Evidence map›Paper›PMID 29572068›Full record

ArticleEuropean journal of pharmacology2018

Polygodial analog induces apoptosis in LNCaP prostate cancer cells.

Subramanyam Dasari, Angela Lincy Prem Antony Samy, Parnal Narvekar, Venkata Satish Dontaraju, Ramesh Dasari, Alexander Kornienko, Gnanasekar Munirathinam

Open access · greenAbstract read
In one paragraph

Article in European journal of pharmacology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.6field-weighted citation impact, top 19% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

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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 1 country.

Subramanyam DasariDepartment of Biomedical Sciences, College of Medicine, University of Illinois, Rockford, IL, USA.
Angela Lincy Prem Antony SamyDepartment of Biomedical Sciences, College of Medicine, University of Illinois, Rockford, IL, USA.
Parnal NarvekarDepartment of Biomedical Sciences, College of Medicine, University of Illinois, Rockford, IL, USA.
Venkata Satish DontarajuInternal Medicine, Rockford Memorial Hospital, Rockford, IL, USA.
Ramesh DasariDepartment of Chemistry and Biochemistry, Texas State University, San Marcos, TX 78666, USA.
Alexander KornienkoDepartment of Chemistry and Biochemistry, Texas State University, San Marcos, TX 78666, USA.
Gnanasekar MunirathinamDepartment of Biomedical Sciences, College of Medicine, University of Illinois, Rockford, IL, USA. Electronic address: mgnanas@uic.edu.
University of Illinois Chicago, Rockford campus · USTexas State University · USJavon Bea Hospital-Rockton · US

Funding

Managing prostate cancer metastasis using vitamin k2R21CA184646 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI MUNIRATHINAM, GNANASEKAR · 2015 to 2016
$382k
Overcoming EMT-driven metastatic castration-resistant prostate cancerR03CA212890 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI MUNIRATHINAM, GNANASEKAR · 2017 to 2018
$160k
NCI NIH HHS R03 CA212890NCI NIH HHS R21 CA184646
6 · The paper itself

Abstract

Prostate cancer (PCa) is the second leading cause of death in American men. The chemotherapeutic treatment strategies are generally not effective and can lead to side effects. Hence, there is an urgent need to identify novel chemotherapeutic agents. The aim of this study was to synthesize and evaluate the therapeutic effects of a synthetic analog of polygodial (PG), a pungent constituent abundantly present in mountain pepper, water pepper and dorrigo pepper, on LNCaP PCa cell line and its anti-cancer mechanisms in a preclinical study. We evaluated the anti-cancer potential of the PG analog namely DRP-27 using various assays such as cell viability by MTT assay, anchorage independent growth by soft agar assay, reactive oxygen species generation by 2',7'-dichlorofluorescein probe-based fluorescence assay, and apoptosis by Annexin-V and TUNEL assays respectively. Western blot analysis was performed to identify the molecular mechanism of DRP-27-induced cell death. Our results showed that DRP-27 significantly inhibited LNCaP cell proliferation in a dose-dependent manner at 48 h treatment in vitro. In addition, DRP-27 potently inhibited anchorage-independent growth of these cells. Flow cytometry, Annexin-V and TUNEL assays confirmed that DRP-27 induces apoptosis in LNCaP cells. DRP-27 also induced the activation of intracellular reactive oxygen species. Western blot analysis revealed that DRP-27 downregulated the expression of survivin, while activating Bax and DNA damage marker pH

Indexed as

Antineoplastic AgentsApoptosisCaspase 3Cell Line, TumorCell ProliferationDNA DamageEnzyme ActivationHumansMaleProstatic NeoplasmsReactive Oxygen SpeciesSesquiterpenesAntineoplastic AgentsCaspase 3polygodialReactive Oxygen SpeciesSesquiterpenesApoptosisPolygodialProstate cancerReactive oxygen species

Identifiers

PMID29572068
PMCPMC5918418
OpenAlexW2789735417

What OpenQuestion holds

Textmetadata
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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.