Evidence map›Paper›PMID 25846734›Full record

ArticleTumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine2015

miR-335 inhibits the proliferation and invasion of clear cell renal cell carcinoma cells through direct suppression of BCL-W.

Kefeng Wang, Xiaonan Chen, Yunhong Zhan, Weiguo Jiang, Xuefeng Liu, Xia Wang, Bin Wu

Abstract read
PubMed Publisher
In one paragraph

Article in Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

32 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
  2. Article
  3. Non-Coding RNAs in Breast Cancer: Diagnostic and Therapeutic Implications.International journal of molecular sciences · 2024
    Review
  4. Article
  5. Article
  6. Article
  7. Functions and Targets of miR-335 in Cancer.OncoTargets and therapy · 2021
    Review
  8. Article
  9. Observational
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. MicroRNA replacement therapy in cancer.Journal of cellular physiology · 2019
    Review
  18. Article
  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

7 authors at 2 institutions in 1 country.

Kefeng WangDepartment of Urology, Sheng Jing Hospital of China Medical University, Shenyang, 110004, Liaoning, People's Republic of China.
Xiaonan ChenDepartment of Urology, Sheng Jing Hospital of China Medical University, Shenyang, 110004, Liaoning, People's Republic of China.
Yunhong ZhanDepartment of Urology, Sheng Jing Hospital of China Medical University, Shenyang, 110004, Liaoning, People's Republic of China.
Weiguo JiangDepartment of Pathology, Sheng Jing Hospital of China Medical University, Shenyang, 110004, Liaoning, People's Republic of China.
Xuefeng LiuDepartment of Urology, Sheng Jing Hospital of China Medical University, Shenyang, 110004, Liaoning, People's Republic of China.
Xia WangDepartment of Urology, Sheng Jing Hospital of China Medical University, Shenyang, 110004, Liaoning, People's Republic of China.
Bin WuDepartment of Urology, Sheng Jing Hospital of China Medical University, Shenyang, 110004, Liaoning, People's Republic of China. wubin1959@163.com.
Sheng Jing Hospital · CNChina Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Increasing evidence has demonstrated that small non-coding microRNAs (miRNAs) play important roles in cancer development and progression. Recent studies have shown that microRNA-335 (miR-335) functions as an oncogene or a tumor suppressor in various human cancer types, but its role in clear cell renal cell carcinoma (ccRCC) remains poorly understood. In our study, we firstly found that the expression level of miR-335 was significantly downregulated in ccRCC tissues versus corresponding non-tumor tissues and the low expression of miR-335 was significantly associated with lymph node metastasis, larger tumor size, and poor T stage. Then, we found that overexpression of miR-335 significantly suppressed the proliferation and invasion of 786-O and CaKi-1 ccRCC cell lines. We subsequently found that miR-335 could interact with the 3'-untranslated regions (3'UTR) of B-cell CLL/lymphoma 2 like 2 (BCL-W or BCL2L2) messenger RNA (mRNA) and repress its expression. In addition, re-expression of BCL-W (without the 3'UTR) could partially abrogate the miR-335-induced 786-O and CaKi-1 ccRCC cell proliferation and invasion inhibition. Furthermore, we found that expression patterns of miR-335 were inversely correlated with those of BCL-W mRNA in ccRCC tissues. Taken together, these results indicate that miR-335 acts as a novel tumor suppressor to regulate ccRCC cell proliferation and invasion through downregulation of BCL-W expression.

Indexed as

AdultAgedApoptosis Regulatory ProteinsCarcinoma, Renal CellCell Line, TumorCell ProliferationFemaleGene Expression Regulation, NeoplasticHumansMaleMicroRNAsMiddle AgedNeoplasm InvasivenessApoptosis Regulatory ProteinsBCL2L2 protein, humanMicroRNAsMIRN335 microRNA, humanBCL-WClear cell renal cell carcinomamiR-335

Identifiers

PMID25846734
OpenAlexW2011192510

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.