Evidence map›Paper›PMID 39292268›Full record

ArticleApplied microbiology and biotechnology2024

A novel dual-epigenetic inhibitor enhances recombinant monoclonal antibody expression in CHO cells.

Ming-Ming Han, Hai-Tong Wang, Hui-Jie Zhang, Jiang-Tao Lu, Jia-Liang Guo, Le-Le Qiu, Xi Zhang, Xiao-Yin Wang, Tian-Yun Wang, Yan-Long Jia

Abstract read
In one paragraph

Article in Applied microbiology and biotechnology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–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

2 citing papers in PubMed.

  1. Article
  2. Cell Engineering for Increasing Production of Recombinant Proteins in Mammalian Cells.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2026
    Review
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

10 authors.

Ming-Ming HanSchool of Pharmacy, Xinxiang Medical University, Xinxiang, 453003, Henan, China.
Hai-Tong WangSchool of Pharmacy, Xinxiang Medical University, Xinxiang, 453003, Henan, China.
Hui-Jie ZhangSchool of Pharmacy, Xinxiang Medical University, Xinxiang, 453003, Henan, China.
Jiang-Tao LuSchool of Pharmacy, Xinxiang Medical University, Xinxiang, 453003, Henan, China.
Jia-Liang GuoJunji College, Xinxiang Medical University, Xinxiang, 453003, Henan, China.
Le-Le QiuSchool of Basic Medicine, Xinxiang Medical University, Xinxiang, 453003, Henan, China.
Xi ZhangSchool of Pharmacy, Xinxiang Medical University, Xinxiang, 453003, Henan, China.
Xiao-Yin WangInternational Joint Research Laboratory for Recombinant Pharmaceutical Protein Expression System of Henan, Xinxiang Medical University, Xinxiang, 453003, Henan, China.
Tian-Yun WangInternational Joint Research Laboratory for Recombinant Pharmaceutical Protein Expression System of Henan, Xinxiang Medical University, Xinxiang, 453003, Henan, China. wtianyuncn@126.com.
Yan-Long JiaSchool of Pharmacy, Xinxiang Medical University, Xinxiang, 453003, Henan, China. yanlongjia@126.com.ORCID http://orcid.org/0000-0002-1462-8902

Funding

Henan Provincial Science and Technology Research Project 232102310309Key Research & Development Projects of Henan Province 241111313000National Natural Science Foundation of China 32071468National Natural Science Foundation of China U23A20270Natural Science Foundation of Henan Province 232300421115Project of Technology Innovation Leading Talent in Central Plain 234200510003the National Training Program of Innovation and Entrepreneurship for Undergraduates of Xinxiang Medical University 202310472014
6 · The paper itself

Abstract

Epigenetic regulation plays a central role in the regulation of a number of cellular processes such as proliferation, differentiation, cell cycle, and apoptosis. In particular, small molecule epigenetic modulators are key elements that can effectively influence gene expression by precisely regulating the epigenetic state of cells. To identify useful small-molecule regulators that enhance the expression of recombinant proteins in Chinese hamster ovary (CHO) cells, we examined a novel dual-HDAC/LSD1 inhibitor I-4 as a supplement for recombinant CHO cells. Treatment with 2 μM I-4 was most effective in increasing monoclonal antibody production. Despite cell cycle arrest at the G1/G0 phase, which inhibits cell growth, the addition of the inhibitor at 2 µM to monoclonal antibody-expressing CHO cell cultures resulted in a 1.94-fold increase in the maximal monoclonal antibody titer and a 2.43-fold increase in specific monoclonal antibody production. In addition, I-4 significantly increased the messenger RNA levels of the monoclonal antibody and histone H3 acetylation and methylation levels. We also investigated the effect on HDAC-related isoforms and found that interference with the HDAC5 gene increased the monoclonal antibody titer by 1.64-fold. The results of this work provide an effective method of using epigenetic regulatory strategies to enhance the expression of recombinant proteins in CHO cells. KEY POINTS: • HDAC/LSD1 dual-target small molecule inhibitor can increase the expression level of recombinant monoclonal antibodies in CHO cells. • By affecting the acetylation and methylation levels of histones in CHO cells and downregulating HDAC5, the production of recombinant monoclonal antibodies increased. • It provides an effective pathway for applying epigenetic regulation strategies to enhance the expression of recombinant proteins.

Indexed as

Antibodies, MonoclonalCricetulusEpigenesis, GeneticRecombinant ProteinsAcetylationAnimalsCHO CellsCricetinaeHistone Deacetylase InhibitorsHistone DeacetylasesHistonesMethylationAntibodies, MonoclonalHistone Deacetylase InhibitorsHistone DeacetylasesHistonesRecombinant ProteinsAcetylation modificationCHO cellsEpigenetic regulationRecombinant protein expressionSmall molecule additives

Identifiers

PMID39292268
PMCPMC11411004

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.