Evidence map›Paper›PMID 41402446›Full record

ArticleCommunications biology2025

Age-related aberrant alternative splicing as a prognostic tool in older breast cancer patients.

Mengxin Chen, Taiping Xiao, Hao Ke, Chun Ye, Fan Yu, Jianbin Su, Shixin Yang, Yun Feng, Huaimeng Xu, Shiting Fu and 13 more

Abstract read
In one paragraph

Article in Communications biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

23 authors.

Mengxin Chen *Human Aging Research Institute (HARI) and School of Life Science, Nanchang University, and Jiangxi Key Laboratory of Human Aging and Disease, Nanchang, Jiangxi, China.ORCID http://orcid.org/0009-0002-8101-2603
Taiping Xiao *Human Aging Research Institute (HARI) and School of Life Science, Nanchang University, and Jiangxi Key Laboratory of Human Aging and Disease, Nanchang, Jiangxi, China.
Hao Ke *Central Laboratory, Jiangxi Maternal and Child Health Hospital, Nanchang, Jiangxi, China.
Chun YeHuman Aging Research Institute (HARI) and School of Life Science, Nanchang University, and Jiangxi Key Laboratory of Human Aging and Disease, Nanchang, Jiangxi, China.
Fan YuHuman Aging Research Institute (HARI) and School of Life Science, Nanchang University, and Jiangxi Key Laboratory of Human Aging and Disease, Nanchang, Jiangxi, China.
Jianbin SuHuman Aging Research Institute (HARI) and School of Life Science, Nanchang University, and Jiangxi Key Laboratory of Human Aging and Disease, Nanchang, Jiangxi, China.
Shixin YangDepartment of Breast Surgery, Jiangxi Maternal and Child Health Hospital, Nanchang, Jiangxi, China.
Yun FengHuman Aging Research Institute (HARI) and School of Life Science, Nanchang University, and Jiangxi Key Laboratory of Human Aging and Disease, Nanchang, Jiangxi, China.
Huaimeng XuHuman Aging Research Institute (HARI) and School of Life Science, Nanchang University, and Jiangxi Key Laboratory of Human Aging and Disease, Nanchang, Jiangxi, China.
Shiting FuHuman Aging Research Institute (HARI) and School of Life Science, Nanchang University, and Jiangxi Key Laboratory of Human Aging and Disease, Nanchang, Jiangxi, China.
Liang LinHuman Aging Research Institute (HARI) and School of Life Science, Nanchang University, and Jiangxi Key Laboratory of Human Aging and Disease, Nanchang, Jiangxi, China.
Junqiang LinHuman Aging Research Institute (HARI) and School of Life Science, Nanchang University, and Jiangxi Key Laboratory of Human Aging and Disease, Nanchang, Jiangxi, China.
Yao XieHuman Aging Research Institute (HARI) and School of Life Science, Nanchang University, and Jiangxi Key Laboratory of Human Aging and Disease, Nanchang, Jiangxi, China.
Qianzhe DingHuman Aging Research Institute (HARI) and School of Life Science, Nanchang University, and Jiangxi Key Laboratory of Human Aging and Disease, Nanchang, Jiangxi, China.
Ye QiuHuankui Academy, Nanchang University, Nanchang, Jiangxi, China.
Ruifan YuHuman Aging Research Institute (HARI) and School of Life Science, Nanchang University, and Jiangxi Key Laboratory of Human Aging and Disease, Nanchang, Jiangxi, China.
Hongyu LvHuman Aging Research Institute (HARI) and School of Life Science, Nanchang University, and Jiangxi Key Laboratory of Human Aging and Disease, Nanchang, Jiangxi, China.
Wulian LiHuman Aging Research Institute (HARI) and School of Life Science, Nanchang University, and Jiangxi Key Laboratory of Human Aging and Disease, Nanchang, Jiangxi, China.
Yuhan ZhangHuman Aging Research Institute (HARI) and School of Life Science, Nanchang University, and Jiangxi Key Laboratory of Human Aging and Disease, Nanchang, Jiangxi, China.
Zhenluo DingGanzhou People's Hospital, Ganzhou, China.
Yang ZouCentral Laboratory, Jiangxi Maternal and Child Health Hospital, Nanchang, Jiangxi, China. zouyang81@163.com.ORCID http://orcid.org/0000-0002-7335-8850
Huozhong YuanGanzhou People's Hospital, Ganzhou, China. yhuozh@163.com.ORCID http://orcid.org/0000-0001-6717-5671
Limin ZhaoHuman Aging Research Institute (HARI) and School of Life Science, Nanchang University, and Jiangxi Key Laboratory of Human Aging and Disease, Nanchang, Jiangxi, China. zhaolimin@ncu.edu.cn.ORCID http://orcid.org/0000-0002-1004-9508

Funding

National Natural Science Foundation of China (National Science Foundation of China) 82260488, 32360164 and 32200679
6 · The paper itself

Abstract

Breast cancer is one of the most prevalent malignancies among women. Although the impact of age on breast cancer progression is well documented, the role of aberrant alternative splicing events in older adults breast cancer patients remains poorly understood. Here, we identified that older adults breast cancer patients exhibit a higher frequency of aberrant alternative splicing events compared to younger patients using public database, a finding that was further validated by data from FUSCC cohorts. A total of 390 high-variability-specific splicing events were observed exclusively in older adults patients. The unsupervised clustering analysis revealed the existence of three distinct subtypes of older adults patients, each displaying significantly different immune cell infiltration profiles and prognostic outcomes. To identify the key regulatory factors of these splicing subtypes, we conducted AS activity score analysis and identified 68 RNA-binding proteins as potential modulators. Subsequently, a machine learning approach using SelectKBest-SVM was employed to construct a predictive model, which demonstrated optimal performance in predicting the prognosis of older adults breast cancer patients, with a high AUC and validation on an independent test set. The developed predictive model offers a promising tool for personalized treatment strategies and accurate prognostication, advancing precision medicine for older adults breast cancer patients.

Indexed as

Alternative SplicingBiomarkers, TumorBreast NeoplasmsAdultAgedAged, 80 and overAge FactorsFemaleGene Expression Regulation, NeoplasticHumansMiddle AgedPrognosisBiomarkers, Tumor

Identifiers

PMID41402446
PMCPMC12804869

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.