Evidence map›Paper›PMID 29362431›Full record

ArticleCell death & disease2018

Dual roles of miR-374a by modulated c-Jun respectively targets CCND1-inducing PI3K/AKT signal and PTEN-suppressing Wnt/β-catenin signaling in non-small-cell lung cancer.

Mengyang Zhao, Ping Xu, Zhen Liu, Yan Zhen, Yiyu Chen, Yiyi Liu, Qiaofen Fu, Xiaojie Deng, Zixi Liang, Yonghao Li and 2 more

RetractedOpen access · goldAbstract readRetracted Publication
In one paragraph

Article in Cell death & disease, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
5.2field-weighted citation impact, top 3% 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

54 citing papers in PubMed, 88 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 1 country.

Mengyang ZhaoCancer Center, Integrated Hospital of Traditional, Chinese Medicine, Southern Medical University, Guangzhou, 510315, China.
Ping XuCancer Center, Integrated Hospital of Traditional, Chinese Medicine, Southern Medical University, Guangzhou, 510315, China.
Zhen LiuKey Laboratory of Protein Modification and Degradation, School of Basic Medical Sciences and Affiliated Cancer Hospital & Institute, Guangzhou Medical University, Guangzhou, 511436, China.
Yan ZhenCancer Center, Integrated Hospital of Traditional, Chinese Medicine, Southern Medical University, Guangzhou, 510315, China.
Yiyu ChenCancer Center, Integrated Hospital of Traditional, Chinese Medicine, Southern Medical University, Guangzhou, 510315, China.
Yiyi LiuCancer Center, Integrated Hospital of Traditional, Chinese Medicine, Southern Medical University, Guangzhou, 510315, China.
Qiaofen FuCancer Center, Integrated Hospital of Traditional, Chinese Medicine, Southern Medical University, Guangzhou, 510315, China.
Xiaojie DengCancer Center, Integrated Hospital of Traditional, Chinese Medicine, Southern Medical University, Guangzhou, 510315, China.
Zixi LiangCancer Center, Integrated Hospital of Traditional, Chinese Medicine, Southern Medical University, Guangzhou, 510315, China.
Yonghao LiCancer Center, Integrated Hospital of Traditional, Chinese Medicine, Southern Medical University, Guangzhou, 510315, China.
Xian LinCancer Center, Integrated Hospital of Traditional, Chinese Medicine, Southern Medical University, Guangzhou, 510315, China.
Weiyi FangCancer Center, Integrated Hospital of Traditional, Chinese Medicine, Southern Medical University, Guangzhou, 510315, China. fangweiyi1975@163.com.
TCM-Intigrated Cancer Center of Southern Medical University · CNGuangzhou Medical University · CNPeking University Shenzhen Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MiR-374a appears to play a complex role in non-small-cell lung cancer (NSCLC). Here, we demonstrate a dual role for miR-374a in NSCLC pathogenesis. The effects and modulatory mechanisms of miR-374a on cell growth, migration, invasion, and in vivo tumorigenesis and metastasis in nude mice were also analyzed. The expression of miR-374a was examined in NSCLC and non-cancerous lung tissues by quantitative real-time reverse transcription-PCR (qRT-PCR), and in situ hybridization, respectively. miR-374a directly targets CCND1 and inactivates PI3K/AKT and Ras-mediated cell cycle signalings, as well as epithelial-mesenchymal transition (EMT). This not only dramatically suppressed cell growth, migration, invasion,and metastasis, but also elevated A549 and pc-9 NSCLC cell sensitivity to cisplatin (DDP) while increasing survival time of tumor-bearing mice. Interestingly, miR-374a serves an inverse function in SPCA-1 and H1975 NSCLC cells by directly targeting PTEN to activate Wnt/β-catenin and Ras signalings and its downstream cascade signals. Surprisingly, transcription factor c-Jun bound to the promoter region of human miR-374a and suppressed miR-374a in A549 and pc-9 cells while inducing it in SPCA-1 and H1975 cells. Increased levels of miR-374a appeared to serve a protective role by targeting CCND1 in early-stage NSCLC (Stages I and II). Inversely, increased miR-374a was an unfavorable factor when targeting PTEN in more advanced staged NSCLC patients. Our studies are the first to demonstrate that miR-374a plays divergent roles in NSCLC pathogenesis at different stages of the disease and implicate the potential application of miR-374a targeting for cancer therapy.

Indexed as

Wnt Signaling Pathway3' Untranslated RegionsAnimalsBase SequenceCarcinoma, Non-Small-Cell LungCell CycleCell Line, TumorCell MovementCell ProliferationCyclin D1Epithelial-Mesenchymal TransitionHumansLung NeoplasmsMaleMice, Inbred BALB CMice, Nude3' Untranslated RegionsCCND1 protein, humanCyclin D1MicroRNAsMIRN374 microRNA 374, humanPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktProto-Oncogene Proteins c-junPTEN Phosphohydrolase

Identifiers

PMID29362431
PMCPMC5833350
OpenAlexW2790629586

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.