Evidence map›Paper›PMID 38230289›Full record

ArticleACS pharmacology & translational science2024

Cell Membrane-Anchored DNA Nanoinhibitor for Inhibition of Receptor Tyrosine Kinase Signaling Pathways via Steric Hindrance and Lysosome-Induced Protein Degradation.

Jinlu Tang, Cuihua Qi, Xue Bai, Mengmeng Ji, Zhaoting Wang, Yanchao Luo, Shanshan Ni, Tianlu Zhang, Kangdong Liu, Baoyin Yuan

Open access · greenAbstract read
In one paragraph

Article in ACS pharmacology & translational science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.2field-weighted citation impact, top 20% of its field
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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Supramolecular Degraders: An Emerging Paradigm in Targeted Protein Degradation.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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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

10 authors at 1 institution in 1 country.

Jinlu TangSchool of Basic Medical Sciences, Zhengzhou University, Zhengzhou 450001, Henan, China.ORCID https://orcid.org/0000-0001-9666-8758
Cuihua QiSchool of Basic Medical Sciences, Zhengzhou University, Zhengzhou 450001, Henan, China.
Xue BaiSchool of Basic Medical Sciences, Zhengzhou University, Zhengzhou 450001, Henan, China.
Mengmeng JiSchool of Basic Medical Sciences, Zhengzhou University, Zhengzhou 450001, Henan, China.
Zhaoting WangSchool of Basic Medical Sciences, Zhengzhou University, Zhengzhou 450001, Henan, China.
Yanchao LuoSchool of Basic Medical Sciences, Zhengzhou University, Zhengzhou 450001, Henan, China.
Shanshan NiSchool of Basic Medical Sciences, Zhengzhou University, Zhengzhou 450001, Henan, China.
Tianlu ZhangSchool of Basic Medical Sciences, Zhengzhou University, Zhengzhou 450001, Henan, China.
Kangdong LiuSchool of Basic Medical Sciences, Zhengzhou University, Zhengzhou 450001, Henan, China.
Baoyin YuanSchool of Basic Medical Sciences, Zhengzhou University, Zhengzhou 450001, Henan, China.ORCID https://orcid.org/0000-0003-4782-1271
Zhengzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Receptor tyrosine kinase (RTK) plays a crucial role in cancer progression, and it has been identified as a key drug target for cancer targeted therapy. Although traditional RTK-targeting drugs are effective, there are some limitations that potentially hinder the further development of RTK-targeting drugs. Therefore, it is urgently needed to develop novel, simple, and general RTK-targeting inhibitors with a new mechanism of action for cancer targeted therapy. Here, a cell membrane-anchored RTK-targeting DNA nanoinhibitor is developed to inhibit RTK function. By using a DNA tetrahedron as a framework, RTK-specific aptamers as the recognition elements, and cholesterol as anchoring molecules, this DNA nanoinhibitor could rapidly anchor on the cell membrane and specifically bind to RTK. Compared with traditional RTK-targeting inhibitors, this DNA nanoinhibitor does not need to bind at a limited domain on RTK, which increases the possibilities of developing RTK inhibitors. With the cellular-mesenchymal to epithelial transition factor (c-Met) as a target RTK, the DNA nanoinhibitor can not only induce steric hindrance effects to inhibit c-Met activation but also reduce the c-Met level via lysosome-mediated protein degradation and thus inhibition of c-Met signaling pathways and related cell behaviors. Moreover, the DNA nanoinhibitor is feasible for other RTKs by just replacing aptamers. This work may provide a novel, simple, and general RTK-targeting nanoinhibitor and possess great value in RTK-targeted cancer therapy.

Identifiers

PMID38230289
PMCPMC10789140
OpenAlexW4389613776

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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.