Evidence map›Paper›PMID 39094512›Full record

ArticleTranslational oncology2024

Ad-VT causes ovarian cancer A2780 cell death via mitochondrial apoptosis and autophagy pathways.

Yingli Cui, Xin Chen, Wenjie Li, Shanzhi Li, Ningyi Jin, Xiao Li, Yiquan Li, Ying Yue

Abstract read
In one paragraph

Article in Translational oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

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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

3 citing papers in PubMed.

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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

8 authors.

Yingli CuiDepartment of Gynecologic Oncology, First Hospital of Jilin University, Changchun 130021, PR China.
Xin ChenEdmond H. Fischer Signal Transduction Laboratory, College of Life Sciences, Jilin University, Changchun, 130021, PR China.
Wenjie LiInstitute of Virology, Wenzhou University, Wenzhou 325035, PR China.
Shanzhi LiChangchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun 130122, PR China; Academician Workstation of Jilin Province, Changchun University of Chinese Medicine, Changchun 130177, PR China.
Ningyi JinChangchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun 130122, PR China; Academician Workstation of Jilin Province, Changchun University of Chinese Medicine, Changchun 130177, PR China; Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou 225009, PR China.
Xiao LiChangchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun 130122, PR China; Academician Workstation of Jilin Province, Changchun University of Chinese Medicine, Changchun 130177, PR China. Electronic address: lixiao06@mails.jlu.edu.cn.
Yiquan LiAcademician Workstation of Jilin Province, Changchun University of Chinese Medicine, Changchun 130177, PR China. Electronic address: liyq01@ccucm.edu.cn.
Ying YueDepartment of Gynecologic Oncology, First Hospital of Jilin University, Changchun 130021, PR China. Electronic address: yuey@jlu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe recombinant adenovirus Ad-apoptin-hTERTp-E1a (Ad-VT) to have a bi-specific oncolytic character in many tumor cells, but its action pathway in killing tumor cells has not been accurately elucidated. Here, we studied the mechanism of apoptosis and autophagy induced by Ad-VT and the interaction between autophagy and apoptosis.

methodsCrystal Violet staining and CCK-8 assays were used to detect the inhibitory effect of Ad-VT on ovarian cancer cells. The antitumor effect of Ad-VT in vivo was analyzed by tumor bearing nude mouse model. Subsequently, flow cytometry and fluorescence staining were used to analyze the main types of apoptosis and autophagy induced by Ad-VT.

resultsIn this study, through the in vitro cell inhibition assays, we found that Ad-VT has a significant inhibitory effect on ovarian cancer A2780 cells, but no significant inhibitory effect on normal ovarian epithelial cells. Then in vivo experiments showed that Ad-VT significantly inhibited tumor growth and extended the survival time of mice. Subsequent detection of the level of apoptosis found that Ad-VT can cause a strong apoptotic response and kill cells mainly through the endogenous apoptotic pathway. Through the staining analysis of LC3 and the analysis of autophagy-related proteins, it was found that Ad-VT could significantly increase the level of autophagy in A2780 cells, and this was a protective mechanism.

conclusionsAd-VT, which replicates under the control of the hTERT promoter and expresses apoptin protein, have significant inhibitory effect on ovarian cancer A2780 cells and promote their apoptosis and autophagy.

Indexed as

ApoptinApoptosisAutophagyOvarian cancerRecombinant adenovirus

Identifiers

PMID39094512
PMCPMC11334942

What Socratic holds

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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 Socratic graph.