Evidence map›Paper›PMID 31938090›Full record

ArticleInternational journal of clinical and experimental pathology2018

siRNA directed against Annexin II receptor inhibits HeLa cell proliferation, migration and invasion and induces apoptosis via suppressing ERK1/2 and Akt signaling pathways.

Zhi-Juan Cao, Xiao-Hang Xu, Tian Gao, Yi Zhang, Hong Xia, Yu-Qing Zhao, Jian-Jun Wang

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.1field-weighted citation impact, top 49% 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

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. Transcriptome sequencing (RNA-Seq) reveals non-coding pseudogene CDC27P9 role in cervical cancer.Apoptosis : an international journal on programmed cell death · 2026
    Article
  2. Article
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

7 authors at 2 institutions in 1 country.

Zhi-Juan CaoDepartment of Gynecology and Obstetrics, The Affiliated Tongji Hospital of Tongji University Shanghai 200065, P. R. China.
Xiao-Hang XuDepartment of Gynecology and Obstetrics, The Affiliated Tongji Hospital of Tongji University Shanghai 200065, P. R. China.
Tian GaoDepartment of Gynecology and Obstetrics, The Affiliated Tongji Hospital of Tongji University Shanghai 200065, P. R. China.
Yi ZhangDepartment of Gynecology and Obstetrics, The Affiliated Tongji Hospital of Tongji University Shanghai 200065, P. R. China.
Hong XiaDepartment of Gynecology and Obstetrics, The Affiliated Tongji Hospital of Tongji University Shanghai 200065, P. R. China.
Yu-Qing ZhaoDepartment of Gynecology, Gynecology and Obstetrics Hospital of Fudan University Shanghai 200090, P. R. China.
Jian-Jun WangDepartment of Gynecology and Obstetrics, The Affiliated Tongji Hospital of Tongji University Shanghai 200065, P. R. China.
Tongji University · CNObstetrics and Gynecology Hospital of Fudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Annexin II receptor (AXIIR) was originally identified as a cell surface receptor for Annexin II and was shown to be involved in the development and progression of multiple cancers, but little was known about its role in cervical cancer. The aim of our study was to investigate the role and the plausible molecular mechanism of AXIIR in regulating apoptosis, invasion and migration of cervical cancer cells. siRNA targeting AXIIR was chemical synthesized and transfected into HeLa cells which with non-specific siRNA tranfection used as a negative control. Cell proliferation, cell migration, cell invasion and cell apoptosis assay were measured by CCK-8, wound healing assay, Transwell invasion assay and flow cytometry, respectively. Tumor-related protein and signaling pathway were also measured by real-time quantitative PCR and western blot assay to investigate the molecular mechanism of AXIIR involved in regulating HeLa cells. Our data showed that AXIIR siRNA significantly inhibited HeLa cell viability and induced cell apoptosis by increases in Caspase-3/-8/-9 mRNA and protein expression, and inhibit HeLa cell migration and invasion by decreased MMP-2/-9 mRNA and protein expression. AXIIR siRNA could also significantly down-regulate Akt, p-Akt, ERK1/2 and p-ERK1/2 expression. In conclusion, AXIIR is of great importance for regulatingcell viability, migration, invasion and apoptosis

Indexed as

AXIIRCervical cancerERK1/2HeLaPI3K/AktsiRNA

Identifiers

PMID31938090
PMCPMC6957953
OpenAlexW3026684818

What OpenQuestion holds

Textmetadata
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.