Evidence map›Paper›PMID 32426269›Full record

ArticleFrontiers in oncology2020

Heterogeneities of Site-Specific

Ting Zhao, Li Jia, Jun Li, Chen Ma, Jingyu Wu, Jiechen Shen, Liuyi Dang, Bojing Zhu, Pengfei Li, Yuan Zhi and 7 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

32 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  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

17 authors at 2 institutions in 1 country.

Ting ZhaoCollege of Life Science, Northwest University, Xi'an, China.
Li JiaCollege of Life Science, Northwest University, Xi'an, China.
Jun LiCollege of Life Science, Northwest University, Xi'an, China.
Chen MaCollege of Life Science, Northwest University, Xi'an, China.
Jingyu WuCollege of Life Science, Northwest University, Xi'an, China.
Jiechen ShenCollege of Life Science, Northwest University, Xi'an, China.
Liuyi DangCollege of Life Science, Northwest University, Xi'an, China.
Bojing ZhuCollege of Life Science, Northwest University, Xi'an, China.
Pengfei LiCollege of Life Science, Northwest University, Xi'an, China.
Yuan ZhiCollege of Life Science, Northwest University, Xi'an, China.
Rongxia LanCollege of Life Science, Northwest University, Xi'an, China.
Yintai XuCollege of Life Science, Northwest University, Xi'an, China.
Zhifang HaoCollege of Life Science, Northwest University, Xi'an, China.
Yichao ChaiDepartment of Hepatobiliary Surgery, Institute of Advanced Surgical Technology and Engineering, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Qingshan LiDepartment of Hepatobiliary Surgery, Institute of Advanced Surgical Technology and Engineering, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Liangshuo HuDepartment of Hepatobiliary Surgery, Institute of Advanced Surgical Technology and Engineering, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Shisheng SunCollege of Life Science, Northwest University, Xi'an, China.
Northwest University · CNFirst Affiliated Hospital of Xi'an Jiaotong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is still one of the malignant tumors with high morbidity and mortality in China and worldwide. Although alpha-fetoprotein (AFP) as well as core fucosylated AFP-L3 have been widely used as important biomarkers for HCC diagnosis and evaluation, the AFP level shows a huge variation among HCC patient populations. In addition, the AFP level has also been proved to be associated with pathological grade, progression, and survival of HCC patients. Understanding the intrinsic heterogeneities of HCC associated with AFP levels is essential for the molecular mechanism studies of HCC with different AFP levels as well as for the potential early diagnosis and personalized treatment of HCC with AFP negative. In this study, an integrated

Indexed as

alpha-fetoproteinglycoproteomehepatocellular carcinomaintact glycopeptidemass spectrometrysite-specific glycosylation

Identifiers

PMID32426269
PMCPMC7212448
OpenAlexW3019798094

What Socratic 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 Socratic graph.