Evidence map›Paper›PMID 29367764›Full record

ArticleOncogene2018

Blockade of insulin-like growth factors increases efficacy of paclitaxel in metastatic breast cancer.

Lucy Ireland, Almudena Santos, Fiona Campbell, Carlos Figueiredo, Dean Hammond, Lesley G Ellies, Ulrike Weyer-Czernilofsky, Thomas Bogenrieder, Michael Schmid, Ainhoa Mielgo

Open access · hybridAbstract read
In one paragraph

Article in Oncogene, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 1 pooled it
6.8field-weighted citation impact, top 2% 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

50 citing papers in PubMed, 1 synthesis or guideline pooled it, 78 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

10 authors at 3 institutions in 4 countries.

Lucy IrelandDepartment of Molecular and Clinical Cancer Medicine, University of Liverpool, Liverpool, UK.
Almudena SantosDepartment of Molecular and Clinical Cancer Medicine, University of Liverpool, Liverpool, UK.
Fiona CampbellDepartment of Molecular and Clinical Cancer Medicine, University of Liverpool, Liverpool, UK.
Carlos FigueiredoDepartment of Molecular and Clinical Cancer Medicine, University of Liverpool, Liverpool, UK.
Dean HammondDepartment of Physiology, University of Liverpool, Liverpool, UK.
Lesley G ElliesDepartment of Pathology, University of California San Diego, La Jolla, USA.
Ulrike Weyer-CzernilofskyBoehringer Ingelheim RCV GmbH & Co KG, Pharmacology and Translational Research, Vienna, Austria.
Thomas BogenriederBoehringer Ingelheim RCV GmbH & Co KG Medicine and Translational Research, Vienna, Austria.
Michael SchmidDepartment of Molecular and Clinical Cancer Medicine, University of Liverpool, Liverpool, UK.
Ainhoa MielgoDepartment of Molecular and Clinical Cancer Medicine, University of Liverpool, Liverpool, UK. amielgo@liverpool.ac.uk.
University of Liverpool · GBBoehringer Ingelheim (Austria) · ATUniversity of California, San Diego · US

Funding

Role of the chronic inflammatory mediator NO in early mammary tumorigenesisK22CA118182 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ELLIES, LESLEY G · 2006 to 2008
$442k
Medical Research Council MR/L000512/1Medical Research Council MR/P018920/1NCI NIH HHS K22 CA118182Wellcome Trust
6 · The paper itself

Abstract

Breast cancer remains the leading cause of cancer death in women owing to metastasis and the development of resistance to established therapies. Macrophages are the most abundant immune cells in the breast tumor microenvironment and can both inhibit and support cancer progression. Thus, gaining a better understanding of how macrophages support cancer could lead to the development of more effective therapies. In this study, we find that breast cancer-associated macrophages express high levels of insulin-like growth factors 1 and 2 (IGFs) and are the main source of IGFs within both primary and metastatic tumors. In total, 75% of breast cancer patients show activation of insulin/IGF-1 receptor signaling and this correlates with increased macrophage infiltration and advanced tumor stage. In patients with invasive breast cancer, activation of Insulin/IGF-1 receptors increased to 87%. Blocking IGF in combination with paclitaxel, a chemotherapeutic agent commonly used to treat breast cancer, showed a significant reduction in tumor cell proliferation and lung metastasis in pre-clinical breast cancer models compared to paclitaxel monotherapy. Our findings provide the rationale for further developing the combination of paclitaxel with IGF blockers for the treatment of invasive breast cancer, and Insulin/IGF1R activation and IGF+ stroma cells as potential biomarker candidates for further evaluation.

Indexed as

AnimalsAntibodies, Monoclonal, HumanizedAntibodies, NeutralizingAntineoplastic Combined Chemotherapy ProtocolsBreast NeoplasmsCells, CulturedDrug Screening Assays, AntitumorDrug SynergismFemaleHumansInsulin-Like Growth Factor IMiceMice, Inbred BALB CMice, Inbred C3HMice, Inbred C57BLPaclitaxelAntibodies, Monoclonal, HumanizedAntibodies, NeutralizingInsulin-Like Growth Factor IPaclitaxelReceptor, IGF Type 1xentuzumab

Identifiers

PMID29367764
PMCPMC5895608
OpenAlexW2953036362

What OpenQuestion holds

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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.