Evidence map›Paper›PMID 31092884›Full record

ArticleCell death and differentiation2019

Translation of yes-associated protein (YAP) was antagonized by its circular RNA via suppressing the assembly of the translation initiation machinery.

Nan Wu, Zhidong Yuan, Kevin Y Du, Ling Fang, Juanjuan Lyu, Chao Zhang, Alina He, Esra Eshaghi, Kaixuan Zeng, Jian Ma and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Cell death and differentiation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 114 papers.

0numbers the graph read from it
0cells of the map it votes in
114citing papers in PubMed
7.5field-weighted citation impact, top 2% 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

114 citing papers in PubMed, 146 citations in OpenAlex.

  1. Review
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  4. Role of non-coding RNAs in OOncology letters · 2026
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54 more citing papers are in PubMed but not listed here.

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

12 authors at 4 institutions in 2 countries.

Nan WuSunnybrook Research Institute, S-Wing Research Building, 2075 Bayview Ave, Toronto, M4N 3M5, Canada.
Zhidong YuanSunnybrook Research Institute, S-Wing Research Building, 2075 Bayview Ave, Toronto, M4N 3M5, Canada.
Kevin Y DuSunnybrook Research Institute, S-Wing Research Building, 2075 Bayview Ave, Toronto, M4N 3M5, Canada.
Ling FangSunnybrook Research Institute, S-Wing Research Building, 2075 Bayview Ave, Toronto, M4N 3M5, Canada.
Juanjuan LyuSunnybrook Research Institute, S-Wing Research Building, 2075 Bayview Ave, Toronto, M4N 3M5, Canada.
Chao ZhangSunnybrook Research Institute, S-Wing Research Building, 2075 Bayview Ave, Toronto, M4N 3M5, Canada.
Alina HeSunnybrook Research Institute, S-Wing Research Building, 2075 Bayview Ave, Toronto, M4N 3M5, Canada.
Esra EshaghiSunnybrook Research Institute, S-Wing Research Building, 2075 Bayview Ave, Toronto, M4N 3M5, Canada.
Kaixuan ZengSunnybrook Research Institute, S-Wing Research Building, 2075 Bayview Ave, Toronto, M4N 3M5, Canada.
Jian MaSunnybrook Research Institute, S-Wing Research Building, 2075 Bayview Ave, Toronto, M4N 3M5, Canada.
William W DuSunnybrook Research Institute, S-Wing Research Building, 2075 Bayview Ave, Toronto, M4N 3M5, Canada.
Burton B YangSunnybrook Research Institute, S-Wing Research Building, 2075 Bayview Ave, Toronto, M4N 3M5, Canada. byang@sri.utoronto.ca.
Sunnybrook Research InstituteUniversity of Toronto · CAJilin University · CNSunnybrook Health Science Centre · CA

Funding

CIHR
6 · The paper itself

Abstract

Yap is the key component of Hippo pathway which plays crucial roles in tumorigenesis. Inhibition of Yap activity could promote apoptosis, suppress proliferation, and restrain metastasis of cancer cells. However, how Yap is regulated is not fully understood. Here, we reported Yap being negatively regulated by its circular RNA (circYap) through the suppression of the assembly of Yap translation initiation machinery. Overexpression of circYap in cancer cells significantly decreased Yap protein but did not affect its mRNA levels. As a consequence, it remarkably suppressed proliferation, migration and colony formation of the cells. We found that circYap could bind with Yap mRNA and the translation initiation associated proteins, eIF4G and PABP. The complex containing overexpressed circYap abolished the interaction of PABP on the poly(A) tail with eIF4G on the 5'-cap of the Yap mRNA, which functionally led to the suppression of Yap translation initiation. Individually blocking the binding sites of circYap on Yap mRNA or respectively mutating the binding sites for PABP and eIF4G derepressed Yap translation. Significantly, breast cancer tissue from patients in the study manifested dysregulation of circYap expression. Collectively, our study uncovered a novel molecular mechanism in the regulation of Yap and implicated a new function of circular RNA, supporting the pursuit of circYap as a potential tool for future cancer intervention.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsBreast NeoplasmsCell Cycle ProteinsCell Line, TumorEukaryotic Initiation Factor-4GHep G2 CellsHumansMelanoma, ExperimentalMiceProtein BiosynthesisRNA, CircularTranscription FactorsTransfectionTranslocation, GeneticYAP-Signaling ProteinsAdaptor Proteins, Signal TransducingCell Cycle ProteinsEukaryotic Initiation Factor-4GRNA, CircularTranscription FactorsYAP1 protein, humanYap1 protein, mouseYAP-Signaling Proteins

Identifiers

PMID31092884
PMCPMC7224378
OpenAlexW2945567360

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.