-3104-1684
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About
Contact & Profiles
Research Areas
  • Cancer Genomics and Diagnostics
  • Neuroblastoma Research and Treatments
  • Immune cells in cancer
  • Ocular Oncology and Treatments
  • Cancer Immunotherapy and Biomarkers
  • Cancer, Hypoxia, and Metabolism
  • Microtubule and mitosis dynamics
  • RNA modifications and cancer
  • Immunotherapy and Immune Responses
  • Cancer Cells and Metastasis
  • Immune Cell Function and Interaction
  • Sarcoma Diagnosis and Treatment
  • Chromatin Remodeling and Cancer
  • RNA Research and Splicing
  • Glioma Diagnosis and Treatment
  • Adipose Tissue and Metabolism
  • Nanoplatforms for cancer theranostics
  • T-cell and B-cell Immunology
  • Cancer-related molecular mechanisms research
  • Genetic factors in colorectal cancer
  • Retinal Development and Disorders
  • RNA and protein synthesis mechanisms
  • Lipid metabolism and biosynthesis
  • Single-cell and spatial transcriptomics
  • Cancer-related gene regulation

Institut Curie
2016-2025

Université Paris Sciences et Lettres
2017-2025

Inserm
2015-2024

Goethe University Frankfurt
2024

Institut Mondor de Recherche Biomédicale
2024

Macquarie University
2024

Genopole (France)
2007-2021

Centre National pour la Recherche Scientifique et Technique (CNRST)
2021

Université Paris Cité
2019

Délégation Paris 5
2019

A subset of cancer-associated fibroblasts (FAP+/CAF-S1) mediates immunosuppression in breast cancers, but its heterogeneity and impact on immunotherapy response remain unknown. Here, we identify 8 CAF-S1 clusters by analyzing more than 19,000 single from cancer. We validate the five most abundant flow cytometry silico analyses other cancer types, highlighting their relevance. Myofibroblasts 0 3, characterized extracellular matrix proteins TGFβ signaling, respectively, are indicative primary...

10.1158/2159-8290.cd-19-1384 article EN Cancer Discovery 2020-05-20

Recent clinical results support the use of new immune checkpoint blockers (ICB), such as anti-PD-1 (e.g. nivolumab and pembrolizumab) anti-PD-L1 antibodies. Radiological evaluation ICB efficacy during therapy is challenging due to tumor infiltration. Changes circulating DNA (ctDNA) levels could be a promising tool for very accurate monitoring treatment efficacy, but data are lacking with ICB.This prospective pilot study was conducted in patients nonsmall cell lung cancer, uveal melanoma, or...

10.1093/annonc/mdx212 article EN publisher-specific-oa Annals of Oncology 2017-04-28

Abstract Purpose: One of the main limitations to anticancer radiotherapy lies in irreversible damage healthy tissues located within radiation field. “FLASH” irradiation at very high dose-rate is a new treatment modality that has been reported specifically spare normal tissue from late radiation-induced toxicity animal models and therefore could be promising strategy reduce toxicity. Experimental Design: Lung responses FLASH were investigated by qPCR, single-cell RNA sequencing (sc-RNA-Seq),...

10.1158/1078-0432.ccr-19-1440 article EN Clinical Cancer Research 2019-12-03

Presentation of exogenous antigens on MHC-I molecules, termed cross-presentation, is essential for cytotoxic CD8+ T cell responses. In mice, dendritic cells (DCs) that arise from monocytes (mo-DCs) during inflammation have a key function in these responses by cross-presenting locally peripheral tissues. Whether human naturally-occurring mo-DCs can cross-present unknown. Here, we use and macrophages directly purified ascites to address this question. Single-cell RNA-seq data show CD1c+ DCs...

10.1038/s41467-018-04985-0 article EN cc-by Nature Communications 2018-06-26

Abstract Tumor-associated macrophages (TAM) play a detrimental role in triple-negative breast cancer (TNBC). In-depth analysis of TAM characteristics and interactions with stromal cells, such as cancer-associated fibroblast (CAF), could provide important biological therapeutic insights. Here we identify at the single-cell level monocyte-derived STAB1+TREM2high lipid-associated macrophage (LAM) subpopulation immune suppressive capacities that is expanded patients resistant to checkpoint...

10.1158/0008-5472.can-22-1427 article EN Cancer Research 2022-07-21

Abstract Inflammation is a complex physiological process triggered in response to harmful stimuli 1 . It involves cells of the immune system capable clearing sources injury and damaged tissues. Excessive inflammation can occur as result infection hallmark several diseases 2–4 The molecular bases underlying inflammatory responses are not fully understood. Here we show that cell surface glycoprotein CD44, which marks acquisition distinct phenotypes context development, immunity cancer...

10.1038/s41586-023-06017-4 article EN cc-by Nature 2023-04-26

Oncogenesis often implicates epigenetic alterations, including derepression of transposable elements (TEs) and defects in alternative splicing. Here, we explore the possibility that noncanonical splice junctions between exons TEs represent a source tumor-specific antigens. We show mouse normal tissues tumor cell lines express wide but distinct ranges mRNA TEs, some which are specific. Immunopeptidome analyses identified peptides derived from exon-TE splicing associated to MHC-I molecules....

10.1126/sciimmunol.abm6360 article EN Science Immunology 2023-02-03

Abstract Noradrenergic and mesenchymal identities have been characterized in neuroblastoma cell lines according to their epigenetic landscapes core regulatory circuitries. However, relationship relative contribution patient tumors remain poorly defined. We now document spontaneous reversible plasticity between the two identities, associated with reprogramming, several models. Interestingly, xenografts cells from each identity eventually harbor a noradrenergic phenotype suggesting that...

10.1038/s41467-023-38239-5 article EN cc-by Nature Communications 2023-05-04
Qinghe Zeng Christophe Klein Stefano Caruso Pascale Maillé Daniela Allende and 95 more Beatriz Mínguez Massimo Iavarone Massih Ningarhari Andrea Casadei‐Gardini Federica Pedica Margherita Rimini Riccardo Perbellini Camille Boulagnon‐Rombi Alexandra Heurgué Marco Maggioni Mohamed Rela Mukul Vij Sylvain Baulande Patricia Legoix Sonia Lameiras Daniela Allende Giuliana Amaddeo Lorenza Rimassa Sylvain Baulande Aurélie Beaufrère María Bermúdez-Ramos Camille Boulagnon‐Rombi Arndt Vogel Josepmaría Argemí Julien Caldéraro Pompilia Radu Stefano Caruso Andrea Casadei‐Gardini A. García Stephen L. Chan María Teresa Salcedo Marı́a Varela Alba Díaz Antonia Digklia Jean‐François Dufour Hyungjin Rhee Narmin Ghaffari Laleh Nicolas Loménie Purva Gopal Rondell P. Graham Alexandra Heurgué Massimo Iavarone Mercedes Iñarrairaegui Jakob Nikolas Kather Christophe Klein Ismaïl Labgaa Sonia Lameiras Patricia Legoix Marie Lequoy Howard Ho‐Wai Leung Nicolas Loménie Marco Maggioni Pascale Maillé Juan Ignacio Marín Guillermo Mendoza-Pacas Sophie Michalak Beatriz Mínguez Omar S.M. El Nahhas Antonia Digklia Pooja Navale Massih Ningarhari Tung‐Hung Su María Reig Jean‐Michel Pawlotsky Federica Pedica Riccardo Perbellini Nguyen H. Tran Bernhard Scheiner Christine Sempoux Pompilia Radu Hélène Regnault María Reig Mohamed Rela Hélène Regnault Lorenza Rimassa Margherita Rimini María Teresa Salcedo Bruno Sangro Bruno Sangro Christine Sempoux Tung‐Hung Su Callie Torres Nguyen H. Tran Eric Trépo Marı́a Varela Gontran Verset Mukul Vij Arndt Vogel Dominique Wendum Qinghe Zeng Qinghe Zeng Josepmaría Argemí Nicolas Loménie Antonia Digklia Pompilia Radu

10.1016/s1470-2045(23)00468-0 article EN publisher-specific-oa The Lancet Oncology 2023-11-08

Abstract Although heterogeneity of FAP+ Cancer-Associated Fibroblasts (CAF) has been described in breast cancer, their plasticity and spatial distribution remain poorly understood. Here, we analyze trajectory inference, deconvolute transcriptomics at single-cell level perform functional assays to generate a high-resolution integrated map cancer (BC), with focus on inflammatory myofibroblastic (iCAF/myCAF) CAF clusters. We identify 10 spatially-organized CAF-related cellular niches, called...

10.1038/s41467-024-47068-z article EN cc-by Nature Communications 2024-04-01

We have used a mRNA differential display technique to identify new genes involved in the reprogramming of gene expression during adipose conversion mouse 3T3 preadipocyte cell lines. report here on identification and cloning novel adipose-specific cDNA encoding predicted membrane protein 413 amino acids. The level corresponding 3.2-kilobase is tremendously increased 3T3-L1 3T3-F442A differentiation into adipocytes. A single, very abundant transcript also found inguinal epididymal white...

10.1074/jbc.m105193200 article EN cc-by Journal of Biological Chemistry 2001-09-01

Purpose: Neuroblastoma displays important clinical and genetic heterogeneity, with emergence of new mutations at tumor progression.Experimental Design: To study clonal evolution during treatment follow-up, an innovative method based on circulating cell-free DNA (cfDNA) analysis by whole-exome sequencing (WES) paired target was realized in sequential liquid biopsy samples 19 neuroblastoma patients.Results: WES the primary cfDNA diagnosis showed overlap single-nucleotide variants (SNV) copy...

10.1158/1078-0432.ccr-17-1586 article EN Clinical Cancer Research 2017-11-30

EWSR1-FLI1, the chimeric oncogene specific for Ewing sarcoma (EwS), induces a cascade of signaling events leading to cell transformation. However, it remains elusive how genetically homogeneous EwS cells can drive heterogeneity transcriptional programs. Here, we combine independent component analysis single-cell RNA sequencing data from diverse types and model systems with time-resolved mapping EWSR1-FLI1 binding sites open chromatin regions characterize dynamic cellular processes associated...

10.1016/j.celrep.2020.01.049 article EN cc-by Cell Reports 2020-02-01

A significant proportion of patients with oestrogen receptor (ER) positive breast cancers (BC) develop resistance to endocrine treatments (ET) and relapse metastatic disease. Here we perform whole exome sequencing gene expression analysis matched primary tumours bone metastasis-derived patient-derived xenografts (PDX). Transcriptomic analyses reveal enrichment the G2/M checkpoint up-regulation Polo-like kinase 1 (PLK1) in PDX. PLK1 inhibition results tumour shrinkage highly proliferating...

10.1038/s41467-020-17697-1 article EN cc-by Nature Communications 2020-08-13

The colon is primarily responsible for absorbing fluids. It contains a large number of microorganisms including fungi, which are enriched in its distal segment. colonic mucosa must therefore tightly regulate fluid influx to control absorption fungal metabolites, can be toxic epithelial cells and lead barrier dysfunction. How this achieved remains unknown. Here, we describe mechanism by the innate immune system allows rapid quality check absorbed fluids avoid intoxication colonocytes. This...

10.1016/j.cell.2020.08.048 article EN cc-by-nc-nd Cell 2020-09-23

Abstract Retinoblastoma is the most frequent intraocular malignancy in children, originating from a maturing cone precursor developing retina. Little known on molecular basis underlying biological and clinical behavior of this cancer. Here, using multi-omics data, we demonstrate existence two retinoblastoma subtypes. Subtype 1, earlier onset, includes heritable forms. It harbors few genetic alterations other than initiating RB1 inactivation corresponds to differentiated tumors expressing...

10.1038/s41467-021-25792-0 article EN cc-by Nature Communications 2021-09-22

In neuroblastoma (NB), the ALK receptor tyrosine kinase can be constitutively activated through activating point mutations or genomic amplification. We studied genetic alterations in high-risk (HR) patients on HR-NBL1/SIOPEN trial to determine their frequency, correlation with clinical parameters, and prognostic impact.Diagnostic tumor samples were available from 1,092 amplification status (n = 330), mutational profile 191), both 571).Genomic (ALKa) was detected 4.5% of cases (41 out 901),...

10.1200/jco.21.00086 article EN cc-by Journal of Clinical Oncology 2021-06-11
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