Evidence map›Paper›PMID 32588529›Full record

ArticleJournal of cellular and molecular medicine2020

TIPE1-mediated autophagy suppression promotes nasopharyngeal carcinoma cell proliferation via the AMPK/mTOR signalling pathway.

Yongliang Liu, Xiangqin Qi, Zhenan Zhao, Daoliang Song, Lianqing Wang, Qiaoli Zhai, Xiaoning Zhang, Peiqing Zhao, Xinxin Xiang

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.2field-weighted citation impact, top 11% 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

10 citing papers in PubMed, 23 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

9 authors at 1 institution in 1 country.

Yongliang LiuDepartment of Otolaryngolgogy, Zibo Central Hospital, Shandong University, Zibo, China.
Xiangqin QiDepartment of Ultrasound, Zibo Central Hospital, Shandong University, Zibo, China.
Zhenan ZhaoDepartment of Otolaryngolgogy, Zibo Central Hospital, Shandong University, Zibo, China.
Daoliang SongDepartment of Otolaryngolgogy, Zibo Central Hospital, Shandong University, Zibo, China.
Lianqing WangCentral of Translation Medicine, Zibo Central Hospital, Shandong University, Zibo, China.
Qiaoli ZhaiCentral of Translation Medicine, Zibo Central Hospital, Shandong University, Zibo, China.
Xiaoning ZhangCentral of Translation Medicine, Zibo Central Hospital, Shandong University, Zibo, China.
Peiqing ZhaoCentral of Translation Medicine, Zibo Central Hospital, Shandong University, Zibo, China.
Xinxin XiangCentral of Translation Medicine, Zibo Central Hospital, Shandong University, Zibo, China.ORCID 0000-0002-4476-3160
Shandong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent studies have shown that tumour necrosis factor-α-induced protein 8 like-1(TIPE1) plays distinct roles in different cancers. TIPE1 inhibits tumour proliferation and metastasis in a variety of tumours but acts as an oncogene in cervical cancer. The role of TIPE1 in nasopharyngeal carcinoma (NPC) remains unknown. Interestingly, TIPE1 expression was remarkably increased in NPC tissue samples compared to adjacent normal nasopharyngeal epithelial tissue samples in our study. TIPE1 expression was positively correlated with that of the proliferation marker Ki67 and negatively correlated with patient lifespan. In vitro, TIPE1 inhibited autophagy and induced cell proliferation in TIPE1-overexpressing CNE-1 and CNE-2Z cells. In addition, knocking down TIPE1 expression promoted autophagy and decreased proliferation, whereas overexpressing TIPE1 increased the levels of pmTOR, pS6 and P62 and decreased the level of pAMPK and the LC3B. Furthermore, the decrease in autophagy was remarkably rescued in TIPE1-overexpressing CNE-1 and CNE-2Z cells treated with the AMPK activator AICAR. In addition, TIPE1 promoted tumour growth in BALB/c nude mice. Taken together, results indicate that TIPE1 promotes NPC progression by inhibiting autophagy and inducing cell proliferation via the AMPK/mTOR signalling pathway. Thus, TIPE1 could potentially be used as a valuable diagnostic and prognostic biomarker for NPC.

Indexed as

AMP-Activated Protein KinasesAnimalsAutophagyBiomarkers, TumorCell Line, TumorCell ProliferationHumansIntracellular Signaling Peptides and ProteinsMaleMiceMice, Inbred BALB CMice, NudeNasopharyngeal CarcinomaNasopharyngeal NeoplasmsSignal TransductionTOR Serine-Threonine KinasesAMP-Activated Protein KinasesBiomarkers, TumorIntracellular Signaling Peptides and ProteinsMTOR protein, humanTNFAIP8L1 protein, humanTOR Serine-Threonine KinasesAMPK/mTOR signalling pathwayautophagycell proliferationnasopharyngeal carcinomaTIPE1

Identifiers

PMID32588529
PMCPMC7417699
OpenAlexW3037884991

What OpenQuestion holds

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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.