Evidence mapPaperPMID 41772135Full record

ArticleNPJ precision oncology2026

HRD in endometrial cancer: LST loss drives distinct genomic profile and platinum response.

Ting Wan, Qiaqia Li, Wen Hao, Ying Xie, Binbin Chen, Mufei Lin, Die Dai, Ziming Du, Jundong Li, Wei Wei

Abstract read
In one paragraph

Article in NPJ precision oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Ting Wan *Department of Gynecologic Oncology, Sun Yat-sen University Cancer Center, Guangzhou, PR China.
Qiaqia Li *Department of Gynecologic Oncology, Sun Yat-sen University Cancer Center, Guangzhou, PR China.
Wen Hao *Department of Gynecological Oncology, Fudan University Shanghai Cancer Center, Shanghai, PR China.
Ying XieBGI Genomics, Shenzhen, PR China.
Binbin ChenBGI Genomics, Shenzhen, PR China.
Mufei LinBGI Genomics, Shenzhen, PR China.
Die DaiBGI Genomics, Shenzhen, PR China.
Ziming DuState Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University Cancer Center, Guangzhou, PR China.
Jundong LiDepartment of Gynecologic Oncology, Sun Yat-sen University Cancer Center, Guangzhou, PR China.
Wei WeiDepartment of Gynecologic Oncology, Sun Yat-sen University Cancer Center, Guangzhou, PR China. weiwei1@sysucc.org.cn.

Funding

Guangdong Basic and Applied Basic Research Foundation No. 2022A1515111160Guangzhou Science and Technology Program No. 2023A04J1784National Natural Science Foundation of China funding No. 82203753
6 · The paper itself

Abstract

While homologous recombination deficiency (HRD) presents therapeutic opportunities in endometrial cancer (EC), its molecular determinants and clinical implications remain poorly characterized. Through genomic analysis of 688 cancer-related genes combined with genomic scar assessment, we investigated HRD molecular features and clinical relevance of HRD across three cohorts: an EC cohort from Sun Yat-sen University Cancer Center (SYSUCC, n = 114), the Cancer Genome Atlas EC cohort (n = 500), and a high-grade serous ovarian cancer (HGSOC) cohort (n = 118). HRD was identified in 23.7% of SYSUCC EC cases, and HRD tumors paradoxically had fewer short-nucleotide variations in HRR genes than proficient (HRP) tumors (18.52% vs. 48.28%, P = 0.007). Mechanistic analysis revealed large-scale transition (LST) losses as the potential predominant HRD driver in EC, occurring significantly more frequently in HRD versus HRP tumors (74.1% vs 5.7%; P < 0.001). Comparative genomics demonstrated enrichment of HRR gene LST losses was EC-specific, contrasting with HGSOC where LST distribution was HRD-independent. Clinically, elevated HRD scores predicted reduced progression-free survival (HR 1.74, 95% CI 1.03-2.94; P = 0.04) yet enhanced platinum sensitivity (HR 0.41, 95% CI 0.18-0.94; P = 0.034). Our findings indicate that the HRD phenotype in EC, driven primarily by LST losses rather than short-nucleotide variations, serves as both a prognostic and predictive biomarker.

Identifiers

PMID41772135
PMCPMC13358079

What Socratic holds

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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 Socratic graph.