Evidence map›Paper›PMID 31709304›Full record

ArticleMolecular therapy oncolytics2019

CBX7 Inhibits Cell Growth and Motility and Induces Apoptosis in Cervical Cancer Cells.

Rong Li, Qi Yan, Ping Tian, Yan Wang, Jing Wang, Ning Tao, Li Ning, Xin Lin, Lu Ding, Jiwen Liu and 1 more

Open access · goldAbstract read
In one paragraph

Article in Molecular therapy oncolytics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

20 citing papers in PubMed, 34 citations in OpenAlex.

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  7. CBX4 deletion promotes tumorigenesis under KrasSignal transduction and targeted therapy · 2023
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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

11 authors at 4 institutions in 1 country.

Rong LiPostdoctoral Research Center on Clinical Medicine, First Affiliated Hospital, Xinjiang Medical University, Xinjiang, China.
Qi YanDepartment of Maternal, Child and Adolescent Health, College of Public Health, Xinjiang Medical University, Xinjiang, China.
Ping TianFifth Affiliated Hospital, Xinjiang Medical University, Xinjiang, China.
Yan WangTumor Hospital Affiliated to Xinjiang Medical University, Xinjiang, China.
Jing WangState Key Laboratory of Pathogenesis, Prevention and Treatment of High Incidence Diseases in Central Asia (PPTHIDCA), Department of Gynecology, First Affiliated Hospital, Xinjiang Medical University, Xinjiang, China.
Ning TaoPostdoctoral Research Center on Clinical Medicine, First Affiliated Hospital, Xinjiang Medical University, Xinjiang, China.
Li NingPostdoctoral Research Center on Clinical Medicine, First Affiliated Hospital, Xinjiang Medical University, Xinjiang, China.
Xin LinPostdoctoral Research Center on Clinical Medicine, First Affiliated Hospital, Xinjiang Medical University, Xinjiang, China.
Lu DingPostdoctoral Research Center on Public Health and Preventive Medicine, Xinjiang Medical University, Xinjiang, China.
Jiwen LiuPostdoctoral Research Center on Clinical Medicine, First Affiliated Hospital, Xinjiang Medical University, Xinjiang, China.
Cailing MaState Key Laboratory of Pathogenesis, Prevention and Treatment of High Incidence Diseases in Central Asia (PPTHIDCA), Department of Gynecology, First Affiliated Hospital, Xinjiang Medical University, Xinjiang, China.
Xinjiang Medical University · CNFirst Affiliated Hospital of Xinjiang Medical University · CNFifth Affiliated Hospital of Xinjiang Medical University · CNTumor Hospital of Xinjiang Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The chromobox protein homolog 7 (CBX7), one member of the polycomb group family, has been characterized mainly to play a tumor-suppressive role in human malignant neoplasias. Moreover, downregulation of CBX7 is correlated with poor prognosis and aggressiveness in a variety of human cancers. However, the biological functions and role of CBX7 in cervical cancer have not been elucidated. In the present study, we explore whether CBX7 exerts its tumor-suppressive function in cervical cancer. To achieve this goal, molecular approaches were used to upregulate the expression of CBX7 or downregulation of CBX7 in cervical cancer cell lines. We observed that overexpression of CBX7 inhibited cell growth and induced apoptosis in cervical cancer cells. CBX7 overexpression retarded cell migration and invasion in cervical cancer cells. In line with this, downregulation of CBX7 promoted cell growth and migration as well as invasion in cervical cancer cells. Our findings suggest that CBX7 might be a tumor suppressor and could be a potential target in cervical cancer.

Indexed as

apoptosisCBX7cell proliferationcervical cancerE-cadherininvasionmigrationmotility

Identifiers

PMID31709304
PMCPMC6834976
OpenAlexW2976427219

What OpenQuestion 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 OpenQuestion graph.