Evidence map›Paper›PMID 31912318›Full record

ArticleAAPS PharmSciTech2020

Liposome-Encapsulated Zoledronate Favors Tumor Vascular Normalization and Enhances Anticancer Efficacy of Cisplatin.

Xin-Jun Cai, Wei-Dong Fei, Ying-Ying Xu, Hong Xu, Gao-Yi Yang, Jia-Wei Cao, Jian-Jun Ni, Kaiyi Tao, Zeng Wang

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In one paragraph

Article in AAPS PharmSciTech, 2020. 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
–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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
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  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

9 authors.

Xin-Jun Cai *Department of Pharmacy, Zhejiang Integrated Traditional and Western Medicine Hospital, Hangzhou, 310003, Zhejiang, People's Republic of China.
Wei-Dong Fei *Department of Pharmacy, Women's Hospital, Zhejiang University School of Medicine, Hangzhou, 310006, Zhejiang, China.
Ying-Ying XuDepartment of Pharmacy, Zhejiang Integrated Traditional and Western Medicine Hospital, Hangzhou, 310003, Zhejiang, People's Republic of China.
Hong XuDepartment of Gastroenterology and Hepatology, Zhejiang Integrated Traditional and Western Medicine Hospital, Hangzhou, 310003, Zhejiang, People's Republic of China.
Gao-Yi YangDepartment of Ultrasound, Zhejiang Integrated Traditional and Western Medicine Hospital, Hangzhou, 310003, Zhejiang, People's Republic of China.
Jia-Wei CaoDepartment of Pharmacy, Zhejiang Integrated Traditional and Western Medicine Hospital, Hangzhou, 310003, Zhejiang, People's Republic of China.
Jian-Jun NiDepartment of Pharmacy, Zhejiang Integrated Traditional and Western Medicine Hospital, Hangzhou, 310003, Zhejiang, People's Republic of China.
Kaiyi TaoDepartment of Thoracic Surgery, Institute of Cancer Research and Basic Medical Sciences of Chinese Academy of Sciences, Cancer Hospital of the University of Chinese Academy of Sciences, Zhejiang Cancer Hospital, Hangzhou, 310022, Zhejiang, People's Republic of China. taoky@zjcc.org.cn.
Zeng WangDepartment of Pharmacy, Institute of Cancer Research and Basic Medical Sciences of Chinese Academy of Sciences, Cancer Hospital of the University of Chinese Academy of Sciences, Zhejiang Cancer Hospital, Hangzhou, 310022, Zhejiang, People's Republic of China. wangzeng@zjcc.org.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study was to examine the effectiveness of alanine-proline-arginine-proline-glycine (APRPG) peptide-conjugated PEGylated cationic liposomes-encapsulated zoledronic acid (ZOL) (APRPG-PEG-ZOL-CLPs) in achieving vascular normalization. Cisplatin (diamminedichloroplatinum, DDP) was used to improve anticancer efficacy. The present study showed that APRPG-PEG-ZOL-CLPs increased anticancer efficacy, which was regarded as vascular normalization. Our results demonstrated that the viability, migration, and tube formation of human umbilical vein endothelial cells (HUVECs) were evidently repressed by APRPG-PEG-ZOL-CLPs. Moreover, APRPG-PEG-ZOL-CLPs could decrease vessel density, as well as hypoxia-inducible factor 1α (HIF-1α), and increase thrombospondin 1 (TSP-1) expression of tumors. Therefore, the anticancer efficacy of APRPG-PEG-ZOL-CLPs combined with DDP was superior to that of PEG-ZOL-CLP or ZOL treatment combined with DDP schemes, as demonstrated by the obviously evident reduction in tumor volume. These results indicated that APRPG-PEG-ZOL-CLPs were most effective in normalizing tumor vasculature to elevate the therapeutic effect of antitumor drugs.

Indexed as

AnimalsAntineoplastic AgentsCells, CulturedCisplatinEndothelial CellsFemaleHumansLiposomesMiceMice, Inbred BALB CNeoplasms, ExperimentalOligopeptidesPolyethylene GlycolsZoledronic Acidalanyl-prolyl-arginyl-prolyl-glycineAntineoplastic AgentsCisplatinLiposomesOligopeptidesPolyethylene GlycolsZoledronic Acidanticancer efficacycisplatinliposomesvascular normalizationzoledronic acid

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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.