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Critical clinical gaps in cancer precision nanomedicine development. | LitMetric

Critical clinical gaps in cancer precision nanomedicine development.

J Control Release

Department of Pharmacy, Faculty of Science, National University of Singapore, 18 Science Drive 4, 117543, Republic of Singapore; Sino-Malaysia Molecular Oncology and Traditional Chinese Medicine Delivery Joint Research Centre, Medical College, Yangzhou University, 136, Jiangyang Middle Road, Yangzhou, Jiangsu Province, China; Non-Destructive Biomedical and Pharmaceutical Research Centre, Smart Manufacturing Research Institute, Universiti Teknologi MARA Selangor, 42300 Puncak Alam, Selangor, Malaysia. Electronic address:

Published: May 2022

AI Article Synopsis

  • Active targeting strategy in nanomedicine for cancer treatment faces challenges related to the selection of targeting ligands and matrix materials that align with patients' omics profiles.
  • Recent literature indicates that these components are often chosen without considering the specific cancer omics of patients, potentially undermining treatment effectiveness.
  • Factors like age, gender, race, and geographical origin significantly influence the expression of important cellular receptors and enzymes, highlighting the need for personalized approaches in nanomedicine to effectively target cancer cells.

Article Abstract

Active targeting strategy is adopted in nanomedicine for cancer treatment. Personalizing the nanomedicine in accordance with patients' omics, under the precision medicine platform, is met with challenges in targeting ligand and matrix material selection at nanoformulation stage. The past 5-year literatures show that the nanoparticulate targeting ligand and matrix material are not selected based upon the cancer omics profiles of patients. The expression of cancer cellular target receptors and metabolizing enzymes is primarily influenced by age, gender, race/ethnic group and geographical origin of patients. The personalized perspective of a nanomedicine cannot be realised with premature digestion of matrix and targeting ligand by specific metabolizing enzymes that are overexpressed by the patients, and unmatched targeting ligand to the majority of cell surface receptors overexpressed in cancer. Omics analysis of individual metabolizing enzyme and cancer cell surface receptor expressed in cancer facilitates targeting ligand and matrix material selection in nanomedicine development.

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Source
http://dx.doi.org/10.1016/j.jconrel.2022.03.055DOI Listing

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