» Articles » PMID: 18061512

Genetic and Epigenetic Alterations in Breast Cancer: What Are the Perspectives for Clinical Practice?

Overview
Publisher Elsevier
Date 2007 Dec 7
PMID 18061512
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

The worldwide incidence of breast cancer affects 1.2 million women each year. In contrast to the high occurrence of this malady, a decline in mortality is reported among industrialized countries. In this respect, both awareness campaigns and substantial progress achieved in therapy and diagnosis allowed for the enhancement of the survival rate in patients with breast cancer. Undoubtedly, oncology research programs played a relevant role in the improvement of therapeutics and diagnostics for breast cancer. Major strides were reported, especially over the last decade and a half, in better understanding molecular and cellular biology events involved in breast cancer pathogenesis and progression of the disease. However, therapeutic approaches for the treatment of patients with breast cancer need further improvement. Therapeutic interventions can chronically compromise both the state of health and quality of life of breast cancer survivors. In addition, current therapeutic approaches have not significantly improved the survival rate in patients with metastatic disease. On these grounds, it is necessary to develop more efficient therapeutics and diagnostic tools, which can improve the health and quality of life of breast cancer survivors and increase the survival rate in patients with metastatic disease. In this respect, the field of cancer research has placed a particular emphasis on the elucidation of genetic and epigenetic alterations that may lead to the pathogenesis of breast cancer and contribute to its progression.

Citing Articles

Dysregulated miRNA Expression and Androgen Receptor Loss in Racially Distinct Triple-Negative Breast Cancer.

Bhattarai S, Sugita B, Nunes-Souza E, Fonseca A, Chandrashekar D, Bhargava M Int J Mol Sci. 2025; 25(24).

PMID: 39769441 PMC: 11679545. DOI: 10.3390/ijms252413679.


Exploring bacterial key genes and therapeutic agents for breast cancer among the Ghanaian female population: Insights from In Silico analyses.

Kibria M, Ali M, Haque Mollah M PLoS One. 2024; 19(11):e0312493.

PMID: 39585882 PMC: 11588272. DOI: 10.1371/journal.pone.0312493.


Tumour suppressor TET2 safeguards enhancers from aberrant DNA methylation and epigenetic reprogramming in ERα-positive breast cancer cells.

Lyu R, Zhu X, Shen Y, Xiong L, Liu L, Liu H Epigenetics. 2021; 17(10):1180-1194.

PMID: 34689714 PMC: 9542862. DOI: 10.1080/15592294.2021.1997405.


SIRT1-dependent epigenetic regulation of H3 and H4 histone acetylation in human breast cancer.

Rifai K, Judes G, Idrissou M, Daures M, Bignon Y, Penault-Llorca F Oncotarget. 2018; 9(55):30661-30678.

PMID: 30093977 PMC: 6078139. DOI: 10.18632/oncotarget.25771.


Decreased expression of the CHD5 gene and its clinicopathological significance in breast cancer: Correlation with aberrant DNA methylation.

Ma Z, Song J, Liu S, Han L, Chen Y, Wang Y Oncol Lett. 2016; 12(5):4021-4026.

PMID: 27895765 PMC: 5104224. DOI: 10.3892/ol.2016.5147.


References
1.
Raaphorst F, Meijer C, Fieret E, Blokzijl T, Mommers E, Buerger H . Poorly differentiated breast carcinoma is associated with increased expression of the human polycomb group EZH2 gene. Neoplasia. 2004; 5(6):481-8. PMC: 1502571. DOI: 10.1016/s1476-5586(03)80032-5. View

2.
Slamon D, Clark G, Wong S, Levin W, Ullrich A, McGuire W . Human breast cancer: correlation of relapse and survival with amplification of the HER-2/neu oncogene. Science. 1987; 235(4785):177-82. DOI: 10.1126/science.3798106. View

3.
Herrera J, Schiltz R, Bustin M . The accessibility of histone H3 tails in chromatin modulates their acetylation by P300/CBP-associated factor. J Biol Chem. 2000; 275(17):12994-9. DOI: 10.1074/jbc.275.17.12994. View

4.
Baxter C, BYVOET P . Intercalating agents as probes of the spatial relationship between chromatin components. Biochem Biophys Res Commun. 1975; 63(1):286-91. DOI: 10.1016/s0006-291x(75)80041-6. View

5.
Radice P . Mutations of BRCA genes in hereditary breast and ovarian cancer. J Exp Clin Cancer Res. 2003; 21(3 Suppl):9-12. View