Evidence map›Paper›PMID 33758600›Full record

ArticleJournal of Cancer2021

The genetic effect and molecular function of the SOCS5 in the prognosis of esophageal squamous cell carcinoma.

Pei-Wen Yang, Ya-Han Chang, Li-Fan Wong, Ching-Ching Lin, Pei-Ming Huang, Min-Shu Hsieh, Jang-Ming Lee

Open access · goldAbstract read
In one paragraph

Article in Journal of Cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 39% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
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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

7 authors at 1 institution in 1 country.

Pei-Wen YangDepartment of Surgery, National Taiwan University Hospital & National Taiwan University College of Medicine.
Ya-Han ChangDepartment of Surgery, National Taiwan University Hospital & National Taiwan University College of Medicine.
Li-Fan WongDepartment of Surgery, National Taiwan University Hospital & National Taiwan University College of Medicine.
Ching-Ching LinDepartment of Surgery, National Taiwan University Hospital & National Taiwan University College of Medicine.
Pei-Ming HuangDepartment of Surgery, National Taiwan University Hospital & National Taiwan University College of Medicine.
Min-Shu HsiehGraduate Institute of Pathology, College of Medicine, National Taiwan University, Taipei, Taiwan.
Jang-Ming LeeDepartment of Surgery, National Taiwan University Hospital & National Taiwan University College of Medicine.
National Taiwan University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Expression of cytokines and growth factors have been shown to be highly correlated with the prognosis of esophageal squamous cell carcinoma (ESCC), a deadly disease with poor prognosis. The suppressor of cytokine signaling (SOCS) family of proteins are key factors in regulating cytokines and growth factors. Yet the role of the SOCS proteins in ESCC is hardly investigated. We currently investigated the prognostic role of SOCS5 in ESCC. We analyzed the prognostic effects of 16 single nucleotide polymorphisms (SNPs) within the SOCS genes in 632 ESCC patients. We repeatedly observed that the 3 SNPs in SOCS5, SOCS5:rs3814039, SOCS5:rs3738890, and SOCS5: rs3768720, were significantly correlated with both overall (OS) and progression-free survival (PFS) of ESCC patients (rs3814039, p=0.032 for OS and p=0.009 for PFS; rs3738890, p=0.016 for OS, and p=0.008 for PFS; rs3768720, p=0.005 for OS and p=0.002 for PFS). SOCS5: rs3768720 was also significantly associated with distant metastasis (Ptrend=0.028). The luciferase assay revealed that SOCS5:rs3814039 and SOCS5: rs3768720 might influence the prognosis by regulating SOCS5 expression. Functional analysis demonstrated SOCS5 was able to regulate epidermal growth factor receptor (EGFR) expression and migration activity of ESCC cells. Furthermore, Patients with strong SOCS5 in normal tissues exhibited significantly better PFS (P=0.049) and reduced risk of distant metastasis (P=0.004) compared to those with weak SOCS5 expression. Overall, our study demonstrates the novel function of SOCS5 in ESCC prognosis. The genetic polymorphisms and expression of SOCS5 could serve as a novel therapeutic biomarker for improving the prognosis of ESCC.

Indexed as

epidermal growth factor receptor (EGFR)esophageal canceresophageal squamous cell carcinoma (ESCC)single nucleotide polymorphisms (SNPs)suppressor of cytokine signaling-5 (SOCS5)

Identifiers

PMID33758600
PMCPMC7974883
OpenAlexW3138521969

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Registered trials

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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.