TY - JOUR
T1 - Dendrimers as nanoscale vectors
T2 - Unlocking the bars of cancer therapy
AU - Dey, Asmita Deka
AU - Bigham, Ashkan
AU - Esmaeili, Yasaman
AU - Ashrafizadeh, Milad
AU - Moghaddam, Farnaz Dabbagh
AU - Tan, Shing Cheng
AU - Yousefiasl, Satar
AU - Sharma, Saurav
AU - Maleki, Aziz
AU - Rabiee, Navid
AU - Kumar, Alan Prem
AU - Thakur, Vijay Kumar
AU - Orive, Gorka
AU - Sharifi, Esmaeel
AU - Kumar, Arun
AU - Makvandi, Pooyan
N1 - Copyright © 2022 Elsevier Ltd. All rights reserved.
PY - 2022/11
Y1 - 2022/11
N2 - Chemotherapy is the first choice in the treatment of cancer and is always preferred to other approaches such as radiation and surgery, but it has never met the need of patients for a safe and effective drug. Therefore, new advances in cancer treatment are now needed to reduce the side effects and burdens associated with chemotherapy for cancer patients. Targeted treatment using nanotechnology are now being actively explored as they could effectively deliver therapeutic agents to tumor cells without affecting normal cells. Dendrimers are promising nanocarriers with distinct physiochemical properties that have received considerable attention in cancer therapy studies, which is partly due to the numerous functional groups on their surface. In this review, we discuss the progress of different types of dendrimers as delivery systems in cancer therapy, focusing on the challenges, opportunities, and functionalities of the polymeric molecules. The paper also reviews the various role of dendrimers in their entry into cells via endocytosis, as well as the molecular and inflammatory pathways in cancer. In addition, various dendrimers-based drug delivery (e.g., pH-responsive, enzyme-responsive, redox-responsive, thermo-responsive, etc.) and lipid-, amino acid-, polymer- and nanoparticle-based modifications for gene delivery, as well as co-delivery of drugs and genes in cancer therapy with dendrimers, are presented. Finally, biosafety concerns and issues hindering the transition of dendrimers from research to the clinic are discussed to shed light on their clinical applications.
AB - Chemotherapy is the first choice in the treatment of cancer and is always preferred to other approaches such as radiation and surgery, but it has never met the need of patients for a safe and effective drug. Therefore, new advances in cancer treatment are now needed to reduce the side effects and burdens associated with chemotherapy for cancer patients. Targeted treatment using nanotechnology are now being actively explored as they could effectively deliver therapeutic agents to tumor cells without affecting normal cells. Dendrimers are promising nanocarriers with distinct physiochemical properties that have received considerable attention in cancer therapy studies, which is partly due to the numerous functional groups on their surface. In this review, we discuss the progress of different types of dendrimers as delivery systems in cancer therapy, focusing on the challenges, opportunities, and functionalities of the polymeric molecules. The paper also reviews the various role of dendrimers in their entry into cells via endocytosis, as well as the molecular and inflammatory pathways in cancer. In addition, various dendrimers-based drug delivery (e.g., pH-responsive, enzyme-responsive, redox-responsive, thermo-responsive, etc.) and lipid-, amino acid-, polymer- and nanoparticle-based modifications for gene delivery, as well as co-delivery of drugs and genes in cancer therapy with dendrimers, are presented. Finally, biosafety concerns and issues hindering the transition of dendrimers from research to the clinic are discussed to shed light on their clinical applications.
KW - Cancer
KW - Chemotherapy
KW - Dendrimers
KW - Drug and gene delivery
KW - Targeted therapy
UR - http://www.scopus.com/inward/record.url?scp=85133225086&partnerID=8YFLogxK
U2 - 10.1016/j.semcancer.2022.06.003
DO - 10.1016/j.semcancer.2022.06.003
M3 - Review article
C2 - 35700939
SN - 1044-579X
VL - 86
SP - 396
EP - 419
JO - Seminars in Cancer Biology
JF - Seminars in Cancer Biology
IS - Pt 2
ER -