Evidence map›Paper›PMID 28451917›Full record

ArticleDigestive diseases and sciences2017

Long Noncoding RNA AFAP1-AS1 Promotes Cell Proliferation and Apoptosis of Gastric Cancer Cells via PTEN/p-AKT Pathway.

Jun-Qiang Guo, Shi-Jie Li, Guo-Xiao Guo

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Article in Digestive diseases and sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
4.0field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

34 citing papers in PubMed, 64 citations in OpenAlex.

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4 · The record

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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

3 authors at 1 institution in 1 country.

Jun-Qiang GuoDepartment of Institute of Traumatic Surgery, Huaihe Hospital, Henan University, Kaifeng, 475000, China.
Shi-Jie LiDepartment of Institute of Traumatic Surgery, Huaihe Hospital, Henan University, Kaifeng, 475000, China.
Guo-Xiao GuoDepartment of General Surgery, Huaihe Hospital, Henan University, No. 1 Baobei Rd., Kaifeng, 475000, Henan, China. guogxiao@126.com.
Henan University Huaihe Hospital and Huaihe Clinical Institute · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLong noncoding RNA (lncRNA) plays critical roles in both tumor-suppressive and oncogenic pathways in the pathological development and prognosis of cancers.

aimsThis study aimed to explore the expression of lncRNA AFAP1-AS1 and its function in gastric cancer (GC).

methodsThe expression of AFAP1-AS1 was detected in GC tissues and GC cells by quantitative real-time reverse-transcription PCR. A small interfering RNA (siRNA) that targeted AFAP1-AS1 was transfected into cells to inhibit the expression of AFAP1-AS1. MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assay and colony formation assay were performed to examine the cell proliferation of SGC7901 cell transfected with si-AFAP1-AS1. Cell apoptosis was detected by flow cytometry. The protein level of cleaved PARP, Caspase 3, Caspase 9, Caspase 8, Bcl-2, Bax, p-AKT, total-AKT, and PTEN were detected by Western blot.

resultsAFAP1-AS1 was up-regulated in GC tissues and GC cells. AFAP1-AS1 knockdown suppressed cell viability of SGC7901 transfected with si-AFAP1-AS1. The number of apoptotic SGC7901 cell transfected with si-AFAP1-AS1 was increased by 3.4-fold comparing to that of control. The protein level of cleaved PARP, Caspase 3, and Caspase 9 were increased in SGC7901 transfected with si-AFAP1-AS1, as well as the expression of Bax. The protein level of Bcl-2 was decreased. AFAP1-AS1 knockdown decreased the protein level of p-AKT and increased the expression of PTEN in SGC7901 cells.

conclusionsAFAP1-AS1 was up-regulated in GC cells and regulated the gastric cancer cell proliferation and apoptosis via PTEN/p-AKT pathway.

Indexed as

ApoptosisCarcinogenesisCell Line, TumorCell ProliferationGene Knockdown TechniquesHumansProto-Oncogene Proteins c-aktPTEN PhosphohydrolaseRNA, Long NoncodingRNA, Small InterferingSignal TransductionStomach NeoplasmsUp-RegulationAFAP1-AS1 long noncoding RNA, humanProto-Oncogene Proteins c-aktPTEN PhosphohydrolasePTEN protein, humanRNA, Long NoncodingRNA, Small InterferingAFAP1-AS1ApoptosisGastric cancerp-AKTProliferationPTEN

Identifiers

PMID28451917
OpenAlexW2610118534

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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 OpenQuestion graph.