Protein biomarkers for subtyping breast cancer and implications for future research: a 2024 update

被引:0
作者
Mueller, Claudius [1 ]
Davis, Justin B. [1 ]
Espina, Virginia [2 ]
机构
[1] Ignite Prote, Lab & Bioinformat Dept, Golden, CO USA
[2] George Mason Univ, Ctr Appl Prote & Mol Med, 10920 George Mason Circle,MS1A9, Manassas, VA 20110 USA
关键词
Antibody-drug conjugate; biomarker; breast cancer; diagnosis; immunohistochemistry; prognosis; reverse-phase protein array; subtype; MOLECULAR-FEATURES; EXPRESSION; GUIDELINE; THERAPY; CHEMOTHERAPY; SURVIVAL; TARGET; IDENTIFICATION; PEMBROLIZUMAB; ACETYLATION;
D O I
10.1080/14789450.2024.2423625
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
IntroductionBreast cancer subtyping is used clinically for diagnosis, prognosis, and treatment decisions. Subtypes are categorized by cell of origin, histomorphology, gene expression signatures, hormone receptor status, and/or protein levels. Categorizing breast cancer based on gene expression signatures aids in assessing a patient's recurrence risk. Protein biomarkers, on the other hand, provide functional data for selecting therapies for primary and recurrent tumors. We provide an update on protein biomarkers in breast cancer subtypes and their application in prognosis and therapy selection.Areas coveredProtein pathways in breast cancer subtypes are reviewed in the context of current protein-targeted treatment options. PubMed, Science Direct, Scopus, and Cochrane Library were searched for relevant studies between 2017 and 17 August 2024.Expert opinionPost-translationally modified proteins and their unmodified counterparts have become clinically useful biomarkers for defining breast cancer subtypes from a therapy perspective. Tissue heterogeneity influences treatment outcomes and disease recurrence. Spatial profiling has revealed complex cellular subpopulations within the breast tumor microenvironment. Deciphering the functional relationships between and within tumor clonal cell populations will further aid in defining breast cancer subtypes and create new treatment paradigms for recurrent, drug resistant, and metastatic disease.
引用
收藏
页码:401 / 416
页数:16
相关论文
共 142 条
[1]   AKT/mTOR signaling modulates resistance to endocrine therapy and CDK4/6 inhibition in metastatic breast cancers [J].
Abu-Khalaf, Maysa M. ;
Alex Hodge, K. ;
Hatzis, Christos ;
Baldelli, Elisa ;
El Gazzah, Emna ;
Valdes, Frances ;
Sikov, William M. ;
Mita, Monica M. ;
Denduluri, Neelima ;
Murphy, Rita ;
Zelterman, Daniel ;
Liotta, Lance ;
Dunetz, Bryant ;
Dunetz, Rick ;
Petricoin, Emanuel F. ;
Pierobon, Mariaelena .
NPJ PRECISION ONCOLOGY, 2023, 7 (01)
[2]   Discovery of 4-Amino-N-[(1S)-1-(4-chlorophenyl)-3-hydroxypropyl]1-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)piperidine-4-carboxamide (AZD5363), an Orally Bioavailable, Potent Inhibitor of Akt Kinases [J].
Addie, Matt ;
Ballard, Peter ;
Buttar, David ;
Crafter, Claire ;
Currie, Gordon ;
Davies, Barry R. ;
Debreczeni, Judit ;
Dry, Hannah ;
Dudley, Philippa ;
Greenwood, Ryan ;
Johnson, Paul D. ;
Kettle, Jason G. ;
Lane, Clare ;
Lamont, Gillian ;
Leach, Andrew ;
Luke, Richard W. A. ;
Morris, Jeff ;
Ogilvie, Donald ;
Page, Ken ;
Pass, Martin ;
Pearson, Stuart ;
Ruston, Linette .
JOURNAL OF MEDICINAL CHEMISTRY, 2013, 56 (05) :2059-2073
[3]   Estrogen and Progesterone Receptor Testing in Breast Cancer: ASCO/CAP Guideline Update [J].
Allison, Kimberly H. ;
Hammond, M. Elizabeth H. ;
Dowsett, Mitchell ;
McKernin, Shannon E. ;
Carey, Lisa A. ;
Fitzgibbons, Patrick L. ;
Hayes, Daniel F. ;
Lakhani, Sunil R. ;
Chavez-MacGregor, Mariana ;
Perlmutter, Jane ;
Perou, Charles M. ;
Regan, Meredith M. ;
Rimm, David L. ;
Symmans, W. Fraser ;
Torlakovic, Emina E. ;
Varella, Leticia ;
Viale, Giuseppe ;
Weisberg, Tracey F. ;
McShane, Lisa M. ;
Wolff, Antonio C. .
JOURNAL OF CLINICAL ONCOLOGY, 2020, 38 (12) :1346-+
[4]   How Many Etiological Subtypes of Breast Cancer: Two, Three, Four, Or More? [J].
Anderson, William F. ;
Rosenberg, Philip S. ;
Prat, Aleix ;
Perou, Charles M. ;
Sherman, Mark E. .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2014, 106 (08)
[5]   Alpelisib for PIK3CA-Mutated, Hormone Receptor-Positive Advanced Breast Cancer [J].
Andre, Fabrice ;
Ciruelos, Eva ;
Rubovszky, Gabor ;
Campone, Mario ;
Loibl, Sibylle ;
Rugo, Hope S. ;
Iwata, Hiroji ;
Conte, Pierfranco ;
Mayer, Ingrid A. ;
Kaufman, Bella ;
Yamashita, Toshinari ;
Lu, Yen-Shen ;
Inoue, Kenichi ;
Takahashi, Masato ;
Papai, Zsuzsanna ;
Longin, Anne-Sophie ;
Mills, David ;
Wilke, Celine ;
Hirawat, Samit ;
Juric, Dejan .
NEW ENGLAND JOURNAL OF MEDICINE, 2019, 380 (20) :1929-1940
[6]  
[Anonymous], Female Breast Cancer Subtypes - Cancer Stat Facts
[7]   Heterogeneity of triple negative breast cancer: Current advances in subtyping and treatment implications [J].
Asleh, Karama ;
Riaz, Nazia ;
Nielsen, Torsten O. .
JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH, 2022, 41 (01)
[8]   Proteomic analysis of archival breast cancer clinical specimens identifies biological subtypes with distinct survival outcomes [J].
Asleh, Karama ;
Negri, Gian Luca ;
Miko, Sandra E. Spencer ;
Colborne, Shane ;
Hughes, Christopher S. ;
Wang, Xiu Q. ;
Gao, Dongxia ;
Gilks, C. Blake ;
Chia, Stephen K. L. ;
Nielsen, Torsten O. ;
Morin, Gregg B. .
NATURE COMMUNICATIONS, 2022, 13 (01)
[9]  
Badve Sunil S, 2022, Am Soc Clin Oncol Educ Book, V42, P1, DOI 10.1200/EDBK_351207
[10]   A comparative study between Ki67 positive versus Ki67 negative females with breast cancer: Cross sectional study [J].
Bahaddin, Mowafak Masoud .
ANNALS OF MEDICINE AND SURGERY, 2020, 60 :232-235