Evidence map›Paper›PMID 25668010›Full record

ArticleBritish journal of cancer2015

High expression of kinesin light chain-2, a novel target of miR-125b, is associated with poor clinical outcome of elderly non-small-cell lung cancer patients.

M Wang, X Zhu, Z Sha, N Li, D Li, L Chen

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

16 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
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  4. Article
  5. Cells · 2022
    Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. The Emerging Roles of miR-125b in Cancers.Cancer management and research · 2020
    Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. miR-125b suppresses the proliferation of hepatocellular carcinoma cells by targeting Sirtuin7.International journal of clinical and experimental medicine · 2015
    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 2 institutions in 1 country.

M WangDepartment of Radiation Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, Republic of China.
X ZhuDepartment of Radiation Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, Republic of China.
Z ShaDepartment of Radiation Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, Republic of China.
N LiDepartment of Radiation Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, Republic of China.
D LiDepartment of Radiation Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, Republic of China.
L ChenDepartment of Radiation Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, Republic of China.
Southern Medical University · CNNanfang Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMiR-125b has critical role in non-small-cell lung cancer (NSCLC) cell migration, and its target genes have not been elucidated. Kinesin-1 light chain (KLC)-2 was predicted as one of miR-125b's targets by bioinformatics analysis. This study is to identify the function of KLC2 and its interaction with miR-125b in NSCLC.

methodsKinesin-1 light chain-2 protein expression and its clinical relevance were analysed in 140 matched NSCLC and adjacent non-neoplastic lung tissues. Both KLC2 gain- and loss-of-function analyses were performed in NSCLC cell lines by transient transfection. The direct interaction between KLC2 and miR-125b was confirmed by a luciferase reporter assay and a transient co-transfection assay as well as an analysis of eight matched clinical samples.

resultsKLC2 protein was upregulated in NSCLC cell lines and tissues, and was an independent predictor of poor prognosis for elderly NSCLC patients. Kinesin-1 light chain-2 remarkably enhanced the invasive and migratory ability of NSCLC cells. MiR-125b inhibited KLC2 3'-untranslated region luciferase activity and protein expression, and inversely correlated with KLC2 expression in clinical samples. Kinesin-1 light chain-2 almost completely reversed miR-125b-induced inhibition on migration and invasion.

conclusionsKinesin-1 light chain-2 protein overexpression predicts poor survival in elderly NSCLC patients. Kinesin-1 light chain-2 acts as a proto-oncogene and a functional target of miR-125b in NSCLC cells.

Indexed as

3' Untranslated RegionsAgedAged, 80 and overCarcinoma, Non-Small-Cell LungCell Line, TumorCell MovementFemaleGene Expression Regulation, NeoplasticHumansKinesinsLung NeoplasmsMaleMicroRNAsMicrotubule-Associated ProteinsMiddle AgedPrognosis3' Untranslated RegionsKinesinsMAS1 protein, humanMicroRNAsMicrotubule-Associated ProteinsMIRN125 microRNA, humanProto-Oncogene Mas

Identifiers

PMID25668010
PMCPMC4453958
OpenAlexW2078543237

What OpenQuestion holds

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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.