Cellular senescence in normal mammary gland and breast cancer: implications for cancer therapy

Cellular senescence (CS) is a major homeostatic biological process, which plays a key role in normal tissue development and provides protection from stressful cell insults. The role of CS in mammary-gland development and breast cancer is not well understood. While there is a lack of experimental dat...

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Hauptverfasser: Sirinian, Chaido (VerfasserIn) , Peroukidis, Stavros (VerfasserIn) , Kriegsmann, Katharina (VerfasserIn) , Chaniotis, Dimitrios (VerfasserIn) , Koutras, Angelos (VerfasserIn) , Kriegsmann, Mark (VerfasserIn) , Papanastasiou, Anastasios D. (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 1 June 2022
In: Genes
Year: 2022, Jahrgang: 13, Heft: 6, Pages: 1-10
ISSN:2073-4425
DOI:10.3390/genes13060994
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.3390/genes13060994
Verlag, lizenzpflichtig, Volltext: https://www.mdpi.com/2073-4425/13/6/994
Volltext
Verfasserangaben:Chaido Sirinian, Stavros Peroukidis, Katharina Kriegsmann, Dimitrios Chaniotis, Angelos Koutras, Mark Kriegsmann and Anastasios D. Papanastasiou

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520 |a Cellular senescence (CS) is a major homeostatic biological process, which plays a key role in normal tissue development and provides protection from stressful cell insults. The role of CS in mammary-gland development and breast cancer is not well understood. While there is a lack of experimental data on the role of CS in the development of the pre-pubertal mammary gland, there is evidence for a biphasic senescence response in adult normal-mammary-epithelial cells, where the bypass of the first senescence barrier (M0) seems to be a key step in the development of premalignant lesions, with genetic abnormalities that resemble in situ breast carcinoma. Further, there is accumulating evidence for the role of cellular senescence in breast-cancer response, regarding treatment and patient outcome. Here, we review the current literature on cellular senescence, in epithelial-mammary cells, breast-cancer cells, and breast-tumor-microenvironment-resident cells. Furthermore, we discuss its putative role in breast-cancer response, regarding treatment and disease progression. In addition, we provide preliminary evidence of CS in breast-cancer-microenvironment cells, such as tumor-associated fibroblasts and tumor-infiltrating lymphocytes, by employing the novel GL13 lipofuscin stain, as a marker of cellular senescence. 
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