Evidence map›Paper›PMID 29549167›Full record

ArticleMolecular cancer therapeutics2018

Tetrandrine (TET) Induces Death Receptors Apo Trail R1 (DR4) and Apo Trail R2 (DR5) and Sensitizes Prostate Cancer Cells to TRAIL-Induced Apoptosis.

Gauri Shishodia, Sweaty Koul, Qin Dong, Hari K Koul

Open access · greenAbstract read
In one paragraph

Article in Molecular cancer therapeutics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

15 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
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  4. Rolapitant treats lung cancer by targeting deubiquitinase OTUD3.Cell communication and signaling : CCS · 2024
    Article
  5. Tetrandrine for Targeting Therapy Resistance in Cancer.Current topics in medicinal chemistry · 2024
    Review
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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

4 authors at 2 institutions in 1 country.

Gauri ShishodiaDepartment of Biochemistry and Molecular Biology, LSU Health Sciences Center, Shreveport, Louisiana.
Sweaty KoulFeist Weiller Cancer Center, Shreveport, Louisiana.
Qin DongDepartment of Biochemistry and Molecular Biology, LSU Health Sciences Center, Shreveport, Louisiana.
Hari K KoulDepartment of Biochemistry and Molecular Biology, LSU Health Sciences Center, Shreveport, Louisiana. hkoul@lsuhsc.edu.
Louisiana State University Health Sciences Center Shreveport · USOverton Brooks VA Medical Center · US

Funding

Tetrandrine for the treatment of Prostate CancerR01CA161880 · NCI · UNIVERSITY OF COLORADO DENVER · PI KOUL, HARI K · 2011 to 2015
$1.5M
BLRD VA I01 BX001258NCI NIH HHS R01 CA161880
6 · The paper itself

Abstract

TNF-related apoptosis-inducing ligand (TRAIL) selectively induces apoptosis in cancer cells, but not in normal cells; as such, it is a promising therapeutic agent. However, therapeutic resistance limits its clinical use in many malignancies, including prostate cancer. Strategies to sensitize cancer cells to TRAIL are urgently needed. We demonstrate here that small-molecule tetrandrine (TET) potentially sensitizes previously resistant (LNCaP and C4-2B cells) and mildly sensitive (PC3 cells) prostate cancer cells to TRAIL-induced apoptosis, and they do so by upregulating mRNA expression and protein levels of death receptors Apo Trail R1 (DR4) and Apo Trail R2 (DR5). Using shRNA knockdown, we show critical requirement of DR4 and DR5 in sensitization of prostate cancer cells to TRAIL. We show that double knockdown of DR4 and DR5 abrogated the apoptotic effects of TET and TRAIL. We also demonstrate that TET-induced DR4 and DR5 expression is independent of p53 status. Given that loss of p53 is associated with progression of prostate cancer to CRPC and NEPC, our results show that TET, by acting as a TRAIL-sensitizing agent in prostate cancer, could serve as a potential therapeutic agent in CRPC and NEPC, for which there is no cure to date.

Indexed as

ApoptosisBenzylisoquinolinesBiobehavioral SciencesCell Line, TumorCell SurvivalGene Expression Regulation, NeoplasticHumansMaleProstatic NeoplasmsReceptors, TNF-Related Apoptosis-Inducing LigandRNA InterferenceRNA, Small InterferingTNF-Related Apoptosis-Inducing LigandBenzylisoquinolinesReceptors, TNF-Related Apoptosis-Inducing LigandRNA, Small InterferingtetrandrineTNF-Related Apoptosis-Inducing LigandTNFRSF10A protein, humanTNFRSF10B protein, human

Identifiers

PMID29549167
PMCPMC10186773
OpenAlexW2793489332

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.