Evidence map›Paper›PMID 35266253›Full record

ArticleCancer science2022

Novel antiangiogenic therapy targeting biglycan using tumor endothelial cell-specific liposomal siRNA delivery system.

Nako Maishi, Yu Sakurai, Hiroto Hatakeyama, Yui Umeyama, Takashi Nakamura, Rikito Endo, Mohammad Towfik Alam, Cong Li, Dorcas Akuba-Muhyia Annan, Hiroshi Kikuchi and 7 more

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

15 citing papers in PubMed, 26 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

17 authors at 4 institutions in 1 country.

Nako MaishiVascular Biology and Molecular Pathology, Hokkaido University Graduate School of Dental Medicine, Sapporo, Japan.
Yu SakuraiFaculty of Pharmaceutical Sciences, Hokkaido University, Sapporo, Japan.
Hiroto HatakeyamaFaculty of Pharmaceutical Sciences, Hokkaido University, Sapporo, Japan.ORCID https://orcid.org/0000-0003-3899-0508
Yui UmeyamaVascular Biology and Molecular Pathology, Hokkaido University Graduate School of Dental Medicine, Sapporo, Japan.
Takashi NakamuraFaculty of Pharmaceutical Sciences, Hokkaido University, Sapporo, Japan.ORCID https://orcid.org/0000-0001-9019-1426
Rikito EndoFaculty of Pharmaceutical Sciences, Hokkaido University, Sapporo, Japan.
Mohammad Towfik AlamVascular Biology and Molecular Pathology, Hokkaido University Graduate School of Dental Medicine, Sapporo, Japan.
Cong LiVascular Biology and Molecular Pathology, Hokkaido University Graduate School of Dental Medicine, Sapporo, Japan.
Dorcas Akuba-Muhyia AnnanVascular Biology and Molecular Pathology, Hokkaido University Graduate School of Dental Medicine, Sapporo, Japan.
Hiroshi KikuchiVascular Biology, Frontier Research Unit, Institute for Genetic Medicine, Hokkaido University, Sapporo, Japan.ORCID https://orcid.org/0000-0003-4999-8994
Hirofumi MorimotoVascular Biology, Frontier Research Unit, Institute for Genetic Medicine, Hokkaido University, Sapporo, Japan.
Masahiro MorimotoVascular Biology and Molecular Pathology, Hokkaido University Graduate School of Dental Medicine, Sapporo, Japan.
Kosuke AkiyamaDepartment of Vascular Biology, Hokkaido University Graduate School of Dental Medicine, Sapporo, Japan.
Noritaka OhgaDepartment of Vascular Biology, Hokkaido University Graduate School of Dental Medicine, Sapporo, Japan.
Yasuhiro HidaDepartment of Cardiovascular and Thoracic Surgery, Faculty of Medicine, Hokkaido University, Sapporo, Japan.ORCID https://orcid.org/0000-0003-1759-4215
Hideyoshi HarashimaFaculty of Pharmaceutical Sciences, Hokkaido University, Sapporo, Japan.
Kyoko HidaVascular Biology and Molecular Pathology, Hokkaido University Graduate School of Dental Medicine, Sapporo, Japan.ORCID https://orcid.org/0000-0002-7968-6062
Hokkaido University · JPChiba University · JPHokkaido University of Science · JPTohoku University · JP

Funding

Japan Agency for Medical Research and Development JP18ck0106198h0003Japan Agency for Medical Research and Development JP20ck0106406h0003JSPS Grants-in-Aid for Scientific Research 19K18549JSPS Grants-in-Aid for Scientific Research 21H03019JSPS Grants-in-Aid for Scientific Research 21H04840JSPS Grants-in-Aid for Scientific Research 21K10107
6 · The paper itself

Abstract

Tumor blood vessels play important roles in tumor progression and metastasis. Targeting tumor endothelial cells (TECs) is one of the strategies for cancer therapy. We previously reported that biglycan, a small leucine-rich proteoglycan, is highly expressed in TECs. TECs utilize biglycan in an autocrine manner for migration and angiogenesis. Furthermore, TEC-derived biglycan stimulates tumor cell migration in a paracrine manner leading to tumor cell intravasation and metastasis. In this study, we explored the therapeutic effect of biglycan inhibition in the TECs of renal cell carcinoma using an in vivo siRNA delivery system known as a multifunctional envelope-type nanodevice (MEND), which contains a unique pH-sensitive cationic lipid. To specifically deliver MEND into TECs, we incorporated cyclo(Arg-Gly-Asp-D-Phe-Lys) (cRGD) into MEND because α

Indexed as

Carcinoma, Renal CellKidney NeoplasmsAngiogenesis InhibitorsAnimalsBiglycanEndothelial CellsHumansLiposomesMiceRNA, Small InterferingAngiogenesis InhibitorsBiglycanLiposomesRNA, Small Interferingbiglycandrug delivery systemtumor angiogenesistumor endothelial celltumor microenvironment

Identifiers

PMID35266253
PMCPMC9128192
OpenAlexW4220916872

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.