期刊论文详细信息
Breast Cancer: Basic and Clinical Research
Breast Cancer Therapeutics and Biomarkers: Past, Present, and Future Approaches
Review
Jason Schick1  Raquel P Ritchie2  Carolina Restini3 
[1] College of Osteopathic Medicine, Michigan State University, Clinton Township, MI, USA;College of Osteopathic Medicine, Michigan State University, Clinton Township, MI, USA;Department of Biochemistry and Molecular Biology, Michigan State University, East Lansing, MI, USA;College of Osteopathic Medicine, Michigan State University, Clinton Township, MI, USA;Department of Pharmacology & Toxicology, Michigan State University, East Lansing, MI, USA;
关键词: Breast cancer;    anti-cancer therapy;    clinical trial;    hormone receptor;    anti-cancer drug resistance;    FDA;   
DOI  :  10.1177/1178223421995854
 received in 2020-08-27, accepted in 2021-01-26,  发布年份 2021
来源: Sage Journals
PDF
【 摘 要 】

Breast cancer (BC) is the leading cause of cancer death in women and the second-most common cancer. An estimated 281 550 new cases of invasive BC will be diagnosed in women in the United States, and about 43 600 will die during 2021. Continual research has shed light on all disease areas, including tumor classification and biomarkers for diagnosis/prognosis. As research investigations evolve, new classes of drugs are emerging with potential benefits in BC treatment that are covered in this manuscript. The initial sections present updated classification and terminology used for diagnosis and prognosis, which leads to the following topics, discussing the past and present treatments available for BC. Our review will generate interest in exploring the complexity of the cell cycle and its association with cancer biology as part of the plethora of target factors toward developing newer drugs and effective therapeutic management of BC.

【 授权许可】

CC BY-NC   
© The Author(s) 2021

【 预 览 】
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RO202212205998888ZK.pdf 1309KB PDF download
Figure 6. 125KB Image download
Figure 8. 171KB Image download
Table 3 84KB Table download
【 图 表 】

Figure 8.

Figure 6.

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