Evidence map›Paper›PMID 36694223›Full record

ArticleHereditas2023

Identification of the prognostic value of Th1/Th2 ratio and a novel prognostic signature in basal-like breast cancer.

Yu Xiao, Yi Huang, Jianping Jiang, Yan Chen, Changyuan Wei

Open access · goldAbstract read
In one paragraph

Article in Hereditas, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

14 citing papers in PubMed, 19 citations in OpenAlex.

  1. A prospective clinical study on the effectiveness ofJournal of traditional and complementary medicine · 2026
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  8. Role, mechanisms and effects ofOncology letters · 2025
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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

5 authors at 2 institutions in 1 country.

Yu XiaoAffiliated Tumor Hospital, Guangxi Medical University, Nanning, Guangxi, China.
Yi HuangDepartment of Research, Affiliated Tumor Hospital, Guangxi Medical University, Nanning, Guangxi, China.
Jianping JiangAffiliated Tumor Hospital, Guangxi Medical University, Nanning, Guangxi, China.
Yan ChenAffiliated Tumor Hospital, Guangxi Medical University, Nanning, Guangxi, China.
Changyuan WeiAffiliated Tumor Hospital, Guangxi Medical University, Nanning, Guangxi, China. changyuanwei@gxmu.edu.cn.
Tumor Hospital of Guangxi Medical University · CNShenzhen Second People's Hospital · CN

Funding

Natural Science Foundation of Guangxi Province 2020GXNSFAA297152
6 · The paper itself

Abstract

backgroundBreast cancer is a heterogeneous group of diseases. The polarization of CD4+ T helper (Th) lymphocytes (mainly Th1 and Th2) may differ in breast cancers with different outcomes, but this has not been fully validated.

methodsThis study is a bioinformatic analysis, in which differentially expressed genes (DEGs) were identified in patients with low and high Th1/Th2 ratios. And then, DEG functions, hub genes and independent predictors were determined.

resultsLow Th1/Th2 ratio was associated with poor outcome in Luminal A and basal-like breast cancer (p < 0.05). GSEA and KEGG analysis of DEGs obtained from comparing low and high Th1/Th2 ratios illuminated downregulation of immune-related gene sets and pathways affecting Th1/Th2 balance toward Th2 polarization (p < 0.05). Survival and Cox analyses of all the DEGs confirmed CCL1 and MYH6 were independent protective factors and IFNK and SOAT2 were independent risk factors for basal-like breast cancer (95%CI: 1.06-2.5, p = 0.026). Then a four-gene signature was constructed and achieved a promising prognostic value (C-index = 0.82; AUC = 0.826).

conclusionsLow Th1/Th2 ratio predicts poor outcome in Luminal A and Basal-like breast cancer, and downregulation of immune-related gene sets and pathways contribute to Th1/Th2 balance toward Th2 polarization. CCL1, MYH6, IFNK, and SOAT2 have an independent prognostic value of survival outcome and might be novel markers in basal-like breast cancer.

Indexed as

Breast NeoplasmsTh1 CellsTh2 CellsCardiac MyosinsChemokine CCL1FemaleHumansInterferon Type IMyosin Heavy ChainsPrognosisSterol O-Acyltransferase 2Cardiac MyosinsCCL1 protein, humanChemokine CCL1interferon kappaInterferon Type IMYH6 protein, humanMyosin Heavy ChainsSterol O-Acyltransferase 2Basal-likeBioinformatic analysisBreast cancerPrognostic modelTh1/Th2 balance

Identifiers

PMID36694223
PMCPMC9875389
OpenAlexW4317877526

What OpenQuestion holds

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LicenceCC BY
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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.