» Articles » PMID: 33603458

Genetic Influences in Breast Cancer Drug Resistance

Overview
Publisher Dove Medical Press
Date 2021 Feb 19
PMID 33603458
Citations 9
Authors
Affiliations
Soon will be listed here.
Abstract

Breast cancer is the most common cancer in adult women aged 20 to 50 years. The therapeutic regimens that are commonly recommended to treat breast cancer are human epidermal growth factor receptor 2 (HER2) targeted therapy, endocrine therapy, and systemic chemotherapy. The selection of pharmacotherapy is based on the characteristics of the tumor and its hormone receptor status, specifically, the presence of HER2, progesterone receptors, and estrogen receptors. Breast cancer pharmacotherapy often gives different results in various populations, which may cause therapeutic failure. Different types of congenital drug resistance in individuals can cause this. Genetic polymorphism is a factor in the occurrence of congenital drug resistance. This review explores the relationship between genetic polymorphisms and resistance to breast cancer therapy. It considers studies published from 2010 to 2020 concerning the relationship of genetic polymorphisms and breast cancer therapy. Several gene polymorphisms are found to be related to longer overall survival, worse relapse-free survival, higher pathological complete response, and increased disease-free survival in breast cancer patients. The presence of these gene polymorphisms can be considered in the treatment of breast cancer in order to shape personalized therapy to yield better results.

Citing Articles

FCGR3A V158F gene polymorphism and trastuzumab response in HER2-positive breast cancer patients.

Abdel-Wahed M, Sabbour G, Hamed A, El Kady M, Mohammed S, Shaaban M Sci Rep. 2024; 14(1):26037.

PMID: 39472454 PMC: 11522560. DOI: 10.1038/s41598-024-76024-6.


Novel associations between MTDH gene polymorphisms and invasive ductal breast cancer: a case-control study.

Huang Y, Dai D, Zhu L, Qi X Discov Oncol. 2024; 15(1):273.

PMID: 38977630 PMC: 11231109. DOI: 10.1007/s12672-024-01086-x.


Synthesis, Characterization, and In Vitro Cytotoxicity Evaluation of Doxorubicin-Loaded Magnetite Nanoparticles on Triple-Negative Breast Cancer Cell Lines.

Markhulia J, Kekutia S, Mikelashvili V, Saneblidze L, Tsertsvadze T, Maisuradze N Pharmaceutics. 2023; 15(6).

PMID: 37376206 PMC: 10304410. DOI: 10.3390/pharmaceutics15061758.


Advances with metal oxide-based nanoparticles as MDR metastatic breast cancer therapeutics and diagnostics.

Subhan M RSC Adv. 2022; 12(51):32956-32978.

PMID: 36425155 PMC: 9670683. DOI: 10.1039/d2ra02005j.


Breast cancer in the era of precision medicine.

Sarhangi N, Hajjari S, Heydari S, Ganjizadeh M, Rouhollah F, Hasanzad M Mol Biol Rep. 2022; 49(10):10023-10037.

PMID: 35733061 DOI: 10.1007/s11033-022-07571-2.


References
1.
Kallel I, Kharrat N, Al-fadhly S, Rebai M, Khabir A, Boudawara T . HER2 polymorphisms and breast cancer in Tunisian women. Genet Test Mol Biomarkers. 2009; 14(1):29-35. DOI: 10.1089/gtmb.2009.0069. View

2.
Xie F, Jin K, Shao L, Fan Y, Tu Y, Li Y . FAF1 phosphorylation by AKT accumulates TGF-β type II receptor and drives breast cancer metastasis. Nat Commun. 2017; 8:15021. PMC: 5414047. DOI: 10.1038/ncomms15021. View

3.
Arnould L, Gelly M, Penault-Llorca F, Benoit L, Bonnetain F, Migeon C . Trastuzumab-based treatment of HER2-positive breast cancer: an antibody-dependent cellular cytotoxicity mechanism?. Br J Cancer. 2006; 94(2):259-67. PMC: 2361112. DOI: 10.1038/sj.bjc.6602930. View

4.
Busch S, Sims A, Stal O, Ferno M, Landberg G . Loss of TGFβ Receptor Type 2 Expression Impairs Estrogen Response and Confers Tamoxifen Resistance. Cancer Res. 2015; 75(7):1457-69. DOI: 10.1158/0008-5472.CAN-14-1583. View

5.
Regan M, Leyland-Jones B, Bouzyk M, Pagani O, Tang W, Kammler R . CYP2D6 genotype and tamoxifen response in postmenopausal women with endocrine-responsive breast cancer: the breast international group 1-98 trial. J Natl Cancer Inst. 2012; 104(6):441-51. PMC: 3309132. DOI: 10.1093/jnci/djs125. View