Evidence map›Paper›PMID 27819329›Full record

ArticleScientific reports2016

mTOR Overactivation in Mesenchymal cells Aggravates CCl

Lanlan Shan, Yan Ding, You Fu, Ling Zhou, Xiaoying Dong, Shunzhi Chen, Hongyuan Wu, Wenqing Nai, Hang Zheng, Wanfu Xu and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

15 citing papers in PubMed, 32 citations in OpenAlex.

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  13. The Roles of Immune Cells in the Pathogenesis of Fibrosis.International journal of molecular sciences · 2020
    Review
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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

13 authors at 3 institutions in 1 country.

Lanlan ShanDepartment of Health Management, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, 510515, China.
Yan DingDepartment of Health Management, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, 510515, China.
You FuDepartment of Health Management, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, 510515, China.
Ling ZhouDepartment of Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, 510515, China.
Xiaoying DongDepartment of Health Management, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, 510515, China.
Shunzhi ChenDepartment of Health Management, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, 510515, China.
Hongyuan WuDepartment of Health Management, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, 510515, China.
Wenqing NaiDepartment of Health Management, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, 510515, China.
Hang ZhengDepartment of Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, 510515, China.
Wanfu XuDepartment of Gastroenterology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, 510623, China.
Xiaochun BaiDepartment of Cell Biology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, Guangdong, 510515, China.
Chunhong JiaDepartment of Cell Biology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, Guangdong, 510515, China.
Meng DaiDepartment of Health Management, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, 510515, China.
Southern Medical University · CNNanfang Hospital · CNGuangzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatic stellate cells are of mesenchymal cell type located in the space of Disse. Upon liver injury, HSCs transactivate into myofibroblasts with increase in expression of fibrillar collagen, especially collagen I and III, leading to liver fibrosis. Previous studies have shown mTOR signaling is activated during liver fibrosis. However, there is no direct evidence in vivo. The aim of this study is to examine the effects of conditional deletion of TSC1 in mesenchymal on pathogenesis of liver fibrosis. Crossing mice bearing the floxed TSC1 gene with mice harboring Col1α2-Cre-ER(T) successfully generated progeny with a conditional knockout of TSC1 (TSC1 CKO) in collagen I expressing mesenchymal cells. TSC1 CKO and WT mice were subjected to CCl

Indexed as

AnimalsCarbon TetrachlorideDisease Models, AnimalGene DeletionLiverLiver CirrhosisMiceMice, KnockoutSirolimusTOR Serine-Threonine KinasesTuberous Sclerosis Complex 1 ProteinTumor Suppressor ProteinsCarbon TetrachloridemTOR protein, mouseSirolimusTOR Serine-Threonine KinasesTsc1 protein, mouseTuberous Sclerosis Complex 1 ProteinTumor Suppressor Proteins

Identifiers

PMID27819329
PMCPMC5098141
OpenAlexW2550350242

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.