Evidence map›Paper›PMID 27600495›Full record

ArticleInternational journal of oncology2016

Heat shock protein 27 is a potential indicator for response to YangZheng XiaoJi and chemotherapy agents in cancer cells.

Sioned Owen, Huishan Zhao, Alwyn Dart, Yamei Wang, Fiona Ruge, Yong Gao, Cong Wei, Yiling Wu, Wen G Jiang

Open access · hybridAbstract read
In one paragraph

Article in International journal of oncology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

8 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Expression of Heat Shock Protein-27 (Hsp27) and P38MAPK in Esophageal Squamous Cell Carcinoma.Medical science monitor : international medical journal of experimental and clinical research · 2017
    Article
  8. Article
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 2 institutions in 2 countries.

Sioned OwenCardiff China Medical Research Collaborative, Cardiff University School of Medicine, Cardiff, UK.
Huishan ZhaoCardiff China Medical Research Collaborative, Cardiff University School of Medicine, Cardiff, UK.
Alwyn DartCardiff China Medical Research Collaborative, Cardiff University School of Medicine, Cardiff, UK.
Yamei WangCardiff China Medical Research Collaborative, Cardiff University School of Medicine, Cardiff, UK.
Fiona RugeCardiff China Medical Research Collaborative, Cardiff University School of Medicine, Cardiff, UK.
Yong GaoYiling Medical Research Institute, Shijiazhuang, Hebei, P.R. China.
Cong WeiYiling Medical Research Institute, Shijiazhuang, Hebei, P.R. China.
Yiling WuYiling Medical Research Institute, Shijiazhuang, Hebei, P.R. China.
Wen G JiangCardiff China Medical Research Collaborative, Cardiff University School of Medicine, Cardiff, UK.
Cardiff University · GBHebei Yiling Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Heat shock protein 27 (HSP27) is a member of the heat shock protein family which has been linked to tumour progression and, most interestingly, to chemotherapy resistance in cancer patients. The present study examined the potential interplay between HSP27 and YangZheng XiaoJi, a traditional Chinese medicine used in cancer treatment. A range of cell lines from different tumour types including pancreatic, lung, gastric, colorectal, breast, prostate and ovarian cancer (both wild-type and resistant) were used. Levels and activation of HSP27 and its potential associated signalling pathways were evaluated by protein array and western blotting. Knockdown of HSP27 in cancer cells was achieved using siRNA. Localisation and co-localisation of HSP27 and other proteins were carried out by immunofluorescence. Cell growth and migration were evaluated in their response to a range of chemotherapeutic agents. The present study first identified, by way of protein array, that YangZheng XiaoJi was able to inhibit the phosphorylation of HSP27 protein in cancer cells. We further demonstrated that HSP27, which is co-localised with caspase-9, can be blocked from localising in focal adhesions and co-localising with caspase-9 by YangZheng XiaoJi. The study also demonstrated that YangZheng XiaoJi was able to sensitise cancer cells including those cells that were resistant to chemotherapy, to chemotherapeutic agents. Finally, knocking down HSP27 markedly reduced the migration of cancer cells and increased the sensitivity of cancer cells to the inhibitory effect on cellular migration by YangZheng XiaoJi. YangZheng XiaoJi can act as an agent in first sensitising cancer cells to chemotherapy and secondly to overcome, to some degree, chemoresistance when used in an appropriate fashion in patients who have active HSP27.

Indexed as

Antineoplastic AgentsApoptosisBlotting, WesternCaspase 9Cell MovementCell ProliferationDrug Resistance, NeoplasmDrugs, Chinese HerbalFluorescent Antibody TechniqueHeat-Shock ProteinsHSP27 Heat-Shock ProteinsHumansMolecular ChaperonesNeoplasmsPhosphorylationPlant ExtractsAntineoplastic AgentsCaspase 9Drugs, Chinese HerbalHeat-Shock ProteinsHSP27 Heat-Shock ProteinsHSPB1 protein, humanMolecular ChaperonesPlant ExtractsRNA, Small Interferingyangzheng xiaoji

Identifiers

PMID27600495
PMCPMC5063420
OpenAlexW2515585752

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.