Evidence map›Paper›PMID 27867568›Full record

ArticleJournal of thoracic disease2016

The overexpression of KIFC1 was associated with the proliferation and prognosis of non-small cell lung cancer.

Yafang Liu, Ping Zhan, Zejun Zhou, Ze Xing, Suhua Zhu, Chenhui Ma, Qian Li, Qingqing Zhu, Yingying Miao, Jianya Zhang and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of thoracic disease, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 14% 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

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 57 citations in OpenAlex.

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  16. High Expression of KIFC1 in Glioma Correlates with Poor Prognosis.Journal of Korean Neurosurgical Society · 2024
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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 3 institutions in 1 country.

Yafang LiuDepartment of Respiratory Medicine, Jinling Hospital, Southern Medical University, Nanjing 210002, China.
Ping ZhanDepartment of Respiratory Medicine, Jinling Hospital, Nanjing University School of Medicine, Nanjing 210002, China.
Zejun ZhouDepartment of Respiratory Medicine, Jinling Hospital, Southern Medical University, Nanjing 210002, China.
Ze XingDepartment of Respiratory Medicine, Jinling Hospital, Nanjing University School of Medicine, Nanjing 210002, China.
Suhua ZhuDepartment of Respiratory Medicine, Jinling Hospital, Southern Medical University, Nanjing 210002, China.
Chenhui MaDepartment of Respiratory Medicine, Jinling Hospital, Southern Medical University, Nanjing 210002, China.
Qian LiDepartment of Respiratory Medicine, Jinling Hospital, Southern Medical University, Nanjing 210002, China.
Qingqing ZhuDepartment of Respiratory Medicine, Jinling Hospital, Southern Medical University, Nanjing 210002, China.
Yingying MiaoDepartment of Respiratory Medicine, Jinling Hospital, Southern Medical University, Nanjing 210002, China.
Jianya ZhangDepartment of Respiratory Medicine, Jinling Hospital, Southern Medical University, Nanjing 210002, China.
Tangfeng LvDepartment of Respiratory Medicine, Jinling Hospital, Southern Medical University, Nanjing 210002, China;; Department of Respiratory Medicine, Jinling Hospital, Nanjing University School of Medicine, Nanjing 210002, China.
Yong SongDepartment of Respiratory Medicine, Jinling Hospital, Southern Medical University, Nanjing 210002, China;; Department of Respiratory Medicine, Jinling Hospital, Nanjing University School of Medicine, Nanjing 210002, China.
Nanjing General Hospital of Nanjing Military Command · CNSouthern Medical University · CNNanjing University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe kinesin family member C1 (KIFC1, also known as HSET) is a kinesin superfamily protein (KIFs). Although KIFC1 acts as a crucial role in the development of several human cancers, the KIFC1 expression profile and functional remain unclear in non-small cell lung cancer (NSCLC).

methodsWe collected the fresh NSCLC samples and paired normal lung tissue in patients with lung cancer operation, and detected KIFC1 expression using quantitative reverse-transcription polymerase chain reaction (qRT-PCR) and Western blotting. To expand on previous smaller-scale studies, NSCLC tissue microarrays (TMA) were analyzed by IHC. Finally, cell lines were employed to further probe the potential mechanisms.

resultsIn this study, we described that KIFC1 was significantly upregulated in NSCLC tissues compared with the corresponding normal tissues. Moreover, KIFC1 overexpression was associated with the poor overall survival (OS) of NSCLC patients, and siRNA-mediated knockdown of KIFC1 significantly suppressed tumor cell proliferation

conclusionswe report that increased KIFC1 expression may promote cell proliferation and identified it as a biomarker of unfavorable prognosis in NSCLC patients.

Indexed as

cell division cycle protein 2 homolog (cdc2)cyclin-dependent kinase inhibitor 1A (p21)Kinesin family member C1 (KIFC1)non-small cell lung cancer (NSCLC)prognostic

Identifiers

PMID27867568
PMCPMC5107536
OpenAlexW2540329287

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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.