Evidence map›Paper›PMID 27775704›Full record

ArticleNature medicine2016

PIM1 kinase regulates cell death, tumor growth and chemotherapy response in triple-negative breast cancer.

Fara Brasó-Maristany, Simone Filosto, Steven Catchpole, Rebecca Marlow, Jelmar Quist, Erika Francesch-Domenech, Darren A Plumb, Leila Zakka, Patrycja Gazinska, Gianmaria Liccardi and 18 more

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Nature medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 138 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
138citing papers in PubMed, 1 pooled it
18.4field-weighted citation impact, top 1% 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

138 citing papers in PubMed, 1 synthesis or guideline pooled it, 240 citations in OpenAlex.

  1. Pooled it
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  4. Review
  5. Article
  6. DamageZhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2026
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  15. Imparting aromaticity to 2-pyridone derivatives byJournal of enzyme inhibition and medicinal chemistry · 2024
    Article
  16. Article
  17. PIM1 kinase and its diverse substrate in solid tumors.Cell communication and signaling : CCS · 2024
    Review
  18. Article
  19. UM171 suppresses breast cancer progression by inducing KLF2.Breast cancer research and treatment · 2024
    Article
  20. Article

78 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

28 authors at 5 institutions in 3 countries.

Fara Brasó-MaristanyBreast Cancer Now Research Unit, Division of Cancer Studies, Faculty of Life Sciences and Medicine, King's College London, Guy's Hospital, London, UK.
Simone FilostoBreast Cancer Now Research Unit, Division of Cancer Studies, Faculty of Life Sciences and Medicine, King's College London, Guy's Hospital, London, UK.
Steven CatchpoleBreast Cancer Now Research Unit, Division of Cancer Studies, Faculty of Life Sciences and Medicine, King's College London, Guy's Hospital, London, UK.
Rebecca MarlowBreast Cancer Now Research Unit, Division of Cancer Studies, Faculty of Life Sciences and Medicine, King's College London, Guy's Hospital, London, UK.
Jelmar QuistBreast Cancer Now Research Unit, Division of Cancer Studies, Faculty of Life Sciences and Medicine, King's College London, Guy's Hospital, London, UK.
Erika Francesch-DomenechBreast Cancer Now Research Unit, Division of Cancer Studies, Faculty of Life Sciences and Medicine, King's College London, Guy's Hospital, London, UK.
Darren A PlumbBreast Cancer Now Research Unit, Division of Cancer Studies, Faculty of Life Sciences and Medicine, King's College London, Guy's Hospital, London, UK.
Leila ZakkaBreast Cancer Now Research Unit, Division of Cancer Studies, Faculty of Life Sciences and Medicine, King's College London, Guy's Hospital, London, UK.
Patrycja GazinskaBreast Cancer Now Research Unit, Division of Cancer Studies, Faculty of Life Sciences and Medicine, King's College London, Guy's Hospital, London, UK.
Gianmaria LiccardiBreast Cancer Now Toby Robins Research Centre, Institute of Cancer Research, London, UK.
Pascal MeierBreast Cancer Now Toby Robins Research Centre, Institute of Cancer Research, London, UK.
Albert Gris-OliverExperimental Therapeutics Group, Vall d'Hebron Institute of Oncology, Barcelona, Spain.ORCID 0000-0003-1802-9541
Maggie Chon U CheangBreast Cancer Now Toby Robins Research Centre, Institute of Cancer Research, London, UK.
Anna Perdrix-RosellBreast Cancer Now Research Unit, Division of Cancer Studies, Faculty of Life Sciences and Medicine, King's College London, Guy's Hospital, London, UK.
Manar ShafatBreast Cancer Now Research Unit, Division of Cancer Studies, Faculty of Life Sciences and Medicine, King's College London, Guy's Hospital, London, UK.
Elodie NoëlBreast Cancer Now Research Unit, Division of Cancer Studies, Faculty of Life Sciences and Medicine, King's College London, Guy's Hospital, London, UK.
Nirmesh PatelBreast Cancer Now Research Unit, Division of Cancer Studies, Faculty of Life Sciences and Medicine, King's College London, Guy's Hospital, London, UK.
Kristen McEachernOncology iMed, AstraZeneca, Waltham, Massachusetts, USA.
Maurizio ScaltritiHuman Oncology and Pathogenesis Program (HOPP), Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Pau CastelHuman Oncology and Pathogenesis Program (HOPP), Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Farzana NoorBreast Cancer Now Research Unit, Division of Cancer Studies, Faculty of Life Sciences and Medicine, King's College London, Guy's Hospital, London, UK.
Richard BuusBreast Cancer Now Toby Robins Research Centre, Institute of Cancer Research, London, UK.ORCID 0000-0002-3386-3465
Sumi MathewBreast Cancer Now Research Unit, Division of Cancer Studies, Faculty of Life Sciences and Medicine, King's College London, Guy's Hospital, London, UK.
Johnathan WatkinsBreast Cancer Now Research Unit, Division of Cancer Studies, Faculty of Life Sciences and Medicine, King's College London, Guy's Hospital, London, UK.
Violeta SerraExperimental Therapeutics Group, Vall d'Hebron Institute of Oncology, Barcelona, Spain.
Pierfrancesco MarraBreast Cancer Now Research Unit, Division of Cancer Studies, Faculty of Life Sciences and Medicine, King's College London, Guy's Hospital, London, UK.
Anita GrigoriadisBreast Cancer Now Research Unit, Division of Cancer Studies, Faculty of Life Sciences and Medicine, King's College London, Guy's Hospital, London, UK.
Andrew N TuttBreast Cancer Now Research Unit, Division of Cancer Studies, Faculty of Life Sciences and Medicine, King's College London, Guy's Hospital, London, UK.ORCID 0000-0001-8715-2901
Guy's Hospital · GBInstitute of Cancer Research · GBMemorial Sloan Kettering Cancer Center · USVall d'Hebron Institute of Oncology · ESAstraZeneca (United States) · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Breast Cancer Now 2011NOVPR10Breast Cancer Now CTR-Q3MEIERDepartment of HealthMedical Research Council G1000089Medical Research Council MR/M019217/1NCI NIH HHS P30 CA008748Worldwide Cancer Research 07-0588Worldwide Cancer Research 14-1328
6 · The paper itself

Abstract

Triple-negative breast cancers (TNBCs) have poor prognosis and lack targeted therapies. Here we identified increased copy number and expression of the PIM1 proto-oncogene in genomic data sets of patients with TNBC. TNBC cells, but not nonmalignant mammary epithelial cells, were dependent on PIM1 for proliferation and protection from apoptosis. PIM1 knockdown reduced expression of the anti-apoptotic factor BCL2, and dynamic BH3 profiling of apoptotic priming revealed that PIM1 prevents mitochondrial-mediated apoptosis in TNBC cell lines. In TNBC tumors and their cellular models, PIM1 expression was associated with several transcriptional signatures involving the transcription factor MYC, and PIM1 depletion in TNBC cell lines decreased, in a MYC-dependent manner, cell population growth and expression of the MYC target gene MCL1. Treatment with the pan-PIM kinase inhibitor AZD1208 impaired the growth of both cell line and patient-derived xenografts and sensitized them to standard-of-care chemotherapy. This work identifies PIM1 as a malignant-cell-selective target in TNBC and the potential use of PIM1 inhibitors for sensitizing TNBC to chemotherapy-induced apoptotic cell death.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsApoptosisBiphenyl CompoundsCell Line, TumorCell ProliferationCell SurvivalDNA Copy Number VariationsFemaleGene Knockdown TechniquesHumansMiceMitochondriaMyeloid Cell Leukemia Sequence 1 ProteinNeoplasm TransplantationProtein Kinase InhibitorsAZD1208BCL2 protein, humanBiphenyl CompoundsMAS1 protein, humanMCL1 protein, humanMYC protein, humanMyeloid Cell Leukemia Sequence 1 ProteinPIM1 protein, humanProtein Kinase InhibitorsProto-Oncogene MasProto-Oncogene Proteins c-bcl-2Proto-Oncogene Proteins c-mycProto-Oncogene Proteins c-pim-1Thiazolidines

Identifiers

PMID27775704
PMCPMC5552044
OpenAlexW2536094308

What OpenQuestion holds

Textmetadata
LicenceTDM
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.