Evidence map›Paper›PMID 34877409›Full record

ArticleOpen medicine (Warsaw, Poland)2021

Prognostic role of oxytocin receptor in colon adenocarcinoma.

Junjie Sun, Zhenyu Xu, Yong Mao, Ting Zhang, Yan Qin, Dong Hua

Open access · goldAbstract read
In one paragraph

Article in Open medicine (Warsaw, Poland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

9 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Cuprotosis clusters predict prognosis and immunotherapy response in low-grade glioma.Apoptosis : an international journal on programmed cell death · 2024
    Article
  8. Article
  9. Roles of the Oxytocin Receptor (OXTR) in Human Diseases.International journal of molecular sciences · 2023
    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

6 authors at 3 institutions in 1 country.

Junjie SunDepartment of Oncology, The Second Affiliated Hospital of Soochow University, Suzhou, 215004, Jiangsu, P. R. China.
Zhenyu XuDepartment of Oncology, The Second Affiliated Hospital of Soochow University, Suzhou, 215004, Jiangsu, P. R. China.
Yong MaoDepartment of Oncology, The Affiliated Hospital of Jiangnan University, No. 200, Huihe Road, Wuxi, 214000, Jiangsu, P. R. China.
Ting ZhangDepartment of Oncology, The Affiliated Hospital of Jiangnan University, No. 200, Huihe Road, Wuxi, 214000, Jiangsu, P. R. China.
Yan QinDepartment of Pathology, The Affiliated Hospital of Jiangnan University, No. 200, Huihe Road, Wuxi, 214000, Jiangsu, P. R. China.
Dong HuaDepartment of Oncology, The Second Affiliated Hospital of Soochow University, Suzhou, 215004, Jiangsu, P. R. China.
Jiangnan University · CNSoochow University · CNWuxi Fourth People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The oxytocin receptor (OXTR) is directly involved in the pathological mechanisms of multiple cancers, including breast cancer, prostate cancer, and ovarian cancer; however, the role of OXTR in the modulation of colon adenocarcinoma (COAD) growth, metastasis, and clinical prognosis remains to be elucidated. This study used systematic bioinformatics analysis to explore the effects of OXTR on modulating COAD growth and prognosis in patients with COAD. Compared with normal tissues, OXTR mRNA level was higher in COAD tissues, which was associated with tumor progression. Elevated mRNA level of OXTR also indicated a poor prognosis in COAD patients. Furthermore, high mRNA level of OXTR was significantly associated with pathways involved in cell cycle regulation and signal transduction pathways, including the hedgehog, mTOR, TGF-β, and Wnt signaling pathways. OXTR expression was significantly correlated with the infiltration level of type 2T helper cell, central memory CD8 T cell, CD56 bright natural killer cell, activated CD8 T cell, activated B cell, and Type 1T helper cell. Moreover, silencing OXTR inhibited cell proliferation, migration, and invasion, and arrested the cell cycle. In conclusion, high mRNA level of OXTR indicates poor prognosis.

Indexed as

colorectal cancerimmune infiltrationoxytocin receptorpoor prognosisThe Cancer Genome Atlas

Identifiers

PMID34877409
PMCPMC8610102
OpenAlexW3216292966

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.