Evidence map›Paper›PMID 39302104›Full record

ArticleCancer research communications2024

Oncogenic Mutant p53 Sensitizes Non-Small Cell Lung Cancer Cells to Proteasome Inhibition via Oxidative Stress-Dependent Induction of Mitochondrial Apoptosis.

Kranthi Kumar Chougoni, Victoria Neely, Boxiao Ding, Eziafa Oduah, Vianna T Lam, Bin Hu, Jennifer E Koblinski, Bradford E Windle, Swati Palit Deb, Sumitra Deb and 4 more

Abstract read
In one paragraph

Article in Cancer research communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
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

14 authors.

Kranthi Kumar Chougoni *Department of Medicine, Keck School of Medicine of USC, USC Norris Comprehensive Cancer Center, University of Southern California, Los Angeles, California.ORCID 0000-0003-4102-8723
Victoria Neely *Philips Institute for Oral Health Research, VCU School of Dentistry, Virginia Commonwealth University, Richmond, Virginia.ORCID 0009-0004-8409-1823
Boxiao DingDepartment of Medicine, Keck School of Medicine of USC, USC Norris Comprehensive Cancer Center, University of Southern California, Los Angeles, California.ORCID 0009-0008-0050-9217
Eziafa OduahDivision of Medical Oncology, Department of Medicine, Duke University School of Medicine, Duke Cancer Institute, Duke University, Durham, North Carolina.ORCID 0000-0001-8517-6360
Vianna T LamPhilips Institute for Oral Health Research, VCU School of Dentistry, Virginia Commonwealth University, Richmond, Virginia.ORCID 0009-0002-9640-2321
Bin HuVCU Cancer Mouse Models Core, Virginia Commonwealth University, Richmond, Virginia.ORCID 0009-0001-1345-9764
Jennifer E KoblinskiVCU Cancer Mouse Models Core, Virginia Commonwealth University, Richmond, Virginia.ORCID 0000-0002-7156-2030
Bradford E WindlePhilips Institute for Oral Health Research, VCU School of Dentistry, Virginia Commonwealth University, Richmond, Virginia.ORCID 0000-0001-9613-7084
Swati Palit DebVCU Massey Comprehensive Cancer Center, Virginia Commonwealth University, Richmond, Virginia.ORCID 0009-0001-4642-6424
Sumitra DebVCU Massey Comprehensive Cancer Center, Virginia Commonwealth University, Richmond, Virginia.ORCID 0009-0000-1008-3100
Jorge J NievaDepartment of Medicine, Keck School of Medicine of USC, USC Norris Comprehensive Cancer Center, University of Southern California, Los Angeles, California.ORCID 0000-0003-1605-4719
Senthil K RadhakrishnanVCU Massey Comprehensive Cancer Center, Virginia Commonwealth University, Richmond, Virginia.ORCID 0000-0002-5211-9498
Hisashi HaradaPhilips Institute for Oral Health Research, VCU School of Dentistry, Virginia Commonwealth University, Richmond, Virginia.ORCID 0000-0001-5993-1289
Steven R GrossmanDepartment of Medicine, Keck School of Medicine of USC, USC Norris Comprehensive Cancer Center, University of Southern California, Los Angeles, California.ORCID 0009-0003-4692-6925

Funding

USC/NORRIS COMPREHENSIVE CANCER CENTER (CORE) SUPPORTP30CA014089 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI MYLES G COCKBURN · 1985 to 2026
$181.4M
Virus Vector Shared ResourceP30CA016059 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI Kim Felder Rhoads · 1985 to 2026
$51.0M
Targeting gain-of-function p53 and BCL-2 for small cell lung cancer treatmentR21CA259782 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI HARADA, HISASHI · 2022 to 2023
$395k
NCI NIH HHS P30 CA014089NCI NIH HHS P30 CA016059NCI NIH HHS R21 CA259782NIH HHS R21 CA259782VCU Massey Comprehensive Cancer Center Team Science Award
6 · The paper itself

Abstract

significanceNSCLC is the leading cause of cancer death due, in part, to a lack of active therapies in advanced disease. We demonstrate that combination therapy with a proteasome inhibitor, BH3-mimetic, and chemotherapy is an active precision therapy in NSCLC cells and tumors expressing Onc-p53 alleles.

Indexed as

ApoptosisCarcinoma, Non-Small-Cell LungLung NeoplasmsMitochondriaOxidative StressProteasome InhibitorsTumor Suppressor Protein p53AnimalsCell Line, TumorHumansMiceMutationXenograft Model Antitumor AssaysProteasome InhibitorsTP53 protein, humanTumor Suppressor Protein p53

Identifiers

PMID39302104
PMCPMC11474859

What Socratic holds

Textmetadata
LicenceCC BY
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.