Evidence map›Paper›PMID 26701717›Full record

ArticleDrug delivery2016

Tumor neovasculature-targeted cationic PEGylated liposomes of gambogic acid for the treatment of triple-negative breast cancer.

Ravi Doddapaneni, Ketan Patel, Ibtisam Hasan Owaid, Mandip Singh

Open access · bronzeAbstract read
In one paragraph

Article in Drug delivery, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
7.8field-weighted citation impact, top 3% 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

35 citing papers in PubMed, 58 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Caged Polyprenylated Xanthones inDrug design, development and therapy · 2023
    Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Role of Exosomes for Delivery of Chemotherapeutic Drugs.Critical reviews in therapeutic drug carrier systems · 2021
    Review
  16. Gambogic acid: A shining natural compound to nanomedicine for cancer therapeutics.Biochimica et biophysica acta. Reviews on cancer · 2020
    Review
  17. Article
  18. Review
  19. Article
  20. Gambogic Acid as a Candidate for Cancer Therapy: A Review.International journal of nanomedicine · 2020
    Review
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.

Ravi Doddapanenia College of Pharmacy and Pharmaceutical Sciences, Florida A&M University , Tallahassee , FL , USA and.
Ketan Patela College of Pharmacy and Pharmaceutical Sciences, Florida A&M University , Tallahassee , FL , USA and.
Ibtisam Hasan Owaidb John D. Dingell VA Medical Center , Detroit , MI , USA.
Mandip Singha College of Pharmacy and Pharmaceutical Sciences, Florida A&M University , Tallahassee , FL , USA and.
Florida Agricultural and Mechanical University · USJohn D. Dingell VA Medical Center · US

Funding

Targeted Nanocarrier Combination Based Therapy for Lung CancerP20MD006738 · NIMHD · FLORIDA AGRICULTURAL AND MECHANICAL UNIV · PI RAHMAN, SALEH MD. MAHMUDUR · 2012 to 2016
$5.6M
Multiphoton Probes for Biomedical ImagingSC1GM092778 · NIGMS · FLORIDA INTERNATIONAL UNIVERSITY · PI MOON, JOONGHO · 2011 to 2014
$829k
NIGMS NIH HHS SC1 GM092778NIMHD NIH HHS P20 MD006738
6 · The paper itself

Abstract

Gambogic acid (GA) is a naturally derived potent anticancer agent with extremely poor aqueous solubility. In the present study, positively charged PEGylated liposomal formulation of GA (GAL) was developed for parenteral delivery for the treatment of triple-negative breast cancer (TNBC). The GAL was formulated with a particle size of 107.3 ± 10.6 nm with +32 mV zeta potential. GAL showed very minimal release of GA over 24 h period confirming the non-leakiness and stability of liposomes. In vitro cytotoxicity assays showed similar cell killing with GA and GAL against MDA-MB-231 cells but significantly higher inhibition of HUVEC growth was observed with GAL. Furthermore, GAL significantly (p < 0.05) inhibited the MDA-MB-231 orthotopic xenograft tumor growth with >50% reduction of tumor volume and reduction in tumor weight by 1.7-fold and 2.2-fold when compared to GA and controls, respectively. Results of western blot analysis indicated that GAL significantly suppressed the expression of apoptotic markers, bcl2, cyclinD1, survivin and microvessel density marker-CD31 and increased the expression of p53 and Bax compared to GA and control. Collectively, these data provide further support for the potential applications of cationic GAL in its intravenous delivery and its significant role in inhibiting angiogenesis against TNBC.

Indexed as

Antineoplastic AgentsBreast NeoplasmsCationsCell Line, TumorDrug Delivery SystemsFemaleHumansLiposomesParticle SizePolyethylene GlycolsTriple Negative Breast NeoplasmsXanthonesXenograft Model Antitumor AssaysAntineoplastic AgentsCationsgambogic acidLiposomesPolyethylene GlycolsXanthonesAngiogenesiscationic liposomeenhanced permeation and retentiongambogic acidtriple-negative breast cancer

Identifiers

PMID26701717
PMCPMC5024788
OpenAlexW2207717930

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.