Evidence map›Paper›PMID 41139457›Full record

ArticleNan fang yi ke da xue xue bao = Journal of Southern Medical University2025

[HOTAIR rs920778 single nucleotide polymorphism is associated with breast cancer susceptibility and HER2-targeted therapy resistance in Chinese population].

Mingliang Zhang, Feifan Sun, Zhuoqi Han, Yue Gao, Yi Luo

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Article in Nan fang yi ke da xue xue bao = Journal of Southern Medical University, 2025. 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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1 · What the graph read from it

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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

5 authors.

Mingliang ZhangDepartment of Surgical Oncology, First Affiliated Hospital of Bengbu Medical University, Bengbu 233000, China.
Feifan SunGraduate School, Bengbu Medical University, Bengbu 233000, China.
Zhuoqi HanGraduate School, Bengbu Medical University, Bengbu 233000, China.
Yue GaoGraduate School, Bengbu Medical University, Bengbu 233000, China.
Yi LuoGraduate School, Bengbu Medical University, Bengbu 233000, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo investigate the association of HOTAIR gene rs920778 single nucleotide polymorphism (SNP) with breast cancer susceptibility and response to HER2-targeted therapy in a Chinese population.

methodsTaqMan probe-based real-time quantitative PCR was used for genotyping of the rs920778 locus (chr12:54,376,218) in peripheral blood genomic DNA from 287 breast cancer patients and 260 healthy individuals from northern Anhui Province. The genotype (GG, GT and TT) and allele (G/T) distribution frequencies were compared between the two groups to evaluate their association with breast cancer risk. Multivariate logistic regression analysis was conducted to assess the relationship between SNP at this locus and aggressive clinicopathological features (including tumor size, lymph node metastasis, ER/PR/HER2 status, and molecular subtypes) of breast cancer. For the HER2-positive subgroup, the association between rs920778 genotype and responses to dual-targeted therapy (trastuzumab [6 mg/kg q3w]+pertuzumab [420 mg q3w] + docetaxel [75 mg/m²]) was analyzed. The primary endpoints included pathological complete response rate (pCR), objective response rate (ORR), and progression-free survival (PFS).

resultsThe TT genotype of rs920778 was associated with a significantly increased breast cancer susceptibility (OR=1.54, 95%

conclusionsThe TT genotype of HOTAIR rs920778 serves as an independent risk factor for breast cancer susceptibility and aggressive progression in Chinese population and may predict the resistance to HER2-targeted therapies, suggesting its potential as a prognostic biomarker for precision oncology.

Indexed as

Breast NeoplasmsDrug Resistance, NeoplasmPolymorphism, Single NucleotideRNA, Long NoncodingAdultAgedCase-Control StudiesChinaEast Asian PeopleErb-b2 Receptor Tyrosine KinasesFemaleGenetic Predisposition to DiseaseGenotypeHumansMiddle AgedERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesHOTAIR long untranslated RNA, humanRNA, Long Noncodingbreast cancer susceptibilityHOTAIRprognostic biomarkersingle nucleotide polymorphismtherapeutic sensitivity

Identifiers

PMID41139457
PMCPMC12568485

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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.