Evidence map›Paper›PMID 32564010›Full record

Observational studyAging2020

Long noncoding RNA KCNQ1OT1 promotes colorectal carcinogenesis by enhancing aerobic glycolysis via hexokinase-2.

Cheng Chen, Meng Wei, Chao Wang, Danping Sun, Peng Liu, Xin Zhong, Wenbin Yu

Open access · greenAbstract readObservational Study
In one paragraph

Observational study in Aging, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
2.6field-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

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 42 citations in OpenAlex.

  1. Long Noncoding RNA KCNQ1OT1 is a Prognostic Biomarker and mediates CD8International journal of biological sciences · 2021
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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

7 authors at 1 institution in 1 country.

Cheng ChenDepartment of General Surgery, Qilu Hospital of Shandong University, Jinan 250012, China.
Meng WeiDepartment of General Surgery, Qilu Hospital of Shandong University, Jinan 250012, China.
Chao WangDepartment of General Surgery, Qilu Hospital of Shandong University, Jinan 250012, China.
Danping SunDepartment of General Surgery, Qilu Hospital of Shandong University, Jinan 250012, China.
Peng LiuDepartment of General Surgery, Qilu Hospital of Shandong University, Jinan 250012, China.
Xin ZhongDepartment of General Surgery, Qilu Hospital of Shandong University, Jinan 250012, China.
Wenbin YuDepartment of General Surgery, Qilu Hospital of Shandong University, Jinan 250012, China.
Qilu Hospital of Shandong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this study, we investigated the mechanistic role and prognostic significance of the long coding RNA (lncRNA) KCNQ1OT1 in colorectal cancer (CRC). KCNQ1OT1 levels were significantly higher in CRC tissues than adjacent normal colorectal tissues (n=79). High KCNQ1OT1 expression correlated with poorer prognosis in CRC patients. KCNQ1OT1-silenced CRC cells showed reduced proliferation, colony formation, extracellular acidification, and lactate and glucose secretion. This suggests KCNQ1OT1 promotes CRC cell proliferation by increasing aerobic glycolysis. RNA pull-down assays with biotinylated KCNQ1OT1 followed by mass spectrometry analysis showed that KCNQ1OT1 directly binds to hexokinase 2 (HK2). This was confirmed by RNA immunoprecipitation assays using anti-hexokinase 2 antibody. HK2 protein levels were reduced in KCNQ1OT1 knockdown CRC cells, but were restored by treatment with the proteasomal inhibitor MG132. KCNQ1OT1 knockdown CRC cells also showed higher ubiquitinated-HK2 levels, suggesting KCNQ1OT1 enhances aerobic glycolysis by stabilizing HK2. HK2 overexpression in KCNQ1OT1 knockdown CRC cells restored proliferation and aerobic glycolysis. KCNQ1OT1 levels correlated positively with HK2 expression and prognosis in CRC patients. These findings show that KCNQ1OT1 promotes colorectal carcinogenesis by increasing aerobic glycolysis through HK2.

Indexed as

Warburg Effect, OncologicCarcinogenesisCell ProliferationColorectal NeoplasmsDisease-Free SurvivalFemaleGene Expression Regulation, NeoplasticGene Knockdown TechniquesGlucoseHCT116 CellsHexokinaseHumansKaplan-Meier EstimateMaleMiddle AgedPotassium Channels, Voltage-GatedGlucoseHexokinaseHK2 protein, humanKCNQ1OT1 long non-coding RNA, humanPotassium Channels, Voltage-Gatedaerobic glycolysiscolorectal cancerHK2lncRNA-KCNQ1OT1

Identifiers

PMID32564010
PMCPMC7343465
OpenAlexW3036616356

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.