Evidence map›Paper›PMID 26341367›Full record

ArticleJournal of neuro-oncology2015

Hugl-1 inhibits glioma cell growth in intracranial model.

Xuejiao Liu, Dong Lu, Peng Ma, Huaqiang Liu, Yuewen Cao, Ben Sang, Xianlong Zhu, Qiong Shi, Jinxia Hu, Rutong Yu and 1 more

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of neuro-oncology, 2015. 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
–field-weighted citation impact
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.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Loss ofCanadian journal of gastroenterology & hepatology · 2019
    Article
  9. Biology open · 2018
    Article
  10. Article
  11. Article
  12. β-catenin-mediated YAP signaling promotes human glioma growth.Journal of experimental & clinical cancer research : CR · 2017
    Article
  13. Article
  14. Article
  15. Article
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

11 authors.

Xuejiao LiuInstitute of Nervous System Diseases, Xuzhou Medical College, 84 West Huai-hai Road, Xuzhou, 221002, Jiangsu, People's Republic of China.
Dong LuInstitute of Nervous System Diseases, Xuzhou Medical College, 84 West Huai-hai Road, Xuzhou, 221002, Jiangsu, People's Republic of China.
Peng MaThe Graduate School, Xuzhou Medical College, Xuzhou, Jiangsu, People's Republic of China.
Huaqiang LiuThe Graduate School, Xuzhou Medical College, Xuzhou, Jiangsu, People's Republic of China.
Yuewen CaoThe Graduate School, Xuzhou Medical College, Xuzhou, Jiangsu, People's Republic of China.
Ben SangThe Graduate School, Xuzhou Medical College, Xuzhou, Jiangsu, People's Republic of China.
Xianlong ZhuThe Graduate School, Xuzhou Medical College, Xuzhou, Jiangsu, People's Republic of China.
Qiong ShiInstitute of Nervous System Diseases, Xuzhou Medical College, 84 West Huai-hai Road, Xuzhou, 221002, Jiangsu, People's Republic of China.
Jinxia HuInstitute of Nervous System Diseases, Xuzhou Medical College, 84 West Huai-hai Road, Xuzhou, 221002, Jiangsu, People's Republic of China.
Rutong YuInstitute of Nervous System Diseases, Xuzhou Medical College, 84 West Huai-hai Road, Xuzhou, 221002, Jiangsu, People's Republic of China. yu.rutong@163.com.
Xiuping ZhouInstitute of Nervous System Diseases, Xuzhou Medical College, 84 West Huai-hai Road, Xuzhou, 221002, Jiangsu, People's Republic of China. xpzhou@xzmc.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Drosophila lethal (2) giant larvae (lgl) has been reported as a tumor suppressor and could regulate the Drosophila hippo signaling. Human giant larvae-1(Hugl-1), one human homologue of Drosophila lgl, also has been reported to be involved in the development of some human cancers. However, whether Hugl-1 is associated with the pathogenesis of malignant gliomas remains poorly understood. In the present work, we examined the effect of Hugl-1 on glioma cell growth both in vitro and in vivo. Firstly, we found that Hugl-1 protein levels decreased in the human glioma tissues, suggesting that Hugl-1 is involved in glioma progression. Unfortunately, either stably or transiently over-expressing Hugl-1 did not affect glioma cell proliferation in vitro. In addition, Hugl-1 over-expression did not regulate hippo signaling pathway. Interestingly, over-expression of Hugl-1 not only inhibited gliomagenesis but also markedly inhibited cell proliferation and promoted the apoptosis of U251 cells in an orthotopic model of nude mice. Taken together, this study provides the evidence that Hugl-1 inhibits glioma cell growth in intracranial model of nude mice, suggesting that Hugl-1 might be a potential tumor target for glioma therapy.

Indexed as

AnimalsAstrocytomaBrain NeoplasmsCell Line, TumorCell ProliferationCytoskeletal ProteinsDisease Models, AnimalFemaleGene Expression Regulation, NeoplasticGreen Fluorescent ProteinsHumansKi-67 AntigenMaleMiceMice, NudePhenylurea CompoundsCytoskeletal Proteinsethylene diureaGreen Fluorescent ProteinsKi-67 AntigenLLGL1 protein, humanPhenylurea CompoundsSincalideGliomasHippoHugl-1Proliferation

Identifiers

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.