Evidence map›Paper›PMID 33213097›Full record

ArticleBiomolecules2020

Transcriptional Profiling Reveals Ribosome Biogenesis, Microtubule Dynamics and Expression of Specific lncRNAs to be Part of a Common Response to Cell-Penetrating Peptides.

Tomas Venit, Moataz Dowaidar, Maxime Gestin, Syed Raza Mahmood, Ülo Langel, Piergiorgio Percipalle

Open access · goldAbstract read
In one paragraph

Article in Biomolecules, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

5 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Review
  3. New approaches to moderate CRISPR-Cas9 activity: Addressing issues of cellular uptake and endosomal escape.Molecular therapy : the journal of the American Society of Gene Therapy · 2022
    Review
  4. Review
  5. 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

6 authors at 2 institutions in 3 countries.

Tomas VenitScience Division, Biology Program, New York University Abu Dhabi (NYUAD), Abu Dhabi P.O. Box 129188, UAE.
Moataz DowaidarDepartment of Biochemistry and Biophysics, Stockholm University, Svante Arrhenius väg 16B, SE-106 91 Stockholm, Sweden.ORCID 0000-0002-6189-3020
Maxime GestinDepartment of Biochemistry and Biophysics, Stockholm University, Svante Arrhenius väg 16B, SE-106 91 Stockholm, Sweden.
Syed Raza MahmoodScience Division, Biology Program, New York University Abu Dhabi (NYUAD), Abu Dhabi P.O. Box 129188, UAE.ORCID 0000-0003-3418-1383
Ülo LangelDepartment of Biochemistry and Biophysics, Stockholm University, Svante Arrhenius väg 16B, SE-106 91 Stockholm, Sweden.
Piergiorgio PercipalleScience Division, Biology Program, New York University Abu Dhabi (NYUAD), Abu Dhabi P.O. Box 129188, UAE.
Stockholm University · SENew York University · US

Funding

Cancerfonden Not applicableNew York University Abu Dhabi Not applicableSheikh Hamdan Bin Rashid Al Maktoum Award for Medical Sciences Not applicableVetenskapsrådet Not applicable
6 · The paper itself

Abstract

Cell-penetrating peptides (CPPs) are short peptides that are able to efficiently penetrate cellular lipid bilayers. Although CPPs have been used as carriers in conjugation with certain cargos to target specific genes and pathways, how rationally designed CPPs per se affect global gene expression has not been investigated. Therefore, following time course treatments with 4 CPPs-penetratin, PepFect14, mtCPP1 and TP10, HeLa cells were transcriptionally profiled by RNA sequencing. Results from these analyses showed a time-dependent response to different CPPs, with specific sets of genes related to ribosome biogenesis, microtubule dynamics and long-noncoding RNAs being differentially expressed compared to untreated controls. By using an image-based high content phenotypic profiling platform we confirmed that differential gene expression in CPP-treated HeLa cells strongly correlates with changes in cellular phenotypes such as increased nucleolar size and dispersed microtubules, compatible with altered ribosome biogenesis and cell growth. Altogether these results suggest that cells respond to different cell penetrating peptides by alteration of specific sets of genes, which are possibly part of the common response to such stimulus.

Indexed as

Cell MembraneCell-Penetrating PeptidesGene ExpressionGene Regulatory NetworksHeLa CellsHumansMicrotubulesRibosomesRNA, Long NoncodingTranscription, GeneticCell-Penetrating PeptidesRNA, Long Noncodingcell-penetrating peptidescentrosomeCPPslncRNAlong noncoding RNAmicrotubulemtCPP1penetratinPepFect14ribosomerRNA ribosome biogenesisTP10

Identifiers

PMID33213097
PMCPMC7698553
OpenAlexW3102562966

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.