Evidence map›Paper›PMID 27508026›Full record

ArticleAmerican journal of translational research2016

MiR-122 targets VEGFC in bladder cancer to inhibit tumor growth and angiogenesis.

Yi Wang, Qing-Fei Xing, Xiao-Qiang Liu, Zhan-Jun Guo, Chang-Ying Li, Guang Sun

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2016. 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
4.3field-weighted citation impact, top 5% 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, 76 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Role of miRNA‑122 in cancer (Review).International journal of oncology · 2024
    Review
  5. Review
  6. Review
  7. Review
  8. Article
  9. The Impact of miR-122 on Cancer.Current pharmaceutical biotechnology · 2024
    Review
  10. Article
  11. Review
  12. An Overview of Angiogenesis in Bladder Cancer.Current oncology reports · 2023
    Review
  13. Article
  14. Review
  15. Review
  16. Review
  17. Article
  18. Article
  19. Review
  20. Article
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 1 institution in 1 country.

Yi WangDepartment of Urology, The Second Hospital of Tianjin Medical University, Tianjin Institute of Urology No. 23, Pingjiang Road, Hexi District, Tianjin 300211, China.
Qing-Fei XingDepartment of Urology, The Second Hospital of Tianjin Medical University, Tianjin Institute of Urology No. 23, Pingjiang Road, Hexi District, Tianjin 300211, China.
Xiao-Qiang LiuDepartment of Urology, The Second Hospital of Tianjin Medical University, Tianjin Institute of Urology No. 23, Pingjiang Road, Hexi District, Tianjin 300211, China.
Zhan-Jun GuoDepartment of Urology, The Second Hospital of Tianjin Medical University, Tianjin Institute of Urology No. 23, Pingjiang Road, Hexi District, Tianjin 300211, China.
Chang-Ying LiDepartment of Urology, The Second Hospital of Tianjin Medical University, Tianjin Institute of Urology No. 23, Pingjiang Road, Hexi District, Tianjin 300211, China.
Guang SunDepartment of Urology, The Second Hospital of Tianjin Medical University, Tianjin Institute of Urology No. 23, Pingjiang Road, Hexi District, Tianjin 300211, China.
Second Hospital of Tianjin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Previous studies indicate that microRNA-122 (miR-122) is down-regulated in several cancer cells and regulates cell apoptosis, proliferation, metastasis, and tumor angiogenesis. However, the mount of miR-122 in bladder cancer and the pivotal molecular mechanisms of miR-122 used to regulate bladder carcinogenesis and angiogenesis remain to be clarified. Here, we reveal that miR-122 expression is down-regulated in human bladder cancer tissues and cell lines. MiR-122 represses vascular endothelial growth factor C (VEGFC) post-transcriptional expression by directly binding to its 3'-UTR. The protein kinase B (AKT) and mammalian target of rapamycin (mTOR), which are the most important downstream molecules of VEGFC, are also decreased in bladder cancer cell after miR-122 overexpression. Furthermore, miR-122 over-expression decreases bladder cancer cell migration, invasion, colony formation in vitro and slow bladder cancer growth and angiogenesis in vivo. Finally, miR-122 sensitizes bladder cancer cells to cisplatin-induced apoptosis. Taken together, these studies suggest that miR-122 serves as a tumor suppressor and down-regulating VEGFC expression, leading to the inhibition of bladder cancer growth and angiogenesis.

Indexed as

angiogenesisbladder cancerMiR-122VEGFC

Identifiers

PMID27508026
PMCPMC4969442
OpenAlexW2519628110

What OpenQuestion holds

Textmetadata
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.