Evidence map›Paper›PMID 36915886›Full record

ArticleTranslational andrology and urology2023

Exosomal miR-93-5p as an important driver of bladder cancer progression.

Feng Yuan, Xiao-Yu Yin, Yu Huang, Xiao-Wei Cai, Lu Jin, Guang-Cheng Dai, Ya-Cheng Zang, Yi Sun, Xiao-Long Liu, Bo-Xin Xue

Open access · diamondAbstract read
In one paragraph

Article in Translational andrology and urology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Bladder cancer: non-coding RNAs and exosomal non-coding RNAs.Functional & integrative genomics · 2024
    Review
  9. Article
  10. Article
  11. Article
  12. 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

10 authors at 2 institutions in 1 country.

Feng Yuan *Department of Urology, The Second Affiliated Hospital of Soochow University, Suzhou, China.
Xiao-Yu Yin *School of Biology and Basic Medical Sciences, Medical College of Soochow University, Suzhou, China.
Yu HuangSchool of Biology and Basic Medical Sciences, Medical College of Soochow University, Suzhou, China.
Xiao-Wei CaiDepartment of Urology, The Second Affiliated Hospital of Soochow University, Suzhou, China.
Lu JinDepartment of Urology, The Second Affiliated Hospital of Soochow University, Suzhou, China.
Guang-Cheng DaiDepartment of Urology, The Second Affiliated Hospital of Soochow University, Suzhou, China.
Ya-Cheng ZangDepartment of Urology, The Second Affiliated Hospital of Soochow University, Suzhou, China.
Yi SunSchool of Biology and Basic Medical Sciences, Medical College of Soochow University, Suzhou, China.
Xiao-Long LiuDepartment of Urology, The Second Affiliated Hospital of Soochow University, Suzhou, China.
Bo-Xin XueDepartment of Urology, The Second Affiliated Hospital of Soochow University, Suzhou, China.
Soochow University · CNSecond Affiliated Hospital of Soochow University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Tumor-derived exosomes are involved in the process of tumor metastasis and angiogenesis. MicroRNAs (miRNAs) are the most widely investigated factors in exosomes. Therefore, we hope to find a new therapeutic target in bladder cancer (BLCA), which has high incidence rate and mortality. Methods: Exosomal microRNA(miR)-93-5p expression level, downstream target molecules, and biological functions were examined with bioinformatics technology. Exosomes were extracted by sequential differential centrifugation and verified by transmission electron microscopy. The exosomal miR-93-5p on cell proliferation, invasion, and angiogenesis abilities in 5637 and T24 cells was determined by Cell Counting Kit 8 (CCK-8), colony-forming assay, Transwell assay, and vascular ring formation assay. A mouse xenograft model with intratumor injection was adopted to evaluate the correlation between BLCA-derived exosomes and tumor growth Results: The results revealed that exosomes play an important role in the biological progression of BLCA, with miR-93-5p being a particularly important molecule. Compared to normal cells, more malignant cells release more exosomal miR-93-5p, and tumor-derived exosomal miR-93-5p could significantly promote cell proliferation, invasion, and angiogenesis Conclusions: Our study successfully revealed the biological role and mechanism of BLCA-derived exosomes in tumor progression. Target at tumor exosomes and exosomal miR-93-5p may be an effective treatment in BLCA.

Indexed as

angiogenesisbladder cancerExosomesmiR-93-5ptumor microenvironment

Identifiers

PMID36915886
PMCPMC10006004
OpenAlexW4321792213

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.