Evidence map›Paper›PMID 30843645›Full record

ArticleCancer science2019

Heat shock factor 1 in cancer-associated fibroblasts is a potential prognostic factor and drives progression of oral squamous cell carcinoma.

Qiong Wang, Yu-Chao Zhang, Li-Fang Zhu, Lu Pan, Miao Yu, Wei-Li Shen, Bang Li, Wei Zhang, Lai-Kui Liu

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 2 pooled it
0.8field-weighted citation impact, top 30% 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

11 citing papers in PubMed, 2 syntheses or guidelines pooled it, 16 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Heat Shock Proteins and HSF1 in Cancer.Frontiers in oncology · 2022
    Review
  9. Review
  10. Review
  11. 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 3 institutions in 1 country.

Qiong WangJiangsu Key Laboratory of Oral Diseases, Nanjing Medical University, Nanjing, China.
Yu-Chao ZhangJiangsu Key Laboratory of Oral Diseases, Nanjing Medical University, Nanjing, China.
Li-Fang ZhuJiangsu Key Laboratory of Oral Diseases, Nanjing Medical University, Nanjing, China.
Lu PanJiangsu Key Laboratory of Oral Diseases, Nanjing Medical University, Nanjing, China.
Miao YuJiangsu Key Laboratory of Oral Diseases, Nanjing Medical University, Nanjing, China.
Wei-Li ShenJiangsu Key Laboratory of Oral Diseases, Nanjing Medical University, Nanjing, China.
Bang LiJiangsu Key Laboratory of Oral Diseases, Nanjing Medical University, Nanjing, China.
Wei ZhangJiangsu Key Laboratory of Oral Diseases, Nanjing Medical University, Nanjing, China.
Lai-Kui LiuJiangsu Key Laboratory of Oral Diseases, Nanjing Medical University, Nanjing, China.ORCID https://orcid.org/0000-0002-6509-922X
Stomatology Hospital · CNNanjing Medical University · CNSoochow University · CN

Funding

Key Project of Health Department of Jiangsu Province CXTDA2017036Natural Science Foundation of Jiangsu Province BK20171483Priority Academic Program Development of Jiangsu Higher Education Institutions PAPD, 2018-87
6 · The paper itself

Abstract

Heat shock factor 1 (HSF1) is highly expressed in various malignancies and is a potential modulator of tumor progression. Emerging evidence suggests that HSF1 activation in stromal cells is closely related to poor patient prognosis. However, the role of HSF1 in oral squamous cell carcinoma (OSCC) remains elusive. We aimed to investigate the function of HSF1 in cancer-associated fibroblasts (CAFs) of the tumor microenvironment (TME) and in tumor development. In the present study, we found that HSF1 was highly expressed in both CAFs and tumor cells, and was significantly correlated with poor prognosis and overall survival. Moreover, HSF1 overexpression in CAFs resulted in a fibroblast-like phenotype of Cal27 cells, induced epithelial-mesenchymal transition (EMT), and promoted proliferation, migration and invasion in Cal27 cells. HSF1 knockdown attenuated features of CAFs and reduced EMT, proliferation, migration and invasion in Cal27 cells. Furthermore, HSF1 in CAFs promoted tumor growth in nude mice. Taken together, these data suggest that HSF1 expression in CAFs drive OSCC progression, and could serve as an independent prognostic marker of patients with OSCC. Thus, HSF1 is a potent mediator of OSCC malignancy.

Indexed as

Up-RegulationAdultAgedAged, 80 and overAnimalsCancer-Associated FibroblastsCarcinoma, Squamous CellCell MovementCell ProliferationEpithelial-Mesenchymal TransitionFemaleGene Expression Regulation, NeoplasticHeat Shock Transcription FactorsHumansMaleMice, NudeHeat Shock Transcription FactorsHSF1 protein, humancancer-associated fibroblastheat shock factor 1invasionmigrationoral squamous cell carcinoma

Identifiers

PMID30843645
PMCPMC6501034
OpenAlexW2921091531

What OpenQuestion holds

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LicenceCC BY-NC
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.