Evidence map›Paper›PMID 31878360›Full record

ReviewCells2019

Heat Shock Proteins: Agents of Cancer Development and Therapeutic Targets in Anti-Cancer Therapy.

Chul Won Yun, Hyung Joo Kim, Ji Ho Lim, Sang Hun Lee

Abstract readReview
In one paragraph

Review in Cells, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 150 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
150citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

150 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Catechol-Proceedings of the National Academy of Sciences of the United States of America · 2026
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90 more citing papers are in PubMed but not listed here.

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

4 authors.

Chul Won YunMedical Science Research Institute, Soonchunhyang University Seoul Hospital, Seoul 04401, Korea.
Hyung Joo KimMedical Science Research Institute, Soonchunhyang University Seoul Hospital, Seoul 04401, Korea.
Ji Ho LimMedical Science Research Institute, Soonchunhyang University Seoul Hospital, Seoul 04401, Korea.
Sang Hun LeeMedical Science Research Institute, Soonchunhyang University Seoul Hospital, Seoul 04401, Korea.

Funding

National Research Foundation of Korea NRF-2016R1D1A3B01007727National Research Foundation of Korea NRF-2017M3A9B4032528
6 · The paper itself

Abstract

Heat shock proteins (HSPs) constitute a large family of molecular chaperones classified by their molecular weights, and they include HSP27, HSP40, HSP60, HSP70, and HSP90. HSPs function in diverse physiological and protective processes to assist in maintaining cellular homeostasis. In particular, HSPs participate in protein folding and maturation processes under diverse stressors such as heat shock, hypoxia, and degradation. Notably, HSPs also play essential roles across cancers as they are implicated in a variety of cancer-related activities such as cell proliferation, metastasis, and anti-cancer drug resistance. In this review, we comprehensively discuss the functions of HSPs in association with cancer initiation, progression, and metastasis and anti-cancer therapy resistance. Moreover, the potential utilization of HSPs to enhance the effects of chemo-, radio-, and immunotherapy is explored. Taken together, HSPs have multiple clinical usages as biomarkers for cancer diagnosis and prognosis as well as the potential therapeutic targets for anti-cancer treatment.

Indexed as

Cell ProliferationDrug Resistance, NeoplasmHeat-Shock ProteinsHSP40 Heat-Shock ProteinsHumansMolecular ChaperonesNeoplasm MetastasisNeoplasmsPrognosisProtein FoldingDNAJB1 protein, humanHeat-Shock ProteinsHSP40 Heat-Shock ProteinsHSPB1 protein, humanMolecular Chaperonescancer therapychemoresistanceheat shock proteinsimmunotherapyradiotherapy

Identifiers

PMID31878360
PMCPMC7017199

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.