Evidence map›Paper›PMID 40611689›Full record

ArticleBiotechnology journal2025

Transcriptomic Insights Into Serum-Free Medium Adaptation and Temperature Reduction in Chinese Hamster Ovary Cell Cultures.

Benjamin F Synoground, Yogender Gowtham, Timothy Lindquist, Junessa Pressley, Derrick C Scott, Christopher S Saski, Sarah W Harcum

Abstract read
In one paragraph

Article in Biotechnology journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Research progress on BTG2 in non‑tumor diseases (Review).International journal of molecular medicine · 2026
    Review
  2. Review
  3. Article
  4. Highly efficient production of HIV-1Journal of virology · 2025
    Article
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

7 authors.

Benjamin F SynogroundDepartment of Bioengineering, Clemson University, Clemson, South Carolina, USA.
Yogender GowthamDepartment of Bioengineering, Clemson University, Clemson, South Carolina, USA.
Timothy LindquistDepartment of Bioengineering, Clemson University, Clemson, South Carolina, USA.
Junessa PressleyDepartment of Biological Sciences, Delaware State University, Dover, Delaware, USA.
Derrick C ScottDepartment of Biological Sciences, Delaware State University, Dover, Delaware, USA.
Christopher S SaskiDepartment of Plant and Environmental Sciences, Clemson University, Clemson, South Carolina, USA.
Sarah W HarcumDepartment of Bioengineering, Clemson University, Clemson, South Carolina, USA.ORCID https://orcid.org/0000-0001-9417-0489

Funding

US National Science Foundation CBET-1218345US National Science Foundation EEC-2100442US National Science Foundation IIP-1624641US National Science Foundation OIA-1736123
6 · The paper itself

Abstract

Chinese hamster ovary (CHO) cells are widely used in recombinant biopharmaceutical production; yet, yields remain low, leading to high market prices. Improving product yield and quality has heavily relied on empirical characterization with limited insight into internal molecular dynamics. RNA-seq offers a powerful alternative to understand intracellular responses to process changes through gene expression measurement. In this study, three RNA-seq datasets across three CHO cell lines and four industrially relevant treatments were integrated to characterize the global transcriptome changes, construct a weighted gene co-expression network, assess the impact on recombinant anti-interleukin 8 (anti-IL8) immunoglobulin heavy and light chain transcript abundance, and expression of glycosylation genes. Treatments included adaptation to serum-free medium, low temperature, low pH, and low glucose concentration in the medium. The findings suggest upregulation of cholesterol biosynthesis is critical for serum-free medium adaptation, and the rate-limiting enzymes in the sterol regulatory element-binding protein pathway (Insig1 and Srebf2) could be targeted to accelerate adaptation. Temperature-induced cell cycle suppression was likely mediated by p53 activation, consistent with previous reports, with the p53-targets, Zmat3 and Btg2, identified as key hub genes. Conversely, glucose and pH were observed to have negligible impacts on the transcriptome. This study uniquely identifies novel genes mediating temperature-induced cell cycle arrest, distinct glycosylation-related gene responses impacting product quality, and new stable housekeeping genes for accurate gene expression normalization in CHO cells.

Indexed as

TranscriptomeAdaptation, PhysiologicalAnimalsCell Culture TechniquesCHO CellsCricetinaeCricetulusCulture Media, Serum-FreeGene Expression ProfilingGlucoseGlycosylationTemperatureCulture Media, Serum-FreeGlucosecholesterol metabolismco‐expression analysisgene expressionRNA‐Seqsterol regulatory element‐binding proteins

Identifiers

PMID40611689
PMCPMC12232170

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.