Evidence map›Paper›PMID 35173146›Full record

ArticleCell death discovery2022

Circ-AFAP1 promote clear cell renal cell carcinoma growth and angiogenesis by the Circ-AFAP1/miR-374b-3p/VEGFA signaling axis.

Yuxi Ou, Xiyu Dai, Xinan Chen, Yiling Chen, Siqi Wu, Quan Zhou, Chen Yang, Haowen Jiang

Open access · goldAbstract read
In one paragraph

Article in Cell death discovery, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

14 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
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  5. World journal of gastroenterology · 2025
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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

8 authors at 1 institution in 1 country.

Yuxi Ou *Department of Urology, Huashan Hospital, Fudan University, Shanghai, China.ORCID http://orcid.org/0000-0001-9812-2521
Xiyu Dai *Department of Urology, Huashan Hospital, Fudan University, Shanghai, China.
Xinan Chen *Department of Urology, Huashan Hospital, Fudan University, Shanghai, China.
Yiling ChenDepartment of Urology, Huashan Hospital, Fudan University, Shanghai, China.
Siqi WuDepartment of Urology, Huashan Hospital, Fudan University, Shanghai, China.
Quan ZhouDepartment of Urology, Huashan Hospital, Fudan University, Shanghai, China.
Chen YangDepartment of Urology, Huashan Hospital, Fudan University, Shanghai, China. YangC_Huashan@163.com.ORCID http://orcid.org/0000-0001-6011-4067
Haowen JiangDepartment of Urology, Huashan Hospital, Fudan University, Shanghai, China. haowj_sh@fudan.edu.cn.ORCID http://orcid.org/0000-0002-5349-1363
Fudan University · CN

Funding

National Natural Science Foundation of China (National Science Foundation of China) 81802569National Natural Science Foundation of China (National Science Foundation of China) 82071703
6 · The paper itself

Abstract

Clear cell renal cell carcinoma (ccRCC) is one of the most common urogenital tumors with high mortality. Circular RNA (circRNA), as an emerging endogenous RNA, has been proved to play a crucial role in the clear cell renal cell carcinoma (ccRCC) progression. In this study, we obtained circAFAP1 upregulated in ccRCC by high-sequencing and verified by qRT-PCR in several renal cancer cell lines. In situ hybridization (ISH) assays and Kaplan-Meier plot showed a higher level of circAFAP1 was linked to shorter overall survival. Moreover, CCK8, colony formation, and EdU experiments showed circAFAP1 promoted ccRCC growth while tube formation displayed circAFAP1 contributed to ccRCC angiogenesis. We predicted the downstream miR-374b-3p and VEGFA by bioinformatic analysis and validated further by qRT-PCR, RNA pull-down, RIP, and dual-luciferase. Downregulation miR-374b-3p or overexpression VEGFA could restore proliferation, vascular formation after circAFAP1 silencing. Consistently with the results in vitro, silencing circAFAP1 suppressed ccRCC growth in vivo. In conclusion, the circAFAP1/miR-374b-3p/VEGFA axis played a critical role in the progression and development of ccRCC which might be novel biological marks and therapeutical targets.

Identifiers

PMID35173146
PMCPMC8850424
OpenAlexW4213260161

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Registered trials

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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.