Exploration of tumor penetrating peptide iRGD as a potential strategy to enhance tumor penetration of cancer nanotherapeutics

被引:21
作者
Saifi, Mohd Aslam [1 ]
Sathish, Gauri [1 ]
Bazaz, Mohd Rabi [2 ]
Godugu, Chandraiah [1 ,3 ]
机构
[1] Natl Inst Pharmaceut Educ & Res NIPER, Dept Biol Sci Regulatory Toxicol, Hyderabad, Telangana, India
[2] Natl Inst Pharmaceut Educ & Res NIPER, Dept Biol Sci Pharmacol & Toxicol, Hyderabad, Telangana, India
[3] Natl Inst Pharmaceut Educ & Res NIPER, Dept Biol Sci Regulatory Toxicol, Hyderabad 500037, Telangana, India
来源
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER | 2023年 / 1878卷 / 03期
关键词
Tumor penetrating peptide; iRGD; Nanoparticles; Tumor penetration; Neuropilins; 3D MULTICELLULAR SPHEROIDS; DRUG-DELIVERY SYSTEM; ANTITUMOR-ACTIVITY; EXTRACELLULAR-MATRIX; ANTI-ANGIOGENESIS; NANOPARTICLES; DOXORUBICIN; EXPRESSION; NEUROPILIN-1; COMBINATION;
D O I
10.1016/j.bbcan.2023.188895
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cancer therapy continues to be a huge challenge as most chemotherapeutic agents exert serious adverse effects on healthy organs. Chemotherapeutic agents lack selective targeting and even the existing target specific therapies are failing due to poor distribution into the tumor microenvironment. Nanotechnology offers multiple advantages to address the limitations encountered by conventional therapy. However, the delivery of nanotherapeutics to tumor tissue has not improved over the years partly due to the poor and inadequate distribution of nanotherapeutics into deeper tumor regions resulting in resistance and relapse. To curb the penetration concerns, iRGD was explored and found to be highly effective in improving the delivery of cancer nanomedicine. The preclinical observations are highly encouraging; however, the clinical translation is at a nascent stage. Based on this, we have made an elaborative effort to give a detailed account of various promising applications of iRGD to increase anticancer and tumor imaging potential. Importantly, we have comprehensively discussed the shortcomings and uncertainties associated with the clinical translation of iRGD-based therapeutic approaches and future directions.
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页数:10
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