Evidence map›Paper›PMID 31766290›Full record

ArticleCancers2019

Histone Demethylase KDM4C Stimulates the Proliferation of Prostate Cancer Cells via Activation of AKT and c-Myc.

Ching-Yu Lin, Bi-Juan Wang, Bo-Chih Chen, Jen-Chih Tseng, Shih Sheng Jiang, Kelvin K Tsai, Ying-Ying Shen, Chiou Hwa Yuh, Zong-Lin Sie, Wen-Ching Wang and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.2field-weighted citation impact, top 11% 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

21 citing papers in PubMed, 41 citations in OpenAlex.

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  8. Association ofmedRxiv : the preprint server for health sciences · 2023
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  18. KDM4C contributes to cytarabine resistance in acute myeloid leukemiaTherapeutic advances in chronic disease · 2021
    Article
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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 4 institutions in 1 country.

Ching-Yu LinInstitute of Cellular and System Medicine, National Health Research Institutes, Miaoli 35053, Taiwan.
Bi-Juan WangInstitute of Cellular and System Medicine, National Health Research Institutes, Miaoli 35053, Taiwan.
Bo-Chih ChenInstitute of Cellular and System Medicine, National Health Research Institutes, Miaoli 35053, Taiwan.
Jen-Chih TsengInstitute of Cellular and System Medicine, National Health Research Institutes, Miaoli 35053, Taiwan.
Shih Sheng JiangNation Institute of Cancer Research, National Health Research Institutes, Miaoli 35053, Taiwan.ORCID 0000-0003-1909-437X
Kelvin K TsaiNation Institute of Cancer Research, National Health Research Institutes, Miaoli 35053, Taiwan.ORCID 0000-0002-1612-2868
Ying-Ying ShenPathology Core Lab, National Health Research Institutes, Miaoli 35053, Taiwan.
Chiou Hwa YuhInstitute of Molecular and Genomic Medicine, National Health Research Institutes, Miaoli 35053, Taiwan.ORCID 0000-0002-2356-1551
Zong-Lin SieInstitute of Molecular and Genomic Medicine, National Health Research Institutes, Miaoli 35053, Taiwan.
Wen-Ching WangInstitute of Molecular & Cellular Biology, National Tsing Hua University, Hsinchu 300, Taiwan.
Hsing-Jien KungGraduate Institute of Cancer Biology and Drug Discovery, Taipei Medical University, Taipei 110, Taiwan.
Chih-Pin ChuuInstitute of Cellular and System Medicine, National Health Research Institutes, Miaoli 35053, Taiwan.
National Health Research Institutes · TWNational Chung Hsing University · TWNational Tsing Hua University · TWTaipei Medical University · TW

Funding

Ministry of Science and Technology, Taiwan MOST 108-2314-B-400-021, MOST 107-2314-B-400-002, MOST 106-2314-B-400-006, MOST 105-2314-B-400-020, MOST 104-2321-B-400-010National Health Research Institutes CS-106-PP-03, CA-106-SP-01, and CS-106-SP-05
6 · The paper itself

Abstract

Our three-dimensional organotypic culture revealed that human histone demethylase (KDM) 4C, a histone lysine demethylase, hindered the acini morphogenesis of RWPE-1 prostate cells, suggesting its potential oncogenic role. Knockdown (KD) of KDM4C suppressed cell proliferation, soft agar colony formation, and androgen receptor (AR) transcriptional activity in PCa cells as well as reduced tumor growth of human PCa cells in zebrafish xenotransplantation assay. Micro-Western array (MWA) analysis indicated that KD of KDM4C protein decreased the phosphorylation of AKT, c-Myc, AR, mTOR, PDK1, phospho-PDK1 S241, KDM8, and proteins involved in cell cycle regulators, while it increased the expression of PTEN. Fluorescent microscopy revealed that KDM4C co-localized with AR and c-Myc in the nuclei of PCa cells. Overexpression of either AKT or c-Myc rescued the suppressive effect of KDM4C KD on PCa cell proliferation. Echoing the above findings, the mRNA and protein expression of KDM4C was higher in human prostate tumor tissues as compared to adjacent normal prostate tissues, and higher KDM4C protein expression in prostate tumors correlated to higher protein expression level of AKT and c-Myc. In conclusion, KDM4C promotes the proliferation of PCa cells via activation of c-Myc and AKT.

Indexed as

AKTc-MycKDM4CMicro-Western Arrayprostate cancer

Identifiers

PMID31766290
PMCPMC6896035
OpenAlexW2987161880

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.