Evidence map›Paper›PMID 34067020›Full record

ArticleInternational journal of molecular sciences2021

Novel Seleno-Aspirinyl Compound AS-10 Induces Apoptosis, G1 Arrest of Pancreatic Ductal Adenocarcinoma Cells, Inhibits Their NF-κB Signaling, and Synergizes with Gemcitabine Cytotoxicity.

Deepkamal N Karelia, Sangyub Kim, Manoj K Pandey, Daniel Plano, Shantu Amin, Junxuan Lu, Arun K Sharma

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

11 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Article
  3. Following the Trace of Cyclodextrins on the Selenium and Tellurium Odyssey.International journal of molecular sciences · 2024
    Review
  4. Review
  5. Formulation Studies with Cyclodextrins for Novel Selenium NSAID Derivatives.International journal of molecular sciences · 2024
    Article
  6. Article
  7. Article
  8. Article
  9. Therapeutic Benefits of Selenium in Hematological Malignancies.International journal of molecular sciences · 2022
    Review
  10. Article
  11. 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 1 institution in 2 countries.

Deepkamal N KareliaDepartment of Pharmacology, Penn State College of Medicine, 500 University Drive, Hershey, PA 17033, USA.
Sangyub KimDepartment of Pharmacology, Penn State College of Medicine, 500 University Drive, Hershey, PA 17033, USA.ORCID 0000-0002-0190-8593
Manoj K PandeyDepartment of Pharmacology, Penn State College of Medicine, 500 University Drive, Hershey, PA 17033, USA.
Daniel PlanoDepartment of Pharmacology, Penn State College of Medicine, 500 University Drive, Hershey, PA 17033, USA.ORCID 0000-0002-8266-0445
Shantu AminDepartment of Pharmacology, Penn State College of Medicine, 500 University Drive, Hershey, PA 17033, USA.
Junxuan LuDepartment of Pharmacology, Penn State College of Medicine, 500 University Drive, Hershey, PA 17033, USA.
Arun K SharmaDepartment of Pharmacology, Penn State College of Medicine, 500 University Drive, Hershey, PA 17033, USA.ORCID 0000-0002-7679-7779
Pennsylvania State University · US

Funding

Targeting AR and AR-Variants in Castration-Resistant Prostate CancerR01CA257370 · NCI · UNIVERSITY OF LOUISVILLE · PI DAMODARAN, CHENDIL, SHARMA, ARUN K · 2021 to 2025
$2.2M
A promising small molecule for pancreatic cancer therapyR21CA234681 · NCI · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI SHARMA, ARUN K · 2019 to 2020
$363k
NCI NIH HHS R01 CA257370NCI NIH HHS R21 CA234681NCI NIH HHS R21 CA234681 and R01CA172169
6 · The paper itself

Abstract

Current available therapies for pancreatic ductal adenocarcinoma (PDAC) provide minimal overall survival benefits and cause severe adverse effects. We have identified a novel molecule AS-10, a selenazolidine-bis-aspirinyl derivative, that was two to three orders of magnitude more potent than aspirin and at least one to two orders of magnitude more potent than gemcitabine in inhibiting PDAC cancer cell growth/viability against three PDAC cell lines while sparing mouse embryonic fibroblasts in the same exposure range. In Panc-1 cells, AS-10 induced apoptosis without necrosis, principally through caspase-3/7 cascade and reactive oxygen species, in addition to an induction of G

Indexed as

ApoptosisG1 Phase Cell Cycle CheckpointsAcetylcysteineAdenocarcinomaAspirinCarcinoma, Pancreatic DuctalCaspasesCell Line, TumorCell ProliferationCytokinesDeoxycytidineEnzyme ActivationGemcitabineGene Expression Regulation, NeoplasticHumansInflammation MediatorsAcetylcysteineAspirinCaspasesCytokinesDeoxycytidineGemcitabineInflammation MediatorsNF-kappa Bapoptosisaspirinpancreatic cancerRNA-Seqselenium

Identifiers

PMID34067020
PMCPMC8124556
OpenAlexW3159385806

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.