Evidence map›Paper›PMID 32164629›Full record

ArticleBMC cancer2020

Alteration in the sensitivity to crizotinib by Na

Fenglian Yang, Mu Hu, Siyuan Chang, Jing Huang, Yang Si, Jinghui Wang, Shan Cheng, Wen G Jiang

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. NaJournal of immunology (Baltimore, Md. : 1950) · 2021
    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

8 authors at 2 institutions in 2 countries.

Fenglian YangSchool of Basic Medical Sciences, Capital Medical University, Beijing, 100069, People's Republic of China.
Mu HuBeijing Key Laboratory of Cancer & Metastasis Research, Capital Medical University, Beijing, China.
Siyuan ChangSchool of Basic Medical Sciences, Capital Medical University, Beijing, 100069, People's Republic of China.
Jing HuangSchool of Basic Medical Sciences, Capital Medical University, Beijing, 100069, People's Republic of China.
Yang SiSchool of Basic Medical Sciences, Capital Medical University, Beijing, 100069, People's Republic of China.
Jinghui WangDepartment of Medical Oncology, Beijing Chest Hospital, Beijing, 101149, P.R. China.
Shan ChengSchool of Basic Medical Sciences, Capital Medical University, Beijing, 100069, People's Republic of China. chengs@ccmu.edu.cn.ORCID http://orcid.org/0000-0002-8658-6916
Wen G JiangSchool of Basic Medical Sciences, Capital Medical University, Beijing, 100069, People's Republic of China.
Capital Medical University · CNBeijing Chest Hospital · CN

Funding

Supporting Project for High Caliber Teachers in Beijing Municipal Universities during the "13th Five-year Plan" IDHT20170516
6 · The paper itself

Abstract

backgroundNa

methodsBoth ALK-translocated and ALK-negative lung adenocarcinoma specimens in tissue sections were collected for immunohistochemistry. The possible mechanisms of NHERF1 and its role in the cell sensitivity to crizotinib were investigated using an ALK-positive and crizotinib-sensitive lung adenocarcinoma cell line H3122. Either a NHERF1 overexpression vector or agents for NHERF1 knockdown was used for crizotinib sensitivity measures, in association with cell viability and apoptosis assays.

resultsThe expression level of NHERF1 in ALK-translocated NSCLC was significantly higher than that in other lung cancer tissues. NHERF1 expression in ALK positive lung cancer cells was regulated by ALK activities, and was in return able to alter the sensitivity to crizotinib. The function of NHERF1 to influence crizotinib sensitivity was depending on its subcellular distribution in cytosol instead of its nucleus localized form.

conclusionEctopically overexpressed NHERF1 could be a functional protein for consideration to suppress lung cancers. The determination of NHERF1 levels in ALK positive NSCLC tissues might be useful to predict crizotinib resistance, especially by distinguishing cytosolic or nuclear localized NHERF1 for the overexpressed molecules.

Indexed as

Up-RegulationAnaplastic Lymphoma KinaseCarcinoma, Non-Small-Cell LungCell Line, TumorCell NucleusCell ProliferationCell SurvivalCrizotinibCytosolDrug Resistance, NeoplasmGene Expression Regulation, NeoplasticHumansLung NeoplasmsPhosphoproteinsSodium-Hydrogen ExchangersALK protein, humanAnaplastic Lymphoma KinaseCrizotinibPhosphoproteinssodium-hydrogen exchanger regulatory factorSodium-Hydrogen ExchangersALKCrizotinibLung cancerNHERF1PDZ protein

Identifiers

PMID32164629
PMCPMC7068933
OpenAlexW3011075452

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.