Evidence map›Paper›PMID 31799200›Full record

ArticleFrontiers in oncology2019

TIGAR Promotes Tumorigenesis and Protects Tumor Cells From Oxidative and Metabolic Stresses in Gastric Cancer.

Zhenhua Liu, Yue Wu, Yingqiu Zhang, Menglang Yuan, Xuelu Li, Jiyue Gao, Shanni Zhang, Chengjuan Xing, Huamin Qin, Hongbo Zhao and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
0.8field-weighted citation impact, top 32% 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

20 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Blockade of TIGAR prevents CD8Cancer immunology, immunotherapy : CII · 2025
    Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Energy metabolism: a new target for gastric cancer treatment.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Glycolysis in the progression of pancreatic cancer.American journal of cancer research · 2022
    Review
  14. Article
  15. Review
  16. Review
  17. Review
  18. Article
  19. Review
  20. 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 at 4 institutions in 1 country.

Zhenhua LiuDepartment of General Surgery, The Second Affiliated Hospital of Dalian Medical University, Dalian, China.
Yue WuInstitute of Cancer Stem Cell, Dalian Medical University, Dalian, China.
Yingqiu ZhangInstitute of Cancer Stem Cell, Dalian Medical University, Dalian, China.
Menglang YuanInstitute of Cancer Stem Cell, Dalian Medical University, Dalian, China.
Xuelu LiDepartment of General Surgery, The Second Affiliated Hospital of Dalian Medical University, Dalian, China.
Jiyue GaoDepartment of General Surgery, The Second Affiliated Hospital of Dalian Medical University, Dalian, China.
Shanni ZhangDepartment of Anesthesia, Dalian Maternal and Child Health Care Hospital, Dalian, China.
Chengjuan XingDepartment of Pathology, The Second Affiliated Hospital of Dalian Medical University, Dalian, China.
Huamin QinDepartment of Pathology, The Second Affiliated Hospital of Dalian Medical University, Dalian, China.
Hongbo ZhaoNational Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital and Shenzhen Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Shenzhen, China.
Zuowei ZhaoDepartment of General Surgery, The Second Affiliated Hospital of Dalian Medical University, Dalian, China.
Dalian Medical University · CNSecond Affiliated Hospital of Dalian Medical University · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNDalian Maternal and Child Health Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer cells adopt glycolysis to facilitate the generation of biosynthetic substrates demanded by cell proliferation and growth, and to adapt to stress conditions such as excessive reactive oxygen species (ROS) accumulation. TIGAR (TP53-induced glycolysis and apoptosis regulator) is a fructose-2,6-bisphosphatase that is regulated by p53. TIGAR functions to inhibit glycolysis and promote antioxidative activities, which assists the generation of NADPH to maintain the levels of GSH and thus reduces intracellular ROS. However, the functions of TIGAR in gastric cancer (GC) remain unclear. TIGAR expression levels were detected by immunoblotting and immunohistochemistry in gastric cancer samples, along with four established cell lines of GC. The functions of TIGAR were determined by utilizing shRNA-mediated knockdown experiments. The NADPH/NADP

Indexed as

apoptosiscell cycle checkpointsglycolysisheterograftsstomach neoplasms

Identifiers

PMID31799200
PMCPMC6878961
OpenAlexW2991206623

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.