Evidence map›Paper›PMID 37240308›Full record

ArticleInternational journal of molecular sciences2023

Spatial Gene Expression Analysis Reveals Characteristic Gene Expression Patterns of De Novo Neuroendocrine Prostate Cancer Coexisting with Androgen Receptor Pathway Prostate Cancer.

Ryuta Watanabe, Noriyoshi Miura, Mie Kurata, Riko Kitazawa, Tadahiko Kikugawa, Takashi Saika

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
10.6field-weighted citation impact, top 1% 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

39 citing papers in PubMed, 41 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

6 authors at 3 institutions in 2 countries.

Ryuta WatanabeDepartment of Urology, Ehime University Hospital, Ehime 791-0204, Japan.ORCID 0000-0001-6656-4261
Noriyoshi MiuraDepartment of Urology, Ehime University Hospital, Ehime 791-0204, Japan.ORCID 0000-0002-2229-0948
Mie KurataDepartment of Analytical Pathology, Ehime University Graduate School of Medicine, Ehime 791-0295, Japan.
Riko KitazawaDivision of Diagnostic Pathology, Ehime University Hospital, Ehime 791-0204, Japan.
Tadahiko KikugawaDepartment of Urology, Ehime University Hospital, Ehime 791-0204, Japan.ORCID 0000-0002-8992-4167
Takashi SaikaDepartment of Urology, Ehime University Hospital, Ehime 791-0204, Japan.
Ehime University Hospital · JPEhime University · JPFred Hutch Cancer Center · US

Funding

Japan Society for the Promotion of Science 22K09449Japan Society for the Promotion of Science 22KK0135Kowa Life Science Foundation noneLife Science Foundation of Japan noneSGH Foundation noneThe Japanese Foundation for Prostate Research none
6 · The paper itself

Abstract

Neuroendocrine prostate carcinoma (NEPC) accounts for less than 1% of prostate neoplasms and has extremely poorer prognosis than the typical androgen receptor pathway-positive adenocarcinoma of the prostate (ARPC). However, very few cases in which de novo NEPC and APRC are diagnosed simultaneously in the same tissue have been reported. We report herein a 78-year-old man of de novo metastatic NEPC coexisting with ARPC treated at Ehime University Hospital. Visium CytAssist Spatial Gene Expression analysis (10× genetics) was performed using formalin-fixed, paraffin-embedded (FFPE) samples. The neuroendocrine signatures were upregulated in NEPC sites, and androgen receptor signatures were upregulated in ARPC sites. TP53, RB1, or PTEN and upregulation of the homologous recombination repair genes at NEPC sites were not downregulated. Urothelial carcinoma markers were not elevated. Meanwhile, Rbfox3 and SFRTM2 levels were downregulated while the levels of the fibrosis markers HGF, HMOX1, ELN, and GREM1 were upregulated in the tumor microenvironment of NEPC. In conclusion, the findings of spatial gene expression analysis in a patient with coexisting ARPC and de novo NEPC are reported. The accumulation of cases and basic data will help with the development of novel treatments for NEPC and improve the prognosis of patients with castration-resistant prostate cancer.

Indexed as

Carcinoma, NeuroendocrineCarcinoma, Transitional CellProstatic NeoplasmsUrinary Bladder NeoplasmsAgedGene ExpressionGene Expression ProfilingHumansMaleReceptors, AndrogenTumor MicroenvironmentReceptors, AndrogenAR pathway prostate cancerCytAssist Visiumde novo NEPCgene expressionsimultaneous occurrencespatial transcriptomicstreatment-induced neuroendocrine prostate cancer

Identifiers

PMID37240308
PMCPMC10219300
OpenAlexW4377108212

What OpenQuestion holds

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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.