Élisabeth Brambilla

ORCID: 0000-0001-7559-2141
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About
Contact & Profiles
Research Areas
  • Lung Cancer Treatments and Mutations
  • Lung Cancer Research Studies
  • RNA modifications and cancer
  • Neuroendocrine Tumor Research Advances
  • Lung Cancer Diagnosis and Treatment
  • Epigenetics and DNA Methylation
  • Cancer Genomics and Diagnostics
  • Cancer-related Molecular Pathways
  • Cancer-related gene regulation
  • Medical Imaging and Pathology Studies
  • Neuroblastoma Research and Treatments
  • Telomeres, Telomerase, and Senescence
  • Cancer-related molecular mechanisms research
  • Cancer, Hypoxia, and Metabolism
  • Cholangiocarcinoma and Gallbladder Cancer Studies
  • Cancer Immunotherapy and Biomarkers
  • Metastasis and carcinoma case studies
  • Radiomics and Machine Learning in Medical Imaging
  • MicroRNA in disease regulation
  • Cancer Research and Treatments
  • PI3K/AKT/mTOR signaling in cancer
  • Ubiquitin and proteasome pathways
  • Ferroptosis and cancer prognosis
  • DNA Repair Mechanisms
  • Colorectal Cancer Treatments and Studies

Université Grenoble Alpes
2014-2025

Inserm
2014-2025

Centre National de la Recherche Scientifique
1993-2025

Centre Hospitalier Universitaire de Grenoble
2012-2023

Institut pour l'avancée des biosciences
2010-2023

Université Joseph Fourier
2008-2023

Institut de Biosciences et Biotechnologies
2019-2023

Hôpital Albert Michallon
2009-2021

University of Missouri–Kansas City
2018

Université Paris-Saclay
2016-2018

10.1038/nature14664 article EN Nature 2015-07-10

Adjuvant cisplatin-based chemotherapy improves survival among patients with completely resected non-small-cell lung cancer, but there is no validated clinical or biologic predictor of the benefit chemotherapy.We used immunohistochemical analysis to determine expression excision repair cross-complementation group 1 (ERCC1) protein in operative specimens cancer. The had been enrolled International Lung Cancer Trial, thereby allowing a comparison effect adjuvant on survival, according ERCC1...

10.1056/nejmoa060570 article EN New England Journal of Medicine 2006-09-06
Martin Peifer Lynnette Fernández-Cuesta Martin L. Sos Julie George Danila Seidel and 88 more Lawryn H. Kasper Dennis Plenker Frauke Leenders Ruping Sun Thomas Zander Roopika Menon Mirjam Koker Ilona Dahmen Christian Müller Vincenzo Di Cerbo Hans‐Ulrich Schildhaus Janine Altmüller Ingelore Baessmann Christian Becker Bram De Wilde Jo Vandesompele Diana Böhm Sascha Ansén Franziska Gabler Ines Wilkening Stefanie Heynck Johannes M. Heuckmann Xin Lü Scott L. Carter Kristian Cibulskis Shantanu Banerji Gad Getz Kwon-Sik Park Daniel Rauh Christian Grütter Matthias Fischer Laura Pasqualucci Gavin Wright Zoe Wainer Prudence A. Russell Iver Petersen Yuan Chen Erich Stoelben Corinna Ludwig Philipp A. Schnabel Hans Hoffmann Thomas Muley Michael Brockmann Walburga Engel-Riedel Lucia Anna Muscarella Vito Michele Fazio Harry J.M. Groen Wim Timens Hannie Sietsma Erik Thunnissen Egbert F. Smit Daniëlle A.M. Heideman Peter J.F. Snijders Federico Cappuzzo Claudia Ligorio Stefania Damiani John K. Field Steinar Solberg Odd Terje Brustugun Marius Lund‐Iversen Jörg Sänger Joachim H. Clement Alex Soltermann Holger Moch Walter Weder Benjamin Solomon Jean‐Charles Soria Pierre Validire Benjamin Besse Élisabeth Brambilla Christian Brambilla Sylvie Lantuéjoul Philippe Lorimier Peter M. Schneider Michael Hallek William Pao Matthew Meyerson Julien Sage Jay Shendure Robert C. Schneider Reinhard Büttner Jürgen Wolf Peter Nürnberg Sven Perner Lukas C. Heukamp Paul K. Brindle Stefan A. Haas Roman K. Thomas

10.1038/ng.2396 article EN Nature Genetics 2012-09-02

The classification of neuroendocrine neoplasms (NENs) differs between organ systems and currently causes considerable confusion. A uniform framework for NENs at any anatomical location may reduce inconsistencies contradictions among the various in use. suggested here is intended to allow pathologists clinicians manage their patients with consistently, while acknowledging organ-specific differences criteria, tumor biology, prognostic factors. based on a consensus conference held International...

10.1038/s41379-018-0110-y article EN cc-by Modern Pathology 2018-08-23

While genomically targeted therapies have improved outcomes for patients with lung adenocarcinoma, little is known about the genomic alterations which drive squamous cell cancer. Sanger sequencing of tyrosine kinome identified mutations in DDR2 kinase gene 3.8% cancers and lines. Squamous cancer lines harboring were selectively killed by knock-down RNAi or treatment multi-targeted inhibitor dasatinib. Tumors established from a mutant line sensitive to dasatinib xenograft models. Expression...

10.1158/2159-8274.cd-11-0005 article EN Cancer Discovery 2011-04-08
Danila Seidel Thomas Zander Lukas C. Heukamp Martin Peifer Marc Bos and 95 more Lynnette Fernández-Cuesta Frauke Leenders Xin Lü Sascha Ansén Masyar Gardizi Chau Nguyen Johannes Berg Prudence A. Russell Zoe Wainer Hans‐Ulrich Schildhaus Toni-Maree Rogers Benjamin Solomon William Pao Scott L. Carter Gad Getz D. Neil Hayes Matthew D. Wilkerson Erik Thunnissen William D. Travis Sven Perner Gavin Wright Élisabeth Brambilla Reinhard Buettner Juergen Wolf Roman K. Thomas Franziska Gabler Ines Wilkening Christian Mueller Ilona Dahmen Roopika Menon Katharina Koenig Kerstin Albus Sabine Merkelbach‐Bruse Jana Fassunke Katja Schmitz Helen Kuenstlinger Michaela Angelika Kleine Elke Binot Silvia Querings Janine Altmueller Ingelore Boessmann Peter Nuemberg Peter M. Schneider Magdalena Bogus Alex Soltermann Holger Moch Odd Terje Brustugun Steinar Solberg Marius Lund‐Iversen Åslaug Helland Thomas Muley Hans Hoffmann Philipp A. Schnabel Yuan Chen Harry J.M. Groen Wim Timens Hannie Sietsma Joachim H. Clement Walter Weder Joerg Saenger Erich Stoelben Corinna Ludwig Walburga Engel-Riedel Egbert F. Smit Danille A. M. Heideman Peter J.F. Snijders Lucia Nogová Martin L. Sos Christian Mattonet Karin Toepelt Matthias Scheffler Eray Goekkurt Rainer Kappes Stefan Krueger Kato Kambartel Dirk Behringer Wolfgang Schulte Wolfgang Galetke Winfried Randerath Matthias Heldwein Andreas Schlesinger Monika Serke Khosro Hekmat Konrad Frank Roland Schnell Marcel Reiser Ali-Nuri Huenerlituerkoglu Stephan Schmitz Lisa Meffert Yon‐Dschun Ko Markus Litt-Lampe Ulrich Gerigk Rainer Fricke Benjamin Besse Christian Brambilla

The pattern of mutations in human lung cancer differs by tumor subtype and is a useful addition to histology for selecting targeted therapy improving patient survival.

10.1126/scitranslmed.3006802 article EN Science Translational Medicine 2013-10-30

The new International Association for the Study of Lung Cancer/American Thoracic Society/European Respiratory Society lung adenocarcinoma classification provides, first time, standardized terminology cancer diagnosis in small biopsies and cytology; this was not primarily addressed by previous World Health Organization classifications. Until recently there have been no therapeutic implications to further NSCLC, so little attention has given distinction squamous cell carcinoma tissue samples....

10.5858/arpa.2012-0263-ra article EN Archives of Pathology & Laboratory Medicine 2012-09-12

We collected 75 primary pulmonary carcinomas with pleomorphic, sarcomatoid, or sarcomatous elements to better define their clinical, histologic, and immunohistochemical profile. The patient's age ranged from 42 81 years (mean 65 years), the male-to-female ratio was 9.7:1. Sixty-nine patients (92%) were smokers. Cough hemoptysis most frequent presenting symptoms. Fifty-nine (65%) died of disease: only stage significantly predicts overall survival (p = 0.0273). Microscopically, based on WHO...

10.1097/00000478-200303000-00004 article EN The American Journal of Surgical Pathology 2003-03-01

The excision repair cross-complementation group 1 (ERCC1) protein is a potential prognostic biomarker of the efficacy cisplatin-based chemotherapy in non–small-cell lung cancer (NSCLC). Although several ongoing trials are evaluating level expression ERCC1, no consensus has been reached regarding method for evaluation.

10.1056/nejmoa1214271 article EN New England Journal of Medicine 2013-03-20

Tumor lymphocytic infiltration (TLI) has differing prognostic value among various cancers. The objective of this study was to assess the effect TLI in lung cancer.A discovery set (one trial, n = 824) and a validation (three trials, 984) that evaluated benefit platinum-based adjuvant chemotherapy non-small-cell cancer were used as part LACE-Bio (Lung Adjuvant Cisplatin Evaluation Biomarker) study. defined intense versus nonintense. main end point overall survival (OS); secondary points...

10.1200/jco.2015.63.0970 article EN Journal of Clinical Oncology 2016-02-02

Pulmonary large-cell neuroendocrine carcinomas (LCNECs) have similarities with other lung cancers, but their precise relationship has remained unclear. Here we perform a comprehensive genomic (n = 60) and transcriptomic 69) analysis of 75 LCNECs identify two molecular subgroups: "type I LCNECs" bi-allelic TP53 STK11/KEAP1 alterations (37%), II enriched for inactivation RB1 (42%). Despite sharing adenocarcinomas squamous cell carcinomas, no transcriptional was found; instead form distinct...

10.1038/s41467-018-03099-x article EN cc-by Nature Communications 2018-03-07

Squamous cell carcinoma (SCC) of the lung is a frequent and aggressive cancer type. Gene amplifications, known activating mechanism oncogenes, target 3q26-qter region as one most frequently gained/amplified genomic sites in SCC various types. Here, we used array comparative hybridization to delineate consensus 3q26.3 amplifications SCC. Recurrent occur 20% (136 tumors total) map core 2 Mb (Megabases) that encompasses SOX2, transcription factor gene. Intense SOX2 immunostaining nuclei SCC,...

10.1371/journal.pone.0008960 article EN cc-by PLoS ONE 2010-01-28
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