Evidence map›Paper›PMID 27145285›Full record

ArticleOncotarget2016

Effective elimination of liver cancer stem-like cells by CD90 antibody targeted thermosensitive magnetoliposomes.

Rui Yang, Li Y An, Qin F Miao, Feng M Li, Yong Han, Hui X Wang, Dang P Liu, Rong Chen, Sha Q Tang

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.0field-weighted citation impact, top 10% 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

19 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
  2. Review
  3. CD90-targeted lentiviral vectors for HSC gene therapy.Molecular therapy : the journal of the American Society of Gene Therapy · 2023
    Article
  4. Review
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  13. Use of magnetic fields and nanoparticles to trigger drug release and improve tumor targeting.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2019
    Review
  14. Article
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  16. Article
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  18. Article
  19. State of the Art of Stimuli-Responsive Liposomes for Cancer Therapy.Iranian journal of pharmaceutical research : IJPR · 2017
    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

9 authors at 2 institutions in 1 country.

Rui YangSchool of Medicine, Southeast University, Nanjing, People's Republic of China.
Li Y AnJiangsu Key Laboratory of Molecular and Fuctional Imaging, Department of Radiology, Zhongda Hospital, Nanjing, People's Republic of China.
Qin F MiaoSchool of Medicine, Southeast University, Nanjing, People's Republic of China.
Feng M LiSchool of Medicine, Southeast University, Nanjing, People's Republic of China.
Yong HanSchool of Medicine, Southeast University, Nanjing, People's Republic of China.
Hui X WangSchool of Medicine, Southeast University, Nanjing, People's Republic of China.
Dang P LiuSchool of Medicine, Southeast University, Nanjing, People's Republic of China.
Rong ChenDepartment of Oncology, Zhongda Hospital, Nanjing, People's Republic of China.
Sha Q TangSchool of Medicine, Southeast University, Nanjing, People's Republic of China.
Southeast University · CNZhongda Hospital Southeast University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo investigate the use of thermosensitive magnetoliposomes (TMs) loaded with magnetic iron oxide (Fe3O4) and the anti-cancer stem cell marker CD90 (CD90@TMs) to target and kill CD90+ liver cancer stem cells (LCSCs).

methodsThe hepatocellular carcinoma cell line Huh7 was used to separate CD90+ LCSCs by magnetic-activated cell sorting. CD90@TMs was characterized and their ability to target CD90+ LCSCs was determined. Experiments were used to investigate whether CD90@TMs combined with magnetic hyperthermia could effectively eliminate CD90+ LCSCs.

resultsThe present study demonstrated that CD90+ LCSCs with stem cells properties were successfully isolated. We also successfully prepared CD90@TMs that was almost spherical and uniform with an average diameter of 130±4.6 nm and determined that magnetic iron oxide could be incorporated and retained a superparamagnetic response. CD90@TMs showed good targeting and increased inhibition of CD90+ LCSCs in vitro and in vivo compared to TMs.

conclusionsCD90@TMs can be used for controlled and targeted delivery of anticancer drugs, which may offer a promising alternative for HCC therapy.

Indexed as

AnimalsAntibodiesApoptosisCarcinoma, HepatocellularCell LineCell Line, TumorCell ProliferationHumansImmunomagnetic SeparationLiver NeoplasmsMice, Inbred NODMice, SCIDNeoplastic Stem CellsTemperatureThy-1 AntigensXenograft Model Antitumor AssaysAntibodiesThy-1 AntigensCD90hyperthermia therapyLCSCstargeting therapyTMs

Identifiers

PMID27145285
PMCPMC5094971
OpenAlexW2344392507

What OpenQuestion 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 OpenQuestion graph.