Evidence map›Paper›PMID 19141648›Full record

ArticleCancer research2009

Multiparametric monitoring of tumor response to chemotherapy by noninvasive imaging.

Zdravka Medarova, Leonid Rashkovetsky, Pamela Pantazopoulos, Anna Moore

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
10.4field-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

33 citing papers in PubMed, 79 citations in OpenAlex.

  1. Trial
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  3. Triple-Negative Breast Cancer: A Review of Conventional and Advanced Therapeutic Strategies.International journal of environmental research and public health · 2020
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  16. Multifunctional nanoparticles for drug delivery and molecular imaging.Annual review of biomedical engineering · 2013
    Review
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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

4 authors at 2 institutions in 1 country.

Zdravka MedarovaDepartment of Radiology, Molecular Imaging Laboratory, MGH/HST Athinoula A Martinos Center for Biomedical Imaging, Massachusetts General Hospital/Harvard Medical School, Boston, Massachusetts 02129, USA.
Leonid Rashkovetsky
Pamela Pantazopoulos
Anna Moore
Athinoula A. Martinos Center for Biomedical Imaging · USHarvard University · US

Funding

Predictive Cancer Diagnostics and Therapy ResponseR01CA135650 · NCI · MICHIGAN STATE UNIVERSITY · PI MEDAROVA, ZDRAVKA O, MOORE, ANNA · 2008 to 2018
$4.6M
In vivo imaging of diabetogenic cytotoxic T-lymphocytesR01DK064850 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI MOORE, ANNA · 2003 to 2006
$1.1M
Novel multi-modal probes for in vivo cancer imagingR21EB001727 · NIBIB · MASSACHUSETTS GENERAL HOSPITAL · PI MOORE, ANNA · 2003 to 2004
$518k
NCI NIH HHS R01 CA135650NIBIB NIH HHS EB001727NIBIB NIH HHS R21 EB001727NIDDK NIH HHS R01 DK064850
6 · The paper itself

Abstract

With the emerging concept of individualized cancer therapy, it becomes crucial to develop methods for the noninvasive assessment of treatment outcome. With this in mind, we designed a novel approach for the comprehensive evaluation of response to chemotherapy with the established agent doxorubicin in a preclinical breast cancer model. This approach delivers information not only about change in tumor size but also about target antigen expression. Our strategy relies on a tumor-specific contrast agent (MN-EPPT) targeting the underglycosylated MUC-1 (uMUC-1) tumor antigen, found on more than 90% of breast cancers and predictive of chemotherapeutic response. MN-EPPT consists of superparamagnetic iron oxide nanoparticles (MN) for magnetic resonance imaging, modified with Cy5.5 dye (for near-IR fluorescence optical imaging), and conjugated to peptides (EPPT), specifically recognizing uMUC-1. In vivo, treatment of mice bearing orthotopic human breast carcinomas with doxorubicin led to a reduction in tumor mass and resulted in down-regulation of uMUC-1. The tumor-specific accumulation of MN-EPPT allowed the assessment of change in tumor volume by noninvasive imaging. Furthermore, in mice injected with MN-EPPT, tumor delta-T2 was significantly reduced after treatment with doxorubicin, indicating a lower accumulation of MN-EPPT and reflecting the reduced expression of uMUC-1. With these studies, we have shown the utility of magnetic resonance imaging for the multiparametric characterization of breast tumor response to chemotherapy. This approach has the potential of significantly advancing our ability to better direct the development of molecularly targeted individualized therapy protocols because it permits the monitoring of therapy on a molecular scale.

Indexed as

AdenocarcinomaAnimalsBiomarkers, TumorBreast NeoplasmsDoxorubicinEnvironmental MonitoringFemaleFluorescein-5-isothiocyanateHumansMagnetic Resonance ImagingMiceMice, NudeMicroscopy, FluorescenceMucin-1PeptidesTreatment OutcomeBiomarkers, TumorDoxorubicinFluorescein-5-isothiocyanateMUC1 protein, humanMucin-1Peptides

Identifiers

PMID19141648
PMCPMC2633414
OpenAlexW2107964698

What OpenQuestion holds

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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.