Aptamers as an approach to targeted cancer therapy

被引:0
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作者
Fatemeh Mahmoudian
Azin Ahmari
Shiva Shabani
Bahman Sadeghi
Shohreh Fahimirad
Fahimeh Fattahi
机构
[1] Semnan University of Medical Sciences,Cancer Research Center
[2] Arak University of Medical Sciences,Clinical Research Development Unit of Ayatollah
[3] Arak University of Medical Sciences,Khansari Hospital
[4] Arak University of Medical Sciences,Department of Radiation Oncology, School of Medicine
[5] Arak University of Medical Sciences,Department of Infectious Diseases, School of Medicine
[6] Arak University of Medical Sciences,Department of Community Medicine, School of Medicine
[7] Oncopathology Research Center,Molecular and Medicine Research Center
[8] Iran University of Medical Sciences,undefined
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关键词
Aptamer; SELEX; Cancer; Targeted therapy;
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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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