Evidence map›Paper›PMID 40588818›Full record

ReviewAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2025

Advancements in DNA-Driven Precision Modulation of Cell Surface Receptor for Programmable Cellular Functions.

Hexin Nan, Ming Cai, Yiyu Wang, Hong-Hui Wang, Zhou Nie

Abstract readReview
In one paragraph

Review in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Hexin NanState Key Laboratory of Chemo and Biosensing, College of Chemistry and Chemical Engineering, College of Biology, Hunan Provincial Key Laboratory of Biomacromolecular Chemical Biology, Hunan University, Changsha, 410082, P. R. China.ORCID https://orcid.org/0009-0002-2943-6943
Ming CaiState Key Laboratory of Chemo and Biosensing, College of Chemistry and Chemical Engineering, College of Biology, Hunan Provincial Key Laboratory of Biomacromolecular Chemical Biology, Hunan University, Changsha, 410082, P. R. China.
Yiyu WangState Key Laboratory of Chemo and Biosensing, College of Chemistry and Chemical Engineering, College of Biology, Hunan Provincial Key Laboratory of Biomacromolecular Chemical Biology, Hunan University, Changsha, 410082, P. R. China.
Hong-Hui WangState Key Laboratory of Chemo and Biosensing, College of Chemistry and Chemical Engineering, College of Biology, Hunan Provincial Key Laboratory of Biomacromolecular Chemical Biology, Hunan University, Changsha, 410082, P. R. China.ORCID https://orcid.org/0000-0002-4420-9733
Zhou NieState Key Laboratory of Chemo and Biosensing, College of Chemistry and Chemical Engineering, College of Biology, Hunan Provincial Key Laboratory of Biomacromolecular Chemical Biology, Hunan University, Changsha, 410082, P. R. China.ORCID https://orcid.org/0000-0001-9864-2965

Funding

Hunan Provincial Natural Science Foundation of China 2023ZJ1120National Key R&D Program of China 2024YFA0916700National Natural Science Foundation of China 22034002National Natural Science Foundation of China 22177030National Natural Science Foundation of China 92253304
6 · The paper itself

Abstract

Precise modulation of receptor-mediated signaling is essential for understanding cellular communication and developing targeted therapeutics. Receptor engineering strategies focus on enhancing specificity, manipulating allosteric effects, and controlling receptor clustering. This review comprehensively summarizes recent advances in DNA-based strategies as versatile platforms for receptor engineering, encompassing both genetic and non-genetic approaches. Genetic approaches leverage DNA's protein-coding capability to reprogram receptor function through techniques like domain fusion and site-directed mutagenesis. Complementarily, non-genetic strategies exploit the structural and functional properties of DNA to achieve multidimensional control over receptor functionalities. Specifically, functional nucleic acids (FNAs) confer novel and customizable molecular recognition responsiveness, while DNA nanostructures, such as DNA origami, provide nanoscale spatial precision for regulating receptor valency and oligomerization. Furthermore, programmable dynamic DNA reactions facilitate the development of nanodevices responsive to diverse stimuli, including proteins, small molecules, ions, light, and mechanical forces. Notably, emerging DNA-based logic circuits and nanorobots offer programmable and autonomous control over receptor signaling. Looking forward, integrating genetic and non-genetic DNA engineering strategies holds significant promise at the interface of synthetic biology and DNA nanotechnology, driving the development of next-generation intelligent cellular systems for precise medicine.

Indexed as

DNAReceptors, Cell SurfaceAnimalsHumansNanostructuresNanotechnologySignal TransductionDNAReceptors, Cell Surfacecellular functionsDNA nanotechnologydynamic DNA reactionsfunctional nucleic acidssynthetic biology

Identifiers

PMID40588818
PMCPMC12407375

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.