Evidence map›Paper›PMID 30378157›Full record

ArticleJournal of cellular biochemistry2019

Endoplasmic reticulum stress, autophagic and apoptotic cell death, and immune activation by a natural triterpenoid in human prostate cancer cells.

Benjamin M Johnson, Faisal F Y Radwan, Azim Hossain, Bently P Doonan, Jessica D Hathaway-Schrader, Jason M God, Christina V Voelkel-Johnson, Narendra L Banik, Sakamuri V Reddy, Azizul Haque

Open access · greenAbstract read
In one paragraph

Article in Journal of cellular biochemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.2field-weighted citation impact, top 46% 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

9 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Review
  3. CanPharmaceuticals (Basel, Switzerland) · 2025
    Review
  4. Article
  5. Review
  6. Review
  7. Peptide Modification Diminishes HLA Class II-restricted CD4International journal of molecular sciences · 2022
    Article
  8. MGMT-inhibitor in combination with TGF-βRI inhibitor or CDK 4/6 inhibitor increases temozolomide sensitivity in temozolomide-resistant glioblastoma cells.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2021
    Article
  9. 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

10 authors at 1 institution in 1 country.

Benjamin M JohnsonDepartment of Microbiology and Immunology and Hollings Cancer Center, Medical University of South Carolina, Charleston, South Carolina.
Faisal F Y RadwanDepartment of Microbiology and Immunology and Hollings Cancer Center, Medical University of South Carolina, Charleston, South Carolina.
Azim HossainDepartment of Microbiology and Immunology and Hollings Cancer Center, Medical University of South Carolina, Charleston, South Carolina.
Bently P DoonanDepartment of Microbiology and Immunology and Hollings Cancer Center, Medical University of South Carolina, Charleston, South Carolina.
Jessica D Hathaway-SchraderDepartment of Microbiology and Immunology and Hollings Cancer Center, Medical University of South Carolina, Charleston, South Carolina.
Jason M GodDepartment of Microbiology and Immunology and Hollings Cancer Center, Medical University of South Carolina, Charleston, South Carolina.
Christina V Voelkel-JohnsonDepartment of Microbiology and Immunology and Hollings Cancer Center, Medical University of South Carolina, Charleston, South Carolina.
Narendra L BanikDepartment of Neurosciences, Medical University of South Carolina, Charleston, South Carolina.
Sakamuri V ReddyChildren's Research Institute, Medical University of South Carolina, Charleston, South Carolina.ORCID 0000-0003-2848-568X
Azizul HaqueDepartment of Microbiology and Immunology and Hollings Cancer Center, Medical University of South Carolina, Charleston, South Carolina.ORCID 0000-0002-6386-9390
Medical University of South Carolina · US

Funding

Translational Science Laboratory Shared ResourceP30CA138313 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI Jian Ouyang · 2009 to 2026
$42.7M
T-COHR: Training in Craniofacial and Oral Health ResearchT32DE017551 · NIDCR · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI YAO, HAI · 2006 to 2025
$10.3M
Disruption of HLA Class II-Mediated Immune Recognition of B-Cell LymphomasR01CA129560 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI HAQUE, AZIZUL · 2009 to 2013
$1.5M
NCI NIH HHS P30 CA138313NCI NIH HHS R01 CA129560NIDCR NIH HHS T32 DE017551
6 · The paper itself

Abstract

Though the current therapies are effective at clearing an early stage prostate cancer, they often fail to treat late-stage metastatic disease. We aimed to investigate the molecular mechanisms underlying the anticancer effects of a natural triterpenoid, ganoderic acid DM (GA-DM), on two human prostate cancer cell lines: the androgen-independent prostate carcinoma (PC-3), and androgen-sensitive prostate adenocarcinoma (LNCaP). Cell viability assay showed that GA-DM was relatively more toxic to LNCaP cells than to PC-3 cells (IC

Indexed as

Antineoplastic AgentsApoptosisAutophagyCalpainCaspase 3Cell Cycle CheckpointsCell SurvivalDNA FragmentationEndoplasmic Reticulum StressHumansMalePC-3 CellsProstatic NeoplasmsProto-Oncogene Proteins c-bcl-2Signal TransductionTriterpenes3,7-dioxolanosta-8,24-dien-26-oic acidAntineoplastic AgentsCalpainCASP3 protein, humanCaspase 3Proto-Oncogene Proteins c-bcl-2TP53 protein, humanTriterpenesTumor Suppressor Protein p53apoptosiscalpainendoplasmic reticulum stressganoderic acid DMimmune activationprostate cancer

Identifiers

PMID30378157
PMCPMC6561659
OpenAlexW2898661588

What OpenQuestion holds

Textmetadata
LicenceTDM
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.