Evidence map›Paper›PMID 28659432›Full record

ArticleMolecular cancer therapeutics2017

A Novel Theranostic Strategy for

Suchismita Mohanty, Zixin Chen, Kai Li, Goreti Ribeiro Morais, Jessica Klockow, Ketan Yerneni, Laura Pisani, Frederick T Chin, Siddharta Mitra, Samuel Cheshier and 6 more

Open access · greenAbstract readComment
In one paragraph

Article in Molecular cancer therapeutics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 2 pooled it
2.6field-weighted citation impact, top 11% 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

27 citing papers in PubMed, 2 syntheses or guidelines pooled it, 42 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. The Proteolytic Landscape of Ovarian Cancer: Applications in Nanomedicine.International journal of molecular sciences · 2022
    Review
  13. Review
  14. Review
  15. Proteases Regulate Cancer Stem Cell Properties and Remodel Their Microenvironment.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2021
    Review
  16. Review
  17. Targeting MMP-14 for dual PET and fluorescence imaging of glioma in preclinical models.European journal of nuclear medicine and molecular imaging · 2020
    Article
  18. Article
  19. Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 4 institutions in 2 countries.

Suchismita MohantyDepartment of Radiology, Molecular Imaging Program at Stanford (MIPS), Stanford University, Stanford, California.
Zixin ChenDepartment of Radiology, Molecular Imaging Program at Stanford (MIPS), Stanford University, Stanford, California.
Kai LiDepartment of Radiology, Molecular Imaging Program at Stanford (MIPS), Stanford University, Stanford, California.
Goreti Ribeiro MoraisInstitute of Cancer Therapeutics, Faculty of Life Sciences, University of Bradford, Bradford, United Kingdom.
Jessica KlockowDepartment of Radiology, Molecular Imaging Program at Stanford (MIPS), Stanford University, Stanford, California.
Ketan YerneniDepartment of Biology, Skidmore College, Saratoga Springs, New York.
Laura PisaniDepartment of Radiology, Molecular Imaging Program at Stanford (MIPS), Stanford University, Stanford, California.
Frederick T ChinDepartment of Radiology, Molecular Imaging Program at Stanford (MIPS), Stanford University, Stanford, California.
Siddharta MitraDepartment of Neurosurgery, Institute for Stem Cell Biology and Regenerative Medicine and Division of Pediatric Neurosurgery, Lucile Packard Children's Hospital, Stanford University, Stanford, California.
Samuel CheshierDepartment of Neurosurgery, Institute for Stem Cell Biology and Regenerative Medicine and Division of Pediatric Neurosurgery, Lucile Packard Children's Hospital, Stanford University, Stanford, California.
Edwin Chang
Sanjiv Sam GambhirDepartment of Radiology, Molecular Imaging Program at Stanford (MIPS), Stanford University, Stanford, California.
Jianghong RaoDepartment of Radiology, Molecular Imaging Program at Stanford (MIPS), Stanford University, Stanford, California.
Paul M LoadmanInstitute of Cancer Therapeutics, Faculty of Life Sciences, University of Bradford, Bradford, United Kingdom.
Robert A FalconerInstitute of Cancer Therapeutics, Faculty of Life Sciences, University of Bradford, Bradford, United Kingdom.
Heike E Daldrup-LinkDepartment of Radiology, Molecular Imaging Program at Stanford (MIPS), Stanford University, Stanford, California. H.E.Daldrup-Link@stanford.edu.
Stanford Medicine · USUniversity of Bradford · GBLucile Packard Children's Hospital · USSkidmore College · US

Funding

Translational Oncology Research Program (Project-005)P30CA124435 · NCI · STANFORD UNIVERSITY · PI Melinda L. Telli · 2007 to 2026
$71.4M
Pilot ProjectsU54CA151459 · NCI · STANFORD UNIVERSITY · PI GAMBHIR, SANJIV S · 2010 to 2014
$12.6M
Nano Characterization and Nano Fabrication CoreU54CA199075 · NCI · STANFORD UNIVERSITY · PI GAMBHIR, SANJIV S · 2015 to 2019
$9.6M
Stanford Molecular Imaging Scholars (SMIS) ProgramT32CA118681 · NCI · STANFORD UNIVERSITY · PI CRAIG S LEVIN · 2016 to 2026
$4.3M
Development of Novel Activatable Theranostic Nanoparticles for combined Cancer MRR21CA176519 · NCI · STANFORD UNIVERSITY · PI DALDRUP-LINK, HEIKE ELIZABETH, RAO, JIANGHONG · 2014 to 2015
$403k
Imaging Tumor Associated Macrophages in Bone SarcomasR21CA190196 · NCI · STANFORD UNIVERSITY · PI DALDRUP-LINK, HEIKE ELIZABETH · 2016 to 2017
$378k
NCI NIH HHS P30 CA124435NCI NIH HHS R21 CA176519NCI NIH HHS R21 CA190196NCI NIH HHS T32 CA118681NCI NIH HHS U54 CA151459NCI NIH HHS U54 CA199075
6 · The paper itself

Abstract

Glioblastoma (GBM) has a dismal prognosis. Evidence from preclinical tumor models and human trials indicates the role of GBM-initiating cells (GIC) in GBM drug resistance. Here, we propose a new treatment option with tumor enzyme-activatable, combined therapeutic and diagnostic (theranostic) nanoparticles, which caused specific toxicity against GBM tumor cells and GICs. The theranostic cross-linked iron oxide nanoparticles (CLIO) were conjugated to a highly potent vascular disrupting agent (ICT) and secured with a matrix-metalloproteinase (MMP-14) cleavable peptide. Treatment with CLIO-ICT disrupted tumor vasculature of

Indexed as

Gene ExpressionTheranostic NanomedicineAnimalsAntineoplastic AgentsApoptosisBrain NeoplasmsCell Line, TumorCell SurvivalDacarbazineDisease Models, AnimalFerric CompoundsFlow CytometryGlioblastomaHumansMagnetic Resonance ImagingMass SpectrometryAntineoplastic AgentsDacarbazineFerric Compoundsferric oxideMatrix Metalloproteinase 14Temozolomide

Identifiers

PMID28659432
PMCPMC5587386
OpenAlexW2728708888

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.