Evidence map›Paper›PMID 35817775›Full record

ArticleScientific data2022

Proteomic characterisation of triple negative breast cancer cells following CDK4/6 inhibition.

Melina Beykou, Mar Arias-Garcia, Theodoros I Roumeliotis, Jyoti S Choudhary, Nicolas Moser, Pantelis Georgiou, Chris Bakal

Open access · goldAbstract readDataset
In one paragraph

Article in Scientific data, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed, 17 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 3 institutions in 1 country.

Melina BeykouImperial College London, Department of Electrical and Electronic Engineering, Circuits and Systems Group, South Kensington Campus, London, SW7 2AZ, UK. melina.beykou19@imperial.ac.uk.ORCID http://orcid.org/0000-0002-2155-1384
Mar Arias-GarciaInstitute of Cancer Research, Division of Cancer Biology, Dynamical Cell Systems, London, SW3 6JB, UK.ORCID http://orcid.org/0000-0003-0130-1107
Theodoros I RoumeliotisInstitute of Cancer Research, Division of Cancer Biology, Functional Proteomics, London, SW3 6JB, UK.
Jyoti S ChoudharyInstitute of Cancer Research, Division of Cancer Biology, Functional Proteomics, London, SW3 6JB, UK.ORCID http://orcid.org/0000-0003-0881-5477
Nicolas MoserImperial College London, Department of Electrical and Electronic Engineering, Circuits and Systems Group, South Kensington Campus, London, SW7 2AZ, UK. nicolas.moser13@imperial.ac.uk.
Pantelis GeorgiouImperial College London, Department of Electrical and Electronic Engineering, Circuits and Systems Group, South Kensington Campus, London, SW7 2AZ, UK. pantelis@imperial.ac.uk.
Chris BakalInstitute of Cancer Research, Division of Cancer Biology, Dynamical Cell Systems, London, SW3 6JB, UK. chris.bakal@icr.ac.uk.ORCID http://orcid.org/0000-0002-0413-6744
Institute of Cancer Research · GBCancer Research UK · GBImperial College London · GB

Funding

Cancer Research UK 20146
6 · The paper itself

Abstract

When used in combination with hormone treatment, Palbociclib prolongs progression-free survival of patients with hormone receptor positive breast cancer. Mechanistically, Palbociclib inhibits CDK4/6 activity but the basis for differing sensitivity of cancer to Palbociclib is poorly understood. A common observation in a subset of Triple Negative Breast Cancers (TNBCs) is that prolonged CDK4/6 inhibition can engage a senescence-like state where cells exit the cell cycle, whilst, remaining metabolically active. To better understand the senescence-like cell state which arises after Palbociclib treatment we used mass spectrometry to quantify the proteome, phosphoproteome, and secretome of Palbociclib-treated MDA-MB-231 TNBC cells. We observed altered levels of cell cycle regulators, immune response, and key senescence markers upon Palbociclib treatment. These datasets provide a starting point for the derivation of biomarkers which could inform the future use CDK4/6 inhibitors in TNBC subtypes and guide the development of potential combination therapies.

Indexed as

Triple Negative Breast NeoplasmsCyclin-Dependent Kinase 4Cyclin-Dependent Kinase 6FemaleHumansProteomeProteomicsCDK4 protein, humanCDK6 protein, humanCyclin-Dependent Kinase 4Cyclin-Dependent Kinase 6Proteome

Identifiers

PMID35817775
PMCPMC9273754
OpenAlexW4285035027

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.