Evidence map›Paper›PMID 33510354›Full record

ArticleOncogene2021

Androgen receptor promotes renal cell carcinoma (RCC) vasculogenic mimicry (VM) via altering TWIST1 nonsense-mediated decay through lncRNA-TANAR.

Bosen You, Yin Sun, Jie Luo, Keliang Wang, Qing Liu, Ruizhe Fang, Bingmei Liu, Fuju Chou, Ronghao Wang, Jialin Meng and 4 more

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in Oncogene, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
4.2field-weighted citation impact, top 4% 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

43 citing papers in PubMed, 57 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Retrospective study assessing the role of the androgen receptor in clear cell renal cell cancer patients treated with VEGFR inhibitors in monotherapy.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
    Article
  13. Review
  14. TRMT10A regulates tRNA-ArgCCT mCell death & disease · 2025
    Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 4 institutions in 3 countries.

Bosen You *Department of Urology, The 4th Affiliated Hospital of Harbin Medical University, Harbin, 150001, China.
Yin Sun *George Whipple Lab for Cancer Research, Departments of Pathology and Urology, and The Wilmot Cancer Institute, University of Rochester Medical Center, Rochester, NY, 14646, USA.
Jie Luo *George Whipple Lab for Cancer Research, Departments of Pathology and Urology, and The Wilmot Cancer Institute, University of Rochester Medical Center, Rochester, NY, 14646, USA.
Keliang Wang *Department of Urology, The 4th Affiliated Hospital of Harbin Medical University, Harbin, 150001, China.
Qing LiuDepartment of Urology, The 2nd Affiliated Hospital of Harbin Medical University, Harbin, 150001, China.
Ruizhe FangDepartment of Urology, The 4th Affiliated Hospital of Harbin Medical University, Harbin, 150001, China.
Bingmei LiuDepartment of Pathology and Cutaneous Oncology, Heilongjiang Provincial Hospital, Harbin, 150001, China.
Fuju ChouGeorge Whipple Lab for Cancer Research, Departments of Pathology and Urology, and The Wilmot Cancer Institute, University of Rochester Medical Center, Rochester, NY, 14646, USA.
Ronghao WangGeorge Whipple Lab for Cancer Research, Departments of Pathology and Urology, and The Wilmot Cancer Institute, University of Rochester Medical Center, Rochester, NY, 14646, USA.
Jialin MengGeorge Whipple Lab for Cancer Research, Departments of Pathology and Urology, and The Wilmot Cancer Institute, University of Rochester Medical Center, Rochester, NY, 14646, USA.
Chi-Ping HuangSex Hormone Research Center and Departments of Urology, China Medical University/Hospital, Taichung, 404, Taiwan.
Shuyuan YehGeorge Whipple Lab for Cancer Research, Departments of Pathology and Urology, and The Wilmot Cancer Institute, University of Rochester Medical Center, Rochester, NY, 14646, USA.ORCID http://orcid.org/0000-0002-5329-2321
Chawnshang ChangGeorge Whipple Lab for Cancer Research, Departments of Pathology and Urology, and The Wilmot Cancer Institute, University of Rochester Medical Center, Rochester, NY, 14646, USA. chang@urmc.rochester.edu.ORCID http://orcid.org/0000-0001-8510-3516
Wanhai XuDepartment of Urology, The 4th Affiliated Hospital of Harbin Medical University, Harbin, 150001, China. xuwanhai@hrbmu.edu.cn.ORCID http://orcid.org/0000-0003-3350-2464
University of Rochester Medical Center · USHarbin Medical University · CNChina Medical University · TWHeilongjiang Provincial Hospital · CN

Funding

Non-AR mediated DHT-promoted Bladder Cancer initiation and progressionR01CA155477 · NCI · UNIVERSITY OF ROCHESTER · PI CHANG, CHAWNSHANG · 2011 to 2015
$1.6M
NCI NIH HHS R01 CA155477
6 · The paper itself

Abstract

While the androgen receptor (AR) may influence the progression of clear cell renal cell carcinoma (ccRCC), its role to impact vasculogenic mimicry (VM) to alter the ccRCC progression and metastasis remains obscure. Here, we demonstrated that elevated AR expression was positively correlated with tumor-originated vasculogenesis in ccRCC patients. Consistently, in vitro research revealed AR promoted VM formation in ccRCC cell lines via modulating lncRNA-TANAR/TWIST1 signals. Mechanism dissection showed that AR could increase lncRNA-TANAR (TANAR) expression through binding to the androgen response elements (AREs) located in its promoter region. Moreover, we found that TANAR could impede nonsense-mediated mRNA decay (NMD) of TWIST1 mRNA by direct interaction with TWIST1 5'UTR. A preclinical study using in vivo mouse model with orthotopic xenografts of ccRCC cells further confirmed the in vitro data. Together, these results illustrated that AR-mediated TANAR signals might play a crucial role in ccRCC VM formation and metastasis, and targeting this newly identified AR/TANAR/TWIST1 signaling may help in the development of a novel anti-angiogenesis therapy to better suppress the ccRCC progression.

Indexed as

AnimalsCarcinoma, Renal CellCell Line, TumorCell MovementCodon, NonsenseGene Expression Regulation, NeoplasticHumansMiceNeovascularization, PathologicNonsense Mediated mRNA DecayNuclear ProteinsReceptors, AndrogenRNA, Long NoncodingSignal TransductionTwist-Related Protein 1AR protein, humanCodon, NonsenseNuclear ProteinsReceptors, AndrogenRNA, Long NoncodingTWIST1 protein, humanTwist-Related Protein 1

Identifiers

PMID33510354
PMCPMC7932923
OpenAlexW3121398019

What OpenQuestion holds

Textmetadata
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.