Evidence map›Paper›PMID 31006167›Full record

ArticleCancer science2019

MicroRNA-204-5p: A novel candidate urinary biomarker of Xp11.2 translocation renal cell carcinoma.

Ryoma Kurahashi, Tsuyoshi Kadomatsu, Masaya Baba, Chiaki Hara, Hitoshi Itoh, Keishi Miyata, Motoyoshi Endo, Jun Morinaga, Kazutoyo Terada, Kimi Araki and 5 more

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

50 citing papers in PubMed, 72 citations in OpenAlex.

  1. Article
  2. Review
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  4. Review
  5. Current issues in molecular biology · 2024
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  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Exosomes in the Diagnosis and Treatment of Renal Cell Cancer.International journal of molecular sciences · 2023
    Review
  13. Review
  14. Extracellular Vesicle MicroRNA in the Kidney.Comprehensive Physiology · 2023
    Article
  15. Article
  16. Review
  17. Biomarkers in renal cell carcinoma and their targeted therapies: a review.Exploration of targeted anti-tumor therapy · 2023
    Review
  18. Review
  19. Article
  20. Review
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

15 authors at 5 institutions in 2 countries.

Ryoma KurahashiDepartment of Molecular Genetics, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
Tsuyoshi KadomatsuDepartment of Molecular Genetics, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.ORCID https://orcid.org/0000-0003-3327-6954
Masaya BabaInternational Research Center for Medical Sciences (IRCMS), Kumamoto University, Kumamoto, Japan.
Chiaki HaraDepartment of Molecular Genetics, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
Hitoshi ItohDepartment of Orthopaedic Surgery, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
Keishi MiyataDepartment of Molecular Genetics, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
Motoyoshi EndoDepartment of Molecular Biology, University of Occupational and Environmental Health, Kitakyushu, Japan.
Jun MorinagaDepartment of Molecular Genetics, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
Kazutoyo TeradaDepartment of Molecular Genetics, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
Kimi ArakiCenter for Metabolic Regulation of Healthy Aging (CMHA), Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
Masatoshi EtoDepartment of Urology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Laura S SchmidtBasic Science Program, Frederick National Laboratory for Cancer Research sponsored by the National Cancer Institute, Frederick, MD, USA.
Tomomi KambaDepartment of Urology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
W Marston LinehanUrologic Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Yuichi OikeDepartment of Molecular Genetics, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
Kumamoto Health Science University · JPKumamoto University · JPNational Institutes of Health · USKyushu University · JPUniversity of Occupational and Environmental Health Japan · JP

Funding

Molecular Therapeutics of Kidney Cancer: VHL Gene and Fumarate Hydratase GeneZIABC011038 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI LINEHAN, WILLIAM MARSTON · 2009 to 2025
$29.8M
CCR NIH HHSCCR NIH HHS HHSN261200800001CCore Research for Evolutional Science and Technology (CREST) program of the Japan Science and Technology Agency (JST) 13417915CREST program of the Japan Agency for Medical Research and Development (AMED) JP18gm0610007Ministry of Education, Culture, Sports, Science and Technology (MEXT) of Japan 17K08663Ministry of Education, Culture, Sports, Science and Technology (MEXT) of Japan 18K07236NCI NIH HHSNCI NIH HHS HHSN261200800001ETakeda Science Foundationthe Center for Metabolic Regulation of Healthy Aging (CMHA)The Shin-Nihon Foundation of Advanced Medical Research
6 · The paper itself

Abstract

Xp11.2 translocation renal cell carcinoma (Xp11 tRCC) is a rare sporadic pediatric kidney cancer caused by constitutively active TFE3 fusion proteins. Tumors in patients with Xp11 tRCC tend to recur and undergo frequent metastasis, in part due to lack of methods available to detect early-stage disease. Here we generated transgenic (Tg) mice overexpressing the human PRCC-TFE3 fusion gene in renal tubular epithelial cells, as an Xp11 tRCC mouse model. At 20 weeks of age, mice showed no histological abnormalities in kidney but by 40 weeks showed Xp11 tRCC development and related morphological and histological changes. MicroRNA (miR)-204-5p levels in urinary exosomes of 40-week-old Tg mice showing tRCC were significantly elevated compared with levels in control mice. MicroRNA-204-5p expression also significantly increased in primary renal cell carcinoma cell lines established both from Tg mouse tumors and from tumor tissue from 2 Xp11 tRCC patients. All of these lines secreted miR-204-5p-containing exosomes. Notably, we also observed increased miR-204-5p levels in urinary exosomes in 20-week-old renal PRCC-TFE3 Tg mice prior to tRCC development, and those levels were equivalent to those in 40-week-old Tg mice, suggesting that miR-204-5p increases follow expression of constitutively active TFE3 fusion proteins in renal tubular epithelial cells prior to overt tRCC development. Finally, we confirmed that miR-204-5p expression significantly increases in noncancerous human kidney cells after overexpression of a PRCC-TFE3 fusion gene. These findings suggest that miR-204-5p in urinary exosomes could be a useful biomarker for early diagnosis of patients with Xp11 tRCC.

Indexed as

Translocation, GeneticAnimalsBasic Helix-Loop-Helix Leucine Zipper Transcription FactorsBiomarkers, TumorCarcinoma, Renal CellCell Cycle ProteinsChromosomes, Human, XExosomesHumansKidneyKidney NeoplasmsMice, Inbred C57BLMice, TransgenicMicroRNAsNeoplasm ProteinsOncogene Proteins, FusionBasic Helix-Loop-Helix Leucine Zipper Transcription FactorsBiomarkers, TumorCell Cycle ProteinsMicroRNAsMIRN204 microRNA, humanNeoplasm ProteinsOncogene Proteins, FusionPRCC protein, humanTFE3 protein, humanbiomarkerexosomemiRNAurineXp11 tRCC

Identifiers

PMID31006167
PMCPMC6549932
OpenAlexW2939270370

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Registered trials

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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.