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Project Information

Category: Other Related Development Researches
Subcategory: Health and Nutrition

DNA Nanostructures As Promising Anticancer Agents: A Review

Conducted by PIT , Started on 2024 - Completed on 2025
Completed Total Page Views : 13 Total Likes : 4 Like

Cancer remains a major global health burden; consequently, the development of more effective and less
toxic treatment options is paramount. DNA nanostructures are a promising platform for cancer therapy
harnessing the unique properties of DNA. They represent an ideal platform for therapeutics, in part
because they are programmable, biocompatible, and possess unique molecular architectures. Structures
such as DNA origami, tetrahedra, polyhedra, and dendrimers can serve as versatile carriers for
chemotherapeutic agents, gene-silencing molecules (such as siRNA and ASOs), photosensitizers, and
immunomodulatory compounds. DNA nanostructures can also enhance traditional chemotherapy and new
strategies, such as gene therapy, phototherapy (PDT/PTT), and immunotherapy, by delivering genetic
material, photosensitizers (PDT or PTT), or immune-response activators (e.g., CpG motifs) directly to the
disease site. Preclinically, DNA nanostructures have demonstrated improved drug bioavailability, significant
tumor regression, and induction of a strong immune response with fewer off-target effects or toxicities
than conventional therapies. This narrative review summarizes the recent advances in DNA nanostructures
as anticancer agents.

Proponents
Murtaza Jafari, Shaiyar Shahryar, Sohameh Mohebbi, Amirhossein Ahmadi, Rahmatullah Nazari, Ahmad Reshad
Haidari, Don Eliseo-Lucero Prisno-III , Brian Gil S. Sarinas, Rose A. Arceno, Shuaibu Saidu Musa,
Mohamed Mustaf Ahmed
Beneficiaries
Cancer Patients, Medical Researchers and Scientists
Fund Source
Internal
No. of Patents
0
No. of Utility Models
0
How to Cite
https://doi.org/10.1016/j.ctarc.2025.101029
Remarks

Agency Details

Palompon Institute of Technology
Evangelista Street, Palompon, Leyte 6538
Phone: (053) 555-9841
Email: [email protected]
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