Dendrimer-mediated targeting of angiogenic biomarkers: therapeutic intervention against cancer

被引:0
作者
Pathak, Anchal [1 ]
Jain, Narendra Kumar [2 ]
Jain, Keerti [1 ]
机构
[1] Natl Inst Pharmaceut Educ & Res NIPER Raebareli, Dept Pharmaceut, Drug Delivery & Nanomed Res Lab, Bijnor Sisendi Rd, Lucknow 226002, UP, India
[2] Dr HS Gour Cent Univ, Dept Pharmaceut Sci, Sagar, India
关键词
Angiogenesis; nanocarriers; dendrimers; chemotherapy; anti-angiogenic agent; ANTICANCER DRUG; POLYAMIDOAMINE DENDRIMER; TUMOR-GROWTH; VEGF SIRNA; IN-VITRO; DELIVERY; SURFACE; NANOPARTICLES; INHIBITION; CHALLENGES;
D O I
10.1080/17425247.2024.2394631
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
IntroductionDevelopment of novel vascular networks is a fundamental requirement for tumor growth and progression. In the last decade, biomarkers and underlying molecular pathways of angiogenesis have been intensely investigated to disrupt the initiation and progression of tumor angiogenesis. However, the clinical applications of anti-angiogenic agents are constrained due to toxic side effects, acquired drug resistance, and unavailability of validated biomarkers.Area coveredThis review discusses the development of dendrimeric nanocarriers that could be a promising domain to explore for the eradication of current challenges associated with angiogenesis-based cancer therapy. Novel drug-delivery approaches with subtle readouts and better understanding of molecular mechanisms have revealed that dendrimers comprise innate anti-angiogenic activity and incorporation of anti-angiogenic agents or gene-silencing RNA could lead to synergistic anti-angiogenic and anticancer effects with reduced side effects.Expert opinionDendrimer-mediated targeting of angiogenic biomarkers has efficiently led to the vascular normalization, and rational linking of dendrimers with anti-angiogenic agent or siRNA or both might be a potential area to eradicate the current challenges of angiogenesis-based cancer therapy. However, drawbacks associated with the dendrimers-mediated targeting of angiogenic biomarkers, such as poor stability or small expression of these biomarkers on the normal cells, limit their application at market scale.
引用
收藏
页码:1235 / 1250
页数:16
相关论文
共 91 条
[1]   Systemic antiangiogenic activity of cationic poly-L-lysine dendrimer delays tumor growth [J].
Al-Jamal, Khuloud T. ;
Al-Jamal, Wafa' T. ;
Akerman, Simon ;
Podesta, Jennifer E. ;
Yilmazer, Acelya ;
Turton, John A. ;
Bianco, Alberto ;
Vargesson, Neil ;
Kanthou, Chryso ;
Florence, Alexander T. ;
Tozer, Gillian M. ;
Kostarelos, Kostas .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (09) :3966-3971
[2]  
Al-Ostoot Fares Hezam, 2021, Cancer Treat Res Commun, V28, P100422, DOI [10.1016/j.ctarc.2021.100422, 10.1016/j.ctarc.2021.100422]
[3]   Curcumin-entrapped MUC-1 aptamer targeted dendrimer-gold hybrid nanostructure as a theranostic system for colon adenocarcinoma [J].
Alibolandi, Mona ;
Hoseini, Fazileh ;
Mohammadi, Marzieh ;
Ramezani, Pouria ;
Einafshar, Elham ;
Taghdisi, Seyed Mohammad ;
Ramezani, Mohammad ;
Abnous, Khalil .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2018, 549 (1-2) :67-75
[4]   VEGF in Signaling and Disease: Beyond Discovery and Development [J].
Apte, Rajendra S. ;
Chen, Daniel S. ;
Ferrara, Napoleone .
CELL, 2019, 176 (06) :1248-1264
[5]   Evaluation of the efficiency of modified PAMAM dendrimer with low molecular weight protamine peptide to deliver IL-12 plasmid into stem cells as cancer therapy vehicles [J].
Azimifar, Mohammad Amin ;
Salmasi, Zahra ;
Doosti, Abbas ;
Babaei, Nahid ;
Hashemi, Maryam .
BIOTECHNOLOGY PROGRESS, 2021, 37 (04)
[6]   Vascular endothelial growth factor selectively targets boronated dendrimers to tumor vasculature [J].
Backer, MV ;
Gaynutdinov, TI ;
Patel, V ;
Bandyopadhyaya, AK ;
Thirumamagal, BTS ;
Tjarks, W ;
Barth, RF ;
Claffey, K ;
Backer, JM .
MOLECULAR CANCER THERAPEUTICS, 2005, 4 (09) :1423-1429
[7]   Nanoparticle and targeted systems for cancer therapy [J].
Brannon-Peppas, L ;
Blanchette, JO .
ADVANCED DRUG DELIVERY REVIEWS, 2004, 56 (11) :1649-1659
[8]   Highly Efficient and Safe Delivery of VEGF siRNA by Bioreducible Fluorinated Peptide Dendrimers for Cancer Therapy [J].
Cai, Xiaojun ;
Zhu, Haofang ;
Zhang, Yanmei ;
Gu, Zhongwei .
ACS APPLIED MATERIALS & INTERFACES, 2017, 9 (11) :9402-9415
[9]   MicroRNA-503 and the Extended MicroRNA-16 Family in Angiogenesis [J].
Caporali, Andrea ;
Emanueli, Costanza .
TRENDS IN CARDIOVASCULAR MEDICINE, 2011, 21 (06) :162-166
[10]   Co-delivery of p53 and MDM2 inhibitor RG7388 using a hydroxyl terminal PAMAM dendrimer derivative for synergistic cancer therapy [J].
Chen, Kang ;
Xin, Xiu ;
Qiu, Lipeng ;
Li, Wenpan ;
Guan, Guannan ;
Li, Gang ;
Qiao, Mingxi ;
Zhao, Xiuli ;
Hu, Haiyang ;
Chen, Dawei .
ACTA BIOMATERIALIA, 2019, 100 :118-131