Evidence map›Paper›PMID 29967343›Full record

ArticleLaboratory investigation; a journal of technical methods and pathology2018

Differential effects of GLI2 and GLI3 in regulating cervical cancer malignancy in vitro and in vivo.

Haiyan Zhu, Lu Xia, Qi Shen, Menghuang Zhao, Xiang Gu, Hakim Bouamar, Bingzhi Wang, Lu-Zhe Sun, Xueqiong Zhu

Open access · greenAbstract read
In one paragraph

Article in Laboratory investigation; a journal of technical methods and pathology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.1field-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

9 citing papers in PubMed, 23 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

9 authors at 3 institutions in 2 countries.

Haiyan ZhuDepartment of Obstetrics and Gynecology, the Second Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Lu XiaDepartments of Cell Systems & Anatomy, School of Medicine, University of Texas Health Science Center, San Antonio, TX, USA.
Qi ShenDepartment of Obstetrics and Gynecology, the Second Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Menghuang ZhaoDepartment of Obstetrics and Gynecology, the Second Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Xiang GuDepartments of Cell Systems & Anatomy, School of Medicine, University of Texas Health Science Center, San Antonio, TX, USA.
Hakim BouamarDepartments of Cell Systems & Anatomy, School of Medicine, University of Texas Health Science Center, San Antonio, TX, USA.
Bingzhi WangDepartments of Cell Systems & Anatomy, School of Medicine, University of Texas Health Science Center, San Antonio, TX, USA.
Lu-Zhe SunDepartment of Obstetrics and Gynecology, the Second Affiliated Hospital of Wenzhou Medical University, Wenzhou, China. sunl@uthscsa.edu.
Xueqiong ZhuDepartment of Obstetrics and Gynecology, the Second Affiliated Hospital of Wenzhou Medical University, Wenzhou, China. zjwzzxq@163.com.ORCID http://orcid.org/0000-0002-8389-928X
The University of Texas Health Science Center at San Antonio · USCentral South University · CNWenzhou Medical University · CN

Funding

TISSUE CULTURE---COREP30CA054174 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Lei Zheng · 1991 to 2026
$59.1M
Connexin hemichannels in suppression of breast cancer bone metastasisR01CA196214 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI JIANG, JEAN X, SUN, LUZHE · 2016 to 2020
$1.8M
Inhibition of the tumor-promoting effects of TGF-beta in advanced prostate cancerR01CA172886 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI HINCK, ANDREW P, SUN, LUZHE · 2013 to 2016
$1.2M
NCI NIH HHS P30 CA054174NCI NIH HHS R01 CA172886NCI NIH HHS R01 CA196214
6 · The paper itself

Abstract

Advanced, recurrent, or persistent cervical cancer is often incurable. Therefore, in-depth insights into the molecular mechanisms are needed for the development of novel therapeutic targets and the improvement of current therapeutic strategies. In this study, we investigated the role of GLI2 and GLI3 in the regulation of the malignant properties of cervical cancer. We showed that down-regulation of GLI2, but not GLI3, with an inducible GLI2 shRNA inhibited the growth and migration of cervical cancer cell lines, which could be rescued by ectopic expression of GLI2. GLI2 appeared to support cell growth by regulating the mitosis, but not the apoptosis, of the cervical cancer cells. Mechanistically, these functions of GLI2 were in part mediated by the activation of AKT pathway. Knockdown of GLI2, but not GLI3, also inhibited xenograft growth of cervical cancer cells in vivo. Finally, analysis of TCGA data showed that high levels of GLI2, but not GLI3, conferred a poor prognosis in cervical cancer patients. These observations for the first time suggest that GLI2, but not GLI3, exerts a tumor-promoting role in cervical cancer and may be targeted as a novel therapeutic strategy.

Indexed as

AnimalsCell MovementCell ProliferationFemaleGene Knockdown TechniquesHeLa CellsHumansMice, NudeNerve Tissue ProteinsNuclear ProteinsProto-Oncogene Proteins c-aktUterine Cervical NeoplasmsZinc Finger Protein Gli2Zinc Finger Protein Gli3GLI2 protein, humanGli2 protein, mouseGLI3 protein, humanGli3 protein, mouseNerve Tissue ProteinsNuclear ProteinsProto-Oncogene Proteins c-aktZinc Finger Protein Gli2Zinc Finger Protein Gli3

Identifiers

PMID29967343
PMCPMC6386554
OpenAlexW2810306624

What OpenQuestion holds

Textmetadata
LicenceTDM
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.