Evidence map›Paper›PMID 32368398›Full record

ArticleAmerican journal of cancer research2020

Cisplatin sensitivity mediated by NKX2-1 in lung adenocarcinoma is dependent on p53 mutational status via modulating TNFSF10 expression.

Ming-Jenn Chen, Po-Ming Chen, Lee Wang, Ching-Ju Shen, Chi-Yi Chen, Huei Lee

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 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 47% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Activation of the TGF-Disease markers · 2022
    Article
  3. 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

6 authors at 4 institutions in 1 country.

Ming-Jenn ChenDepartment of Surgery, Chi Mei Medical Center Tainan, Taiwan.
Po-Ming ChenGraduate Institute of Cancer Biology and Drug Discovery, Taipei Medical University Taipei, Taiwan.
Lee WangDepartment of Public Health, Chung Shan Medical University Taichung, Taiwan.
Ching-Ju ShenDepartment of Gynecology and Obstetrics, Kaohsiung Medical University Hospital, College of Medicine, Kaohsiung Medical University Kaohsiung, Taiwan.
Chi-Yi ChenDepartment of Surgery, Chung Shan Medical University Hospital Taichung, Taiwan.
Huei LeeGraduate Institute of Cancer Biology and Drug Discovery, Taipei Medical University Taipei, Taiwan.
Chia Nan University of Pharmacy and Science · TWChung Shan Medical University · TWChung Shan Medical University Hospital · TWKaohsiung Medical University Chung-Ho Memorial Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

NKX2-1 was shown to enhance cisplatin sensitivity in KRAS-mutated cells, but it conferred cisplatin resistance in EGFR-mutated lung adenocarcinoma cells. However, NKX2-1 as a dual role in tumor progression depended on p53 mutational status via modulation of the NF-κB pathway. We hypothesized that NKX2-1 may confer cisplatin resistance in p53-mutated (p53-MT) lung adenocarcinoma cells but may enhance cisplatin sensitivity in wild-type (p53-WT) cells. In the present study, six p53-MT and -p53-WT cell lines were treated with various concentrations of cisplatin to calculate the inhibitory concentration of cisplatin for 50% cell viability (IC

Indexed as

cisplatinlung adenocarcinomaNKX2-1p53 mutational statusTNFSF10

Identifiers

PMID32368398
PMCPMC7191106
OpenAlexW3021258262

What OpenQuestion 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 OpenQuestion graph.