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Dendrimeric nanosystem consistently circumvents heterogeneous drug response and resistance in pancreatic cancer.
Liu, Juan; Chen, Chao; Wei, Tuo; Gayet, Odile; Loncle, Céline; Borge, Laurence; Dusetti, Nelson; Ma, Xiaowei; Marson, Domenico; Laurini, Erik; Pricl, Sabrina; Gu, Zhongwei; Iovanna, Juan; Peng, Ling; Liang, Xing-Jie.
Affiliation
  • Liu J; CNRS, Centre Interdisciplinaire de Nanoscience de Marseille, UMR 7325, Equipe Labellisée Ligue Contre le Cancer Aix-Marseille Université Marseille France.
  • Chen C; Laboratory of Controllable Nanopharmaceuticals Chinese Academy of Sciences (CAS) Center for Excellence in Nanoscience Beijing China.
  • Wei T; CAS Key Laboratory for Biomedical Effects of Nanomaterials and Nanosafety National Center for Nanoscience and Technology of China Beijing China.
  • Gayet O; University of Chinese Academy of Sciences Beijing China.
  • Loncle C; Hepato-Pancreato-Biliary Center, Beijing Tsinghua Changgung Hospital, School of Medicine Tsinghua University Beijing China.
  • Borge L; CNRS, Centre Interdisciplinaire de Nanoscience de Marseille, UMR 7325, Equipe Labellisée Ligue Contre le Cancer Aix-Marseille Université Marseille France.
  • Dusetti N; CNRS, Centre Interdisciplinaire de Nanoscience de Marseille, UMR 7325, Equipe Labellisée Ligue Contre le Cancer Aix-Marseille Université Marseille France.
  • Ma X; Laboratory of Controllable Nanopharmaceuticals Chinese Academy of Sciences (CAS) Center for Excellence in Nanoscience Beijing China.
  • Marson D; CAS Key Laboratory for Biomedical Effects of Nanomaterials and Nanosafety National Center for Nanoscience and Technology of China Beijing China.
  • Laurini E; University of Chinese Academy of Sciences Beijing China.
  • Pricl S; Centre de Recherche en Cancérologie de Marseille, INSERM, UMR1068 Marseille France.
  • Gu Z; Centre de Recherche en Cancérologie de Marseille, INSERM, UMR1068 Marseille France.
  • Iovanna J; Centre de Recherche en Cancérologie de Marseille, INSERM, UMR1068 Marseille France.
  • Peng L; Centre de Recherche en Cancérologie de Marseille, INSERM, UMR1068 Marseille France.
  • Liang XJ; Laboratory of Controllable Nanopharmaceuticals Chinese Academy of Sciences (CAS) Center for Excellence in Nanoscience Beijing China.
Exploration (Beijing) ; 1(1): 21-34, 2021 Aug.
Article in En | MEDLINE | ID: mdl-37366462
ABSTRACT
Pancreatic ductal adenocarcinoma (PDAC) is a deadly cancer with no efficacious treatment. The application of nanomedicine is expected to bring new hope to PDAC treatment. In this study, we report a novel supramolecular dendrimeric nanosystem carrying the anticancer drug doxorubicin, which demonstrated potent anticancer activity, markedly overcoming the heterogeneity of drug response and resistance of primary cultured tumor cells derived from PDAC patients. This dendrimer nanodrug was constructed with a fluorinated amphiphilic dendrimer, which self-assembled into micelles nanostructure and encapsulated doxorubicin with high loading. Because of the fine nanosize, stable formulation and acid-promoted drug release, this dendrimeric nanosystem effectively accumulated in tumor, with deep penetration in tumor tissue and rapid drug uptake/release profile in cells, ultimately resulting in potent anticancer activity and complete suppression of tumor growth in patient-derived xenografts. Most importantly, this dendrimer nanodrug generated uniform and effective response when treating 35 primary pancreatic cancer cell lines issued from patient samples as a robust platform for preclinical drug efficacy testing. In addition, this dendrimer nanodrug formulation was devoid of adverse effects and showed excellent tolerability. Given all these uniquely advantageous features, this simple and convenient dendrimer nanodrug holds great promise as a potential candidate to treat the deadly PDAC.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Exploration (Beijing) Year: 2021 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Exploration (Beijing) Year: 2021 Document type: Article