Evidence map›Paper›PMID 35711824›Full record

ArticleJournal of Cancer2022

ADAR1 Prevents R-loop Accumulation-Driven ATR Pathway Activation in Ovarian Cancer.

Hanwei Cui, Qian Yi, Min Tian, Hai Ting Yang, Yuteng Liang, Jie Huang, Qi Zeng, Weichao Sun, Jian Han, Jianxin Guo and 3 more

Open access · goldAbstract read
In one paragraph

Article in Journal of Cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 22% 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, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

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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

13 authors at 2 institutions in 1 country.

Hanwei CuiCentral Laboratory, Shenzhen Samii Medical Center, Shenzhen, Guangdong 518118, P.R. China.
Qian YiThe Central Laboratory, Shenzhen Second People's Hospital/the First Affiliated Hospital of Shenzhen University Health Science Center, Shenzhen 518035, P.R. China.
Min TianThe Department of Gynecology & Obstetrics, Daping Hospital, Army Medical University, Chongqing 400042, P.R. China.
Hai Ting YangDepartment of Reproductive Medicine, The First Affiliated hospital of Jinan University, Guang zhou, Guangdong, China, 510000.
Yuteng LiangThe Central Laboratory, Shenzhen Second People's Hospital/the First Affiliated Hospital of Shenzhen University Health Science Center, Shenzhen 518035, P.R. China.
Jie HuangThe Department of Gynecology & Obstetrics, Daping Hospital, Army Medical University, Chongqing 400042, P.R. China.
Qi ZengThe Department of Gynecology & Obstetrics, Daping Hospital, Army Medical University, Chongqing 400042, P.R. China.
Weichao SunThe Central Laboratory, Shenzhen Second People's Hospital/the First Affiliated Hospital of Shenzhen University Health Science Center, Shenzhen 518035, P.R. China.
Jian HanThe Department of Gynecology & Obstetrics, Daping Hospital, Army Medical University, Chongqing 400042, P.R. China.
Jianxin GuoThe Department of Gynecology & Obstetrics, Daping Hospital, Army Medical University, Chongqing 400042, P.R. China.
Zhiying YuThe Department of Gynecology, Shenzhen Second People's Hospital/the First Affiliated Hospital of Shenzhen University Health Science Center, Shenzhen 518035, P.R. China.
Wenlan LiuThe Central Laboratory, Shenzhen Second People's Hospital/the First Affiliated Hospital of Shenzhen University Health Science Center, Shenzhen 518035, P.R. China.
Xiufeng YeThe Department of Gynecology, Shenzhen Second People's Hospital/the First Affiliated Hospital of Shenzhen University Health Science Center, Shenzhen 518035, P.R. China.
Shenzhen Genoimmune Medical Institute · CNSouthwest Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adenosine (A)-to-inosine (I) RNA editing is the most prevalent RNA editing mechanism, in which adenosine deaminase acting on RNA 1 (ADAR1) is a major adenosine deaminase. Increasing evidence suggests that editing dysregulation of ADAR1 plays an important role in human tumorigenesis, while the underlying mechanism remains elusive. Here, we demonstrated that ADAR1 was highly expressed in ovarian cancer tissues and negatively correlated with progression free survival of ovarian cancer patients. Importantly, silence of ADAR1 repressed ovarian cancer cell growth and colony formation

Indexed as

ADAR1DNA DamageOvarian CancerR-Loop

Identifiers

PMID35711824
PMCPMC9174845
OpenAlexW4285181146

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.