Evidence map›Paper›PMID 32775000›Full record

ArticleAmerican journal of cancer research2020

Repurposing antidepressant sertraline as a pharmacological drug to target prostate cancer stem cells: dual activation of apoptosis and autophagy signaling by deregulating redox balance.

Somaiah Chinnapaka, Velavan Bakthavachalam, Gnanasekar Munirathinam

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
3.5field-weighted citation impact, top 6% 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

33 citing papers in PubMed, 1 synthesis or guideline pooled it, 45 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

3 authors at 1 institution in 1 country.

Somaiah ChinnapakaDepartment of Biomedical Sciences, College of Medicine, University of Illinois Rockford, IL, USA.
Velavan BakthavachalamDepartment of Biomedical Sciences, College of Medicine, University of Illinois Rockford, IL, USA.
Gnanasekar MunirathinamDepartment of Biomedical Sciences, College of Medicine, University of Illinois Rockford, IL, USA.
University of Illinois Chicago, Rockford campus · US

Funding

Targeting TCTP Signaling to Control Castration-Resistant Prostate CancerR03CA230829 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI MUNIRATHINAM, GNANASEKAR · 2018 to 2019
$160k
NCI NIH HHS R03 CA230829
6 · The paper itself

Abstract

Cancer stem cells play a major role in tumor initiation, progression, and tumor relapse of prostate cancer (PCa). Recent studies suggest that Translationally Controlled Tumor Protein (TCTP) is a critical survival factor of stem cells including cancer stem cells. Here, we aimed to determine whether the TCTP inhibitor sertraline (STL) could target prostate cancer stem cells (PCSC). In colony formation, spheroidogenesis, angiogenesis, and wound healing assays STL showed a robust inhibition of tumorigenic (colony growth), angiogenic (endothelial tube formation) and metastatic (wound healing and migration) potential of PCSC. Interestingly, antioxidants such as N-acetyl cysteine (NAC), Glutathione (GSH) and catalase effectively blocked the cytotoxicity effect of STL on PCSC implicating oxidative stress as the underlying anti-PCSC targeting mechanism. Cell cycle analysis showed a robust G

Indexed as

angiogenesisantidepressantapoptosisautophagyoxidative stressprostate cancerprostate cancer stem cellsSertralineTCTP

Identifiers

PMID32775000
PMCPMC7407340
OpenAlexW3049415421

What Socratic 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 Socratic graph.