Evidence map›Paper›PMID 40292228›Full record

ArticleBreast cancer : basic and clinical research2025

A Comparative Study on Copy Number Variation in Subtypes of Breast Phyllodes Tumors.

Yuqiong Liu, Min Zhang, Huifen Huang, Huayan Ren, Huixiang Li, Chenran Wang

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Article in Breast cancer : basic and clinical research, 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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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Yuqiong LiuDepartment of Pathology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Min ZhangDepartment of Pathology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Huifen HuangDepartment of Pathology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Huayan RenDepartment of Pathology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Huixiang LiDepartment of Pathology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Chenran WangDepartment of Cancer Biology, University of Cincinnati College of Medicine, Cincinnati, OH, USA.ORCID https://orcid.org/0000-0003-4181-2729

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Breast phyllodes tumor (PT) is a biphasic tumor and constitutes about 0.3% to 1% of all breast tumors. The PT is histologically classified as benign, borderline, and malignant subtypes. Unlike epithelial breast cancers, PT is derived from breast fibroepithelial tissues, and the genomic information of PT subtypes is still limited. Objectives: The objectives were to gain a deeper understanding of genomic changes in the progression of PTs from benign and borderline to malignant. Design: In this study, we used an Affymetrix OncoScan Array to analyze the genome-wide copy number variations (CNVs) and nucleotide point mutations from 3 benign PTs, 3 borderline PTs, and 3 malignant PTs collected from the First Affiliated Hospital of Zhengzhou University. Methods: DNA was extracted from formalin-fixed paraffin-embedded (FFPE) specimens using the TIANamp FFPE DNA Kit. The DNA was profiled for genome-wide CNV using the Affymetrix OncoScan Array and analyzed using the Nexus Express Chromosome Analysis Suite. Results: Our in silico variation analysis indicated copy number loss in Xp11.22 to q22.1 of all benign PTs (χ Conclusions: Our data suggested that CNV at 7p11.2, 22q11.23, and Xq23 together with a point mutation in

Indexed as

Breastcopy number variationmissense mutationphyllodes tumorpoint mutation

Identifiers

PMID40292228
PMCPMC12033413

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