Mineralized human primary osteoblast matrices as a model system to analyse interactions of prostate cancer cells with the bone microenvironment

Biomaterials ◽  
2010 ◽  
Vol 31 (31) ◽  
pp. 7928-7936 ◽  
Author(s):  
Johannes C. Reichert ◽  
Verena M.C. Quent ◽  
Leslie J. Burke ◽  
Scott H. Stansfield ◽  
Judith A. Clements ◽  
...  
MRS Advances ◽  
2019 ◽  
Vol 4 (21) ◽  
pp. 1207-1213 ◽  
Author(s):  
MD Shahjahan Molla ◽  
Dinesh R. Katti ◽  
Kalpana S. Katti

ABSTRACTProstate cancer has a strong preference for metastasizing to bone which is the primary cause of prostate cancer-related morbidity and mortality. The complex nature of cancer metastasis requires the development of translational models that recapitulate a specific metastatic stage. Herein, we report the mimicking of mesenchymal to epithelial transition (MET) of prostate cancer cells using highly metastatic and a non-metastatic prostate cancer cell lines. A unique cell culture technique that we termed as ‘sequential culture’ was used to create a biomimetic bone microenvironment for metastasized prostate cancer cells by introducing bioactive factors from osteogenic induction of human mesenchymal stem cells (MSCs) within the porous 3D scaffolds. The in vitro 3D tumor model can be used as a testbed to study the interaction between prostate cancer and bone microenvironment and for the design of novel therapeutic studies.


The Prostate ◽  
2004 ◽  
Vol 59 (2) ◽  
pp. 120-131 ◽  
Author(s):  
Roxane Tenta ◽  
Despina Tiblalexi ◽  
Evangelia Sotiriou ◽  
Peter Lembessis ◽  
Menelaos Manoussakis ◽  
...  

2014 ◽  
Vol 191 (4S) ◽  
Author(s):  
Palamadai N. Venkatasubramanian ◽  
Massa Mafi ◽  
Charles B. Brendler ◽  
Beth A. Plunkett ◽  
Jennifer Doll

2014 ◽  
Vol 2014 ◽  
pp. 1-14 ◽  
Author(s):  
Nadia Rucci ◽  
Adriano Angelucci

The onset of metastases dramatically changes the prognosis of prostate cancer patients, determining increased morbidity and a drastic fall in survival expectancy. Bone is a common site of metastases in few types of cancer, and it represents the most frequent metastatic site in prostate cancer. Of note, the prevalence of tumor relapse to the bone appears to be increasing over the years, likely due to a longer overall survival of prostate cancer patients. Bone tropism represents an intriguing challenge for researchers also because the preference of prostate cancer cells for the bone is the result of a sequential series of targetable molecular events. Many factors have been associated with the peculiar ability of prostate cancer cells to migrate in bone marrow and to determine mixed osteoblastic/osteolytic lesions. As anticipated by the success of current targeted therapy aimed to block bone resorption, a better understanding of molecular affinity between prostate cancer and bone microenvironment will permit us to cure bone metastasis and to improve prognosis of prostate cancer patients.


The Prostate ◽  
2006 ◽  
Vol 66 (1) ◽  
pp. 32-48 ◽  
Author(s):  
Sreenivasa R. Chinni ◽  
Sivasakthy Sivalogan ◽  
Zhong Dong ◽  
J. Carlos Trindade Filho ◽  
Xiyun Deng ◽  
...  

2007 ◽  
Vol 35 (4) ◽  
pp. 701-703 ◽  
Author(s):  
I. Podgorski ◽  
B.E. Linebaugh ◽  
B.F. Sloane

The skeleton is the most common site of metastasis in patients with advanced prostate cancer. Despite many advances in targeting skeletal metastases, the mechanisms behind the attraction of prostate cancer cells to the bone are not known. Osteoclast cathepsin K, due to its ability to effectively degrade bone matrix collagen I, has been implicated in colonization and growth of prostate tumours in the bone. Identification of new cathepsin K substrates in the bone microenvironment and the recent findings demonstrating its involvement in obesity and inflammation suggest additional roles for this enzyme in skeletal metastases of prostate cancer.


2014 ◽  
Vol 6 (6) ◽  
pp. 627-635 ◽  
Author(s):  
Lauren L. Bischel ◽  
Benjamin P. Casavant ◽  
Pamela A. Young ◽  
Kevin W. Eliceiri ◽  
Hirak S. Basu ◽  
...  

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