Critical clinical gaps in cancer precision nanomedicine development

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...

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Bibliographic Details
Published in:Journal of Controlled Release
Main Author: Gan W.W.; Chan L.W.; Li W.; Wong T.W.
Format: Review
Language:English
Published: Elsevier B.V. 2022
Online Access:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85127814501&doi=10.1016%2fj.jconrel.2022.03.055&partnerID=40&md5=71b6f899537e58020fe912e7ffd21014
id 2-s2.0-85127814501
spelling 2-s2.0-85127814501
Gan W.W.; Chan L.W.; Li W.; Wong T.W.
Critical clinical gaps in cancer precision nanomedicine development
2022
Journal of Controlled Release
345

10.1016/j.jconrel.2022.03.055
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85127814501&doi=10.1016%2fj.jconrel.2022.03.055&partnerID=40&md5=71b6f899537e58020fe912e7ffd21014
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. © 2022 Elsevier B.V.
Elsevier B.V.
01683659
English
Review

author Gan W.W.; Chan L.W.; Li W.; Wong T.W.
spellingShingle Gan W.W.; Chan L.W.; Li W.; Wong T.W.
Critical clinical gaps in cancer precision nanomedicine development
author_facet Gan W.W.; Chan L.W.; Li W.; Wong T.W.
author_sort Gan W.W.; Chan L.W.; Li W.; Wong T.W.
title Critical clinical gaps in cancer precision nanomedicine development
title_short Critical clinical gaps in cancer precision nanomedicine development
title_full Critical clinical gaps in cancer precision nanomedicine development
title_fullStr Critical clinical gaps in cancer precision nanomedicine development
title_full_unstemmed Critical clinical gaps in cancer precision nanomedicine development
title_sort Critical clinical gaps in cancer precision nanomedicine development
publishDate 2022
container_title Journal of Controlled Release
container_volume 345
container_issue
doi_str_mv 10.1016/j.jconrel.2022.03.055
url https://www.scopus.com/inward/record.uri?eid=2-s2.0-85127814501&doi=10.1016%2fj.jconrel.2022.03.055&partnerID=40&md5=71b6f899537e58020fe912e7ffd21014
description 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. © 2022 Elsevier B.V.
publisher Elsevier B.V.
issn 01683659
language English
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