Emerging Role of Genomics and Cell-Free DNA in Breast Cancer

Author(s):  
Lorenzo Gerratana ◽  
Andrew A. Davis ◽  
Ami N. Shah ◽  
Chenyu Lin ◽  
Carla Corvaja ◽  
...  
Keyword(s):  
2015 ◽  
Vol 106 (11) ◽  
pp. 1582-1589 ◽  
Author(s):  
Takashi Takeshita ◽  
Yutaka Yamamoto ◽  
Mutsuko Yamamoto‐Ibusuki ◽  
Toko Inao ◽  
Aiko Sueta ◽  
...  

2020 ◽  
Vol 20 (5) ◽  
pp. 413-421.e1
Author(s):  
Mathilde Ritter ◽  
Viola Paradiso ◽  
Patrik Widmer ◽  
Andrea Garofoli ◽  
Luca Quagliata ◽  
...  

2021 ◽  
Vol 197 ◽  
pp. 113959
Author(s):  
Chen Wang ◽  
Huijuan Zeng ◽  
Luning Zhang ◽  
Yiyun Shen ◽  
Bingjie Zou ◽  
...  

2021 ◽  
Vol 17 (1) ◽  
pp. 12-17
Author(s):  
Yang Zhou ◽  
Dongrui Cheng ◽  
Tingya Jiang

2021 ◽  
Vol 35 (4) ◽  
Author(s):  
Alexis Murillo Carrasco ◽  
Oscar Acosta ◽  
Jaime Ponce ◽  
José Cotrina ◽  
Alfredo Aguilar ◽  
...  

Cancers ◽  
2021 ◽  
Vol 13 (4) ◽  
pp. 728
Author(s):  
Maria Panagopoulou ◽  
Manel Esteller ◽  
Ekaterini Chatzaki

Breast cancer (BC) is a leading cause of death between women. Mortality is significantly raised due to drug resistance and metastasis, while personalized treatment options are obstructed by the limitations of conventional biopsy follow-up. Lately, research is focusing on circulating biomarkers as minimally invasive choices for diagnosis, prognosis and treatment monitoring. Circulating cell-free DNA (ccfDNA) is a promising liquid biopsy biomaterial of great potential as it is thought to mirror the tumor’s lifespan; however, its clinical exploitation is burdened mainly by gaps in knowledge of its biology and specific characteristics. The current review aims to gather latest findings about the nature of ccfDNA and its multiple molecular and biological characteristics in breast cancer, covering basic and translational research and giving insights about its validity in a clinical setting.


2021 ◽  
Vol 6 (1) ◽  
Author(s):  
Brian C.-H. Chiu ◽  
Chang Chen ◽  
Qiancheng You ◽  
Rudyard Chiu ◽  
Girish Venkataraman ◽  
...  

AbstractThe 5-methylcytosines (5mC) have been implicated in the pathogenesis of diffuse large B-cell lymphoma (DLBCL) and follicular lymphoma (FL). However, the role of 5-hydroxymethylcytosines (5hmC) that are generated from 5mC through active demethylation, in lymphomagenesis is unknown. We profiled genome-wide 5hmC in circulating cell-free DNA (cfDNA) from 73 newly diagnosed patients with DLBCL and FL. We identified 294 differentially modified genes between DLBCL and FL. The differential 5hmC in the DLBCL/FL-differentiating genes co-localized with enhancer marks H3K4me1 and H3K27ac. A four-gene panel (CNN2, HMG20B, ACRBP, IZUMO1) robustly represented the overall 5hmC modification pattern that distinguished FL from DLBCL with an area under curve of 88.5% in the testing set. The median 5hmC modification levels in signature genes showed potential for separating patients for risk of all-cause mortality. This study provides evidence that genome-wide 5hmC profiles in cfDNA differ between DLBCL and FL and could be exploited as a non-invasive approach.


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