Evidence map›Paper›PMID 34516672›Full record

ArticleThe Prostate2021

PSMA-positive membranes secreted from prostate cancer cells have potency to transform vascular endothelial cells into an angiogenic state.

Ryuta Watanabe, Masashi Maekawa, Takeshi Kiyoi, Mie Kurata, Noriyoshi Miura, Tadahiko Kikugawa, Shigeki Higashiyama, Takashi Saika

Open access · hybridAbstract read
In one paragraph

Article in The Prostate, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

17 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
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  7. PSMA-targeted combination brusatol and docetaxel nanotherapeutics for the treatment of prostate cancer.Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 2024
    Article
  8. Article
  9. Membrane-derived particles shed by PSMA-positive cells function as pro-angiogenic stimuli in tumors.Journal of controlled release : official journal of the Controlled Release Society · 2023
    Article
  10. Review
  11. Article
  12. Review
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  14. The clinical application ofTranslational oncology · 2023
    Article
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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

8 authors at 2 institutions in 1 country.

Ryuta WatanabeDepartment of Urology, Ehime University Graduate School of Medicine, Matsuyama, Ehime, Japan.ORCID 0000-0001-6656-4261
Masashi MaekawaDepartment of Biochemistry and Molecular Genetics, Ehime University Graduate School of Medicine, Matsuyama, Ehime, Japan.ORCID 0000-0002-9574-1906
Takeshi KiyoiDivision of Analytical Bio-medicine, Advanced Research Support Center, Ehime University, Ehime, Japan.
Mie KurataDepartment of Pathology, Ehime University Graduate School of Medicine and Proteo-Science Center, Ehime, Japan.
Noriyoshi MiuraDepartment of Urology, Ehime University Graduate School of Medicine, Matsuyama, Ehime, Japan.
Tadahiko KikugawaDepartment of Urology, Ehime University Graduate School of Medicine, Matsuyama, Ehime, Japan.
Shigeki HigashiyamaDepartment of Biochemistry and Molecular Genetics, Ehime University Graduate School of Medicine, Matsuyama, Ehime, Japan.
Takashi SaikaDepartment of Urology, Ehime University Graduate School of Medicine, Matsuyama, Ehime, Japan.
Ehime University · JPOsaka International Cancer Institute · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundProstate-specific membrane antigen (PSMA) is highly expressed in poorly differentiated, metastatic, and castration-resistant prostate cancers. Recently, 68Ga-PSMA positron emission tomography/computed tomography has been successfully developed as an effective diagnostic tool for prostate cancer. However, the pathophysiological functions of PSMA in prostate tumors remain unclear.

methodsWe examined the protein expression of PSMA in tumor endothelial cells in human prostate tumors by immunohistochemistry. Prostate cancer tissues were resected by robotic surgery in 2019 at Ehime University from patients with prostate cancer. In vitro, we prepared conditioned medium (CM) derived from a PSMA-positive human prostate cancer cell line, LNCaP, cultured on collagen I gels. We then examined PSMA expression in human umbilical vascular endothelial cells (HUVECs) cultured with the CM. We assessed angiogenic activities by treatment of HUVECs with LNCaP-derived CM using a tube formation assay that mimics angiogenesis.

resultsImmunohistochemistry of PSMA and CD31, a marker of endothelial cells, and PSMA-expressing tumor endothelial cells were observed in 4 of 33 prostate cancer patients (12.1%). We also found that the 10,000g pellet fraction of the LNCaP-derived CM containing PSMA-positive membranes, such as microvesicles transformed HUVECs "PSMA-negative" into "PSMA-positive." Furthermore, treatment of HUVECs with the 10,000g pellet fraction of the LNCaP-derived CM significantly promoted tube formation, mimicking angiogenesis in a PSMA-dependent manner.

conclusionsOur findings revealed the existence of PSMA-positive tumor endothelial cells in human prostate tumors, which enhances tumor angiogenesis in prostate cancer tissues.

Indexed as

AgedAntigens, SurfaceCell Transformation, NeoplasticCulture Media, ConditionedEndothelial CellsGene Expression ProfilingGlutamate Carboxypeptidase IIHumansHuman Umbilical Vein Endothelial CellsImmunohistochemistryMaleNeoplasm GradingNeovascularization, PathologicProstateProstatic Neoplasms, Castration-ResistantTumor Cells, CulturedAntigens, SurfaceCulture Media, ConditionedFOLH1 protein, humanGlutamate Carboxypeptidase IIhuman umbilical vascular endothelial cells (HUVECs)LNCaPprostate cancer specimenprostate-specific membrane antigen (PSMA)tube formationtumor endothelial cells

Identifiers

PMID34516672
PMCPMC9292811
OpenAlexW3200187442

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.