Critical clinical gaps in cancer precision nanomedicine development

被引:18
作者
Gan, Wendy Wei [1 ]
Chan, Lai Wah [1 ]
Li, Wenji [2 ,3 ]
Wong, Tin Wui [1 ,2 ,4 ]
机构
[1] Natl Univ Singapore, Fac Sci, Dept Pharm, 18 Sci Dr 4, Singapore 117543, Singapore
[2] Yangzhou Univ, Med Coll, Sino Malaysia Mol Oncol & Tradit Chinese Med Deli, 136 Jiangyang Middle Rd, Yangzhou, Jiangsu, Peoples R China
[3] Yangzhou Univ, Affiliated Hosp, Dept TCM, Yangzhou 225000, Jiangsu, Peoples R China
[4] Univ Teknol MARA Selangor, Nondestruct Biomed & Pharmaceut Res Ctr, Smart Mfg Res Inst, Puncak Alam 42300, Selangor, Malaysia
关键词
Cancer; Cellular receptor; Metabolizing enzyme; Nanomedicine; Omics; Precision medicine; TARGETING TUMOR MICROENVIRONMENT; BREAST-CANCER; DRUG-DELIVERY; HUMAN-LIVER; METABOLIZING ENZYME; EXPRESSION; RECEPTOR; NANOPARTICLES; THERAPY; GENDER;
D O I
10.1016/j.jconrel.2022.03.055
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
引用
收藏
页码:811 / 818
页数:8
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