Evidence map›Paper›PMID 40927672›Full record

ArticleBiochemistry and biophysics reports2025

Collagen proteins, thrombospondin 1 and lumican are differentially expressed across breast cancer subtypes by functional proteomics from core needle biopsy samples of Taiwanese breast cancer.

Wei-Chi Ku, Nam Nhut Phan, Chih-Yi Liu, Chi-Jung Huang, Chen-Chung Liao, Yen-Chun Huang, Po-Hsin Kong, Ling-Ming Tseng, Chi-Cheng Huang

Abstract read
In one paragraph

Article in Biochemistry and biophysics reports, 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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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

9 authors.

Wei-Chi KuSchool of Medicine, College of Medicine, Fu-Jen Catholic University, New Taipei, 242, Taiwan.
Nam Nhut PhanGreehey's Children Cancer Research Institute, University of Texas Health at San Antonio, San Antonio, TX, USA, 78229.
Chih-Yi LiuSchool of Medicine, College of Medicine, Fu-Jen Catholic University, New Taipei, 242, Taiwan.
Chi-Jung HuangDepartment of Medical Research, Cathay General Hospital, Taipei, 106, Taiwan.
Chen-Chung LiaoCancer and Immunology Research Center, National Yang Ming Chiao Tung University, Taipei, 112, Taiwan.
Yen-Chun HuangMarker Exploration Corporation, Taipei, 112, Taiwan.
Po-Hsin KongMarker Exploration Corporation, Taipei, 112, Taiwan.
Ling-Ming TsengDivision of Breast Surgery, Department of Surgery, Taipei Veterans General Hospital, Taipei, 112, Taiwan.
Chi-Cheng HuangDivision of Breast Surgery, Department of Surgery, Taipei Veterans General Hospital, Taipei, 112, Taiwan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: This study aimed to conduct functional proteomics across breast cancer subtypes with bioinformatics analyses. Methods: Candidate proteins were identified using nanoscale liquid chromatography with tandem mass spectrometry (NanoLC-MS/MS) from core needle biopsy samples of early stage (0-III) breast cancers, followed by external validation with public domain gene-expression datasets (TCGA TARGET GTEx and TCGA BRCA). Results: Seventeen proteins demonstrated significantly differential expression and protein-protein interaction (PPI) found the strong networks including COL2A1, COL11A1, COL6A1, COL6A2, THBS1 and LUM. Public domain databases also showed that Conclusion: Functional proteomics suggested that collagen proteins, thrombospondin 1 and lumican are differentially expressed across breast cancer subtypes.

Indexed as

Breast neoplasmsCollagenLumicanProteomicsThrombospondin 1

Identifiers

PMID40927672
PMCPMC12414843

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