Evidence map›Paper›PMID 26359455›Full record

ArticleCancer research2015

Combining miR-10b-Targeted Nanotherapy with Low-Dose Doxorubicin Elicits Durable Regressions of Metastatic Breast Cancer.

Byunghee Yoo, Amol Kavishwar, Alana Ross, Ping Wang, Doris P Tabassum, Kornelia Polyak, Natalia Barteneva, Victoria Petkova, Pamela Pantazopoulos, Aseda Tena and 2 more

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2015. 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 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

57 citing papers in PubMed, 75 citations in OpenAlex.

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  12. Monitoring of Nanodrug Accumulation in Murine Breast Cancer Metastases.Journal of visualized experiments : JoVE · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 5 institutions in 1 country.

Byunghee YooMolecular Imaging Laboratory, MGH/MIT/HMS Athinoula A. Martinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
Amol KavishwarMolecular Imaging Laboratory, MGH/MIT/HMS Athinoula A. Martinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
Alana RossMolecular Imaging Laboratory, MGH/MIT/HMS Athinoula A. Martinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
Ping WangMolecular Imaging Laboratory, MGH/MIT/HMS Athinoula A. Martinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
Doris P TabassumDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts.
Kornelia PolyakDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts.
Natalia BartenevaProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts.
Victoria PetkovaMolecular Medicine Core, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts.
Pamela PantazopoulosMolecular Imaging Laboratory, MGH/MIT/HMS Athinoula A. Martinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
Aseda TenaTransplantation Biology Research Center, Massachusetts General Hospital/Harvard Medical School, Boston, Massachusetts.
Anna MooreMolecular Imaging Laboratory, MGH/MIT/HMS Athinoula A. Martinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts. zmedarova@partners.org amoore@helix.mgh.harvard.edu.
Zdravka MedarovaMolecular Imaging Laboratory, MGH/MIT/HMS Athinoula A. Martinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts. zmedarova@partners.org amoore@helix.mgh.harvard.edu.
Athinoula A. Martinos Center for Biomedical Imaging · USDana-Farber Cancer Institute · USBeth Israel Deaconess Medical Center · USBoston Children's Hospital · USMassachusetts General Hospital · US

Funding

NUCLEAR MAGNETIC RESONANCE RESEARCHT32CA009502 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI MOORE, ANNA · 1985 to 2013
$2.0M
MicroRNA Therapy for Lymph Node Metastatic Breast CancerR01CA163461 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI MEDAROVA, ZDRAVKA O · 2012 to 2016
$1.9M
Target-Specific Imaging and Delivery of siRNA to TumorsR00CA129070 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI MEDAROVA, ZDRAVKA O · 2009 to 2011
$739k
IVIS Spectrum Imaging SystemS10RR025504 · NCRR · MASSACHUSETTS GENERAL HOSPITAL · PI MOORE, ANNA · 2009 to 2009
$341k
NCI NIH HHS 5T32CA009502NCI NIH HHS R00 CA129070NCI NIH HHS R00CA129070NCI NIH HHS R01 CA163461NCI NIH HHS R01CA16346101A1NCI NIH HHS T32 CA009502NCRR NIH HHS S10 RR025504
6 · The paper itself

Abstract

The therapeutic promise of microRNA (miRNA) in cancer has yet to be realized. In this study, we identified and therapeutically exploited a new role for miR-10b at the metastatic site, which links its overexpression to tumor cell viability and proliferation. In the protocol developed, we combined a miR-10b-inhibitory nanodrug with low-dose anthracycline to achieve complete durable regressions of metastatic disease in a murine model of metastatic breast cancer. Mechanistic investigations suggested a potent antiproliferative, proapoptotic effect of the nanodrug in the metastatic cells, potentiated by a cell-cycle arrest produced by administration of the low-dose anthracycline. miR-10b was overexpressed specifically in cells with high metastatic potential, suggesting a role for this miRNA as a metastasis-specific therapeutic target. Taken together, our results implied the existence of pathways that regulate the viability and proliferation of tumor cells only after they have acquired the ability to grow at distant metastatic sites. As illustrated by miR-10b targeting, such metastasis-dependent apoptotic pathways would offer attractive targets for further therapeutic exploration.

Indexed as

NanoparticlesAnimalsAntibiotics, AntineoplasticApoptosisBreast NeoplasmsCell CycleCell Line, TumorCell MovementCell ProliferationDisease Models, AnimalDoxorubicinFemaleGene Knockout TechniquesHumansMiceMicroRNAsAntibiotics, AntineoplasticDoxorubicinMicroRNAsMIRN10 microRNA, human

Identifiers

PMID26359455
PMCPMC4609288
OpenAlexW2173409576

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.