Evidence map›Paper›PMID 32982236›Full record

ArticleInternational journal of nanomedicine2020

Salinomycin-Loaded Small-Molecule Nanoprodrugs Enhance Anticancer Activity in Hepatocellular Carcinoma.

Jianguo Wang, Jianyong Zhuo, Yaoye Tao, Shengjun Xu, Zun Chen, Fan Yang, Qinghong Ke, Haiyang Xie, Shusen Zheng, Hangxiang Wang and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

7 citing papers in PubMed, 16 citations in OpenAlex.

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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

11 authors at 2 institutions in 1 country.

Jianguo Wang *Department of Hepatobiliary and Pancreatic Surgery, Affiliated Hangzhou First People's Hospital, Zhejiang University School of Medicine, Hangzhou 310006, People's Republic of China.
Jianyong Zhuo *NHC Key Laboratory of Combined Multi-Organ Transplantation, Hangzhou 310003, People's Republic of China.
Yaoye TaoNHC Key Laboratory of Combined Multi-Organ Transplantation, Hangzhou 310003, People's Republic of China.
Shengjun XuNHC Key Laboratory of Combined Multi-Organ Transplantation, Hangzhou 310003, People's Republic of China.
Zun ChenNHC Key Laboratory of Combined Multi-Organ Transplantation, Hangzhou 310003, People's Republic of China.
Fan YangNHC Key Laboratory of Combined Multi-Organ Transplantation, Hangzhou 310003, People's Republic of China.
Qinghong KeNHC Key Laboratory of Combined Multi-Organ Transplantation, Hangzhou 310003, People's Republic of China.
Haiyang XieNHC Key Laboratory of Combined Multi-Organ Transplantation, Hangzhou 310003, People's Republic of China.
Shusen ZhengNHC Key Laboratory of Combined Multi-Organ Transplantation, Hangzhou 310003, People's Republic of China.
Hangxiang WangNHC Key Laboratory of Combined Multi-Organ Transplantation, Hangzhou 310003, People's Republic of China.ORCID 0000-0001-6370-9728
Xiao XuDepartment of Hepatobiliary and Pancreatic Surgery, Affiliated Hangzhou First People's Hospital, Zhejiang University School of Medicine, Hangzhou 310006, People's Republic of China.
First Affiliated Hospital Zhejiang University · CNHangzhou First People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThere is currently no effective treatment for advanced hepatocellular carcinoma (HCC), and chemotherapy has little effect on long-term survival of HCC patients, largely due to the cancer stem cell (CSC) chemoresistance of HCC.

methodsWe constructed a small-molecule nanometer-sized prodrug (nanoprodrug) loaded with salinomycin (SAL) for the treatment of HCC. SAL was encapsulated by the prodrug LA-SN38 (linoleic acid modified 7-ethyl-10-hydroxycamptothecin) to construct a self-assembled nanoprodrug further PEGylated with DSPE-PEG

resultsDelivery of the SAL- and LA-SN38-based nanoprodrugs effectively promoted apoptosis of HCC cells, exerted inhibition of HCC tumor-sphere formation as well as HCC cell motility and invasion, and reduced the proportion of CD133+ HCC-CSC cells. In nude mice, the nanoprodrug suppressed growth of tumor xenografts derived from human cell lines and patient.

conclusionOur results show that SAL-based nanoprodrugs are a promising platform for treating patients with HCC and a novel strategy for combination therapy of cancers.

Indexed as

AnimalsAntineoplastic AgentsCarcinoma, HepatocellularCell Line, TumorHumansIrinotecanLinoleic AcidLiver NeoplasmsMaleMice, Inbred BALB CMice, NudeNanoparticlesNeoplastic Stem CellsPhosphatidylethanolaminesPolyether PolyketidesPolyethylene Glycols1,2-distearoyl-sn-glycero-3-phosphoethanolamine-N-methoxy-poly(ethylene glycol 2000)Antineoplastic AgentsIrinotecanLA-SN38Linoleic AcidPhosphatidylethanolaminesPolyether PolyketidesPolyethylene GlycolsProdrugsPyranssalinomycincancer stem cellshepatocellular carcinomasalinomycinself-assemblesmall-molecule prodrugs

Identifiers

PMID32982236
PMCPMC7501963
OpenAlexW3086684690

What OpenQuestion holds

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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 OpenQuestion graph.