Evidence map›Paper›PMID 35990250›Full record

ArticleDisease markers2022

Interleukin-8 Regulates the Autophagy and Apoptosis in Gastric Cancer Cells via Regulating PI3K/Akt Signaling Pathway.

Liang Yu, Guoqiang Zhou, Zhiliang Shi, Jian Guo, Shengyuan Yu, Cheng Yu, Chenglong Shen

Open access · hybridAbstract read
In one paragraph

Article in Disease markers, 2022. 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
0.6field-weighted citation impact, top 32% 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, 4 citations in OpenAlex.

  1. Review
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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

7 authors at 1 institution in 1 country.

Liang YuDepartment of General Surgery, Changshu No. 2 People's Hospital, China.ORCID https://orcid.org/0000-0003-0644-9557
Guoqiang ZhouDepartment of General Surgery, Changshu No. 2 People's Hospital, China.ORCID https://orcid.org/0000-0002-5905-8595
Zhiliang ShiDepartment of General Surgery, Changshu No. 2 People's Hospital, China.ORCID https://orcid.org/0000-0003-2384-0339
Jian GuoDepartment of General Surgery, Changshu No. 2 People's Hospital, China.ORCID https://orcid.org/0000-0002-7956-353X
Shengyuan YuDepartment of General Surgery, Changshu No. 2 People's Hospital, China.ORCID https://orcid.org/0000-0001-5258-9804
Cheng YuDepartment of General Surgery, Changshu No. 2 People's Hospital, China.ORCID https://orcid.org/0000-0002-9546-948X
Chenglong ShenDepartment of General Surgery, Changshu No. 2 People's Hospital, China.ORCID https://orcid.org/0000-0003-3234-9648
Changshu No.1 People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To explore the role and mechanism of interleukin-8-mediated autophagy regulation of gastric cancer (GC) cells in GC. Methods: After cell culture, the SGC7901 cell line was separated into the control group and IL-8 (20 ng/mL) group, IL-8 (40 ng/mL) group, and IL-8 (60 ng/mL) group, to verify the effects of the PI3K/Akt signal path on the modulation of autophagy in GC cells. Western blot detected autophagy markers, ATG12-ATG5 complexes, autophagy-associated pathways, and apoptosis-associated factors in GC cells. Transwell was utilized to identify invasion capability. Results: Compared with the control group, the expression of LC3II, Atg5, ATG7, Beclin1, Bax, C-cas3, C-cas9, P-PI3K, P-Akt, and ATG12-ATG5 was remarkably elevated in the IL-8 (60 ng/mL) group, IL-8 (20 ng/mL) group, and the IL-8 (40 ng/mL) group. The expression of P62 and Bcl-2 in the IL-8 (60 ng/mL) group was also lower than that of the IL-8 (20 ng/mL) group and IL-8 (40 ng/mL) group, in contrast to the controls. The invasive quantity of GC SGC7901 cells in the IL-8 (60 ng/mL) group was also remarkably higher in contrast to the IL-8 (20 ng/mL) and IL-8 (40 ng/mL) groups. The relative expressions of LC3II, Atg5, ATG7, Beclin1, Bax, C-cas3, C-cas9, P-PI3K, P-Akt, and ATG12-ATG5 complex proteins in LY294002 group were considerably elevated. LC3II, Atg5, ATG7, Beclin1, Bax, C-cas3, C-cas9, P-PI3K, P-Akt, and ATG12-ATG5 were decreased in the IL-8 + LY294002 group. The relative expressions of P62 and Bcl-2 proteins in the IL-8 + LY294002 group were remarkably elevated, and the invasion of SGC7901 cells in the IL-8 group was elevated. In contrast to the IL-8 group, the invasion quantity of gastric cancer SGC7901 cells in the IL-8 + LY294002 group was considerably decreased. Conclusion: IL-8 promotes autophagy and aggression and suppresses apoptosis of GC SGC7901 cells by regulating PI3K/AKT pathway phosphorylation.

Indexed as

ApoptosisAutophagyInterleukin-8Phosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktStomach NeoplasmsAutophagy-Related Protein 5bcl-2-Associated X ProteinBeclin-1CRISPR-Associated ProteinsHumansProto-Oncogene Proteins c-bcl-2Signal TransductionAutophagy-Related Protein 5bcl-2-Associated X ProteinBeclin-1CRISPR-Associated ProteinsInterleukin-8Phosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktProto-Oncogene Proteins c-bcl-2

Identifiers

PMID35990250
PMCPMC9388311
OpenAlexW4291009259

What OpenQuestion holds

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LicenceCC BY
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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.