Evidence map›Paper›PMID 25085205›Full record

ArticleInvestigational new drugs2014

CG100649, a novel COX-2 inhibitor, inhibits colorectal adenoma and carcinoma growth in mouse models.

Sun-Hee Kim, Ofer Margalit, Hiroshi Katoh, Dingzhi Wang, Hong Wu, Dianren Xia, Vijaykumar R Holla, Peiying Yang, Raymond N DuBois

Open access · greenAbstract read
In one paragraph

Article in Investigational new drugs, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 14% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. The effect of prediagnostic aspirin use on the prognosis of stage III colorectal cancer.International journal of clinical and experimental medicine · 2015
    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 2 institutions in 1 country.

Sun-Hee Kim *Arizona State University Biodesign Institute, Tempe, Arizona (O.M., D.W., R.N.D); Departments of Cancer Biology (S.H.K, H.W., D.X., V.R.H), and General Oncology (P.Y.), The University of Texas MD Anderson Cancer Center, Houston, Texas.
Ofer Margalit *Arizona State University Biodesign Institute, Tempe, Arizona (O.M., D.W., R.N.D); Departments of Cancer Biology (S.H.K, H.W., D.X., V.R.H), and General Oncology (P.Y.), The University of Texas MD Anderson Cancer Center, Houston, Texas.
Hiroshi KatohArizona State University Biodesign Institute, Tempe, Arizona (O.M., D.W., R.N.D); Departments of Cancer Biology (S.H.K, H.W., D.X., V.R.H), and General Oncology (P.Y.), The University of Texas MD Anderson Cancer Center, Houston, Texas.
Dingzhi WangArizona State University Biodesign Institute, Tempe, Arizona (O.M., D.W., R.N.D); Departments of Cancer Biology (S.H.K, H.W., D.X., V.R.H), and General Oncology (P.Y.), The University of Texas MD Anderson Cancer Center, Houston, Texas.
Hong WuArizona State University Biodesign Institute, Tempe, Arizona (O.M., D.W., R.N.D); Departments of Cancer Biology (S.H.K, H.W., D.X., V.R.H), and General Oncology (P.Y.), The University of Texas MD Anderson Cancer Center, Houston, Texas.
Dianren XiaArizona State University Biodesign Institute, Tempe, Arizona (O.M., D.W., R.N.D); Departments of Cancer Biology (S.H.K, H.W., D.X., V.R.H), and General Oncology (P.Y.), The University of Texas MD Anderson Cancer Center, Houston, Texas.
Vijaykumar R HollaArizona State University Biodesign Institute, Tempe, Arizona (O.M., D.W., R.N.D); Departments of Cancer Biology (S.H.K, H.W., D.X., V.R.H), and General Oncology (P.Y.), The University of Texas MD Anderson Cancer Center, Houston, Texas.
Peiying YangArizona State University Biodesign Institute, Tempe, Arizona (O.M., D.W., R.N.D); Departments of Cancer Biology (S.H.K, H.W., D.X., V.R.H), and General Oncology (P.Y.), The University of Texas MD Anderson Cancer Center, Houston, Texas.
Raymond N DuBoisArizona State University Biodesign Institute, Tempe, Arizona (O.M., D.W., R.N.D); Departments of Cancer Biology (S.H.K, H.W., D.X., V.R.H), and General Oncology (P.Y.), The University of Texas MD Anderson Cancer Center, Houston, Texas.
The University of Texas MD Anderson Cancer Center · USArizona State University · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
THE ROLE OF ENDOCANNABINOIDS AND THEIR RECEPTORS IN COLORECTAL CANCERP01CA077839 · NCI · VANDERBILT UNIVERSITY · PI DUBOIS, RAYMOND N. · 1999 to 2016
$17.8M
Eicosanoids and Intestinal Epithelial Growth RegulationR37DK047297 · NIDDK · VANDERBILT UNIVERSITY · PI DUBOIS, RAYMOND N. · 2003 to 2012
$3.8M
Nuclear Hormone Receptors in Intestinal BiologyR01DK062112 · NIDDK · VANDERBILT UNIVERSITY · PI DUBOIS, RAYMOND N. · 2002 to 2010
$3.0M
Role of Eicosanoids in Intestinal BiologyR01DK047297 · NIDDK · VANDERBILT UNIVERSITY · PI DUBOIS, RAYMOND N. · 1994 to 2018
$2.6M
(PQA1)The Molecular Mechanisms Underlying Effects of Aspirin on Colorectal CancerR01CA184820 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI DUBOIS, RAYMOND N. · 2014 to 2017
$1.6M
NCI NIH HHS P01 CA077839NCI NIH HHS P01-CA077839NCI NIH HHS R01 CA184820NIDDK NIH HHS R01 DK047297NIDDK NIH HHS R01 DK062112NIDDK NIH HHS R37 DK047297NIDDK NIH HHS R37-DK047297
6 · The paper itself

Abstract

Nonsteroidal anti-inflammatory drugs (NSAIDs) and selective cyclooxygenase-2 (COX-2) inhibitors (COXIBs) can reduce the risk of developing colorectal cancer (CRC) and are being considered for use as adjuvant therapy for treatment of CRC patients. However, long-term use of most NSAIDs, except aspirin, increases cardiovascular risk, hampering use of these drugs in CRC prevention and possibly for treatment. CG100649 is a new member of the COXIB family, which is proposed to inhibit both COX-2 and carbonic anhydrase-I/-II (CA-I/-II) activity. Using mouse models, we show here that CG100649 inhibits premalignant and malignant colorectal lesions in mouse models, partly through inhibiting tumor cell proliferation. These pre-clinical findings suggest a need for further exploration of CG100649 for CRC prevention and treatment. The long-term safety profile of CG100649, particularly regarding its effect on cardiovascular risk, is yet to be determined.

Indexed as

AdenomaAnimalsAntineoplastic AgentsCarcinomaCell Line, TumorCell ProliferationColorectal NeoplasmsCyclooxygenase 2 InhibitorsDinoprostoneFuransHumansMiceSulfonamidesXenograft Model Antitumor AssaysAntineoplastic AgentsCG100649Cyclooxygenase 2 InhibitorsDinoprostoneFuransSulfonamides

Identifiers

PMID25085205
PMCPMC4356209
OpenAlexW1971926696

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.