Evidence map›Paper›PMID 29890852›Full record

ArticleDrug delivery2018

Selective delivery of PLXDC1 small interfering RNA to endothelial cells for anti-angiogenesis tumor therapy using CD44-targeted chitosan nanoparticles for epithelial ovarian cancer.

Ga Hee Kim, Ji Eun Won, Yeongseon Byeon, Min Gi Kim, Tae In Wi, Jae Myeong Lee, Yun-Yong Park, Jeong-Won Lee, Tae Heung Kang, In Duk Jung and 6 more

Open access · goldAbstract read
In one paragraph

Article in Drug delivery, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

34 citing papers in PubMed, 73 citations in OpenAlex.

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  11. TME-Related Biomimetic Strategies Against Cancer.International journal of nanomedicine · 2024
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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

16 authors at 5 institutions in 2 countries.

Ga Hee Kima Department of Immunology School of Medicine , Konkuk University , Chungju , South Korea.
Ji Eun Wona Department of Immunology School of Medicine , Konkuk University , Chungju , South Korea.
Yeongseon Byeona Department of Immunology School of Medicine , Konkuk University , Chungju , South Korea.
Min Gi Kima Department of Immunology School of Medicine , Konkuk University , Chungju , South Korea.
Tae In Wia Department of Immunology School of Medicine , Konkuk University , Chungju , South Korea.
Jae Myeong Leea Department of Immunology School of Medicine , Konkuk University , Chungju , South Korea.
Yun-Yong Parkb Asan Institute for Life Sciences, Asan Medical Center , University of Ulsan College of Medicine , Seoul , Republic of Korea.
Jeong-Won Leed Department of Obstetrics and Gynecology , Samsung Medical Center , Sungkyunkwan University School of Medicine , Seoul , Republic of Korea.
Tae Heung Kanga Department of Immunology School of Medicine , Konkuk University , Chungju , South Korea.ORCID http://orcid.org/0000-0002-9853-913X
In Duk Junga Department of Immunology School of Medicine , Konkuk University , Chungju , South Korea.
Byung Cheol Shine Bio & Drug Discovery Division, Korea Research Institute of Chemical Technology , Daejeon , Republic of Korea.
Hyung Jun Ahnf Center for Theragnosis, Biomedical Research Institute, Korea Institute of Science and Technology , Seoul, Republic of Korea.
Young Joo Leeg Department of Bioscience and Biotechnology , Sejong University , Kwang-Jin-Gu , Seoul , Republic of Korea.
Anil K Soodh Department of Gynecologic Oncology and Reproductive Medicine , The University of Texas MD Anderson Cancer Center , Houston , TX , USA.
Hee Dong Hana Department of Immunology School of Medicine , Konkuk University , Chungju , South Korea.ORCID http://orcid.org/0000-0002-3300-5575
Yeong-Min Parka Department of Immunology School of Medicine , Konkuk University , Chungju , South Korea.
Konkuk University · KRUlsan College · KRThe University of Texas MD Anderson Cancer Center · USKorea Research Institute of Chemical Technology · KRSejong University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Angiogenesis plays an essential role in the growth and metastasis of tumor cells, and the modulation of angiogenesis can be an effective approach for cancer therapy. We focused on silencing the angiogenic gene PLXDC1 as an important factor for anti-angiogenesis tumor therapy. Herein, we developed PLXDC1 small interfering siRNA (siRNA)-incorporated chitosan nanoparticle (CH-NP/siRNA) coated with hyaluronic acid (HA) to target the CD44 receptor on tumor endothelial cells. This study aimed to improve targeted delivery and enhance therapeutic efficacy for tumor anti-angiogenesis. The HA-CH-NP/siRNA was 200 ± 10 nm in size with a zeta potential of 26.4 mV. The loading efficiency of siRNA to the HA-CH-NP/siRNA was up to 60%. The selective binding of HA-CH-NP/siRNA to CD44-positive tumor endothelial cells increased by 2.1-fold compared with that of the CD44 nontargeted CH-NP/siRNA. PLXDC1 silencing by the HA-CH-NP/siRNA significantly inhibited tumor growth in A2780 tumor-bearing mice compared with that in the control group (p < .01), and mRNA expression of PLXDC1 was significantly reduced in the HA-CH-NP/siRNA-treated group. Furthermore, treatment with HA-CH-NP/siRNA resulted in significant inhibition of cell proliferation (p < .001), reduced microvessel density (p < .001), and increased cell apoptosis (p < .001). This study demonstrates that HA-CH-NP/siRNA is a highly selective delivery platform for siRNA, and has broad potential to be used in anti-angiogenesis tumor therapy.

Indexed as

Angiogenesis InhibitorsAnimalsAntineoplastic AgentsApoptosisCarcinoma, Ovarian EpithelialCell LineCell Line, TumorCell ProliferationChitosanDrug Delivery SystemsEndothelial CellsFemaleGene SilencingHumansHuman Umbilical Vein Endothelial CellsHyaluronan ReceptorsAngiogenesis InhibitorsAntineoplastic AgentsCD44 protein, humanChitosanHyaluronan ReceptorsHyaluronic AcidNeoplasm ProteinsPLXDC1 protein, humanReceptors, Cell SurfaceRNA, MessengerRNA, Small Interferingangiogenesis tumor therapyChitosan nanoparticlesepithelial ovarian cancerPLXDC1 siRNAtargeted delivery

Identifiers

PMID29890852
PMCPMC6096458
OpenAlexW2807764057

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.