Aurélie Dumont

ORCID: 0009-0004-7665-7815
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About
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Research Areas
  • PARP inhibition in cancer therapy
  • BRCA gene mutations in cancer
  • Ovarian cancer diagnosis and treatment
  • Microtubule and mitosis dynamics
  • Cancer Treatment and Pharmacology
  • Lung Cancer Treatments and Mutations
  • Advanced Breast Cancer Therapies
  • Cancer-related Molecular Pathways
  • Cancer Genomics and Diagnostics
  • HER2/EGFR in Cancer Research
  • Breast Cancer Treatment Studies
  • Genetic factors in colorectal cancer
  • Wnt/β-catenin signaling in development and cancer
  • Advancements in Semiconductor Devices and Circuit Design
  • Breast Lesions and Carcinomas
  • Brain Metastases and Treatment
  • Pharmacogenetics and Drug Metabolism
  • Radio Frequency Integrated Circuit Design
  • Clinical Laboratory Practices and Quality Control
  • Data Quality and Management
  • DNA Repair Mechanisms
  • Ancient and Medieval Archaeology Studies
  • Cancer therapeutics and mechanisms
  • Protein Kinase Regulation and GTPase Signaling
  • Skin and Cellular Biology Research

Assistance Publique – Hôpitaux de Paris
2024

Centre Oscar Lambret
2013-2023

Institut Curie
2012-2018

Université Paris Sciences et Lettres
2018

Bristol-Myers Squibb (France)
2018

Comprehensive Cancer Center Vienna
2017

Translational Research in Oncology
2013

Inserm
2012

École Nationale Supérieure des Mines de Paris
2012

AgroParisTech
2012

Breast cancers are composed of molecularly distinct subtypes with different clinical outcomes and responses to therapy. To discover potential therapeutic targets for the poor prognosis-associated triple-negative breast cancer (TNBC), gene expression profiling was carried out on a cohort 130 samples. Polo-like kinase 1 (PLK1) found be significantly overexpressed in TNBC compared other subtypes. High PLK1 confirmed by reverse phase protein tissue microarrays. In cell lines, RNAi-mediated...

10.1158/0008-5472.can-12-2633 article EN Cancer Research 2012-11-11

Triple-negative breast cancer (TNBC) represents a subgroup of cancers (BC) associated with the most aggressive clinical behavior. No targeted therapy is currently available for treatment patients TNBC. In order to discover potential therapeutic targets, we searched protein kinases that are overexpressed in human TNBC biopsies and whose silencing cell lines causes death. A cohort including BC obtained at Institut Curie as well normal tissues has been analyzed gene-expression level. The data...

10.1371/journal.pone.0063712 article EN cc-by PLoS ONE 2013-05-20
Raphaël Leman Etienne Müller Angélina Legros Nicolas Goardon Imène Chentli and 95 more Alexandre Atkinson Aurore Tranchant Laurent Castéra Sophie Krieger Agathe Ricou Flavie Boulouard Florence Joly Romain Boucly Aurélie Dumont Noémie Basset Florence Coulet Louise-Marie Chevalier Étienne Rouleau Katharina Leitner Antonio González‐Martín Piera Gargiulo Hans‐Joachim Lück Catherine Genestie Gerhard Bogner Christian Marth Edgar Petru Alexander Reinthaller Christian Schauer P. Sevelda Lionel D’Hondt Ignace Vergote Peter Vuylsteke Sakari Hietanen Gabriel Lindahl Johanna Mäenpää Trine Jakobi Nøttrup Ulla Puistola Sophie Abadie‐Lacourtoisie Jérôme Alexandre Émilie Boissier Hugues Bourgeois Annick Chevalier-Place Pierre Judet de La Combe Cristina Costan Jérôme Dauba Laure De Cock Christophe Desauw Raymond Despax Nadine Dohollou Coraline Dubot Michel Fabbro Laure Favier Anne Floquet Philippe Follana Claire Garnier Tixidre Georges Garnier Laurence Gladieff Julien Grenier Cécile Guillemet Anne‐Claire Hardy‐Bessard Florence Joly Elsa Kalbacher Marie‐Christine Kaminsky Jean‐Emmanuel Kurtz Rémy Largillier Claudia Lefeuvre‐Plesse Anne Lesoin Charles-Briac Levaché Tifenn L’Haridon Alain Lortholary Jean‐Pierre Lotz Jérôme Meunier M Mousseau Marie‐Ange Mouret‐Reynier Patricia Pautier Thierry Petit Magali Provansal Éric Pujade-Lauraine Nadia Raban Isabelle Ray‐Coquard Manuel Rodrigues Frédèric Selle Robert Sverdlin Youssef Tazi Benoît You Bahriye Aktas Dirk Bauerschlag Thomas Beck Antje Belau Holger Bronger Stefan Buchholz Paul Buderath Alexander Burges Ulrich Canzler Nikolaus de Gregorio Dominik Denschlag Max Dieterich Michael Eichbaum Ayşe Balat Günter Emons

The optimal application of maintenance PARP inhibitor therapy for ovarian cancer requires accessible, robust, and rapid testing homologous recombination deficiency (HRD). However, in many countries, access to HRD is problematic the failure rate high. We developed an academic test support treatment decision-making.Genomic Instability Scar (GIScar) was through targeted sequencing a 127-gene panel determine status. GIScar trained from noninterventional study with 250 prospectively collected...

10.1158/1078-0432.ccr-23-0898 article EN cc-by-nc-nd Clinical Cancer Research 2023-09-26

c-Yes, a member of the Src tyrosine kinase family, is found highly activated in colon carcinoma but its importance relative to c-Src has remained unclear. Here we show that, HT29 cells, silencing not c-Src, selectively leads an increase cell clustering associated with localisation β-catenin at membranes and reduction expression target genes. c-Yes induced apoptosis, inhibition growth soft-agar mouse xenografts, migration loss capacity generate liver metastases mice. Re-introduction c -Src,...

10.1371/journal.pone.0017237 article EN cc-by PLoS ONE 2011-02-24
Juliette Coignard Michael Lush Jonathan Beesley Tracy A. O’Mara Joe Dennis and 95 more Jonathan P. Tyrer Daniel R. Barnes Lesley McGuffog Goska Leslie Manjeet K. Bolla Muriel A. Adank Simona Agata Thomas U. Ahearn Kristiina Aittomäki Irene L. Andrulis Hoda Anton‐Culver Volker Arndt Norbert Arnold Kristan J. Aronson Banu Arun Annelie Augustinsson Jacopo Azzollini Daniel Barrowdale Caroline Baynes Heiko Becher Marina Bermisheva Leslie Bernstein Katarzyna Białkowska Carl Blomqvist Stig E. Bojesen Bernardo Bonanni Åke Borg Hiltrud Brauch Hermann Brenner Barbara Burwinkel Saundra S. Buys Trinidad Caldés Maria A. Caligo Daniele Campa Brian D. Carter Jose E. Castelao Jenny Chang‐Claude Stephen J. Chanock Wendy K. Chung Kathleen Claes Christine L. Clarke Ophélie Bertrand Sandrine M. Caputo Anaïs Dupré Marine Le Mentec Muriel Belotti Anne-Marie Birot Bruno Buecher Emmanuelle Fourme Marion Gauthier-Villars Lisa Golmard Claude Houdayer Virginie Moncoutier Antoine de Pauw Claire Saule Olga Sinilnikova Sylvie Mazoyer Francesca Damiola Laure Barjhoux Carole Verny-Pierre Mélanie Léone Nadia Boutry-Kryza Alain Calender Sophie Giraud Olivier Caron Marine Guillaud-Bataille Brigitte Bressac–de Paillerets Yves- Jean Bignon Nancy Uhrhammer Christine Lasset Valérie Bonadona Pascaline Berthet Dominique Vaur Laurent Castéra Tetsuro Noguchi Cornel Popovici Hagay Sobol Violaine Bourdon Tetsuro Noguchi Audrey Remenieras Catherine Noguès Isabelle Coupier Pascal Pujol Aurélie Dumont Françoise Révillion Claude Adenis Danièle Muller Emmanuelle Barouk-Simonet Françoise Bonnet Virginie Bubien Nicolas Sevenet Michel Longy Christine Toulas Rosine Guimbaud Laurence Gladieff

Breast cancer (BC) risk for BRCA1 and BRCA2 mutation carriers varies by genetic familial factors. About 50 common variants have been shown to modify BC carriers. All but three, were identified in general population studies. Other carrier-specific susceptibility may exist studies of so far underpowered. We conduct a novel case-only genome-wide association study comparing genotype frequencies between 60,212 cases 13,007 with or mutations. identify robust associations 2 3 carriers, P < 10-8, at...

10.1038/s41467-020-20496-3 article EN cc-by Nature Communications 2021-02-17

// Sylvie Maubant 1, * , Tania Tahtouh Amélie Brisson 1 Virginie Maire Fariba Némati 2 Bruno Tesson 3 Mengliang Ye Guillem Rigaill 4, 5 Maïté Noizet Aurélie Dumont David Gentien 6 Bérengère Marty-Prouvost Leanne de Koning 7 Sardar Faisal Mahmood Didier Decaudin Francisco Cruzalegui 8 Gordon C. Tucker Sergio Roman-Roman 9 and Thierry Dubois Institut Curie, PSL Research University, Translational Department, Breast Cancer Biology Group, Paris, France Preclinical Investigation Laboratory, INSERM...

10.18632/oncotarget.25187 article EN Oncotarget 2018-04-27

Neoadjuvant chemotherapy (NCT) using anthracyclines and taxanes is a standard treatment for locally advanced breast cancer. Efficacy of NCT however variable among patients predictive markers are expected to guide the selection who will benefit from NCT. A promising approach stand with polymorphisms located in genes encoding drug transporters, metabolizing enzymes target which can affect efficacy. Our study investigated potential 37 predict response cancer.118 women adenocarcinoma were...

10.1186/s40064-015-1053-0 article EN SpringerPlus 2015-07-06
Yue Jiao Fabienne Lesueur Chloé‐Agathe Azencott M Laurent Noura Mebirouk and 95 more Lilian Laborde Juana Beauvallet Marie‐Gabrielle Dondon Séverine Eon‐Marchais Anthony Laugé Nadia Boutry‐Kryza Alain Calender Sophie Giraud Mélanie Léoné Brigitte Bressac–de Paillerets Olivier Caron Marine Guillaud-Bataille Yves‐Jean Bignon Nancy Uhrhammer Valérie Bonadona Christine Lasset Pascaline Berthet Laurent Castéra Dominique Vaur Violaine Bourdon Catherine Noguès Tetsuro Noguchi Cornel Popovici Audrey Remenieras Hagay Sobol Isabelle Coupier Pierre-Olivier Harmand Pascal Pujol Paul Vilquin Aurélie Dumont Françoise Révillion Danièle Muller Emmanuelle Barouk-Simonet Françoise Bonnet Virginie Bubien Michel Longy Nicolas Sévenet Laurence Gladieff Rosine Guimbaud V. Feillel Christine Toulas Hélène Dreyfus Dominique Leroux Magalie Peysselon Christine Rebischung Amandine Baurand Geoffrey Bertolone Fanny Coron Laurence Faivre Vincent Goussot Caroline Jacquot Caroline Sawka Caroline Kientz Marine Lebrun Fabienne Prieur Sandra Fert‐Ferrer Véronique Mari Laurence Venat‐Bouvet Stéphane Bézieau Capucine Delnatte Isabelle Mortemousque Florence Coulet Florent Soubrier Mathilde Warcoin Myriam Bronner Sarab Lizard Johanna Sokolowska Marie‐Agnès Collonge‐Rame Alexandre Damette Paul Gesta Hakima Lallaoui Jean Chiésa Denise Molina‐Gomes Olivier Ingster Sylvie Manouvrier‐Hanu Sophie Lejeune Catherine Noguès Lilian Laborde Pauline Pontois Dominique Stoppa‐Lyonnet Marion Gauthier‐Villars Bruno Buecher Olivier Caron Emmanuelle Mouret‐Fourme Jean‐Pierre Fricker Christine Lasset Valérie Bonadona Pascaline Berthet Laurence Faivre Élisabeth Luporsi Marc Frénay Laurence Gladieff Paul Gesta Hagay Sobol François Eisinger

Abstract Background Linking independent sources of data describing the same individuals enable innovative epidemiological and health studies but require a robust record linkage approach. We describe hybrid process to link databases from two ongoing French national studies, GEMO (Genetic Modifiers BRCA1 BRCA2 ), which focuses on identification genetic factors modifying cancer risk mutation carriers, GENEPSO (prospective cohort BRCAx carriers), environmental lifestyle factors. Methods To...

10.1186/s12874-021-01299-6 article EN cc-by BMC Medical Research Methodology 2021-07-29

Edoxaban is a direct oral anticoagulant available in Europe but not France. Given the high tourist traffic France, understanding pharmacology of edoxaban and availability its laboratory testing seemed crucial emergency situations. The aim this work was to describe methodology for measuring anti-Xa activity edoxaban, highlighting pre-analytical analytical aspects, along with essential clinico-biological data therapeutic guidance. analysis performed using chromogenic method on STAR-Max...

10.1684/abc.2024.1910 article EN Annales de biologie clinique 2024-08-01

536 Background: Pathological complete response (pCR) is the main prognostic factor after preoperative chemotherapy. Predictive factors of pCR are mainly histological type, hormonal status, HER2 overexpression. Single nucleotide polymorphisms (SNP) in genes encoding drug transporters, metabolizing enzymes and target can affect efficacy may explain therapeutic failures. The aim study was to identify SNPs associated with breast cancer (BC) patients (PTS) HER-2 overexpression treated sequential...

10.1200/jco.2013.31.15_suppl.536 article EN Journal of Clinical Oncology 2013-05-20

Abstract Background: Adjuvant chemotherapy (ACT) using anthracyclines and taxanes is a standard treatment for BC. Usual criteria as age, SBR grade, HER2 or hormonal status (HS), estrogen receptor (ER), triple negative BC, histological type, lymphovascular invasion (LVI), Ki67, tumor size lymph node involvement are not yet sufficient ACT decision. As SNPs located in genes involved metabolism transport of cytotoxic drugs may affect efficacy ACT, we investigated the potential 49 to predict...

10.1158/1538-7445.sabcs15-p5-08-24 article EN Cancer Research 2016-02-15

&lt;div&gt;Abstract&lt;p&gt;Breast cancers are composed of molecularly distinct subtypes with different clinical outcomes and responses to therapy. To discover potential therapeutic targets for the poor prognosis-associated triple-negative breast cancer (TNBC), gene expression profiling was carried out on a cohort 130 samples. Polo-like kinase 1 (PLK1) found be significantly overexpressed in TNBC compared other subtypes. High PLK1 confirmed by reverse phase protein tissue microarrays. In...

10.1158/0008-5472.c.6505248 preprint EN 2023-03-30

&lt;div&gt;Abstract&lt;p&gt;Breast cancers are composed of molecularly distinct subtypes with different clinical outcomes and responses to therapy. To discover potential therapeutic targets for the poor prognosis-associated triple-negative breast cancer (TNBC), gene expression profiling was carried out on a cohort 130 samples. Polo-like kinase 1 (PLK1) found be significantly overexpressed in TNBC compared other subtypes. High PLK1 confirmed by reverse phase protein tissue microarrays. In...

10.1158/0008-5472.c.6505248.v1 preprint EN 2023-03-30

Abstract Introduction. Treatment of patients with triple-negative breast cancers (TNBCs) remains a major challenge for oncologists. Although they respond well to the current therapeutic strategies based on conventional chemotherapies, represent large proportion cancer death due high recurrence rate. Alternative treatments are needed improve survival these patients. The Wnt/beta-catenin signaling, recently reported be activated in TNBCs, may an interesting pathway target. Methods. We analyzed...

10.1158/1535-7163.targ-13-b233 article EN Molecular Cancer Therapeutics 2013-11-01

544 Background: Neoadjuvant chemotherapy (NCT) using anthracyclines and taxanes is a standard treatment for locally advanced breast cancer pathologic complete response (pCR) major prognostic factor survival. Gene polymorphisms have been identified as modulators of response. Our study investigated constitutional variants genes associated with change in the to neoadjuvant and/or patients adenocarcinoma. Methods: From November 2007 January 2012, 118 women adenocarcinoma histologically proven,...

10.1200/jco.2013.31.15_suppl.544 article EN Journal of Clinical Oncology 2013-05-20
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