Aptamers as an approach to targeted cancer therapy

被引:24
作者
Mahmoudian, Fatemeh [1 ,2 ]
Ahmari, Azin [2 ,3 ]
Shabani, Shiva [2 ,4 ]
Sadeghi, Bahman [2 ,5 ]
Fahimirad, Shohreh [6 ]
Fattahi, Fahimeh [2 ,7 ]
机构
[1] Semnan Univ Med Sci, Canc Res Ctr, Semnan, Iran
[2] Arak Univ Med Sci, Ayatollah Khansari Hosp, Clin Res Dev Unit, Arak, Iran
[3] Arak Univ Med Sci, Sch Med, Dept Radiat Oncol, Arak, Iran
[4] Arak Univ Med Sci, Sch Med, Dept Infect Dis, Arak, Iran
[5] Arak Univ Med Sci, Sch Med, Dept Community Med, Arak, Iran
[6] Arak Univ Med Sci, Mol & Med Res Ctr, Arak, Iran
[7] Iran Univ Med Sci, Oncopathol Res Ctr, Tehran, Iran
关键词
Aptamer; SELEX; Cancer; Targeted therapy; NUCLEIC-ACID APTAMERS; G-QUADRUPLEX APTAMER; CHITOSAN NANOPARTICLES; DRUG-DELIVERY; COLON-CANCER; NEXT-GENERATION; RNA APTAMERS; TUMOR-GROWTH; DNA APTAMER; T-CELLS;
D O I
10.1186/s12935-024-03295-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Conventional cancer treatments can cause serious side effects because they are not specific to cancer cells and can damage healthy cells. Aptamers often are single-stranded oligonucleotides arranged in a unique architecture, allowing them to bind specifically to target sites. This feature makes them an ideal choice for targeted therapeutics. They are typically produced through the systematic evolution of ligands by exponential enrichment (SELEX) and undergo extensive pharmacological revision to modify their affinity, specificity, and therapeutic half-life. Aptamers can act as drugs themselves, directly inhibiting tumor cells. Alternatively, they can be used in targeted drug delivery systems to transport drugs directly to tumor cells, minimizing toxicity to healthy cells. In this review, we will discuss the latest and most advanced approaches to using aptamers for cancer treatment, particularly targeted therapy overcoming resistance to conventional therapies.
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页数:22
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