Evidence map›Paper›PMID 27347318›Full record

ArticleAmerican journal of translational research2016

Inhibiting CREPT reduces the proliferation and migration of non-small cell lung cancer cells by down-regulating cell cycle related protein.

Tao Liu, Wei-Miao Li, Wu-Ping Wang, Ying Sun, Yun-Feng Ni, Hao Xing, Jing-Hua Xia, Xue-Jiao Wang, Zhi-Pei Zhang, Xiao-Fei Li

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

17 citing papers in PubMed, 28 citations in OpenAlex.

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  12. Long Chain Non-Coding RNA (lncRNA) HOTAIR Knockdown Increases miR-454-3p to Suppress Gastric Cancer Growth by Targeting STAT3/Cyclin D1.Medical science monitor : international medical journal of experimental and clinical research · 2019
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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

10 authors at 1 institution in 1 country.

Tao LiuDepartment of Thoracic Surgery, Tangdu Hospital, The Fourth Military Medical University Xi'an 710038, China.
Wei-Miao LiDepartment of Thoracic Surgery, Tangdu Hospital, The Fourth Military Medical University Xi'an 710038, China.
Wu-Ping WangDepartment of Thoracic Surgery, Tangdu Hospital, The Fourth Military Medical University Xi'an 710038, China.
Ying SunDepartment of Thoracic Surgery, Tangdu Hospital, The Fourth Military Medical University Xi'an 710038, China.
Yun-Feng NiDepartment of Thoracic Surgery, Tangdu Hospital, The Fourth Military Medical University Xi'an 710038, China.
Hao XingDepartment of Thoracic Surgery, Tangdu Hospital, The Fourth Military Medical University Xi'an 710038, China.
Jing-Hua XiaDepartment of Thoracic Surgery, Tangdu Hospital, The Fourth Military Medical University Xi'an 710038, China.
Xue-Jiao WangDepartment of Thoracic Surgery, Tangdu Hospital, The Fourth Military Medical University Xi'an 710038, China.
Zhi-Pei ZhangDepartment of Thoracic Surgery, Tangdu Hospital, The Fourth Military Medical University Xi'an 710038, China.
Xiao-Fei LiDepartment of Thoracic Surgery, Tangdu Hospital, The Fourth Military Medical University Xi'an 710038, China.
Air Force Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It has been reported that CREPT acts as a highly expressed oncogene in a variety of tumors, affecting cyclin D1 signal pathways. However, the distribution and clinical significance of CREPT in NSCLC remains poorly understood. Our study focused on the role of CREPT on the regulation ofnon-small cell lung cancer (NSCLC). We found that CREPT mRNA and protein expression was significantly increased in NSCLC compared with adjacent lung tissues and was increased in various NSCLC cell lines compared with the normal human bronchial epithelial (HBE) cell line. siRNA-induced knockingdown of CREPT significantly inhibited the proliferation and migration of NSCLC cell lines by arresting cell cycle in S phase. Moreover, CREPT knocking down affected the expression of cell cycle proteins including c-mycand CDC25A. Finally, we found there were obvious correlations between CREPT with c-myc expression in histological type, differentiation, and pTNM stages of NSCLC (P<0.05, rs>0.3). Immunohistofluorescence studies demonstrated a co-localization phenomenon when CREPT and c-myc were expressed. Thus, we propose that CREPT may promote NSCLC cell growth and migration through the c-myc and CDC25A signaling molecules.

Indexed as

CDC25Ac-mycco-localizationCREPTmigrationproliferation

Identifiers

PMID27347318
PMCPMC4891423
OpenAlexW2473581090

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.