Evidence map›Paper›PMID 40968751›Full record

ArticleJournal of gynecologic oncology2026

Suppressor of TCR signaling 2 (Sts-2) as a potential immunotherapy target and prognostic biomarker in cervical cancer.

Yinlong Chen, Qin Chen, Xiaoqing Guo, Qingliang Zheng

Abstract read
In one paragraph

Article in Journal of gynecologic oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. 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

4 authors.

Yinlong ChenPrenatal Diagnosis Center, The Eighth Affiliated Hospital, Sun Yat-sen University, Shenzhen, P.R. China.ORCID 0009-0001-4604-7192
Qin ChenPrenatal Diagnosis Center, The Eighth Affiliated Hospital, Sun Yat-sen University, Shenzhen, P.R. China.ORCID 0009-0007-9243-2677
Xiaoqing GuoDepartment of Gynecological Oncology, Shanghai First Maternity and Infant Hospital, Tongji University School of Medicine, Shanghai, PR China. guoxiaoqing@51mch.com.ORCID 0000-0002-2493-5156
Qingliang ZhengPrenatal Diagnosis Center, The Eighth Affiliated Hospital, Sun Yat-sen University, Shenzhen, P.R. China. zhengqliang@mail.sysu.edu.cn.ORCID 0000-0002-5626-8423

Funding

Futian Healthcare Research Project FTWS012Futian Healthcare Research Project FTWS2022005Natural Science Foundation of Guangdong 2024A1515013144NNSFC 82071644NNSFC 82371677Shenzhen Science and Technology Program JCYJ20220530144208019Shenzhen Science and Technology Program JCYJ20230807111301004Shenzhen Science and Technology Program JCYJ20240813150622030
6 · The paper itself

Abstract

objectiveMore efficient immune targets are needed for the treatment of cervical cancer. This study aimed to identify potential targets for immunotherapy and prediction in cervical squamous cell carcinoma and endocervical adenocarcinoma (CESC) by conducting bioinformatics analysis and verifying the results with clinical tissue samples.

methodsA retrospective analysis of RNA sequencing data from 304 patients sourced from The Cancer Genome Atlas (TCGA) and another 300 patients from the Gene Expression Omnibus (GEO) was performed to investigate the correlation between suppressor of TCR signaling 2 (Sts-2) expression and clinical parameters in cervical cancer. To authenticate our findings, we utilized a combination of immunohistochemistry, quantitative polymerase chain reaction, and western blotting techniques in a separate cohort consisting of 6 cervical cancer tissue samples.

resultsThe Sts-2 gene was discovered to be substantially co-expressed with a multitude of immune checkpoint molecules, including programmed cell death protein 1 (r=0.8, p<0.001), TIGIT (r=0.87, p<0.001), LAG3 (r=0.71, p<0.001), and CTLA4 (r=0.74, p<0.001), in CESC patients. Both the TCGA and GEO datasets have independently validated that Sts-2 expression levels significantly correlate with overall survival rates, thus demonstrating its prognostic importance. A single-gene Gene Set Enrichment Analysis indicated that Sts-2 was highly enriched in T cell-related immune pathways. Moreover, using the Tumor Immune Dysfunction and Exclusion algorithm, it was suggested that high Sts-2 expression might predict a more favorable response to immunotherapy.

conclusionThe heightened expression of Sts-2 serves as a dual indicator of elevated T cell content and a favorable prognosis in cervical cancer.

Indexed as

AdenocarcinomaBiomarkers, TumorCarcinoma, Squamous CellUterine Cervical NeoplasmsAdultAgedFemaleHumansImmunotherapyMiddle AgedPrognosisRetrospective StudiesBiomarkers, TumorCervical CancerImmunotherapyPrognosis

Identifiers

PMID40968751
PMCPMC13009699

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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.