Evidence map›Paper›PMID 32365111›Full record

ArticlePloS one2020

Treatment of cancer cells with Lapatinib negatively regulates general translation and induces stress granules formation.

Pauline Adjibade, Bryan Simoneau, Nassim Ledoux, William-Naud Gauthier, Melisse Nkurunziza, Edouard W Khandjian, Rachid Mazroui

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

22 citing papers in PubMed, 40 citations in OpenAlex.

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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

7 authors at 2 institutions in 1 country.

Pauline AdjibadeDépartement de Biologie Moléculaire, Biochimie Médicale et Pathologie, Centre de Recherche en Cancérologie, Centre de Recherche du CHU de Québec, Faculté de Médecine, Université Laval, Québec, Parti Québécois, Canada.
Bryan SimoneauDépartement de Biologie Moléculaire, Biochimie Médicale et Pathologie, Centre de Recherche en Cancérologie, Centre de Recherche du CHU de Québec, Faculté de Médecine, Université Laval, Québec, Parti Québécois, Canada.
Nassim LedouxDépartement de Biologie Moléculaire, Biochimie Médicale et Pathologie, Centre de Recherche en Cancérologie, Centre de Recherche du CHU de Québec, Faculté de Médecine, Université Laval, Québec, Parti Québécois, Canada.
William-Naud GauthierDépartement de Biologie Moléculaire, Biochimie Médicale et Pathologie, Centre de Recherche en Cancérologie, Centre de Recherche du CHU de Québec, Faculté de Médecine, Université Laval, Québec, Parti Québécois, Canada.
Melisse NkurunzizaDépartement de Biologie Moléculaire, Biochimie Médicale et Pathologie, Centre de Recherche en Cancérologie, Centre de Recherche du CHU de Québec, Faculté de Médecine, Université Laval, Québec, Parti Québécois, Canada.
Edouard W KhandjianDépartement de Psychiatrie et de Neurosciences, Centre de Recherche, Institut Universitaire en Santé mentale de Québec, Faculté de Médecine, Université Laval, Québec, Parti Québécois, Canada.
Rachid MazrouiDépartement de Biologie Moléculaire, Biochimie Médicale et Pathologie, Centre de Recherche en Cancérologie, Centre de Recherche du CHU de Québec, Faculté de Médecine, Université Laval, Québec, Parti Québécois, Canada.ORCID 0000-0001-7796-2740
Université Laval · CAInstitut Universitaire en Santé Mentale de Québec · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Stress granules (SG) are cytoplasmic RNA granules that form during various types of stress known to inhibit general translation, including oxidative stress, hypoxia, endoplasmic reticulum stress (ER), ionizing radiations or viral infection. Induction of these SG promotes cell survival in part through sequestration of proapoptotic molecules, resulting in the inactivation of cell death pathways. SG also form in cancer cells, but studies investigating their formation upon treatment with chemotherapeutics are very limited. Here we identified Lapatinib (Tykerb / Tyverb®), a tyrosine kinase inhibitor used for the treatment of breast cancers as a new inducer of SG in breast cancer cells. Lapatinib-induced SG formation correlates with the inhibition of general translation initiation which involves the phosphorylation of the translation initiation factor eIF2α through the kinase PERK. Disrupting PERK-SG formation by PERK depletion experiments sensitizes resistant breast cancer cells to Lapatinib. This study further supports the assumption that treatment with anticancer drugs activates the SG pathway, which may constitute an intrinsic stress response used by cancer cells to resist treatment.

Indexed as

Cell Line, TumorCytoplasmic GranulesDrug Resistance, NeoplasmeIF-2 KinaseEndoplasmic Reticulum StressEukaryotic Initiation Factor-2HumansLapatinibMCF-7 CellsNeoplasmsPhosphorylationProtein BiosynthesisUp-RegulationeIF-2 KinaseEukaryotic Initiation Factor-2Lapatinib

Identifiers

PMID32365111
PMCPMC7197775
OpenAlexW3021353580

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.