Evidence map›Paper›PMID 38665667›Full record

ArticleJACS Au2024

A Reconfigurable DNA Framework Nanotube-Assisted Antiangiogenic Therapy.

Wei Li, Zhongliang Wang, Qing Su, Jie Chen, Qian Wu, Xue Sun, Shuhan Zhu, Xiaodie Li, Hao Wei, Jialin Zeng and 3 more

Open access · goldAbstract read
In one paragraph

Article in JACS Au, 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 23% 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, 5 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
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

13 authors at 6 institutions in 1 country.

Wei LiDepartment of Oncology, Zhujiang Hospital, Southern Medical University, Guangzhou, Guangdong 510282, China.
Zhongliang WangDepartment of Pathology, Zhujiang Hospital, Southern Medical University, Guangzhou, Guangdong 510282, China.
Qing SuDepartment of Pharmacy, Zhujiang Hospital, Southern Medical University, Guangzhou, Guangdong 510282, China.
Jie ChenDepartment of Radiation Oncology, Cancer Hospital of Shantou University Medical College, Shantou, Guangdong 515000, China.
Qian WuDepartment of Pathology, Beijing Sixth Hospital, Beijing University, Beijing 100080, China.
Xue SunDepartment of Pathology, Zhujiang Hospital, Southern Medical University, Guangzhou, Guangdong 510282, China.
Shuhan ZhuDepartment of Pathology, Zhujiang Hospital, Southern Medical University, Guangzhou, Guangdong 510282, China.
Xiaodie LiDepartment of Oncology, Zhujiang Hospital, Southern Medical University, Guangzhou, Guangdong 510282, China.
Hao WeiDepartment of Urology, Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, Shandong 266000, China.
Jialin ZengDepartment of Oncology, Zhujiang Hospital, Southern Medical University, Guangzhou, Guangdong 510282, China.
Linlang GuoDepartment of Pathology, Zhujiang Hospital, Southern Medical University, Guangzhou, Guangdong 510282, China.
Chao ZhangDepartment of Oncology, Zhujiang Hospital, Southern Medical University, Guangzhou, Guangdong 510282, China.
Jian HeDepartment of Nuclear Medicine, Nanjing Drum Tower Hospital, The Affiliated Hospital of Nanjing University Medical School, Nanjing 210008, China.ORCID https://orcid.org/0000-0003-4580-1381
Zhujiang Hospital · CNNanjing Drum Tower Hospital · CNPeking University · CNQingdao University · CNShantou University · CNSichuan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A major limitation of tumor antiangiogenic therapy is the pronounced off-target effect, which can lead to unavoidable injury in multiple organs. Ensuring sufficient delivery and controlled release of these antiangiogenic agents at tumor sites is crucial for realizing their clinical application. Here, we develop a smart DNA-based nanodrug, termed Endo-rDFN, by precisely assembling the antiangiogenic agent, endostar (Endo), into a reconfigurable DNA framework nanotube (rDFN) that could recognize tumor-overexpressed nucleolin to achieve the targeted delivery and controllable release of Endo. Endo-rDFN can not only effectively enhance the tumor-targeting capability of Endo and maintain its efficient accumulation in tumor tissues but also achieve on-demand release of Endo at tumor sites via the specific DNA aptamer for tumor-overexpressed nucleolin, named AS1411. We also found that Endo-rDFN exhibited significant inhibition of angiogenesis and tumor growth, while also providing effective protection against multiorgan injury (heart, liver, spleen, kidney, lung, etc.) to some extent, without compromising the function of these organs. Our study demonstrates that rDFN represents a promising vector for reducing antiangiogenic therapy-induced multiorgan injury, highlighting its potential for promoting the clinical application of antiangiogenic agents.

Identifiers

PMID38665667
PMCPMC11040663
OpenAlexW4393307639

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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 OpenQuestion graph.