Evidence map›Paper›PMID 38735920›Full record

ArticleJournal of nanobiotechnology2024

MSC microvesicles loaded G-quadruplex-enhanced circular single-stranded DNA-9 inhibits tumor growth by targeting MDSCs.

Jingxia Han, Rong Qin, Shaoting Zheng, Xiaohui Hou, Xiaorui Wang, Huihui An, Zhongwei Li, Yinan Li, Heng Zhang, Denghui Zhai and 3 more

Erratum issuedAbstract read
In one paragraph

Article in Journal of nanobiotechnology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Jingxia Han *State Key Laboratory of Medicinal Chemical Biology and College of Pharmacy, Nankai University, Tianjin, China.
Rong Qin *State Key Laboratory of Medicinal Chemical Biology and College of Pharmacy, Nankai University, Tianjin, China.
Shaoting ZhengState Key Laboratory of Medicinal Chemical Biology and College of Pharmacy, Nankai University, Tianjin, China.
Xiaohui HouState Key Laboratory of Medicinal Chemical Biology and College of Pharmacy, Nankai University, Tianjin, China.
Xiaorui WangPrecision Medicine Center, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Huihui AnState Key Laboratory of Medicinal Chemical Biology and College of Pharmacy, Nankai University, Tianjin, China.
Zhongwei LiState Key Laboratory of Medicinal Chemical Biology and College of Pharmacy, Nankai University, Tianjin, China.
Yinan LiState Key Laboratory of Medicinal Chemical Biology and College of Pharmacy, Nankai University, Tianjin, China.
Heng ZhangState Key Laboratory of Medicinal Chemical Biology and College of Pharmacy, Nankai University, Tianjin, China.
Denghui ZhaiCollege of Life Sciences, Nankai University, Tianjin, China.
Huijuan LiuState Key Laboratory of Medicinal Chemical Biology and College of Pharmacy, Nankai University, Tianjin, China. huijuan.liu@nankai.edu.cn.
Jing MengState Key Laboratory of Food Nutrition and Safety, Tianjin University of Science and Technology, Tianjin, China. jing.meng@tust.edu.cn.
Tao SunState Key Laboratory of Medicinal Chemical Biology and College of Pharmacy, Nankai University, Tianjin, China. tao.sun@nankai.edu.cn.

Funding

China Postdoctoral Science Foundation 2022M712374 and 2021M701778Fundamental Research Funds for the Central Universities 63233164the National Natural Science Foundation of China 82073205, 82272934, 82273237, 82072709 and 81902441the Natural Science Foundation of Tianjin 21JCZDJC00930
6 · The paper itself

Abstract

backgroundMyeloid-derived suppressor cells (MDSCs) promote tumor growth, metastasis, and lead to immunotherapy resistance. Studies revealed that miRNAs are also expressed in MDSCs and promote the immunosuppressive function of MDSCs. Currently, few studies have been reported on inducible cellular microvesicle delivery of nucleic acid drugs targeting miRNA in MDSCs for the treatment of malignant tumors. RESULTS AND

conclusionIn this study, we designed an artificial DNA named G-quadruplex-enhanced circular single-stranded DNA-9 (G4-CSSD9), that specifically adsorbs the miR-9 sequence. Its advanced DNA folding structure, rich in tandem repeat guanine (G-quadruplex), also provides good stability. Mesenchymal stem cells (MSCs) were prepared into nanostructured vesicles by membrane extrusion. The MSC microvesicles-encapsulated G4-CSSD9 (MVs@G4-CSSD9) was delivered into MDSCs, which affected the downstream transcription and translation process, and reduced the immunosuppressive function of MDSCs, so as to achieve the purpose of treating melanoma. In particular, it provides an idea for the malignant tumor treatment.

Indexed as

DNA, Single-StrandedG-QuadruplexesMesenchymal Stem CellsMicroRNAsMyeloid-Derived Suppressor CellsAnimalsCell-Derived MicroparticlesCell Line, TumorDNA, CircularHumansMelanomaMiceMice, Inbred C57BLDNA, CircularDNA, Single-StrandedMicroRNAsG-quadruplex-enhanced circular single-stranded DNA-9MelanomamiR-9Myeloid-derived suppressor cellsUmbilical cord mesenchymal stem cells

Identifiers

PMID38735920
PMCPMC11089713

What OpenQuestion holds

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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.