Evidence map›Paper›PMID 34257534›Full record

ArticlePathology oncology research : POR2021

Increasing Embryonic Morphogen Nodal Expression Suggests Malignant Transformation in Colorectal Lesions and as a Potential Marker for CMS4 Subtype of Colorectal Cancer.

Xiaopai Wang, Shousheng Liu, Huijiao Cao, Xiubo Li, Yuming Rong, Guorong Liu, Hong Du, Hong Shen

Open access · goldAbstract read
In one paragraph

Article in Pathology oncology research : POR, 2021. 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
0.2field-weighted citation impact, top 52% 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, 2 citations in OpenAlex.

  1. Article
  2. Review
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 5 institutions in 1 country.

Xiaopai WangDepartment of Pathology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Shousheng LiuDepartment of General Medicine, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University Cancer Center, Guangzhou, China.
Huijiao CaoDepartment of General Medicine, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University Cancer Center, Guangzhou, China.
Xiubo LiDepartment of Pathology, Guangzhou First People's Hospital, School of Medicine, South China University of Technology, Guangzhou, China.
Yuming RongDepartment of General Medicine, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University Cancer Center, Guangzhou, China.
Guorong LiuDepartment of Pathology, Guangzhou First People's Hospital, School of Medicine, South China University of Technology, Guangzhou, China.
Hong DuDepartment of Pathology, Guangzhou First People's Hospital, School of Medicine, South China University of Technology, Guangzhou, China.
Hong ShenDepartment of Pathology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Sun Yat-sen University · CNSouth China University of Technology · CNGuangzhou First People's Hospital · CNGuangzhou Medical University · CNSouthern Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nodal, an embryonic morphogen in TGF-β family, is related with tumorigenicity and progression in various tumors including colorectal cancer (CRC). However, the difference of Nodal expression between CRC and colorectal polyps has not yet been investigated. Besides, whether Nodal can be used as a marker for consensus molecular subtype classification-4 (CMS4) of CRC is also worth studying. We analyzed Nodal expression in patients of CRC (161), high-grade intraepithelial neoplasia (HGIN, 28) and five types of colorectal polyps (116). The Nodal expression difference among groups and the association between Nodal expression and clinicopathological features were analyzed. Two categories logistic regression model was used to predict the odds ratio (OR) of risk factors for high tumor-stroma percentage (TSP), and ROC curve was used to assess the diagnostic value of Nodal in predicting high TSP in CRC. We found that Nodal expression was significantly elevated in CRC and HGIN (

Indexed as

Biomarkers, TumorCarcinoma in SituCell Transformation, NeoplasticColonic PolypsColorectal NeoplasmsFemaleHumansLymphatic MetastasisMaleMiddle AgedNodal ProteinRisk FactorsROC CurveStromal CellsBiomarkers, TumorNodal ProteinNODAL protein, humanCMS-4colorectal cancerNodalTGF-βtumor-stroma percentage

Identifiers

PMID34257534
PMCPMC8262187
OpenAlexW3137260818

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.