Evidence map›Paper›PMID 22842609›Full record

ArticleInternational journal of oncology2012

Topical phospho-sulindac (OXT-328) is effective in the treatment of non-melanoma skin cancer.

Ka Wing Cheng, George Mattheolabakis, Chi C Wong, Nengtai Ouyang, Liqun Huang, Panayiotis P Constantinides, Basil Rigas

Open access · hybridAbstract read
In one paragraph

Article in International journal of oncology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

10 citing papers in PubMed, 16 citations in OpenAlex.

  1. The Antiangiogenic Effect and Ocular Pharmacology of Novel Modified Nonsteroidal Anti-Inflammatory Drugs in the Treatment of Oxygen-Induced Retinopathy.Journal of ocular pharmacology and therapeutics : the official journal of the Association for Ocular Pharmacology and Therapeutics · 2023
    Article
  2. Article
  3. Article
  4. Article
  5. Use of rodents as models of human diseases.Journal of pharmacy & bioallied sciences · 2014
    Review
  6. Article
  7. Article
  8. Nanoemulsions and nanoparticles for non-melanoma skin cancer: effects of lipid materials.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2013
    Article
  9. Article
  10. 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

7 authors at 1 institution in 1 country.

Ka Wing ChengDivision of Cancer Prevention, Department of Medicine, Stony Brook University, Stony Brook, NY, USA.
George Mattheolabakis
Chi C Wong
Nengtai Ouyang
Liqun Huang
Panayiotis P Constantinides
Basil Rigas
Stony Brook University · US

Funding

No-Releasing Aspirin and Colon Cancer PreventionR01CA092423 · NCI · STATE UNIVERSITY NEW YORK STONY BROOK · PI RIGAS, BASIL · 2001 to 2011
$4.1M
Colon Cancer Prevention with Phospho-SulindacR01CA139454 · NCI · STATE UNIVERSITY NEW YORK STONY BROOK · PI RIGAS, BASIL · 2009 to 2013
$1.6M
Phospho-valproic acid for pancreatic cancer preventionR01CA154172 · NCI · STATE UNIVERSITY NEW YORK STONY BROOK · PI RIGAS, BASIL · 2010 to 2014
$1.6M
NCI NIH HHS R01 CA092423NCI NIH HHS R01CA09242308NCI NIH HHS R01 CA139454NCI NIH HHS R01CA139454NCI NIH HHS R01 CA154172NCI NIH HHS R01CA154172
6 · The paper itself

Abstract

Phospho-sulindac (P-S, OXT-328), a novel sulindac derivative, has shown superior anticancer efficacy and safety compared to sulindac. In this study, we investigated the efficacy of topical P-S hydrogel in the treatment of non-melanoma skin cancer in preclinical models. P-S is a potent inhibitor of A431 epidermoid carcinoma in vitro and achieves this effect by inhibiting cell proliferation and inducing apoptosis. The anticancer efficacy of topical and oral P-S was further evaluated in mice bearing A431 intradermal xenografts. Compared to the controls, topical P-S hydrogel inhibited the A431 xenografts by 70.5% (p<0.01), while oral P-S inhibited it by 43.4% (p<0.05), being significantly less effective than topical P-S (p=0.017). Topical P-S hydrogel generated significant levels (>500 nmol/g tumor tissue) of intact P-S in the tumors, accounting for 92.5% of the total metabolites in the A431 xenografts. This local delivery of high levels of intact P-S to the A431 xenografts is an important contributor to the potent activity of topical P-S and no local or systemic side effects were noted in the treatment group. Thus, topical P-S is a promising treatment modality against non-melanoma skin cancer and merits further evaluation.

Indexed as

Administration, TopicalAnimalsApoptosisCarcinoma, Squamous CellCell Line, TumorCell ProliferationHumansMiceOrganophosphorus CompoundsSkin NeoplasmsSulindacXenograft Model Antitumor AssaysOrganophosphorus CompoundsOXT-328Sulindac

Identifiers

PMID22842609
PMCPMC3583614
OpenAlexW2064483818

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.