Bone cancer

Bone cancer

Bone cancer, also known as primary bone cancer, develops in the cells of bone or cartilage. It is a cancerous (malignant) tumour formed by a group of cancerous cells that can invade and destroy neighbouring bone tissue.

 Often derived from osteoblasts or osteoclasts, they disrupt the delicate balance of bone remodelling, inducing pathological changes. The main varieties include osteogenic sarcoma and multiple myeloma, each with distinct patterns of development and progression. Genetic alterations, such as mutations in tumour suppressor genes, are often key instigators of these bone cancers. This type of cancer is very rare in adults over the age of 40, but is more common in children, adolescents and young adults.

There are different types of bone tumours, including osteosarcoma, Ewing's sarcoma, chondrosarcoma, fibrosarcoma, angiosarcoma and high-grade undifferentiated polymorphous sarcoma.  It is important to note that bone cancer is different from bone metastases, which are secondary tumours arising from cancers of other organs that spread to the bone.

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300433
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300447
 1cryovial 
C0004007
 OneFrozenvial 
330447
 1cellcultureflask 
300289
-
305096
-
T0004005
 OneFrozenvial 
300127
 1cryovial 
C0004004
 OneFrozenvial 
330127
 1cellcultureflask 
300136
 1cryovial 
300435
 1cryovial 
300235
 1cryovial 
300440
-
330136
 1cellcultureflask 
330235
 1cellcultureflask 
330435
 1cellcultureflask 
300441
 1cryovial 
330441
 1cellcultureflask 
300331
 1cryovial