Evidence map›Paper›PMID 34131805›Full record

ArticleBiotechnology letters2021

Differential expression of miRNAs and functional role of mir-200a in high and low productivity CHO cells expressing an Fc fusion protein.

Laura Bryan, Michael Henry, Niall Barron, Clair Gallagher, Ronan M Kelly, Christopher C Frye, Matthew D Osborne, Martin Clynes, Paula Meleady

Open access · hybridAbstract read
In one paragraph

Article in Biotechnology letters, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
0.3field-weighted citation impact, top 44% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

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

9 authors at 4 institutions in 2 countries.

Laura BryanNational Institute for Cellular Biotechnology, Dublin City University, Glasnevin, Dublin 9, Ireland. laura.bryan2@mail.dcu.ie.ORCID http://orcid.org/0000-0003-0013-137X
Michael HenryNational Institute for Cellular Biotechnology, Dublin City University, Glasnevin, Dublin 9, Ireland.
Niall BarronNational Institute for Bioprocessing Research and Training, Dublin 4, Ireland.
Clair GallagherNational Institute for Cellular Biotechnology, Dublin City University, Glasnevin, Dublin 9, Ireland.
Ronan M KellyEli Lilly and Company, LTC-North, 1200 Kentucky Avenue, Indianapolis, IN, 46225, USA.
Christopher C FryeEli Lilly and Company, LTC-North, 1200 Kentucky Avenue, Indianapolis, IN, 46225, USA.
Matthew D OsborneEli Lilly, Kinsale Limited, Cork, Ireland.
Martin ClynesNational Institute for Cellular Biotechnology, Dublin City University, Glasnevin, Dublin 9, Ireland.
Paula MeleadyNational Institute for Cellular Biotechnology, Dublin City University, Glasnevin, Dublin 9, Ireland.
Dublin City University · IEEli Lilly (United States) · USEli Lilly (Ireland) · IEUniversity College Dublin · IE

Funding

Irish Research Council for Science, Engineering and Technology EPSPG/2016/10Science Foundation Ireland 16/RI/3701
6 · The paper itself

Abstract

objectivesWe used miRNA and proteomic profiling to understand intracellular pathways that contribute to high and low specific productivity (Qp) phenotypes in CHO clonally derived cell lines (CDCLs) from the same cell line generation project.

resultsDifferentially expressed (DE) miRNAs were identified which are predicted to target several proteins associated with protein folding. MiR-200a was found to have a number of predicted targets associated with the unfolded protein response (UPR) which were shown to have decreased expression in high Qp CDCLs and have no detected change at the mRNA level. MiR-200a overexpression in a CHO CDCL was found to increase recombinant protein titer by 1.2 fold and Qp by 1.8 fold.

conclusionThese results may suggest a role for miR-200a in post-transcriptional regulation of the UPR, presenting miR-200a as a potential target for engineering industrially attractive CHO cell phenotypes.

Indexed as

Immunoglobulin Fc FragmentsMicroRNAsRecombinant Fusion ProteinsAnimalsCHO CellsCricetinaeCricetulusHumansProtein FoldingProteomicsImmunoglobulin Fc FragmentsMicroRNAsMIRN200 microRNA, humanRecombinant Fusion ProteinsBiopharmaceuticalsCell specific productivity (Qp)Chinese hamster ovary (CHO) cellsLabel free quantitative proteomicsMiRNA

Identifiers

PMID34131805
PMCPMC8254715
OpenAlexW3166232637

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.