Evidence map›Paper›PMID 31179189›Full record

ArticlePeerJ2019

Fisher linear discriminant analysis for classification and prediction of genomic susceptibility to stomach and colorectal cancers based on six STR loci in a northern Chinese Han population.

Shuhong Hao, Ming Ren, Dong Li, Yujie Sui, Qingyu Wang, Gaoyang Chen, Zhaoyan Li, Qiwei Yang

Open access · goldAbstract read
In one paragraph

Article in PeerJ, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. 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

8 authors at 1 institution in 1 country.

Shuhong HaoDepartment of Hematology and Oncology, The Second Hospital of Jilin University, Changchun, Jilin Province, China.
Ming RenDepartment of Orthopedics, The Second Hospital of Jilin University, Changchun, Jilin Province, China.
Dong LiDepartment of Obstetrics and Gynecology, The Second Hospital of Jilin University, Changchun, Jilin Province, China.
Yujie SuiMedical Research Center, The Second Hospital of Jilin University, Changchun, Jilin Province, China.
Qingyu WangDepartment of Orthopedics, The Second Hospital of Jilin University, Changchun, Jilin Province, China.
Gaoyang ChenDepartment of Orthopedics, The Second Hospital of Jilin University, Changchun, Jilin Province, China.
Zhaoyan LiDepartment of Orthopedics, The Second Hospital of Jilin University, Changchun, Jilin Province, China.
Qiwei YangMedical Research Center, The Second Hospital of Jilin University, Changchun, Jilin Province, China.
Second Affiliated Hospital of Jilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveGastrointestinal cancer is the leading cause of cancer-related death worldwide. The aim of this study was to verify whether the genotype of six short tandem repeat (STR) loci including AR, Bat-25, D5S346, ER1, ER2, and FGA is associated with the risk of gastric cancer (GC) and colorectal cancer (CRC) and to develop a model that allows early diagnosis and prediction of inherited genomic susceptibility to GC and CRC.

methodsAlleles of six STR loci were determined using the peripheral blood of six colon cancer patients, five rectal cancer patients, eight GC patients, and 30 healthy controls. Fisher linear discriminant analysis (FDA) was used to establish the discriminant formula to distinguish GC and CRC patients from healthy controls. Leave-one-out cross validation and receiver operating characteristic (ROC) curves were used to validate the accuracy of the formula. The relationship between the STR status and immunohistochemical (IHC) and tumor markers was analyzed using multiple correspondence analysis.

resultsD5S346 was confirmed as a GC- and CRC-related STR locus. For the first time, we established a discriminant formula on the basis of the six STR loci, which was used to estimate the risk coefficient of suffering from GC and CRC. The model was statistically significant (Wilks' lambda = 0.471,

conclusionsThe results of this study complement clinical diagnostic criteria and present markers for early prediction of GC and CRC. This approach will aid in improving risk awareness of susceptible individuals and contribute to reducing the incidence of GC and CRC by prevention and early detection.

Indexed as

Fisher linear discriminant analysisGastrointestinal cancerGenomic susceptibility predictionMolecular diagnosisSTR

Identifiers

PMID31179189
PMCPMC6544021
OpenAlexW2947859587

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.