Evidence map›Paper›PMID 31789388›Full record

ArticleInternational journal of oncology2020

Clinical importance of long non‑coding RNA LINC00460 expression in EGFR‑mutant lung adenocarcinoma.

Yuta Nakano, Kazutoshi Isobe, Hiroshi Kobayashi, Kyohei Kaburaki, Takuma Isshiki, Susumu Sakamoto, Yujiro Takai, Naobumi Tochigi, Tetsuo Mikami, Akira Iyoda and 2 more

Open access · hybridAbstract read
In one paragraph

Article in International journal of oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

25 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
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  8. Tumor-Suppressive and Oncogenic Roles of microRNA-149-5p in Human Cancers.International journal of molecular sciences · 2022
    Review
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  10. Article
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  13. Article
  14. Functions of non-coding RNAs in regulating cancer drug targets.Acta biochimica et biophysica Sinica · 2022
    Review
  15. Review
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  18. Article
  19. A Review on the Role of miR-149-5p in the Carcinogenesis.International journal of molecular sciences · 2021
    Review
  20. 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

12 authors at 1 institution in 1 country.

Yuta NakanoDepartment of Respiratory Medicine, Toho University School of Medicine, Tokyo 143‑8541, Japan.
Kazutoshi IsobeDepartment of Respiratory Medicine, Toho University School of Medicine, Tokyo 143‑8541, Japan.
Hiroshi KobayashiDepartment of Respiratory Medicine, Toho University School of Medicine, Tokyo 143‑8541, Japan.
Kyohei KaburakiDepartment of Respiratory Medicine, Toho University School of Medicine, Tokyo 143‑8541, Japan.
Takuma IsshikiDepartment of Respiratory Medicine, Toho University School of Medicine, Tokyo 143‑8541, Japan.
Susumu SakamotoDepartment of Respiratory Medicine, Toho University School of Medicine, Tokyo 143‑8541, Japan.
Yujiro TakaiDepartment of Respiratory Medicine, Toho University School of Medicine, Tokyo 143‑8541, Japan.
Naobumi TochigiDepartment of Surgical Pathology, Toho University School of Medicine, Tokyo 143‑8541, Japan.
Tetsuo MikamiDepartment of Pathology, Toho University School of Medicine, Tokyo 143‑8541, Japan.
Akira IyodaDepartment of Chest Surgery, Toho University School of Medicine, Tokyo 143‑8541, Japan.
Sakae HommaDepartment of Respiratory Medicine, Toho University School of Medicine, Tokyo 143‑8541, Japan.
Kazuma KishiDepartment of Respiratory Medicine, Toho University School of Medicine, Tokyo 143‑8541, Japan.
Toho University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long non‑coding RNAs (lncRNAs) have been reported to be involved in the physiological and pathological processes of tumor pathogenesis, including epithelial‑mesenchymal transition (EMT). However, epidermal growth factor receptor (EGFR)‑tyrosine kinase inhibitor (TKI) resistance is a major challenge in the treatment of advanced and recurrent EGFR‑mutant lung adenocarcinoma. An increased understanding of the underlying mechanisms would aid in the development of effective therapeutic strategies against EGFR‑TKI resistance, strategies which are urgently required for clinical therapy. In this study, long non‑coding RNA LINC00460 was identified as a novel marker of a poor response to EGFR‑TKI and prognosis. In lung cancer cells, LINC00460 promoted EGFR‑TKI resistance as a competitive decoy for miR‑149‑5p, thereby facilitating interleukin (IL)‑6 expression and inducing EMT‑like phenotypes. The knockdown or knockout of LINC00460 in gefitinib‑resistant non‑small cell lung cancer cells restored the response to EGFR‑TKI. In addition, as compared with patients with a low LINC00460 expression in tumors, those with a high LINC00460 expression had a significantly shorter progression‑free survival following gefitinib therapy, and a shorter overall survival. Therefore, LINC00460 may be a predictor of and potential therapeutic target for EGFR‑TKI resistance.

Indexed as

MutationAdenocarcinoma of LungApoptosisBiomarkers, TumorCarcinoma, Non-Small-Cell LungCell ProliferationDrug Resistance, NeoplasmErbB ReceptorsFollow-Up StudiesGene Expression Regulation, NeoplasticHumansLung NeoplasmsPrognosisProtein Kinase InhibitorsRNA, Long NoncodingSurvival RateBiomarkers, TumorEGFR protein, humanErbB ReceptorsProtein Kinase InhibitorsRNA, Long Noncoding

Identifiers

PMID31789388
PMCPMC6910175
OpenAlexW2990557156

What OpenQuestion holds

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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.