Evidence map›Paper›PMID 34949659›Full record

ArticleCancer genomics & proteomics

SIRT5 Directly Inhibits the PI3K/AKT Pathway in Prostate Cancer Cell Lines.

So Young Choi, Ju Mi Jeon, Ann Yae Na, Oh Kwang Kwon, In Hyuk Bang, Yun-Sok Ha, Eun Ju Bae, Byung-Hyun Park, Eun Hye Lee, Tae Gyun Kwon and 2 more

Open access · diamondAbstract read
In one paragraph

Article in Cancer genomics & proteomics. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

17 citing papers in PubMed, 30 citations in OpenAlex.

  1. Molecules (Basel, Switzerland) · 2026
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  14. Targeting PI3K/Akt signaling in prostate cancer therapy.Journal of cell communication and signaling · 2023
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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

12 authors at 2 institutions in 1 country.

So Young Choi *BK21 Plus KNU Multi-Omics Based Creative Drug Research Team, College of Pharmacy, Research Institute of Pharmaceutical Sciences, Kyungpook National University, Daegu, Republic of Korea.
Ju Mi Jeon *BK21 Plus KNU Multi-Omics Based Creative Drug Research Team, College of Pharmacy, Research Institute of Pharmaceutical Sciences, Kyungpook National University, Daegu, Republic of Korea.
Ann Yae NaBK21 Plus KNU Multi-Omics Based Creative Drug Research Team, College of Pharmacy, Research Institute of Pharmaceutical Sciences, Kyungpook National University, Daegu, Republic of Korea.
Oh Kwang KwonBK21 Plus KNU Multi-Omics Based Creative Drug Research Team, College of Pharmacy, Research Institute of Pharmaceutical Sciences, Kyungpook National University, Daegu, Republic of Korea.
In Hyuk BangDepartment of Biochemistry and Molecular Biology, Chonbuk National University Medical School, Jeonbuk, Republic of Korea.
Yun-Sok HaDepartment of Urology, School of Medicine, Kyungpook National University, Daegu, Republic of Korea.
Eun Ju BaeCollege of Pharmacy, Chonbuk National University, Jeonbuk, Republic of Korea.
Byung-Hyun ParkDepartment of Biochemistry and Molecular Biology, Chonbuk National University Medical School, Jeonbuk, Republic of Korea.
Eun Hye LeeJoint Institute for Regenerative Medicine, Kyungpook National University, Daegu, Republic of Korea.
Tae Gyun KwonDepartment of Urology, School of Medicine, Kyungpook National University, Daegu, Republic of Korea.
Jun Nyung LeeDepartment of Urology, School of Medicine, Kyungpook National University, Daegu, Republic of Korea; ljnlover@gmail.com.
Sangkyu LeeBK21 Plus KNU Multi-Omics Based Creative Drug Research Team, College of Pharmacy, Research Institute of Pharmaceutical Sciences, Kyungpook National University, Daegu, Republic of Korea; sangkyu@knu.ac.kr ljnlover@gmail.com.
Kyungpook National University · KRJeonbuk National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimProstate cancer (PCa) is the most commonly diagnosed genital cancer in men globally. Among patients who develop advanced PCa, 80% are affected by bone metastasis, with a sharp drop in survival rate. Despite efforts, the details of mechanisms of metastasis of PCa remain unclear. SIRT5, an NAD MATERIALS AND

methodsWe characterized the differentially expressed proteins between parental and SIRT5 KO PC-3 cells using quantitative proteomics analysis.

resultsA significant increase in expression of interleukin-1β (IL-1β) in SIRT5 KO cells was observed, and the PI3K/AKT/NF-ĸB signaling pathway was found significantly elevated in SIRT5 KO cells by the Gene Ontology annotation and KEGG pathway functional enrichment analysis. Moreover, we confirmed that SIRT5 can bind PI3K by immunoprecipitation analysis.

conclusionThis study is the first to demonstrate a relationship between SIRT5 and PCa metastasis, suggesting that SIRT5-mediated inhibition of the PI3K/AKT/NK-kB pathway is reduced for secondary metastasis from bone to other tissues.

Indexed as

Epigenesis, GeneticGene Expression Regulation, NeoplasticAcetylationApoptosisCell Line, TumorCell MovementCell ProliferationGene Knockout TechniquesHumansMalePhosphatidylinositol 3-KinasesProstatic NeoplasmsProteomicsProto-Oncogene Proteins c-aktSignal TransductionSirtuinsAKT1 protein, humanPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktSIRT5 protein, humanSirtuinsIL-1BmetastasisPI3K/AKT pathwayProstate cancerSIRT5

Identifiers

PMID34949659
PMCPMC8717960
OpenAlexW4200387017

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.