Evidence map›Paper›PMID 34629889›Full record

ArticlePharmacogenomics and personalized medicine2021

Nuclear Pore Glycoprotein 62 Genetic Variant rs9523 is Associated with Clinical Outcomes of Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors in Lung Adenocarcinoma Patients.

Ji Eun Park, Mi Jeong Hong, Shin Yup Lee, Jang Hyuck Lee, Jin Eun Choi, Hyo-Gyoung Kang, Sook Kyung Do, Ji Yun Jeong, Kyung Min Shin, Won Kee Lee and 8 more

Open access · goldAbstract read
In one paragraph

Article in Pharmacogenomics and personalized medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 91% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

18 authors at 1 institution in 1 country.

Ji Eun Park *Department of Internal Medicine, School of Medicine, Kyungpook National University, Daegu, Republic of Korea.
Mi Jeong Hong *Department of Biochemistry, School of Medicine, Kyungpook National University, Daegu, Republic of Korea.
Shin Yup LeeDepartment of Internal Medicine, School of Medicine, Kyungpook National University, Daegu, Republic of Korea.
Jang Hyuck LeeDepartment of Biochemistry, School of Medicine, Kyungpook National University, Daegu, Republic of Korea.
Jin Eun ChoiDepartment of Biochemistry, School of Medicine, Kyungpook National University, Daegu, Republic of Korea.
Hyo-Gyoung KangDepartment of Biochemistry, School of Medicine, Kyungpook National University, Daegu, Republic of Korea.
Sook Kyung DoDepartment of Biochemistry, School of Medicine, Kyungpook National University, Daegu, Republic of Korea.
Ji Yun JeongDepartment of Pathology, School of Medicine, Kyungpook National University, Daegu, Republic of Korea.ORCID 0000-0001-6167-4998
Kyung Min ShinDepartment of Radiology, School of Medicine, Kyungpook National University, Daegu, Republic of Korea.
Won Kee LeeDepartment of Medical Informatics, School of Medicine, Kyungpook National University, Daegu, Republic of Korea.
Sun Ha ChoiDepartment of Internal Medicine, School of Medicine, Kyungpook National University, Daegu, Republic of Korea.
Yong Hoon LeeDepartment of Internal Medicine, School of Medicine, Kyungpook National University, Daegu, Republic of Korea.
Hye Won SeoDepartment of Internal Medicine, School of Medicine, Kyungpook National University, Daegu, Republic of Korea.
Seung Soo YooDepartment of Internal Medicine, School of Medicine, Kyungpook National University, Daegu, Republic of Korea.
Jaehee LeeDepartment of Internal Medicine, School of Medicine, Kyungpook National University, Daegu, Republic of Korea.ORCID 0000-0001-8111-7320
Seung Ick ChaDepartment of Internal Medicine, School of Medicine, Kyungpook National University, Daegu, Republic of Korea.
Chang Ho KimDepartment of Internal Medicine, School of Medicine, Kyungpook National University, Daegu, Republic of Korea.
Jae Yong ParkDepartment of Internal Medicine, School of Medicine, Kyungpook National University, Daegu, Republic of Korea.
Kyungpook National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionEpidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) have represented the prototype of targeted therapy in NSCLC. Patients with EGFR-mutant lung adenocarcinoma extract an extraordinary clinical benefit from EGFR-TKIs. However, the extent and duration of these responses are heterogeneous, suggesting the existence of genetic modifiers affecting an individual's response to TKIs. We investigated whether genetic variants in miRNA binding sites are associated with the clinical outcome of EGFR-TKIs in lung adenocarcinoma patients.

methodsOne hundred SNPs at miRNA binding sites in cancer-related genes were selected for the analysis using the crosslinking, ligation and sequencing of hybrids (CLASH) and CancerGenes database. qRT-PCR and luciferase assays were conducted to evaluate the functional relevance of the SNPs.

results

conclusionGenetic variants in miRNA binding sites, especially

Indexed as

clinical outcomeEGFR-TKIlung adenocarcinomamiRNA binding sitepolymorphism

Identifiers

PMID34629889
PMCPMC8493114
OpenAlexW3202551131

What OpenQuestion holds

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LicenceCC BY-NC
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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.