Evidence map›Paper›PMID 25170759›Full record

ArticlePloS one2014

Insulin-like growth factor 1 receptor and response to anti-IGF1R antibody therapy in osteosarcoma.

Yu Cao, Michael Roth, Sajida Piperdi, Kristofer Montoya, Rebecca Sowers, Pulivarthi Rao, David Geller, Peter Houghton, E Anders Kolb, Jonathan Gill and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

32 citing papers in PubMed, 47 citations in OpenAlex.

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  17. IGF-1R inhibitor PQ401 inhibits osteosarcoma cell proliferation, migration and colony formation.International journal of clinical and experimental pathology · 2019
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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

11 authors at 5 institutions in 1 country.

Yu CaoDivision of Pediatric Hematology/Oncology, Children's Hospital at Montefiore, Albert Einstein College of Medicine, Bronx, New York, United States of America.
Michael RothDivision of Pediatric Hematology/Oncology, Children's Hospital at Montefiore, Albert Einstein College of Medicine, Bronx, New York, United States of America.
Sajida PiperdiDivision of Pediatric Hematology/Oncology, Children's Hospital at Montefiore, Albert Einstein College of Medicine, Bronx, New York, United States of America.
Kristofer MontoyaDivision of Pediatric Hematology/Oncology, Children's Hospital at Montefiore, Albert Einstein College of Medicine, Bronx, New York, United States of America.
Rebecca SowersDivision of Pediatric Hematology/Oncology, Children's Hospital at Montefiore, Albert Einstein College of Medicine, Bronx, New York, United States of America.
Pulivarthi RaoDivision of Pediatric Hematology/Oncology, Texas Children's Cancer Center, Baylor College of Medicine, Houston, Texas, United States of America.
David GellerDepartment of Orthopedic Surgery, Montefiore Medical Center and the Children's Hospital at Montefiore, Albert Einstein College of Medicine, Bronx, New York, United States of America.
Peter HoughtonCenter for Childhood Cancer and Blood Diseases, Nationwide Children's Hospital, Columbus, Ohio, United States of America.
E Anders KolbDivision of Pediatric Hematology/Oncology, A.I. duPont Hospital for Children, Wilmington, Delaware, United States of America.
Jonathan GillDivision of Pediatric Hematology/Oncology, Children's Hospital at Montefiore, Albert Einstein College of Medicine, Bronx, New York, United States of America.
Richard GorlickDivision of Pediatric Hematology/Oncology, Children's Hospital at Montefiore, Albert Einstein College of Medicine, Bronx, New York, United States of America; Department of Molecular Pharmacology, Albert Einstein College of Medicine, Bronx, New York, United States of America.
Children's Hospital at Montefiore · USAlbert Einstein College of Medicine · USChildren's Cancer Center · USCommunity Health Systems - Dupont Hospital · USNationwide Children's Hospital · US

Funding

Paul Calabresis Career Development Award For Clinical Oncology K12CA132783 · NCI · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI PEREZ-SOLER, ROMAN, VERMA, AMIT K. · 2009 to 2019
$8.2M
NCI NIH HHS K12 CA132783NCI NIH HHS K12 CA-132783-04
6 · The paper itself

Abstract

backgroundSurvival outcomes for patients with osteosarcoma (OS) have remained stagnant over the past three decades. Insulin-like growth factor 1 receptor (IGF1R) is over-expressed in a number of malignancies, and anti-IGF1R antibodies have and are currently being studied in clinical trials. Understanding the molecular aberrations which result in increased tumor response to anti-IGF1R therapy could allow for the selection of patients most likely to benefit from IGF1R targeted therapy.

methodsIGF1R mRNA expression was assessed by RT PCR in OS patient primary tumors, cell lines, and xenograft tumors. IGF1R copy number was assessed by 3 approaches: PCR, FISH, and dot blot analysis. Exons 1-20 of IGF1R were sequenced in xenograft tumors and 87 primary OS tumors, and surface expression of IGF1R was assessed by flow cytometry. Levels of mRNA and protein expression, copy number, and mutation status were compared with tumor response to anti-IGF1R antibody therapy in 4 OS xenograft models.

resultsIGF1R mRNA is expressed in OS. Primary patient samples and xenograft samples had higher mRNA expression and copy number compared with corresponding cell lines. IGF1R mRNA expression, cell surface expression, copy number, and mutation status were not associated with tumor responsiveness to anti-IGF1R antibody therapy.

conclusionsIGF1R is expressed in OS, however, no clear molecular markers predict response to IGF1R antibody-mediated therapy. Additional pre-clinical studies assessing potential predictive biomarkers and investigating targetable molecular pathways critical to the proliferation of OS cells are needed.

Indexed as

AnimalsAntibodies, NeoplasmAntineoplastic AgentsCell Line, TumorFemaleGene Expression Regulation, NeoplasticHumansMaleMiceMice, SCIDNeoplasm ProteinsOsteosarcomaReceptor, IGF Type 1RNA, MessengerRNA, NeoplasmXenograft Model Antitumor AssaysAntibodies, NeoplasmAntineoplastic AgentsNeoplasm ProteinsReceptor, IGF Type 1RNA, MessengerRNA, Neoplasm

Identifiers

PMID25170759
PMCPMC4149550
OpenAlexW2007274108

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.