Evidence map›Paper›PMID 24113515›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2014

The clinical potential of targeted nanomedicine: delivering to cancer stem-like cells.

Sang-Soo Kim, Antonina Rait, Farwah Rubab, Abhi K Rao, Michael C Kiritsy, Kathleen F Pirollo, Shangzi Wang, Louis M Weiner, Esther H Chang

Open access · hybridAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

29 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Viruses · 2022
    Article
  7. Review
  8. Article
  9. Review
  10. Nanotherapeutics for Gene Modulation that Prevents Apoptosis in the Brain and Fatal Neuroinflammation.Molecular therapy : the journal of the American Society of Gene Therapy · 2018
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Nanomaterial-Enabled Cancer Therapy.Molecular therapy : the journal of the American Society of Gene Therapy · 2017
    Review
  16. Tumor-targeted nanotherapeutics: overcoming treatment barriers for glioblastoma.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2017
    Review
  17. Review
  18. Review
  19. Review
  20. Article
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

9 authors at 3 institutions in 1 country.

Sang-Soo KimDepartment of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, District of Columbia, USA.
Antonina RaitDepartment of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, District of Columbia, USA.
Farwah RubabSynerGene Therapeutics, Inc., Potomac, Maryland, USA.
Abhi K RaoDepartment of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, District of Columbia, USA.
Michael C KiritsyDepartment of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, District of Columbia, USA.
Kathleen F PirolloDepartment of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, District of Columbia, USA.
Shangzi WangDepartment of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, District of Columbia, USA.
Louis M WeinerDepartment of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, District of Columbia, USA.
Esther H ChangDepartment of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, District of Columbia, USA. Electronic address: change@georgetown.edu.
Georgetown University · USGeorgetown University Medical Center · USAllogene Therapeutics (United States) · US

Funding

Tissue Culture Shared ResourceP30CA051008 · NCI · GEORGETOWN UNIVERSITY · PI STEPHEN W BYERS · 1990 to 2026
$71.5M
TRAINING GRANT IN TUMOR BIOLOGYT32CA009686 · NCI · GEORGETOWN UNIVERSITY · PI ANNA Tate RIEGEL, DAVID J ROBBINS · 1996 to 2026
$10.8M
Nanoimmunoliposome-Complexed SPIO: Tumor-Specific Detection of Early Lung CancerR01CA132012 · NCI · GEORGETOWN UNIVERSITY · PI CHANG, ESTHER H, FREEDMAN, MATTHEW T · 2008 to 2010
$1.9M
FLUORESCENCE IMAGING OF LIVE CELLS AND TISSUESS10RR015768 · NCRR · GEORGETOWN UNIVERSITY · PI MUELLER, SUSETTE C · 2001 to 2001
$221k
EXTRAMURAL RESEARCH FACILITIES CONSTRUCTION PROJECTSC06RR014567 · NCRR · GEORGETOWN UNIVERSITY · PI PESTELL, RICHARD G · 1999 to 1999
–
NCI NIH HHS 2P30-CA-51008NCI NIH HHS 5R01CA132012-02NCI NIH HHS P30 CA051008NCI NIH HHS R01 CA132012NCI NIH HHS T32 CA009686NCRR NIH HHS 1 S10 RR 15768-01NCRR NIH HHS C06 RR014567NCRR NIH HHS C06RR14567
6 · The paper itself

Abstract

Cancer stem-like cells (CSCs) have been implicated in recurrence and treatment resistance in many human cancers. Thus, a CSC-targeted drug delivery strategy to eliminate CSCs is a desirable approach for developing a more effective anticancer therapy. We have developed a tumor-targeting nanodelivery platform (scL) for systemic administration of molecular medicines. Following treatment with the scL nanocomplex carrying various payloads, we have observed exquisite tumor-targeting specificity and significant antitumor response with long-term survival benefit in numerous animal models. We hypothesized that this observed efficacy might be attributed, at least in part, to elimination of CSCs. Here, we demonstrate the ability of scL to target both CSCs and differentiated nonstem cancer cells (non-CSCs) in various mouse models including subcutaneous and intracranial xenografts, syngeneic, and chemically induced tumors. We also show that systemic administration of scL carrying the wtp53 gene was able to induce tumor growth inhibition and the death of both CSCs and non-CSCs in subcutaneous colorectal cancer xenografts suggesting that this could be an effective method to reduce cancer recurrence and treatment resistance. This scL nanocomplex is being evaluated in a number of clinical trials where it has been shown to be well tolerated with indications of anticancer activity.

Indexed as

Drug Delivery SystemsNanomedicineAnimalsApoptosisBrainCell Line, TumorCell SurvivalColorectal NeoplasmsDisease Models, AnimalFemaleGene ExpressionGene Transfer TechniquesHumansImmunophenotypingLiposomesMiceLiposomesReceptors, TransferrinTumor Suppressor Protein p53

Identifiers

PMID24113515
PMCPMC3916038
OpenAlexW1974692537

What OpenQuestion holds

Textmetadata
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.