scholarly journals Pregnancy-associated breast cancer: the risky status quo and new concepts of predictive medicine

2018 ◽  
Vol 9 (1) ◽  
pp. 1-13 ◽  
Author(s):  
Jiri Polivka ◽  
Irem Altun ◽  
Olga Golubnitschaja
Cancers ◽  
2019 ◽  
Vol 11 (10) ◽  
pp. 1451 ◽  
Author(s):  
Erika Bandini ◽  
Tania Rossi ◽  
Giulia Gallerani ◽  
Francesco Fabbri

Breast cancer (BC) is a disease characterized by a high grade of heterogeneity. Consequently, despite the great achievements obtained in the last decades, most of the current therapeutic regimens still fail. The identification of new molecular mechanisms that will increase the knowledge of all steps of tumor initiation and growth is mandatory in finding new clinical strategies. The BC microenvironment, consisting of endothelial cells, fibroblasts, immune cells and adipocytes, plays an essential role in regulating BC development, and recently it has gained great attention in the scientific community. In particular, adipose tissue is emerging as an important target to investigate among mammary gland components. The mechanisms underlying BC progression driven by adipocytes are predominantly unexplored, especially that involving the switch from normal adipocytes to the so-called cancer-associated adipocytes (CAAs). MicroRNAs (miRNAs), a class of gene expression modulators, have emerged as the regulators of key oncogenes and tumor suppressor genes that affect multiple pathways of the tumor microenvironment and adipose tissue. This review concerns a presentation of the role of adipocytes in breast tissue, and describes the most recent discoveries about the interplay between adipocytes and miRNAs, which collaborate in the arrangement of a pro-inflammatory and cancerous microenvironment, laying the foundations for new concepts in the prevention and treatment of BC.


2018 ◽  
Vol 9 (4) ◽  
pp. 403-419 ◽  
Author(s):  
Sona Uramova ◽  
Peter Kubatka ◽  
Zuzana Dankova ◽  
Andrea Kapinova ◽  
Barbora Zolakova ◽  
...  

2004 ◽  
Vol 22 (13) ◽  
pp. 2554-2566 ◽  
Author(s):  
Jeanne S. Mandelblatt ◽  
Clyde B. Schechter ◽  
K. Robin Yabroff ◽  
William Lawrence ◽  
James Dignam ◽  
...  

Purpose Historically, African American women have experienced higher breast cancer mortality than white women, despite lower incidence. Our objective was to evaluate whether costs of increasing rates of screening or application of intensive treatment will be off-set by survival benefits for African American women. Methods We use a stochastic simulation model of the natural history of breast cancer to evaluate the incremental societal costs and benefits of status quo versus targeted biennial screening or treatment improvements among African Americans 40 years of age and older. Main outcome measures were number of mammograms, stage, all-cause mortality, and discounted costs per life year saved (LYS). Results At the current screening rate of 76%, there is little incremental benefit associated with further increasing screening, and the costs are high: $124,053 and $124,217 per LYS for lay health worker and patient reminder interventions, respectively, compared with the status quo. Using reminders would cost $51,537 per LYS if targeted to virtually unscreened women or $78,130 per LYS if targeted to women with a two-fold increase in baseline risk. If all patients received the most intensive treatment recommended, costs increase but deaths decrease, for a cost of $52,678 per LYS. Investments of up to $6,000 per breast cancer patient could be used to enhance treatment and still yield cost-effectiveness ratios of less than $75,000 per LYS. Conclusion Except in pockets of unscreened or high-risk women, further investments in interventions to increase screening are unlikely to be an efficient use of resources. Ensuring that African American women receive intensive treatment seems to be the most cost-effective approach to decreasing the disproportionate mortality experienced by this population.


2010 ◽  
Vol 27 (2) ◽  
pp. 31
Author(s):  
MHJ Ariyaratne ◽  
WL Dilesha
Keyword(s):  

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