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Epitranscriptomics & Cancer Adaptation : A.David

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Our research work focuses on the contribution of post-transcriptional mechanisms on cancer cell adaptation, in particular RNA epigenetic & translational control.

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Added by standudu
Group name EquipeCTCS
Item Type Journal Article
Title Gadolinium-Based Nanoparticles Sensitize Ovarian Peritoneal Carcinomatosis to Targeted Radionuclide Therapy
Creator Garcia-Prada et al.
Author Clara Diaz Garcia-Prada
Author Léna Carmes
Author Salima Atis
Author Ali Parach
Author Alejandro Bertolet
Author Marta Jarlier
Author Sophie Poty
Author Daniel Suarez Garcia
Author Wook-Geun Shin
Author Jan Schuemann
Author Olivier Tillement
Author François Lux
Author Julie Constanzo
Author Jean-Pierre Pouget
Abstract Ovarian cancer (OC) is the most lethal gynecologic malignancy (5-y overall survival rate, 46%). OC is generally detected when it has already spread to the peritoneal cavity (peritoneal carcinomatosis). This study investigated whether gadolinium-based nanoparticles (Gd-NPs) increase the efficacy of targeted radionuclide therapy using [177Lu]Lu-DOTA-trastuzumab (an antibody against human epidermal growth factor receptor 2). Gd-NPs have radiosensitizing effects in conventional external-beam radiotherapy and have been tested in clinical phase II trials. Methods: First, the optimal activity of [177Lu]Lu-DOTA-trastuzumab (10, 5, or 2.5 MBq) combined or not with 10?mg of Gd-NPs (single injection) was investigated in athymic mice bearing intraperitoneal OC cell (human epidermal growth factor receptor 2-positive) tumor xenografts. Next, the therapeutic efficacy and toxicity of 5 MBq of [177Lu]Lu-DOTA-trastuzumab with Gd-NPs (3 administration regimens) were evaluated. NaCl, trastuzumab plus Gd-NPs, and [177Lu]Lu-DOTA-trastuzumab alone were used as controls. Biodistribution and dosimetry were determined, and Monte Carlo simulation of energy deposits was performed. Lastly, Gd-NPs' subcellular localization and uptake, and the cytotoxic effects of the combination, were investigated in 3 cancer cell lines to obtain insights into the involved mechanisms. Results: The optimal [177Lu]Lu-DOTA-trastuzumab activity when combined with Gd-NPs was 5 MBq. Moreover, compared with [177Lu]Lu-DOTA-trastuzumab alone, the strongest therapeutic efficacy (tumor mass reduction) was obtained with 2 injections of 5?mg of Gd-NPs/d (separated by 6?h) at 24 and 72?h after injection of 5 MBq of [177Lu]Lu-DOTA-trastuzumab. In vitro experiments showed that Gd-NPs colocalized with lysosomes and that their radiosensitizing effect was mediated by oxidative stress and inhibited by deferiprone, an iron chelator. Exposure of Gd-NPs to 177Lu increased the Auger electron yield but not the absorbed dose. Conclusion: Targeted radionuclide therapy can be combined with Gd-NPs to increase the therapeutic effect and reduce the injected activities. As Gd-NPs are already used in the clinic, this combination could be a new therapeutic approach for patients with ovarian peritoneal carcinomatosis.
Publication Journal of Nuclear Medicine: Official Publication, Society of Nuclear Medicine
Pages jnumed.123.265418
Date 2023-10-19
Journal Abbr J Nucl Med
Language eng
DOI 10.2967/jnumed.123.265418
ISSN 1535-5667
Library Catalog PubMed
Extra PMID: 37857502
Tags Auger electrons, original, radioimmunotherapy, radiopharmaceutical, radiosensitization, TRT
Date Added 2023/11/14 - 13:40:15
Date Modified 2023/11/14 - 13:40:44
Notes and Attachments PubMed entry (Attachment)


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