Author

Tâp Ha‐Duong

Centre National de la Recherche ScientifiqueORCID 0000-0002-0847-2948Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Biophysics· 1 Cancer Biology· 1 Pharmacology & Toxicology· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Research Focus:cancer & tumor microenvironment· 2 Research Focus:drug response / drug discovery· 2 Approach:experimental assay· 2 Assay:metabolomics· 2 Assay:proteomics· 2 Approach:deep learning· 1 Research Focus:metabolism & bioenergetics· 1

Frequent Co-Authors

Antonin MarchaisiD· 2 shared Birgit GeoergeriD· 2 shared Catherine BrenneriD· 2 shared Daniela Dias‐PedrosoiD· 2 shared Guido KroemeriD· 2 shared Hong-Toan LaiiD· 2 shared Liuba MazzantiiD· 2 shared Maria Eugénia Marques Da CostaiD· 2 shared

Activity by Year

2026-2026 · peak 3/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersPharmacology & Toxicology

Antonin MarchaisORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Engineered flavonoid disrupts mitochondrial AIF/CHCHD4 complex for targeted cancer therapy

Hong-Toan Lai, Daniela Dias‐Pedroso, Maria Eugénia Marques Da Costa, Romain Fernandes, Tran Ngoc Anh Nguyen, Olivia Bawa, Pierre Khneisser, João Gabriel Silva, Yassine Khalij, Michelangelo Campanella, John Griffith Jones, Svetlana Dokudovskaya, Guido Kroemer, Antonin Marchais, Nathalie Gaspar, , Catherine Brenner

This paper identifies M30-E05, an engineered flavonoid that disrupts the AIF/CHCHD4 mitochondrial complex, reducing cancer cell viability and tumor growth in xenograft models.

Acta Pharmaceutica Sinica B · Jun 15, 2026Peer-reviewedPharmacology & Toxicology

Computational Design and Biophysical Validation of Macrocyclic Peptides as Inhibitors of SLIT2/ROBO1 interaction

Somaya A. Abdel‐Rahman, Maxence Delaunay, Tâp Ha‐Duong, Moustafa Tarek Gabr

This paper computationally designs and experimentally validates macrocyclic peptides that inhibit SLIT2/ROBO1 interaction, showing promising in vitro properties.

Bioorganic & Medicinal Chemistry Letters · Apr 10, 2026Peer-reviewedBiophysics

Combined inhibition of AIF/CHCHD4 interaction and GLS1 to exploit metabolic vulnerabilities in pediatric osteosarcoma

Hong-Toan Lai, Tran Ngoc Anh Nguyen, Maria Eugénia Marques Da Costa, Romain Fernandes, Daniela Dias‐Pedroso, Sylvère Durand, Guido Kroemer, Reynand Jay Canoy, Liuba Mazzanti, Yegor S Vassetzky, Nathalie Gaspar, Antonin Marchais, Birgit Geoerger, Tâp Ha‐Duong, Catherine Brenner

This study identifies a metabolic vulnerability in osteosarcoma by combining AIF/CHCHD4 inhibition and GLS1 suppression, showing synergy between mitoxantrone and telaglenastat in vitro and in vivo.

bioRxiv · Apr 7, 2026 · PreprintCancer Biology