Evidence map›Paper›PMID 31207989›Full record

ArticleInternational journal of molecular sciences2019

Chromogranin-A Expression as a Novel Biomarker for Early Diagnosis of Colon Cancer Patients.

Xueli Zhang, Hong Zhang, Bairong Shen, Xiao-Feng Sun

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

35 citing papers in PubMed, 62 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Anticolon Cancer Targets and Molecular Mechanisms of Tao-He-Cheng-Qi Formula.Evidence-based complementary and alternative medicine : eCAM · 2022
    Article
  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

4 authors at 3 institutions in 2 countries.

Xueli ZhangSchool of Medicine, Institute of Medical Sciences, Örebro University, SE-70182 Örebro, Sweden. zhang.xueli@oru.se.
Hong ZhangSchool of Medicine, Institute of Medical Sciences, Örebro University, SE-70182 Örebro, Sweden. hong.zhang@oru.se.
Bairong ShenCentre for Systems Biology, Soochow University, Suzhou 215006, China. bairong.shen@suda.edu.cn.
Xiao-Feng SunDepartment of Oncology and Clinical and Experimental Medicine, Linköping University, SE-58183 Linköping, Sweden. xiao-feng.sun@liu.se.
Örebro University · SELinköping University · SESoochow University · CN

Funding

Svenska Forskningsrådet Formas CAN 2016/341Vetenskapsrådet 2016-01098
6 · The paper itself

Abstract

Colon cancer is one of the major causes of cancer death worldwide. The five-year survival rate for the early-stage patients is more than 90%, and only around 10% for the later stages. Moreover, half of the colon cancer patients have been clinically diagnosed at the later stages. It is; therefore, of importance to enhance the ability for the early diagnosis of colon cancer. Taking advantages from our previous studies, there are several potential biomarkers which have been associated with the early diagnosis of the colon cancer. In order to investigate these early diagnostic biomarkers for colon cancer, human chromogranin-A (CHGA) was further analyzed among the most powerful diagnostic biomarkers. In this study, we used a logistic regression-based meta-analysis to clarify associations of CHGA expression with colon cancer diagnosis. Both healthy populations and the normal mucosa from the colon cancer patients were selected as the double normal controls. The results showed decreased expression of CHGA in the early stages of colon cancer as compared to the normal controls. The decline of CHGA expression in the early stages of colon cancer is probably a new diagnostic biomarker for colon cancer diagnosis with high predicting possibility and verification performance. We have also compared the diagnostic powers of CHGA expression with the typical oncogene KRAS, classic tumor suppressor TP53, and well-known cellular proliferation index MKI67, and the CHGA showed stronger ability to predict early diagnosis for colon cancer than these other cancer biomarkers. In the protein-protein interaction (PPI) network, CHGA was revealed to share some common pathways with KRAS and TP53. CHGA might be considered as a novel, promising, and powerful biomarker for early diagnosis of colon cancer.

Indexed as

Biomarkers, TumorChromogranin AColonic NeoplasmsGene Regulatory NetworksHumansMeta-Analysis as TopicProtein Interaction MapsProto-Oncogene Proteins p21(ras)Sensitivity and SpecificityTumor Suppressor Protein p53Biomarkers, TumorChromogranin AKRAS protein, humanProto-Oncogene Proteins p21(ras)TP53 protein, humanTumor Suppressor Protein p53biomarkerCHGAcolon cancerearly diagnosislogistic regressionmeta-analysisPPI

Identifiers

PMID31207989
PMCPMC6628020
OpenAlexW2950646821

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.