Evidence map›Paper›PMID 35996134›Full record

ArticleBMC urology2022

Effect of AKT silence on malignant biological behavior of renal cell carcinoma cells.

Zuan Li, DeYong Nong, Bincai Li, Haojian Wang, Chunlin Li, Zhi Chen, Ximing Li, Guihai Huang, Junhao Lin, Nan Hao and 1 more

Open access · goldAbstract read
In one paragraph

Article in BMC urology, 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
0.3field-weighted citation impact, top 41% 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, 2 citations in OpenAlex.

  1. Mechanism ofFrontiers in pharmacology · 2026
    Article
  2. Article
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 1 institution in 1 country.

Zuan LiDepartment of Urology, The People's Hospital of Guangxi Zhuang Autonomous Region, Nanning, China.
DeYong NongDepartment of Urology, The People's Hospital of Guangxi Zhuang Autonomous Region, Nanning, China.
Bincai LiDepartment of Urology, The People's Hospital of Guangxi Zhuang Autonomous Region, Nanning, China.
Haojian WangDepartment of Urology, The People's Hospital of Guangxi Zhuang Autonomous Region, Nanning, China.
Chunlin LiDepartment of Urology, The People's Hospital of Guangxi Zhuang Autonomous Region, Nanning, China.
Zhi ChenDepartment of Urology, The People's Hospital of Guangxi Zhuang Autonomous Region, Nanning, China.
Ximing LiDepartment of Urology, The People's Hospital of Guangxi Zhuang Autonomous Region, Nanning, China.
Guihai HuangDepartment of Urology, The People's Hospital of Guangxi Zhuang Autonomous Region, Nanning, China.
Junhao LinDepartment of Urology, The People's Hospital of Guangxi Zhuang Autonomous Region, Nanning, China.
Nan HaoDepartment of Urology, The People's Hospital of Guangxi Zhuang Autonomous Region, Nanning, China.
Wei LiDepartment of Urology, The People's Hospital of Guangxi Zhuang Autonomous Region, Nanning, China. liwei95_2000@163.com.
The People's Hospital of Guangxi Zhuang Autonomous Region · CN

Funding

National Natural Science Foundation of China 81760456
6 · The paper itself

Abstract

backgroundAs the most common malignant tumor of primary renal tumor, renal cell carcinoma (RCC) is the highly invasive disease with high mortality. AKT is a serine/threonine kinase that play a critical role in the phosphoinositide 3-kinase (PI3K) signaling pathway, and it is an attractive target for RCC treatment. The aim of present study was to investigate the effect of AKT silence on malignant behavior of renal cell carcinoma cells.

methodsAKT expression was quantified by immunohistochemistry in tumor tissues and normal tissues. The human RCC cell lines Caki-2 cell were chosen for this study. The optimal silencing siRNA was subsequently selected by RT-qPCR and western blot. The effect of AKT silence on RCC cells was investigated by CCK8 assay, transwell assay, scratch test and flow cytometry. The AKT1 expression in human renal cell carcinoma tissue was detected by immunohistochemical staining.

resultsThe AKT in Caki-2 cells was silenced successfully. The results shown AKT silence could inhibit cell proliferation, invasion, and, migration. In addition, AKT silence could promote Caki-2 cell apoptosis with prevention of RCC cells move from G1 phase to S phase. Immunohistochemical staining revealed significant difference of expression of AKT1 in RCC tissues and normal renal tissues. Taken together, AKT family members might involve in malignant growth of RCC, and might be a potential therapeutic target.

conclusionOur data show that AKT silence inhibited cell proliferation, invasion, and, migration of Caki-2 cell, and promoted Caki-2 cell apoptosis. Moreover, AKT silence prevented RCC cells move from G1 phase to S phase. Therefore, AKT may act as an effective therapeutic target for RCC.

Indexed as

Carcinoma, Renal CellKidney NeoplasmsProto-Oncogene Proteins c-aktCell Line, TumorCell ProliferationGene Expression Regulation, NeoplasticGene SilencingHumansPhosphatidylinositol 3-KinasesAKT1 protein, humanPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktAKTBiological behaviorRenal cell carcinomaSilence

Identifiers

PMID35996134
PMCPMC9396790
OpenAlexW4293277619

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.