Evidence map›Paper›PMID 31777993›Full record

ArticleCancer science2020

RPV-modified epirubicin and dioscin co-delivery liposomes suppress non-small cell lung cancer growth by limiting nutrition supply.

Liang Kong, Fu-Yi Cai, Xue-Min Yao, Ming Jing, Min Fu, Jing-Jing Liu, Si-Yu He, Lu Zhang, Xin-Ze Liu, Rui-Jun Ju and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

11 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
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  9. In vivo gene delivery mediated by non-viral vectors for cancer therapy.Journal of controlled release : official journal of the Controlled Release Society · 2020
    Review
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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.

Liang KongSchool of Pharmacy, Liaoning University of Traditional Chinese Medicine, Dalian, China.
Fu-Yi CaiSchool of Pharmacy, Liaoning University of Traditional Chinese Medicine, Dalian, China.
Xue-Min YaoSchool of Pharmacy, Liaoning University of Traditional Chinese Medicine, Dalian, China.
Ming JingSchool of Pharmacy, Liaoning University of Traditional Chinese Medicine, Dalian, China.
Min FuSchool of Pharmacy, Liaoning University of Traditional Chinese Medicine, Dalian, China.
Jing-Jing LiuSchool of Pharmacy, Liaoning University of Traditional Chinese Medicine, Dalian, China.
Si-Yu HeSchool of Pharmacy, Liaoning University of Traditional Chinese Medicine, Dalian, China.
Lu ZhangSchool of Pharmacy, Liaoning University of Traditional Chinese Medicine, Dalian, China.
Xin-Ze LiuSchool of Pharmacy, Liaoning University of Traditional Chinese Medicine, Dalian, China.
Rui-Jun JuDepartment of Pharmaceutical Engineering, Beijing Institute of Petrochemical Technology, Beijing, China.
Xue-Tao LiSchool of Pharmacy, Liaoning University of Traditional Chinese Medicine, Dalian, China.ORCID https://orcid.org/0000-0002-0608-4669
Liaoning University of Traditional Chinese Medicine · CNBeijing Institute of Petrochemical Technology · CN

Funding

National Natural Science Foundation of China 81673603National Natural Science Foundation of China 81703453National Natural Science Foundation of China 81874347
6 · The paper itself

Abstract

Chemotherapy for non-small cell lung cancer (NSCLC) is far from satisfactory, mainly due to poor targeting of antitumor drugs and self-adaptations of the tumors. Angiogenesis, vasculogenic mimicry (VM) channels, migration, and invasion are the main ways for tumors to obtain nutrition. Herein, RPV-modified epirubicin and dioscin co-delivery liposomes were successfully prepared. These liposomes showed ideal physicochemical properties, enhanced tumor targeting and accumulation in tumor sites, and inhibited VM channel formation, tumor angiogenesis, migration and invasion. The liposomes also downregulated VM-related and angiogenesis-related proteins in vitro. Furthermore, when tested in vivo, the targeted co-delivery liposomes increased selective accumulation of drugs in tumor sites and showed extended stability in blood circulation. In conclusion, RPV-modified epirubicin and dioscin co-delivery liposomes showed strong antitumor efficacy in vivo and could thus be considered a promising strategy for NSCLC treatment.

Indexed as

A549 CellsAnimalsAntineoplastic Combined Chemotherapy ProtocolsCarcinoma, Non-Small-Cell LungCell Line, TumorCell-Penetrating PeptidesCell ProliferationCell SurvivalDiosgeninEpirubicinGene Expression Regulation, NeoplasticHumansLiposomesLung NeoplasmsMaleMiceCell-Penetrating PeptidesdioscinDiosgeninEpirubicinLiposomesangiogenesiscell-penetrating peptideco-delivery liposomenon-small cell lung cancervasculogenic mimicry

Identifiers

PMID31777993
PMCPMC7004549
OpenAlexW2989929431

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.