Literature DB >> 28669337

Synthetic Lethality: From Research to Precision Cancer Nanomedicine.

Anuradha Gupta1, Anas Ahmad1, Aqib Iqbal Dar1, Rehan Khan1.   

Abstract

Cancer is an evolutionary disease with multiple genetic alterations, accumulated due to chromosomal instability and/or aneuploidy and it sometimes acquires drug-resistant phenotype also. Whole genome sequencing and mutational analysis helped in understanding the differences among persons for predisposition of a disease and its treatment non-responsiveness. Thus, molecular targeted therapies came into existence. Among them, the concept of synthetic lethality have enthralled great attention as it is a pragmatic approach towards exploiting cancer cell specific mutations to specifically kill cancer cells without affecting normal cells and thus enhancing anti-cancer drug therapeutic index. Thus, this approach helped in discovering new therapeutic molecules for development of precision medicine. Nanotechnology helped in delivering these molecules to the target site in an effective concentration thus reducing off target effects of drugs, dose and dosage frequency drugs. Researchers have tried to deliver siRNA targeting synthetic lethal partner for target cancer cell killing by incorporating it in nanoparticles and it has shown efficacy by preventing tumor progression. This review summarizes the brief introduction of synthetic lethality, and synthetic lethal gene interactions, with a major focus on its therapeutic anticancer potential with the application of nanotechnology for development of personalized medicine. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.org.

Entities:  

Keywords:  Synthetic lethality; drug-resistant phenotype; efficacy; nanotechnology; precision nanomedicine; targeted drug delivery.

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Year:  2018        PMID: 28669337     DOI: 10.2174/1568009617666170630141931

Source DB:  PubMed          Journal:  Curr Cancer Drug Targets        ISSN: 1568-0096            Impact factor:   3.428


  2 in total

1.  The double edge of anti-CD40 siRNA therapy: It increases renal microcapillar density but favours the generation of an inflammatory milieu in the kidneys of ApoE -/- mice.

Authors:  Miguel Hueso; Angela Casas; Adrian Mallén; Laura de Ramón; Nuria Bolaños; Cristian Varela; Josep M Cruzado; Joan Torras; Estanislao Navarro
Journal:  J Inflamm (Lond)       Date:  2019-12-16       Impact factor: 4.981

Review 2.  Thymoquinone (2-Isoprpyl-5-methyl-1, 4-benzoquinone) as a chemopreventive/anticancer agent: Chemistry and biological effects.

Authors:  Anas Ahmad; Rakesh Kumar Mishra; Akshay Vyawahare; Ajay Kumar; Muneeb U Rehman; Wajhul Qamar; Abdul Quaiyoom Khan; Rehan Khan
Journal:  Saudi Pharm J       Date:  2019-09-25       Impact factor: 4.330

  2 in total

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