Evidence map›Paper›PMID 22726459›Full record

ArticleCancer science2012

Comparative proteomic profiles indicating genetic factors may involve in hepatocellular carcinoma familial aggregation.

Da-Ni Zhong, Qiu-Yue Ning, Ji-Zhou Wu, Ning Zang, Jian-Lin Wu, Die-Fei Hu, Shuang-Yan Luo, Ai-Chun Huang, Lan-Lan Li, Guo-Jian Li

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Cancer science, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.3field-weighted citation impact, top 42% 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

12 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Tracking the important role ofOncology letters · 2020
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Familial Hepatocellular Carcinoma- First Reported Case from India.Journal of clinical and diagnostic research : JCDR · 2016
    Article
  11. Article
  12. 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

10 authors at 2 institutions in 1 country.

Da-Ni ZhongDepartment of Infectious Diseases, First Affiliated Hospital, Guangxi Medical University, Nanning, China.
Qiu-Yue Ning
Ji-Zhou Wu
Ning Zang
Jian-Lin Wu
Die-Fei Hu
Shuang-Yan Luo
Ai-Chun Huang
Lan-Lan Li
Guo-Jian Li
Guangxi Medical University · CNThe People's Hospital of Guangxi Zhuang Autonomous Region · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Familial aggregation of hepatocellular carcinoma (HCC), the third leading cause of cancer death worldwide, has shown to be a common phenomenon. We investigated the association between the genetic background and HCC familial aggregation. Serum samples were collected from HCC family members and normal control family members for screening the differentially expressed protein peaks with the approach of surface-enhanced laser desorption ionization time-of-flight mass spectrometry. Potential genetically associated protein peaks were selected and further identified by matrix assisted laser desorption ionization-time of flight mass spectrometry. A panel of six protein peaks (m/z 6432.94, 8478.35, 9381.91, 17284.67, 17418.34, and 18111.04) were speculated to reflect the genetic susceptibility of HCC familial aggregation. Three of them (m/z 6432.94, 8478.35, and 9381.91) were selected to identify as the candidate proteins. Nine identified proteins, including mostly apolipoprotein family (ApoA1, ApoA2, ApoC3, ApoE) and serum amyloid A protein (SAA), were found overexpressed in the multiple HCC cases family members. The comparative proteomic profiles have suggested that genetic factors ought to be taken into account for familial aggregation of HCC.

Indexed as

AdultCarcinoma, HepatocellularFemaleGenetic Predisposition to DiseaseHumansInfantLiver NeoplasmsMalePedigreeProteomicsSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationTranscriptome

Identifiers

PMID22726459
PMCPMC7659362
OpenAlexW2083995892

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.