Evidence map›Paper›PMID 27626679›Full record

ArticleOncotarget2016

HSPB1 deficiency sensitizes melanoma cells to hyperthermia induced cell death.

He-Xiao Wang, Yang Yang, Hao Guo, Dian-Dong Hou, Song Zheng, Yu-Xiao Hong, Yun-Fei Cai, Wei Huo, Rui-Qun Qi, Li Zhang and 2 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.7field-weighted citation impact, top 25% 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

10 citing papers in PubMed, 20 citations in OpenAlex.

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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

12 authors at 2 institutions in 1 country.

He-Xiao WangDepartment of Dermatology, The First Hospital of China Medical University, Shenyang 110001, P.R. China.
Yang YangDepartment of Dermatology, The First Hospital of China Medical University, Shenyang 110001, P.R. China.
Hao GuoDepartment of Dermatology, The First Hospital of China Medical University, Shenyang 110001, P.R. China.
Dian-Dong HouDepartment of Dermatology, The First Hospital of China Medical University, Shenyang 110001, P.R. China.
Song ZhengDepartment of Dermatology, The First Hospital of China Medical University, Shenyang 110001, P.R. China.
Yu-Xiao HongDepartment of Dermatology, The First Hospital of China Medical University, Shenyang 110001, P.R. China.
Yun-Fei CaiDepartment of Dermatology, The First Hospital of China Medical University, Shenyang 110001, P.R. China.
Wei HuoDepartment of Dermatology, The First Hospital of China Medical University, Shenyang 110001, P.R. China.
Rui-Qun QiDepartment of Dermatology, The First Hospital of China Medical University, Shenyang 110001, P.R. China.
Li ZhangDepartment of Dermatology, The First Hospital of China Medical University, Shenyang 110001, P.R. China.
Hong-Duo ChenDepartment of Dermatology, The First Hospital of China Medical University, Shenyang 110001, P.R. China.
Xing-Hua GaoDepartment of Dermatology, The First Hospital of China Medical University, Shenyang 110001, P.R. China.
China Medical University · CNFirst Hospital of China Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hyperthermia has shown clinical potency as a single agent or as adjuvant to other therapies in cancer treatment. However, thermotolerance induced by thermosensitive genes such as the heat shock proteins can limit the efficacy of hyperthermic treatment. In the present study, we identified HSPB1 (HSP27) is hyperthermically inducible or endogenously highly expressed in both murine and human melanoma cell lines. We used a siRNA strategy to reduce HSPB1 levels and showed increased intolerance to hyperthermia via reduced cell viability and/or proliferation of cells. In the investigation of underlying mechanisms, we found knock down of HSPB1 further increased the proportion of apoptotic cells in hyperthermic treated melanoma cells when compared with either single agent alone, and both agents leaded to cell cycle arrest at G0/G1 or G2/M phases. We concluded that hyperthermia combined with silencing of HSPB1 enhanced cell death and resulted in failure to thrive in melanoma cell lines, implying the potential clinical utility of hyperthermia in combination with HSPB1 inhibition in cancer treatment.

Indexed as

Hyperthermia, InducedAnimalsApoptosisCell Line, TumorCell SurvivalGene Knockdown TechniquesHeat-Shock ProteinsHSP27 Heat-Shock ProteinsHumansMelanomaMiceMolecular ChaperonesNeoplasm ProteinsHeat-Shock ProteinsHsbp1 protein, mouseHSP27 Heat-Shock ProteinsHSPB1 protein, humanMolecular ChaperonesNeoplasm Proteinscombination strategyHSPB1hyperthermiamelanomathermotolerance

Identifiers

PMID27626679
PMCPMC5341888
OpenAlexW2510002246

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.