Evidence map›Paper›PMID 28152343›Full record

ArticleNucleus (Austin, Tex.)2017

Transcriptomes reflect the phenotypes of undifferentiated, granulocyte and macrophage forms of HL-60/S4 cells.

David B Mark Welch, Anna Jauch, Jörg Langowski, Ada L Olins, Donald E Olins

Open access · goldAbstract read
In one paragraph

Article in Nucleus (Austin, Tex.), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.3field-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

13 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. Nuclear Pore Complexes in Various States of HL-60/S4 Cells.bioRxiv : the preprint server for biology · 2026
    Article
  4. Article
  5. Article
  6. Imidazo[1,2-International journal of molecular sciences · 2020
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Defining the epichromatin epitope.Nucleus (Austin, Tex.) · 2017
    Article
  13. 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

5 authors at 4 institutions in 2 countries.

David B Mark Welcha Josephine Bay Paul Center for Comparative Molecular Biology and Evolution , Marine Biological Laboratory , Woods Hole , MA , USA.
Anna Jauchb Institute of Human Genetics, University of Heidelberg , Heidelberg , Germany.
Jörg Langowskic Division Biophysics of Macromolecules, B040 , German Cancer Research Center (DKFZ), TP3 , Heidelberg , Germany.
Ada L Olinsd University of New England, College of Pharmacy , Department of Pharmaceutical Sciences , Portland , ME , USA.
Donald E Olinsd University of New England, College of Pharmacy , Department of Pharmaceutical Sciences , Portland , ME , USA.
Heidelberg University · DEMarine Biological Laboratory · USNew England College · USUniversity of New England · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To understand the chromatin changes underlying differential gene expression during induced differentiation of human leukemic HL-60/S4 cells, we conducted RNA-Seq analysis on quadruplicate cultures of undifferentiated, granulocytic- and macrophage-differentiated cell forms. More than half of mapped genes exhibited altered transcript levels in the differentiated cell forms. In general, more genes showed increased mRNA levels in the granulocytic form and in the macrophage form, than showed decreased levels. The majority of Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways were significantly enriched in genes that exhibited differential transcript levels after either RA or TPA treatment. Changes in transcript levels for groups of genes with characteristic protein phenotypes, such as genes encoding cytoplasmic granular proteins, nuclear envelope and cytoskeletal proteins, cell adhesion proteins, and proteins involved in the cell cycle and apoptosis illustrate the profound differences among the various cell states. In addition to the transcriptome analyses, companion karyotyping by M-FISH of undifferentiated HL-60/S4 cells revealed a plethora of chromosome alterations, compared with normal human cells. The present mRNA profiling provides important information related to nuclear shape changes (e.g., granulocyte lobulation), deformability of the nuclear envelope and linkage between the nuclear envelope and cytoskeleton during induced myeloid chromatin differentiation.

Indexed as

PhenotypeTranscriptomeApoptosisCell AdhesionCell CycleCell DifferentiationCytoskeletal ProteinsGranulocytesHL-60 CellsHumansMacrophagesNuclear EnvelopePhorbol EstersRNA, MessengerTretinoinCytoskeletal ProteinsPhorbol EstersRNA, MessengerTretinoinAcute myeloid leukemaapoptosiscell attachmentcell differentiationcell divisioncytoskeletongranulocytekaryotypemacrophagemRNA levelsnuclear envelope

Identifiers

PMID28152343
PMCPMC5403136
OpenAlexW2585615819

What OpenQuestion holds

Textmetadata
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.