Evidence map›Paper›PMID 27880730›Full record

ArticleOncotarget2016

Loss of ZG16 is regulated by miR-196a and contributes to stemness and progression of colorectal cancer.

Xiaobing Chen, Peng Du, Junjun She, Liang Cao, Yingchao Li, Hongping Xia

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

24 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Identification of hub genes in colon cancer via bioinformatics analysis.The Journal of international medical research · 2020
    Article
  17. Article
  18. A Novel Prognostic Score Based onPharmacogenomics and personalized medicine · 2020
    Article
  19. Article
  20. Review
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

6 authors at 3 institutions in 1 country.

Xiaobing ChenDepartment of Oncology, Henan Cancer Hospital, The Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou 450008, China.
Peng DuDepartment of Colorectal Surgery, Xinhua Hospital, Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai 200092, China.
Junjun SheDepartment of General Surgery, The First Affiliated Hospital of Xi'An Jiaotong University, Xi'An 710061, China.
Liang CaoDepartment of Oncology, Henan Cancer Hospital, The Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou 450008, China.
Yingchao LiDepartment of Gastroenterology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an 710061, China.
Hongping XiaDepartment of General Surgery, The First Affiliated Hospital of Xi'An Jiaotong University, Xi'An 710061, China.
First Affiliated Hospital of Xi'an Jiaotong University · CNZhengzhou University · CNXinHua Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal cancer (CRC) is one of the most common malignant tumour and the leading cause of cancer-related mortality worldwide. Clarification of the mechanism that underlies CRC tumorigenesis and progression therefore is urgently needed ffor developing novel therapies. Through analysis of The Cancer Genome Atlas (TCGA) dataset, we identified an interesting gene, ZG16, which is significantly decreased in CRC samples compared to adjacent non-tumor tissues and associated with prognosis of patients. We found that the expression of ZG16 correlated with CRC related genes which were regulated by APC/CTNNB1 pathway. Interestingly, the expression of ZG16 was negatively correlated with CRC stem cell marker, LGR5. Overexpression of ZG16 significantly inhibits growth and sphere formation of stem-like CRC cells. Moreover, we also identified an upstream regulator of ZG16, miR-196a, which was significantly overexpressed in CRC and promotes cell growth and stemness. In conclusion, this study demonstrated that loss of ZG16 is regulated by miR-196a and contributes to stemness and progression of CRC, which may provide a promising therapeutic strategy for advanced CRCs.

Indexed as

Gene Expression Regulation, Neoplastic3' Untranslated RegionsAnimalsCell ProliferationColorectal NeoplasmsDisease ProgressionHT29 CellsHumansLectinsMice, Inbred BALB CMice, NudeMicroRNAsNeoplastic Stem CellsReceptors, G-Protein-CoupledSignal TransductionTransplantation, Heterologous3' Untranslated RegionsLectinsLGR5 protein, humanMicroRNAsMIRN196 microRNA, humanReceptors, G-Protein-CoupledZG16 protein, humanColorectal cancerLGR5miR-196astemnessZG16

Identifiers

PMID27880730
PMCPMC5349946
OpenAlexW2556424962

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.