Evidence map›Paper›PMID 35537818›Full record

ArticleAging2022

LncRNA CRART16/miR-122-5p/FOS axis promotes angiogenesis of gastric cancer by upregulating VEGFD expression.

Junling Zhang, Xiaocong Pang, Lili Lei, Jixin Zhang, Xiaoqian Zhang, Ziyi Chen, Jing Zhu, Yong Jiang, Guowei Chen, Yingchao Wu and 5 more

Open access · hybridAbstract read
In one paragraph

Article in Aging, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 14% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 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

15 authors at 4 institutions in 1 country.

Junling ZhangDepartment of General Surgery, Peking University First Hospital, Beijing 100034, China.
Xiaocong PangInstitute of Clinical Pharmacology, Peking University, Beijing 100034, China.
Lili LeiInstitute of Clinical Pharmacology, Peking University, Beijing 100034, China.
Jixin ZhangDepartment of Pathology, Peking University First Hospital, Beijing 100034, China.
Xiaoqian ZhangDepartment of General Surgery, The Cancer Hospital of the Chinese Academy of Medical Sciences and China National Cancer Center, Beijing 100034, China.
Ziyi ChenLiver Transplantation Center, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.
Jing ZhuDepartment of General Surgery, Peking University First Hospital, Beijing 100034, China.
Yong JiangDepartment of General Surgery, Peking University First Hospital, Beijing 100034, China.
Guowei ChenDepartment of General Surgery, Peking University First Hospital, Beijing 100034, China.
Yingchao WuDepartment of General Surgery, Peking University First Hospital, Beijing 100034, China.
Tao WuDepartment of General Surgery, Peking University First Hospital, Beijing 100034, China.
Yisheng PanDepartment of General Surgery, Peking University First Hospital, Beijing 100034, China.
Yucun LiuDepartment of General Surgery, Peking University First Hospital, Beijing 100034, China.
Yimin CuiInstitute of Clinical Pharmacology, Peking University, Beijing 100034, China.
Xin WangDepartment of General Surgery, Peking University First Hospital, Beijing 100034, China.
Peking University First Hospital · CNPeking University · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNNanjing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWe previously identified a novel lncRNA, CRART16, that could induce cetuximab resistance in colorectal cancer cells. This study explored the relationship of CRART16 expression to gastric cancer progression and the molecular mechanisms involved.

methodsWe evaluated CRART16 expression in gastric cancer tissues and adjacent normal tissues from the TCGA database and our hospital. Besides, we assessed its relationship with the overall survival (OS) of patients with gastric cancer. The effects of CRART16 on gastric cancer angiogenesis were determined by endothelial tube formation assay, spheroid sprouting assay, HUVEC invasion assay, and chick embryo chorioallantoic membrane (CAM) assay. The involvement of the lncRNA CRART16/miR-122-5p/FOS axis was analyzed by western blotting and dual-luciferase reporter assay. The functions of CRART16 were confirmed in xenograft mouse models.

resultsWe found that CRART16 was substantially overexpressed in gastric cancer tissues compared with normal tissues, based on the TCGA database and our clinical samples. High expression of CRART16 correlated with more advanced tumor stages and poor prognosis. Overexpression of CRART16 in gastric cancer cells promoted proliferation, colony formation, angiogenesis, and bevacizumab resistance

conclusionOur findings demonstrate that CRART16 promotes angiogenesis

Indexed as

MicroRNAsProto-Oncogene Proteins c-fosRNA, Long NoncodingStomach NeoplasmsVascular Endothelial Growth Factor DAnimalsCell Line, TumorCell ProliferationChick EmbryoGene Expression Regulation, NeoplasticHumansHuman Umbilical Vein Endothelial CellsMiceNeovascularization, PathologicFOS protein, humanMicroRNAsMIRN122 microRNA, humanProto-Oncogene Proteins c-fosRNA, Long NoncodingVascular Endothelial Growth Factor DVEGFD protein, humanangiogenesisCRART16gastric cancerlong non-coding RNAmicroRNA

Identifiers

PMID35537818
PMCPMC9134963
OpenAlexW4280538856

What OpenQuestion holds

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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.