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Attilio Di Pietro

Attilio Di Pietro

Overview

Attilio Di Pietro is a researcher affiliated with the University of Lyon System in France. Their work primarily spans the interdisciplinary fields of Biochemistry, Genetics and Molecular Biology, and Medicine. Within these fields, they focus on subfields such as Molecular Biology and Oncology, addressing molecular mechanisms relevant to health and disease.

The researcher's recent scholarly contributions include investigations into drug resistance in cancer therapeutics. One notable publication is titled "Uncompetitive nanomolar dimeric indenoindole inhibitors of the human breast cancer resistance pump ABCG2", published in 2020 in the European Journal of Medicinal Chemistry. This paper explores chemical inhibitors targeting the ABCG2 protein, a pump involved in multidrug resistance in breast cancer cells.

Attilio Di Pietro's work encompasses various scientific topics, including:

  • Drug Transport and Resistance Mechanisms
  • DNA and Nucleic Acid Chemistry
  • Cancer therapeutics and mechanisms

Their collaboration network involves several frequent co-authors who have contributed to this work, such as:

  • Nathalie Guragossian
  • Billel Belhani
  • Alexis Moréno
  • Magda Teixeira Nunes
  • Lucía González-Lobato

Publication venues for Di Pietro's research mainly include the European Journal of Medicinal Chemistry, where they have at least one documented publication. This venue aligns with their focus on molecular compounds and their biochemical properties related to medical applications.

Best Publications

  • Flavonoids: A class of modulators with bifunctional interactions at vicinal ATP- and steroid-binding sites on mouse P-glycoprotein

    Gwenaelle Conseil;Helene Baubichon-Cortay;Guila Dayan;Jean-Michel Jault

  • Flavonoid structure-activity studies identify 6-prenylchrysin and tectochrysin as potent and specific inhibitors of breast cancer resistance protein ABCG2.

    Abdelhakim Ahmed-Belkacem;Alexandre Pozza;Francisco Muñoz-Martínez;Susan E. Bates

  • Targeting the Achilles Heel of Multidrug-Resistant Cancer by Exploiting the Fitness Cost of Resistance

    Gergely Szakács;Matthew D. Hall;Michael M. Gottesman;Ahcène Boumendjel

  • Recent advances in the discovery of flavonoids and analogs with high-affinity binding to P-glycoprotein responsible for cancer cell multidrug resistance

    Ahcène Boumendjel;Attilio Di Pietro;Charles Dumontet;Denis Barron

  • Characterization of YvcC (BmrA), a multidrug ABC transporter constitutively expressed in Bacillus subtilis.

    Emmanuelle Steinfels;Cédric Orelle;‖ Jean-Raphaël Fantino;Olivier Dalmas

  • The HPr kinase from Bacillus subtilis is a homo-oligomeric enzyme which exhibits strong positive cooperativity for nucleotide and fructose 1,6-bisphosphate binding.

    Jean-Michel Jault;Sonia Fieulaine;Sylvie Nessler;Philippe Gonzalo

  • C-Isoprenylation of flavonoids enhances binding affinity toward P-glycoprotein and modulation of cancer cell chemoresistance.

    Gilles Comte;# Jean-Baptiste Daskiewicz;Christine Bayet;Gwenaëlle Conseil

  • "Hysteretic" behavior and nucleotide binding sites of pig heart mitochondrial F1 adenosine 5'-triphosphatase

    Attilio Di Pietro;Francois Penin;Catherine Godinot;Daniele C. Gautheron

  • Verapamil and its derivative trigger apoptosis through glutathione extrusion by multidrug resistance protein MRP1.

    Doriane Trompier;Xiu Bao Chang;Régis Barattin;Amaury Du Moulinet D'Hardemare

  • Acridone derivatives: Design, synthesis, and inhibition of breast cancer resistance protein ABCG2

    Ahcene Boumendjel;Sira Macalou;Abdelhakim Ahmed-Belkacem;Madeleine Blanc

  • Nonprenylated Rotenoids, a New Class of Potent Breast Cancer Resistance Protein Inhibitors

    Abdelhakim Ahmed-Belkacem;X Sira Macalou;X Francesca Borrelli;Raffaele Capasso

  • Jatrophane diterpenes as modulators of multidrug resistance. Advances of structure-activity relationships and discovery of the potent lead pepluanin A.

    Gabriella Corea;Ernesto Fattorusso;Virginia Lanzotti;Riccardo Motti

  • Investigation of Chalcones as Selective Inhibitors of the Breast Cancer Resistance Protein: Critical Role of Methoxylation in both Inhibition Potency and Cytotoxicity

    Glaucio Valdameri;Glaucio Valdameri;Charlotte Gauthier;Raphaël Terreux;Rémy Kachadourian

  • ABCG2 Transports and Transfers Heme to Albumin through Its Large Extracellular Loop

    Elodie Desuzinges-Mandon;Ophélie Arnaud;Lorena Martinez;Frédéric Huché

  • Jatrophane diterpenes as P-glycoprotein inhibitors. First insights of structure-activity relationships and discovery of a new, powerful lead.

    Gabriella Corea;Ernesto Fattorusso;Virginia Lanzotti;Orazio Taglialatela-Scafati

  • Three-dimensional structure by cryo-electron microscopy of YvcC, an homodimeric ATP-binding cassette transporter from Bacillus subtilis.

    Mohamed Chami;Emmanuelle Steinfels;Cédric Orelle;Jean-Michel Jault

  • Jatrophane diterpenes from Euphorbia spp. as modulators of multidrug resistance in cancer therapy

    G. Corea;A. Di Pietro;C. Dumontet;C. Dumontet;E. Fattorusso

  • Substituted chromones as highly potent nontoxic inhibitors, specific for the breast cancer resistance protein.

    Glaucio Valdameri;Glaucio Valdameri;Estelle Genoux-Bastide;Basile Peres;Charlotte Gauthier

  • Binding of steroid modulators to recombinant cytosolic domain from mouse P-glycoprotein in close proximity to the ATP site.

    Guila Dayan;§ Jean-Michel Jault;§ Hélène Baubichon-Cortay;Loris G. Baggetto

  • (R)- and (S)-verapamil differentially modulate the multidrug-resistant protein MRP1

    Thomas Perrotton;Doriane Trompier;Xiu Bao Chang;Attilio Di Pietro

Frequent Co-Authors

Rajendra Prasad
Rajendra Prasad Amity University
Balázs Sarkadi
Balázs Sarkadi TTK Research Centre for Natural Sciences
Pierre Boulanger
Pierre Boulanger Claude Bernard University Lyon 1
François Penin
François Penin Claude Bernard University Lyon 1
André Goffeau
André Goffeau Université Catholique de Louvain
Susan E. Bates
Susan E. Bates Columbia University
Suresh V. Ambudkar
Suresh V. Ambudkar National Institutes of Health
Alain Puisieux
Alain Puisieux Claude Bernard University Lyon 1
Gilles Divita
Gilles Divita Centre national de la recherche scientifique, CNRS

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