Evidence map›Paper›PMID 33860796›Full record

ArticleBioscience reports2021

HDAC6 inhibitor WT161 performs anti-tumor effect on osteosarcoma and synergistically interacts with 5-FU.

Jun Sun, Wei Wu, Xiaofeng Tang, Feifei Zhang, Cheng Ju, Renfeng Liu, Yiping Liang, Bo Yu, Bin Lv, Yuhong Guo and 6 more

Open access · goldAbstract read
In one paragraph

Article in Bioscience reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

14 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. HDAC6: A unique HDAC family member as a cancer target.Cellular oncology (Dordrecht, Netherlands) · 2022
    Review
  11. Targeting HDAC6 to Overcome Autophagy-Promoted Anti-Cancer Drug Resistance.International journal of molecular sciences · 2022
    Review
  12. The roles of glycolysis in osteosarcoma.Frontiers in pharmacology · 2022
    Review
  13. Article
  14. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 4 institutions in 1 country.

Jun Sun *Jiangxi Key Laboratory of Cancer Metastasis and Precision Treatment, Center Laboratory, The Third Affiliated Hospital of Nanchang University, Nanchang 330008, China.
Wei Wu *Hubei Key Laboratory of Economic Forest Germplasm Improvement and Resources Comprehensive Utilization, Huanggang Normal University, Huangzhou, Hubei 438000, China.
Xiaofeng Tang *Jiangxi Key Laboratory of Cancer Metastasis and Precision Treatment, Center Laboratory, The Third Affiliated Hospital of Nanchang University, Nanchang 330008, China.
Feifei ZhangJiangxi Key Laboratory of Cancer Metastasis and Precision Treatment, Center Laboratory, The Third Affiliated Hospital of Nanchang University, Nanchang 330008, China.
Cheng JuJiangxi Key Laboratory of Cancer Metastasis and Precision Treatment, Center Laboratory, The Third Affiliated Hospital of Nanchang University, Nanchang 330008, China.
Renfeng LiuJiangxi Key Laboratory of Cancer Metastasis and Precision Treatment, Center Laboratory, The Third Affiliated Hospital of Nanchang University, Nanchang 330008, China.
Yiping LiangJiangxi Key Laboratory of Cancer Metastasis and Precision Treatment, Center Laboratory, The Third Affiliated Hospital of Nanchang University, Nanchang 330008, China.
Bo YuJiangxi Key Laboratory of Cancer Metastasis and Precision Treatment, Center Laboratory, The Third Affiliated Hospital of Nanchang University, Nanchang 330008, China.
Bin LvJiangxi Key Laboratory of Cancer Metastasis and Precision Treatment, Center Laboratory, The Third Affiliated Hospital of Nanchang University, Nanchang 330008, China.
Yuhong GuoJiangxi Key Laboratory of Cancer Metastasis and Precision Treatment, Center Laboratory, The Third Affiliated Hospital of Nanchang University, Nanchang 330008, China.
Duo ZengJiangxi Key Laboratory of Cancer Metastasis and Precision Treatment, Center Laboratory, The Third Affiliated Hospital of Nanchang University, Nanchang 330008, China.
Xuchang TaoDepartment of Nuclear Medicine, The Third Affiliated Hospital of Nanchang University, Nanchang 330008, China.
Min WangDepartment of Orthopedics, Tianjin General Hospital, Tianjin 300052, China.
Zhiping ZhangNanchang Key Laboratory of Orthopedics, The Third Affiliated Hospital of Nanchang University, Nanchang 330008, China.
Changhua ZhangCollege of Pharmacy, Jiangxi University of Traditional Chinese Medicine, Nanchang 330004, China.
Xiao-Bin LvJiangxi Key Laboratory of Cancer Metastasis and Precision Treatment, Center Laboratory, The Third Affiliated Hospital of Nanchang University, Nanchang 330008, China.
Nanchang University · CNJiangxi University of Traditional Chinese Medicine · CNHuanggang Normal University · CNTianjin Medical University General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWT161, as a selective HDAC6 inhibitor, has been shown to play anti-tumor effects on several kinds of cancers. The aim of the present study is to explore the roles of WT161 in osteosarcoma and its underlying mechanisms.

methodsThe anti-proliferative effect of WT161 on osteosarcoma cells was examined using MTT assay and colony formation assay. Cell apoptosis was analyzed using flow cytometer. The synergistic effect was evaluated by isobologram analysis using CompuSyn software. The osteosarcoma xenograft models were established to evaluate the anti-proliferative effect of WT161 in vivo.

resultsWT161 suppressed the cell growth and induced apoptosis of osteosarcoma cells in a dose- and time-dependent manner. Mechanistically, we found that WT161 treatment obviously increased the protein level of PTEN and decreased the phosphorylation level of protein kinase-B (AKT). More importantly, WT161 showed synergistic inhibition with 5-FU on osteosarcoma cells in vitro and in vivo.

conclusionsThese results indicate that WT161 inhibits the growth of osteosarcoma through PTEN and has a synergistic efficiency with 5-FU.

Indexed as

AnimalsAntineoplastic AgentsApoptosisCell Line, TumorCell ProliferationDrug SynergismFemaleFluorouracilHistone Deacetylase 6Histone Deacetylase InhibitorsHumansHydroxamic AcidsMiceMice, NudeOsteosarcomaProto-Oncogene Proteins c-aktAntineoplastic AgentsFluorouracilHDAC6 protein, humanHistone Deacetylase 6Histone Deacetylase InhibitorsHydroxamic AcidsProto-Oncogene Proteins c-aktPTEN PhosphohydrolaseTerphenyl CompoundsWT1615-FUapoptosisosteosarcomaPTENsynergistic inhibitionWT161

Identifiers

PMID33860796
PMCPMC8150159
OpenAlexW3138875952

What OpenQuestion holds

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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.