Evidence map›Paper›PMID 31257493›Full record

ArticleMolecular medicine reports2019

SIRT6 regulates the proliferation and apoptosis of hepatocellular carcinoma via the ERK1/2 signaling pathway.

Cuisheng Zhang, Ying Yu, Qingxian Huang, Kun Tang

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

39 citing papers in PubMed, 62 citations in OpenAlex.

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  16. The sirtuin family in health and disease.Signal transduction and targeted therapy · 2022
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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

4 authors at 1 institution in 1 country.

Cuisheng ZhangDepartment of Hepatobiliary Surgery, Yuhuangding Hospital of Yantai, Yantai, Shandong 264000, P.R. China.
Ying YuDepartment of Vascular Surgery, Yuhuangding Hospital of Yantai, Yantai, Shandong 264000, P.R. China.
Qingxian HuangDepartment of Hepatobiliary Surgery, Yuhuangding Hospital of Yantai, Yantai, Shandong 264000, P.R. China.
Kun TangDepartment of Hepatobiliary Surgery, Yuhuangding Hospital of Yantai, Yantai, Shandong 264000, P.R. China.
Yuhuangding Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is the most common type of liver cancer, and exhibits a high mortality rate. Sirtuin (SIRT)6 is a member of the sirtuin family, which may be useful targets in the treatment of tumors. The present study aimed to explore the expression of SIRT6 in numerous HCC cell lines and investigate the role of SIRT6 in the proliferation and apoptosis of the HCC cells, and the underlying mechanisms. Overexpression and silencing of SIRT6 were performed by transfection of Huh‑7 cells with synthetic overexpression and small interfering RNA (siRNA) plasmids. Cell proliferation was evaluated using a Cell Counting Kit‑8 assay. The apoptosis rate was measured via flow cytometry. Cloning efficiency was assessed using plate clone formation assays. The expression of mRNAs and proteins were determined via reverse transcription‑quantitative PCR and western blot analyses, respectively. SIRT6 was overexpressed in Hep3B, Huh‑7, MHCC‑97H, MHCC‑97L, MHCC‑LM6, MHCC‑LM3, YY‑8103 and SK‑hep‑1 cell lines, compared with MIHA and HL‑7702 normal liver cell lines. Overexpression of SIRT6 increased the proliferation of Huh‑7 cells, upregulated the expression of Bcl‑2 and phosphorylation of extracellular‑signal regulated protein kinase (ERK), and decreased the expression of cleaved‑caspase‑3 and Bcl‑2‑associated X protein (Bax) in Huh‑7 cells. siRNA‑mediated silencing of SIRT6 decreased the proliferation and increased the apoptosis of Huh‑7 cells, downregulated the expression of Bcl‑2 and phosphorylated‑ERK, and promoted the expression of cleaved‑caspase‑3 and Bax. The proliferation of Huh‑7 cells was decreased using the ERK1/2 inhibitor U0126. The results suggested that SIRT6 affected the proliferation and apoptosis of HCC cells via the regulation of the ERK1/2 pathway, altering the activation of the intrinsic apoptosis pathway. SIRT6 may be a potential target for the treatment of HCC; however, its role requires further investigation.

Indexed as

Gene Expression Regulation, NeoplasticApoptosisbcl-2-Associated X ProteinCell Line, TumorCell MovementCell ProliferationClone CellsHepatocytesHumansMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Proto-Oncogene Proteins c-bcl-2RNA, MessengerRNA, Small InterferingSignal TransductionSirtuinsBAX protein, humanbcl-2-Associated X ProteinBCL2 protein, humanMAPK1 protein, humanMAPK3 protein, humanMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Proto-Oncogene Proteins c-bcl-2RNA, MessengerRNA, Small InterferingSIRT6 protein, humanSirtuins

Identifiers

PMID31257493
PMCPMC6625461
OpenAlexW2952901180

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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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.