Evidence map›Paper›PMID 31533634›Full record

ArticleBMC gastroenterology2019

SNHG 6 promotes the progression of Colon and Rectal adenocarcinoma via miR-101-3p and Wnt/β-catenin signaling pathway.

Qianwen Shao, Jing Xu, Rong Deng, Wei Wei, Bing Zhou, Chao Yue, Miaoling Zhu, Haitao Zhu

Open access · goldAbstract read
In one paragraph

Article in BMC gastroenterology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.4field-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

26 citing papers in PubMed, 41 citations in OpenAlex.

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  14. The Hypoxia-Long Noncoding RNA Interaction in Solid Cancers.International journal of molecular 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

8 authors at 2 institutions in 1 country.

Qianwen ShaoDepartment of oncology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, People's Republic of China, 210029.
Jing XuGenetic testing center, department of oncology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, People's Republic of China, 210029.
Rong DengGeneral Department, Cancer hospital of NanJing Medical University, Nanjing, Jiangsu, People's Republic of China, 210009.
Wei WeiGeneral Department, Cancer hospital of NanJing Medical University, Nanjing, Jiangsu, People's Republic of China, 210009.
Bing ZhouGeneral Department, Cancer hospital of NanJing Medical University, Nanjing, Jiangsu, People's Republic of China, 210009.
Chao YueGeneral Department, Cancer hospital of NanJing Medical University, Nanjing, Jiangsu, People's Republic of China, 210009.
Miaoling ZhuPathology department, Cancer hospital of NanJing Medical University, Nanjing, Jangsu, People's Republic of China, 210009.
Haitao ZhuColorectal cancer center, general surgery department, Jiangsu province cancer hospital, Affiliated Cancer hospital of NanJing Medical University, Jiangsu Cancer Institute, No 42, Baiziting road, NanJing, Nanjing, Jiangsu, People's Republic of China, 210009. co87r5@163.com.ORCID http://orcid.org/0000-0002-1424-6840
Jiangsu Province Hospital · CNJiangsu Cancer Hospital · CN

Funding

Key Project of and Technology Department of Jiangsu Province of China BL2014092Key Project of Cancer hospital of NanJing Medical University noneProvincial Natural Science Foundation BK20131438Six Talent Peaks Project in Jiangsu Province WSW-038
6 · The paper itself

Abstract

backgroundSmall nucleolar RNA host gene 6 (SNHG6) regulates diverse biological processes in cancers. Potential function of SNHG6 in human colon and rectal adenocarcinoma (CRC) was evaluated.

methodsQuantitative real-time polymerase chain reaction, MTT assays, Colony formation assays, Transwell assay, Western Blotting and Luciferase reporter assays were performed to measure the biological functions and potential molecular mechanisms of SNHG6 in CRC.

resultsSNHG6 was over-expressed in CRC, and high expression of s SNHG6 were associated with short survival times. We then identified miR-101-3p as an inhibitory target of SNHG6. Knockdown of SNHG6 significantly decreased miR-101-3p expression. Moreover, silenced SNHG6 obviously inhibited CRC cell growth, weakened cell invasion capacity and blocked the Wnt/β-catenin signaling pathway.

conclusionSNHG6 could regulate the progression of CRC via modulating the expression levels of miR-101-3p and the activity of Wnt/β-catenin signaling.

Indexed as

AdenocarcinomaCell Line, TumorCell MovementCell ProliferationColorectal NeoplasmsDisease ProgressionGene Knockdown TechniquesHCT116 CellsHT29 CellsHumansMicroRNAsReal-Time Polymerase Chain ReactionRNA, Long NoncodingSurvival RateWnt Signaling Pathwaylong non-coding RNA SNHG6, humanMicroRNAsMIRN101 microRNA, humanRNA, Long NoncodingCell signal pathwayceRNASmall nucleolar RNA host gene 6SpongingTarget therapy

Identifiers

PMID31533634
PMCPMC6749705
OpenAlexW2973811147

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.