Evidence map›Paper›PMID 33941853›Full record

ArticleOncogene2021

EphA2-YES1-ANXA2 pathway promotes gastric cancer progression and metastasis.

Linfeng Mao, Weijie Yuan, Kaimei Cai, Chen Lai, Changhao Huang, Yi Xu, Shangwei Zhong, Chen Yang, Ran Wang, Pengwei Zeng and 3 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 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
6.2field-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

50 citing papers in PubMed, 82 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 2 institutions in 1 country.

Linfeng MaoDepartment of General Surgery, Xiangya Hospital, Central South University (CSU), Hunan, Changsha, China.ORCID http://orcid.org/0000-0001-8113-1253
Weijie YuanDepartment of General Surgery, Xiangya Hospital, Central South University (CSU), Hunan, Changsha, China.
Kaimei CaiThe Hunan Provincial Key Lab of Precision Diagnosis and Treatment for Gastrointestinal Tumor, Xiangya Hospital, CSU, Hunan, Changsha, China.
Chen LaiDepartment of General Surgery, Xiangya Hospital, Central South University (CSU), Hunan, Changsha, China.
Changhao HuangDepartment of General Surgery, Xiangya Hospital, Central South University (CSU), Hunan, Changsha, China.
Yi XuThe Hunan Provincial Key Lab of Precision Diagnosis and Treatment for Gastrointestinal Tumor, Xiangya Hospital, CSU, Hunan, Changsha, China.
Shangwei ZhongThe Hunan Provincial Key Lab of Precision Diagnosis and Treatment for Gastrointestinal Tumor, Xiangya Hospital, CSU, Hunan, Changsha, China.
Chen YangDepartment of General Surgery, Xiangya Hospital, Central South University (CSU), Hunan, Changsha, China.
Ran WangDepartment of General Surgery, Xiangya Hospital, Central South University (CSU), Hunan, Changsha, China.
Pengwei ZengDepartment of General Surgery, Xiangya Hospital, Central South University (CSU), Hunan, Changsha, China.
Heyuan HuangDepartment of General Surgery, Xiangya Hospital, Central South University (CSU), Hunan, Changsha, China.
Zhikang ChenDepartment of General Surgery, Xiangya Hospital, Central South University (CSU), Hunan, Changsha, China.
Zihua ChenDepartment of General Surgery, Xiangya Hospital, Central South University (CSU), Hunan, Changsha, China. zihuachenxy@126.com.ORCID http://orcid.org/0000-0002-8467-7742
Central South University · CNHunan Cancer Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Erythropoietin-producing hepatocellular receptor A2 (EphA2) is a key member of the receptor tyrosine kinase (RTK) family, while YES Proto-Oncogene 1 (YES1) is a non-receptor tyrosine kinase (nRTK) and annexin A2 (ANXA2) belongs to the calcium-dependent phospholipid-binding protein family annexins. Here, we show that EphA2, YES1, and ANXA2 form a signal axis, in which YES1 activated by EphA2 phosphorylates ANXA2 at Tyr24 site, leading to ANXA2 activation and increased ANXA2 nuclear distribution in gastric cancer (GC) cells. Overexpression (OE) of YES1 increases, while knockdown (KD) of YES1 or ANXA2 decreases GC cell invasion and migration in vitro and tumor growth in mouse models. Reexpression of wildtype (WT) rather than mutant ANXA2 (Tyr24F) in ANXA2 knockdown (ANXA2-KD) GC cells restores YES1-induced cell invasion and migration, while neither WT nor mutant ANXA2 (Tyr24F) can restore cell invasion and migration in YES1-KD GC cells. In addition, the activation of EphA2-YES1-ANXA2 pathway is correlated with poor prognosis. Thus, our results establish EphA2-YES1-ANXA2 axis as a novel pathway that drives GC invasion and metastasis, targeting this pathway would be an efficient way for the treatment of GC.

Indexed as

AnimalsAnnexin A2Cell Line, TumorCell ProliferationHumansMiceMice, Inbred NODMice, SCIDNeoplasm MetastasisPhosphorylationProto-Oncogene Proteins c-yesReceptor, EphA2Signal TransductionStomach NeoplasmsSurvival RateXenograft Model Antitumor AssaysAnnexin A2ANXA2 protein, humanEPHA2 protein, humanProto-Oncogene Proteins c-yesReceptor, EphA2YES1 protein, human

Identifiers

PMID33941853
PMCPMC8134040
OpenAlexW3159081741

What Socratic 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 Socratic graph.