Evidence map›Paper›PMID 29872866›Full record

ArticleJournal of molecular medicine (Berlin, Germany)2018

The lncRNA MIR4435-2HG promotes lung cancer progression by activating β-catenin signalling.

Haiyun Qian, Li Chen, Jiangping Huang, Xianghui Wang, Shengwei Ma, Fenghe Cui, Liyun Luo, Li Ling, Kai Luo, Guopei Zheng

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of molecular medicine (Berlin, Germany), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
3.9field-weighted citation impact, top 5% 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

55 citing papers in PubMed, 81 citations in OpenAlex.

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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 4 institutions in 1 country.

Haiyun QianDepartment of Cardiothoracic Surgery, Jingzhou Central Hospital, The Second Clinical Medical College, Yangtze University, Renming Road 1#, Jingzhou, 434020, Hubei, China.
Li ChenDepartment of Endocrinology, Jingzhou Central Hospital, The Second Clinical Medical College, Yangtze University, Renming Road 1#, Jingzhou, 434020, Hubei, China.
Jiangping HuangDepartment of Cardiothoracic Surgery, Jingzhou Central Hospital, The Second Clinical Medical College, Yangtze University, Renming Road 1#, Jingzhou, 434020, Hubei, China.
Xianghui WangDepartment of Cardiothoracic Surgery, Jingzhou Central Hospital, The Second Clinical Medical College, Yangtze University, Renming Road 1#, Jingzhou, 434020, Hubei, China.
Shengwei MaDepartment of Cardiothoracic Surgery, Jingzhou Central Hospital, The Second Clinical Medical College, Yangtze University, Renming Road 1#, Jingzhou, 434020, Hubei, China.
Fenghe CuiDepartment of Cardiothoracic Surgery, Jingzhou Central Hospital, The Second Clinical Medical College, Yangtze University, Renming Road 1#, Jingzhou, 434020, Hubei, China.
Liyun LuoGuangzhou Key Laboratory of "Translational Medicine on Malignant Tumor Treatment", Affiliated Cancer Hospital & Institute of Guangzhou Medical University, Hengzhigang Road 78#, Guangzhou, 510095, Guangdong, China.
Li LingGuangzhou Key Laboratory of "Translational Medicine on Malignant Tumor Treatment", Affiliated Cancer Hospital & Institute of Guangzhou Medical University, Hengzhigang Road 78#, Guangzhou, 510095, Guangdong, China.
Kai LuoGuangzhou Key Laboratory of "Translational Medicine on Malignant Tumor Treatment", Affiliated Cancer Hospital & Institute of Guangzhou Medical University, Hengzhigang Road 78#, Guangzhou, 510095, Guangdong, China. luokainan@126.com.
Guopei ZhengGuangzhou Key Laboratory of "Translational Medicine on Malignant Tumor Treatment", Affiliated Cancer Hospital & Institute of Guangzhou Medical University, Hengzhigang Road 78#, Guangzhou, 510095, Guangdong, China. zhengguopei@126.com.
Jingzhou Central Hospital · CNGuangzhou Medical University · CNYangtze University · CNGuangzhou Medical University Cancer Hospital · CN

Funding

National Natural Science Foundation of China 81402196National Natural Science Foundation of China 81672616
6 · The paper itself

Abstract

Recently, emerging evidence has suggested that long noncoding RNAs (lncRNAs) have crucial roles in cancer progression. Here, we demonstrated that the lncRNA MIR4435-2HG was highly expressed in lung cancer tissues and correlated with histological grades and lymph node metastasis. Phenotypic analysis indicated that MIR4435-2HG knockdown inhibited lung cancer cell proliferation and invasion in vitro and in vivo. Notably, MIR4435-2HG knockdown suppressed the EMT (epithelial-mesenchymal transition) process and cancer stem cell traits of lung cancer cells. Mechanistically, MIR4435-2HG knockdown decreased the transactivation of β-catenin. MIR4435-2HG interacted with β-catenin and thus prevented its degradation by the proteasome system. Our findings highlight the important roles and mechanisms of MIR4435-2HG in lung cancer progression. High expression of lncRNA MIR4435-2HG correlates with lung cancer progression MIR4435-2HG promotes lung cancer cells proliferation and invasion MIR4435-2HG knockdown suppresses the EMT process and cancer stem cell traits MIR4435-2HG knockdown inhibits the β-catenin signalling.

Indexed as

Gene Expression Regulation, NeoplasticSignal TransductionAdultAgedAnimalsbeta CateninCell Line, TumorCell MovementDisease Models, AnimalDisease ProgressionEpithelial-Mesenchymal TransitionFemaleHumansLung NeoplasmsMiceMiddle Agedbeta CateninRNA, Long NoncodingEMTlncRNAsLung cancerβ-catenin

Identifiers

PMID29872866
OpenAlexW2807231290

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.