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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Elsevier B.V.
2022
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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 |
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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 |
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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 |
format |
Review |
accesstype |
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record_format |
scopus |
collection |
Scopus |
_version_ |
1814778503945519104 |