Evidence map›Paper›PMID 36076996›Full record

ReviewInternational journal of molecular sciences2022

Targeting HDAC6 to Overcome Autophagy-Promoted Anti-Cancer Drug Resistance.

Hyein Jo, Kyeonghee Shim, Dooil Jeoung

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

19 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
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  4. Review
  5. Role of HDAC6 in carcinomas.Discover oncology · 2026
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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

3 authors at 1 institution in 1 country.

Hyein JoDepartment of Biochemistry, College of Natural Sciences, Kangwon National University, Chuncheon 24341, Korea.
Kyeonghee ShimDepartment of Biochemistry, College of Natural Sciences, Kangwon National University, Chuncheon 24341, Korea.
Dooil JeoungDepartment of Biochemistry, College of Natural Sciences, Kangwon National University, Chuncheon 24341, Korea.
Kangwon National University · KR

Funding

National Research Foundation of Korea 2017M3A9G7072417National Research Foundation of Korea 2020R1A2C1006996National Research Foundation of Korea 2022R1F1A1060031National Research Foundation of Korea BK21 Plus Program
6 · The paper itself

Abstract

Histone deacetylases (HDACs) regulate gene expression through the epigenetic modification of chromatin structure. HDAC6, unlike many other HDACs, is present in the cytoplasm. Its deacetylates non-histone proteins and plays diverse roles in cancer cell initiation, proliferation, autophagy, and anti-cancer drug resistance. The development of HDAC6-specific inhibitors has been relatively successful. Mechanisms of HDAC6-promoted anti-cancer drug resistance, cancer cell proliferation, and autophagy are discussed. The relationship between autophagy and anti-cancer drug resistance is discussed. The effects of combination therapy, which includes HDAC6 inhibitors, on the sensitivity of cancer cells to chemotherapeutics and immune checkpoint blockade are presented. A summary of clinical trials involving HDAC6-specific inhibitors is also presented. This review presents HDAC6 as a valuable target for developing anti-cancer drugs.

Indexed as

Antineoplastic AgentsHistone Deacetylase InhibitorsAutophagyHistone Deacetylase 6Histone DeacetylasesAntineoplastic AgentsHistone Deacetylase 6Histone Deacetylase InhibitorsHistone Deacetylasesanti-cancer drug resistanceautophagyclinical trialscombination therapyHDAC6HDAC6 inhibitorsimmune checkpoint

Identifiers

PMID36076996
PMCPMC9455701
OpenAlexW4293000973

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.