Evidence map›Paper›PMID 39819545›Full record

ArticleCurrent cancer drug targets2026

Advances in Understanding How RhoB Regulates Akt Inhibition Efficacy in NSCLC.

Nurullah Akgun, Zekai Halici, Elif Cadirci

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Article in Current cancer drug targets, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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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

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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

2 citing papers in PubMed.

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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.

Nurullah AkgunDepartment of Pharmacology, Faculty of Medicine, Ataturk University, 25240, Erzurum, Turkey.ORCID 0000-0003-2703-9872
Zekai HaliciDepartment of Pharmacology, Faculty of Medicine, Ataturk University, 25240, Erzurum, Turkey.
Elif CadirciDepartment of Pharmacology, Faculty of Medicine, Ataturk University, 25240, Erzurum, Turkey.

Funding

Ataturk University Scientific Research Projects Coordination Unit TDK-2021-8900
6 · The paper itself

Abstract

objectivesIncreasing the effectiveness and reliability of Akt inhibition in lung cancer treatment may pave the way for a more favorable use of this method in the future. Therefore, we aimed to evaluate the possible role of RhoB in the regulation of Akt inhibition in NSCLC. MATERIALS AND

methodsThe study was conducted using the NSCLC cell line A549. Small interfering RNA (siRNA)-mediated RhoB knockdown was performed and combined with perifosine (Akt inhibitor) treatment. Cell proliferation was detected by xCELLigence® RTCA. RhoB, pAkt, and Bcl2l11 expressions were analyzed by ELISA. Apoptosis rates were determined by flow cytometry.

resultsWe knocked down RhoB in A549 cells using siRNA. According to the results of the 72-hour experiment, RhoB upregulation was observed to reduce the antiproliferative activity of the Akt inhibitor. The pAkt level was significantly lower in the group where the Akt inhibitor was applied to RhoB-silenced cells via siRNA compared to other treatment groups. The percentage of apoptosis in the group where the Akt inhibitor was applied to RhoBsilenced cells was found to be significantly higher than in the RhoB-suppressed group.

conclusionBoth proliferation and apoptosis tests determined that the RhoB molecule is a negative regulator of the anti-tumor activity of Akt inhibition in non-small cell lung cancer. This study suggests that RhoB expression may play a critical role in the regulation of Akt inhibition in NSCLC, potentially opening new avenues for treatment strategies.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsPhosphorylcholineProto-Oncogene Proteins c-aktrhoB GTP-Binding ProteinA549 CellsApoptosisCell ProliferationGene Expression Regulation, NeoplasticHumansRNA, Small InterferingperifosinePhosphorylcholineProto-Oncogene Proteins c-aktrhoB GTP-Binding ProteinRHOB protein, humanRNA, Small InterferingAktApoptosisBcl2l11ELISAlung cancerRhoBxCELLigence

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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.