Evidence map›Paper›PMID 34584409›Full record

ArticleInternational journal of nanomedicine2021

Synthesis and Characterization of Salinomycin-Loaded High-Density Lipoprotein and Its Effects on Cervical Cancer Cells and Cervical Cancer Stem Cells.

Xirui Yin, Yuhui Lu, Miao Zou, Liuli Wang, Xuan Zhou, Yingyu Zhang, Manman Su

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.4field-weighted citation impact, top 37% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Review
  3. Advanced drug delivery platforms target cancer stem cells.Asian journal of pharmaceutical sciences · 2025
    Review
  4. Review
  5. Article
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

7 authors at 1 institution in 1 country.

Xirui YinDepartment of Regenerative Medicine, School of Pharmaceutical Sciences, Jilin University, Changchun, People's Republic of China.
Yuhui LuDepartment of Regenerative Medicine, School of Pharmaceutical Sciences, Jilin University, Changchun, People's Republic of China.
Miao ZouDepartment of Regenerative Medicine, School of Pharmaceutical Sciences, Jilin University, Changchun, People's Republic of China.
Liuli WangDepartment of Regenerative Medicine, School of Pharmaceutical Sciences, Jilin University, Changchun, People's Republic of China.
Xuan ZhouDepartment of Regenerative Medicine, School of Pharmaceutical Sciences, Jilin University, Changchun, People's Republic of China.
Yingyu ZhangDepartment of Medical Science, Chang Chun Medical College, Changchun, People's Republic of China.
Manman SuDepartment of Regenerative Medicine, School of Pharmaceutical Sciences, Jilin University, Changchun, People's Republic of China.
Jilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCervical cancer stem cells (CCSCs), a small part of tumor population, are one of the important reasons for metastasis and recurrence of cervical cancer. Targeting CCSCs may be an effective way to eliminate tumors. Salinomycin (Sal) has been proved to be an effective anticancer drug in many studies, especially for cancer stem cells (CSCs). However, the cytotoxicity of salinomycin limits its further research as an anticancer drug. High-density lipoprotein (HDL) nanoparticles are an excellent drug carrier, which can reduce the toxicity of Sal, have a certain targeting effect and improve the clinical benefit of Sal.

methodsSalinomycin-loaded high-density lipoprotein (S-HDL) was synthesized and characterized by various analytical techniques. CD44

resultsS-HDL had a particle size of 38.98 ± 1.78 nm and an encapsulation efficiency of 50.73 ± 4.29%. Cell uptake analysis showed that HDL nanoparticles could enhance the drug uptake of CCCs and CCSCs and may target CCCs and CCSCs. In cell viability analysis, CCCs and CCSCs showed high sensitivity to S-HDL. S-HDL can more efficiently prevent CCSCs from developing tumorspheres than Sal in tumorsphere formation study. S-HDL had stronger ability to induce cell cycle arrest, promote cell apoptosis and inhibit cell migration compared with free Sal, which was consistent with the results of Genome Wide analysis.

conclusionS-HDL can effectively target and eliminate CCCs and CCSCs, which is a potential drug for the treatment of cervical cancer.

Indexed as

Uterine Cervical NeoplasmsCell Line, TumorFemaleHeLa CellsHumansLipoproteins, HDLNeoplastic Stem CellsPolyether PolyketidesPyransLipoproteins, HDLPolyether PolyketidesPyranssalinomycincellular uptakecervical cancer stem cellsHDLLPR1salinomycin

Identifiers

PMID34584409
PMCPMC8459968
OpenAlexW3199947521

What Socratic holds

Textmetadata
LicenceCC BY-NC
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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.