Evidence map›Paper›PMID 29728874›Full record

ArticleInflammopharmacology2019

Antineoplastic influence of nimesulide in chemically induced hepatocellular carcinoma by inhibition of DNA synthesis.

M Afzal, D P Bhardwaj, R Khan, Imran Kazmi, S Saleem, F A Al-Abbasi, Firoz Anwar

Abstract read
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In one paragraph

Article in Inflammopharmacology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
0.5field-weighted citation impact, top 33% 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

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. 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

7 authors at 3 institutions in 2 countries.

M AfzalDepartment of Pharmacology, College of Pharmacy, Jouf University, Sakaka, Kingdom of Saudi Arabia.
D P BhardwajSiddhartha Institute of Pharmacy, Near I.T. Park, Sahastradhara Road, Dehradun, Uttarakhand, India.
R KhanSiddhartha Institute of Pharmacy, Near I.T. Park, Sahastradhara Road, Dehradun, Uttarakhand, India.
Imran KazmiDepartment of Biochemistry, Faculty of Science, King Abdulaziz University, Jeddah, Saudi Arabia. kazmiimran2005@gmail.com.ORCID http://orcid.org/0000-0003-1881-5219
S SaleemSiddhartha Institute of Pharmacy, Near I.T. Park, Sahastradhara Road, Dehradun, Uttarakhand, India.
F A Al-AbbasiDepartment of Biochemistry, Faculty of Science, King Abdulaziz University, Jeddah, Saudi Arabia.
Firoz AnwarDepartment of Biochemistry, Faculty of Science, King Abdulaziz University, Jeddah, Saudi Arabia. firoz_anwar2000@yahoo.com.
King Abdulaziz University · SASiddhartha Medical College · INJouf University · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma is emerging as one of the most common forms of cancer resulting in thousands of death worldwide. The purpose of this study was to screen nimesulide for anticancer activity in chemically induced hepatocellular carcinoma in Wistar rats as well as in BEL 7402 and HEP G2 cell lines. HCC in rats was induced by administering a single dose of diethyl nitrosamine (150 mg/kg) intraperitoneally. Duration of the in vivo study was 12 weeks and the anticancer potential was further confirmed by in vitro cell line study. Administration of DENA in Wistar rats significantly elevated the levels of serum biochemical parameters and α-feto protein. Treatment with different dose of nimesulide significantly decreased the markedly raised serum levels of biochemical parameters as well as maintained the histology of the liver tissues nearly similar to the normal. Further study of hepatocytes enzymes showed that treatment with nimesulide also improved the antioxidant enzyme levels. Our study also examined the cytotoxicity and DNA synthesis inhibition by nimesulide in BEL 7402 and Hep G2 cell lines. Cell viability was assessed by [

Indexed as

AnimalsAntineoplastic AgentsAntioxidantsCarcinoma, HepatocellularCell Line, TumorCell SurvivalDNAFemaleHep G2 CellsHumansLiverLiver NeoplasmsMaleRatsRats, WistarReactive Oxygen SpeciesAntineoplastic AgentsAntioxidantsDNAnimesulideReactive Oxygen SpeciesSulfonamidesBiochemical parametersCOX-2 inhibitorDiethylnitrosamineHepatoprotective

Identifiers

PMID29728874
OpenAlexW2802764230

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.