Evidence map›Paper›PMID 28737827›Full record

ArticleOncology reports2017

Cytotoxic and chemosensitization effects of Scutellarin from traditional Chinese herb Scutellaria altissima L. in human prostate cancer cells.

Chen Gao, Yinglu Zhou, Zhongling Jiang, Yuan Zhao, Dongjun Zhang, Xia Cong, Rongfeng Cao, Huatao Li, Wenru Tian

Open access · hybridAbstract read
In one paragraph

Article in Oncology reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
5.0field-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

23 citing papers in PubMed, 58 citations in OpenAlex.

  1. Article
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  4. Review
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  8. Article
  9. Autophagy Induction byPharmaceuticals (Basel, Switzerland) · 2023
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Combined Scutellarin and CFrontiers in oncology · 2021
    Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. Review
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

9 authors at 1 institution in 1 country.

Chen GaoCollege of Animal Science and Veterinary Medicine, Qingdao Agricultural University, Qingdao, Shandong 266109, P.R. China.
Yinglu ZhouCollege of Animal Science and Veterinary Medicine, Qingdao Agricultural University, Qingdao, Shandong 266109, P.R. China.
Zhongling JiangCollege of Animal Science and Veterinary Medicine, Qingdao Agricultural University, Qingdao, Shandong 266109, P.R. China.
Yuan ZhaoShu Lan Animal Husbandry Bureau, Shulan, Jilin 132600, P.R. China.
Dongjun ZhangFeicheng Animal Husbandry and Veterinary Bureau, Feicheng, Shandong 271600, P.R. China.
Xia CongCollege of Animal Science and Veterinary Medicine, Qingdao Agricultural University, Qingdao, Shandong 266109, P.R. China.
Rongfeng CaoCollege of Animal Science and Veterinary Medicine, Qingdao Agricultural University, Qingdao, Shandong 266109, P.R. China.
Huatao LiCollege of Animal Science and Veterinary Medicine, Qingdao Agricultural University, Qingdao, Shandong 266109, P.R. China.
Wenru TianCollege of Animal Science and Veterinary Medicine, Qingdao Agricultural University, Qingdao, Shandong 266109, P.R. China.
Qingdao Agricultural University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Scutellaria altissima L. is a common traditional Chinese medicine used to treat inflammation in some countries. Scutellarin, an active major flavone glycoside isolated from the traditional Chinese medicine Scutellaria altissima L., has been shown to offer various beneficial biochemical effects on cerebrovascular diseases and inflammation. However, the antiproliferative effects of Scutellarin in prostate cancer and the underlying mechanism are not fully elucidated. In the present study, we aimed to ascertain whether Scutellarin inhibits cancer cell growth and to further explore the molecular mechanism. Scutellarin enhanced the sensitivity of prostate cancer cells to cisplatin. MTT assays revealed that cell viability was significantly decreased in the prostate cancer cells treated with Scutellarin. Flow cytometric analysis indicated that Scutellarin suppressed cell proliferation by promoting G2/M arrest and inducing apoptosis. We employed western blotting to delineate the underlying mechanisms involved in the G2/M arrest and apoptosis. Comet assay and γH2AX immunocytochemistry were used to detect levels of DNA damage in PC3 cells exposed to Scutellarin and/or cisplatin. Our data revealed that Scutellarin significantly induced prostate cancer cell apoptosis by activating the caspase cascade. An increase in the Bax/Bcl-2 ratio, depolarization of mitochondrial membrane potential and cell cycle arrest at G2/M phase were accompanied by the apoptosis induction. Additionally, Scutellarin altered the protein expression of cell cycle and apoptosis regulatory genes by downregulating Cdc2, cyclin B1 and Bcl-2 and upregulating caspase-3, caspase-9 and Bax in prostate cancer cells. Furthermore, Scutellarin sensitized PC3 cells to cisplastin treatment in a dose-dependent manner. Taken together, our data confirmed the cytotoxicity of Scutellarin against prostate cancer PC3 cells and provide new findings in regards to Scutellarin sensitizing prostate cancer cells to chemotherapy. Our findings suggest that Scutellarin has potential to be used as a novel antineoplastic therapeutic candidate for prostate cancer patients.

Indexed as

ApigeninApoptosisCDC2 Protein KinaseCell Cycle CheckpointsCell Line, TumorCell ProliferationCyclin B1CytotoxinsDrug Resistance, NeoplasmDrugs, Chinese HerbalFlow CytometryGene Expression Regulation, NeoplasticGlucuronatesHumansMaleProstatic NeoplasmsApigeninCDC2 Protein KinaseCDK1 protein, humanCyclin B1CytotoxinsDrugs, Chinese HerbalGlucuronatesProto-Oncogene Proteins c-bcl-2scutellarin

Identifiers

PMID28737827
PMCPMC5549025
OpenAlexW2737284239

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.