Evidence map›Paper›PMID 42212167›Full record

ArticleFrontiers in bioengineering and biotechnology2026

Cell surface engineering via self-assembly DNA networks for cell behavior control.

Tianshu Chen, Xuexue Liu, Xiaochen Tang, Ji Ma, Siwei Mao, Miao Ding, Ni Zhen, Qizhi Diao, Qiuhui Pan

Abstract read
In one paragraph

Article in Frontiers in bioengineering and biotechnology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Tianshu Chen *Department of Clinical Laboratory, Hainan Branch, Shanghai Children's Medical Center, School of Medicine, Shanghai Jiao Tong University, Sanya, China.
Xuexue Liu *School of Pharmacy, Faculty of Medicine, Macau University of Science and Technology, Macau, China.
Xiaochen TangClinical Laboratory, Shanghai Children's Medical Center, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
Ji MaClinical Laboratory, Shanghai Children's Medical Center, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
Siwei MaoClinical Laboratory, Shanghai Children's Medical Center, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
Miao DingClinical Laboratory, Shanghai Children's Medical Center, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
Ni ZhenClinical Laboratory, Shanghai Children's Medical Center, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
Qizhi DiaoDepartment of Clinical Laboratory, Hainan Branch, Shanghai Children's Medical Center, School of Medicine, Shanghai Jiao Tong University, Sanya, China.
Qiuhui PanDepartment of Clinical Laboratory, Hainan Branch, Shanghai Children's Medical Center, School of Medicine, Shanghai Jiao Tong University, Sanya, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Synthesis of the extracellular matrix provides a novel opportunity to cell behavior control. However, exploration of the application of nucleic acid materials for cell surface engineering to achieve physical regulation of migration remains relatively limited. In this study, a self-assembled DNA network anchored to the cell membrane was constructed as a synthetic matrix mimic, which has been shown to inhibit cancer cell migration and invasion through physical confinement. The DNA network forms a dense and uniform engineering on the surface of tumor cells through a process of self-assembly. This study found that coating with RCA1/2 network led to a significant reduction in wound healing rate of approximately 49.19% and invasion rate of approximately 44.49%. The study also indicates that the potential mechanism for inhibiting cell migration and invasion is that coating of the DNA network on the membrane significantly limits membrane fluidity and promotes integrin retention on the membrane, thus interfering with its dynamic circulation. The spatial confinement in this study provides a novel DNA-based platform for controlling cell behavior as well as opening up a new paradigm for anti-migratory and anti-invasive strategies.

Indexed as

cell migration and invasioncell surface engineeringDNA networksextracellular matrix mimicintegrin

Identifiers

PMID42212167
PMCPMC13212446

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.