breast cancer bone metastasis lytic or blastic

Those leading to excess bone deposition are considered osteoblastic. It is impossible to understand the growth and progression of cancer cells in the bone marrow without consideration of the interaction between osteoblasts and osteoclasts. Multiple myeloma is a malignant tumor of plasma cells that causes lytic bone damage. In males, prostate and lung cancers make up 80% of carcinomas metastasising to bone. WebMetastasis and multiple myeloma are common malignant diseases involving the bone marrow. Osteoblasts derive from mesenchymal stem cells in the marrow under control of Runx2, a key osteoblastic transcription factor. A working model to describe the bone remodeling compartment in the presence of metastatic cancer cells has been referred to as the 'vicious cycle of bone metastasis' [13] (Figure 1B). COX-2 inhibition also partially attenuated the ability of two breast cancer cell lines to degrade and invade extracellular matrix components such as laminin and collagen [47]. Where 10.1158/0008-5472.CAN-09-2758. Bisphosphonates binding to hydroxyapatite are ingested by osteoclasts and cause their apoptosis. Stopeck [74] recently reported the results of a clinical trial in which denosumab was found to be superior to zoledronic acid in preventing skeletal-related events in breast, prostate and multiple myeloma patients. Cancer can cause bone to break down and leak calcium. Rucci N, Teti A: Osteomimicry: how tumor cells try to deceive the bone. 10.1016/S8756-3282(03)00086-3. There are two types of lesions: lytic lesions, which destroy bone material; and blastic lesions, which fill the Breast cancer metastasis to the bone: mechanisms of bone loss, http://breast-cancer-research.com/series/metastasis_pathway. Jemal A, Siegel R, Ward E, Murray T, Xu J, Thun MJ: Cancer Statistics, 2007.

WebWhen cancer cells spread to the bones (bone metastases), they can cause many problems such as pain, broken bones, or more serious problems. 10.1016/S0531-5565(03)00069-X. When treated with neutralizing antibody to PDGF, the osteoblasts assumed normal morphology. Clinical evidence indicates that this drug can reduce the rate of bone loss, but is not curative. 10.1023/A:1026526703898. Exp Cell Res. Osteoclasts derive from hematopoietic stem cells. Mixed lesions may also occur. Thus, cathepsin K is a key molecule not only in osteoclastic breakdown of collagen but also in angiogenesis and production of proinflammatory cytokines. 10.1007/s10585-007-9112-8. Juarez P, Guise TA: TGF-beta in cancer and bone: Implications for treatment of bone metastases. Metastastic human breast cancer cells (MDA-MB-231) added to this culture attach, penetrate the tissue and form single cell files characteristic of metastases seen in pathologic tissues. 1970, 86: 1436-1440. The use of blocking antibodies to placental growth factor in two xenograft mouse/human models greatly decreased the numbers and size of osteolytic lesions [61]. 2006, 85: 584-595. Tumours that metastasise to bonemay be remembered using the mnemonic "PBKTL",rendered as "lead kettle", as "Pb"is the standard abbreviation for the chemical element, lead. WebThe lesions can often be blastic but may also appear purely lytic, with poor margination, no matrix and cortical destruction.

N Engl J Med. Because of its significant role, TGF- has been a tempting therapeutic target. 10.1038/35036374. Cancer Res. Nat Cell Biol. Runx2 also promotes PTHrP expression in breast cancer cells, which in turn stimulates other cells, such as osteoblasts, to produce more RANKL, leading to further osteoclast activation. Andrea M Mastro. Active TGF- is involved in tumor growth, osteoblast retraction from the bone surface, inhibition of osteoblast differentiation [52, 53] and promotion of osteoclast differentiation. Hung JJ, Jeng WJ, Hsu WH et-al. Breast cancer frequently metastasizes to the skeleton. Mol Cancer. Bergers G, Brekken R, McMahon G, Vu TH, Itoh T, Tamaki K, Tanzawa K, Thorpe P, Itohara S, Werb Z, Hanahan D: Matrix metalloproteinase-9 triggers the angiogenic switch during carcinogenesis. Interestingly, many osteomimetic factors are regulated by the same transcription factor, Runx2, considered to be the major regulator of osteoblast commitment and differentiation [39]. The clinical outcomes of bone pain, pathologic fractures, nerve compression syndrome, and metabolic disturbances leading to hypercalcemia and acid/base imbalance severely reduce the quality of life [3]. 10.1158/0008-5472.CAN-08-4437. Biochem Biophys Res Commun. Springer Nature. The hypoactivity of osteoblasts has been known for some time in multiple myeloma. 1999, London: Martin Dunitz Ltd. Raisz LG, Mundy GR, Luben RA: Skeletal reactions to neoplasms. There were 22 lytic, 15 mixed, 6 diffuse, and 5 blastic metastatic cases. Below are the links to the authors original submitted files for images. 2003, 300: 957-964. Clinical studies of newly diagnosed breast cancer patients have revealed that high bone turnover correlates with a higher risk of skeletal complications [62]. There are currently drugs in preclinical and clinical stages of testing that are directed to homing, adhesion, and vascularization of tumors [70]. Mets (adults) lytic Lung Kidney colon Thyroid blastic Prostate Stomach Bladder Breast cancer cause both lytic and blastic 6. WebIf resectable, Males with bone metastasis and elevated PSA In all adjuvant chemotherapy should be considered, whereas patients with bone metastases from adenocarcinoma, neoadjuvant treatment with platinum and taxanes may serum PSA should be quantified. Lynch CC: Matrix metalloproteinases as master regulators of the vicious cycle of bone metastasis. Provided by the Springer Nature SharedIt content-sharing initiative. 2008, 34 (Suppl 1): S25-30. PGs produced from this arachidonic acid conversion are both autocrine and paracrine factors that help to govern physiologic homeostasis. 10.1158/1535-7163.MCT-07-0234. SPARC cleavage also coincides with an increase in inflammatory cytokines such as IL-6 and IL-8 [51]. AMM, the senior investigator and corresponding author, has worked in the area of breast cancer metastasis to bone for over 12 years. As the most common nonepithelial malignancy, prostate adenocarcinoma (PRAD) is the fifth chief cause of cancer mortality in men. These results signify an important role for cancer cell-derived Runx2 in the osteolytic process. Cancer Res. However, both drugs are associated with low incidence of osteonecrosis of the jaw [75]. Eur J Cancer. Metastases leading to overall bone loss are classified as osteolytic. Blastic lesions are caused by new bone being made without old bone breaking It is the most common of primary bone tumors and found in the spine, pelvis skull, sternum, and ribs. Neutralization of TGF- in conditioned medium from human metastatic MDA-MB-231 breast cancer cells permitted the differentiation of osteoblasts in culture, suggesting that TGF- negatively affects osteoblasts while promoting growth of the metastatic cells [33]. It is estimated that osteolytic lesions occur in 60 to 95% of myeloma patients [1, 27]. PubMed Central Part of statement and

It has high affinity for type I collagen, the most abundant matrix protein. 2004, 21: 427-435. Clin Cancer Res. Bone.

Recently we have begun developing an in vitro bioreactor [78]. Once osteoblasts finish bone deposition, they undergo apoptosis, remain in the matrix as osteocytes or revert to thin bone-lining cells. 2010, 70: 6537-6547.

Bone is the most common site to which breast cancer metastasizes. instability (CIN) compared to metastasis of know origin. By knowing the typical behaviour of the metastatic lesion - lytic or blastic -you can help sort between the types to make the mnemonic even more useful. ADVERTISEMENT: Radiopaedia is free thanks to our supporters and advertisers. Radiograph shows a destructive expanded osteolytic lesion in the metacarpal of the thumb in a 55-year- old man with lung carcinoma.

WebBone Metastasis Cancer cells that break off from a primary tumor and enter the bloodstream or lymph vessels can reach nearly all tissues of the body. 2010, 70: 6150-6160. Thus, inflammation is likely to be important in cancer initiation, metastasis and the resulting osteolysis. PDGF is a dimeric protein consisting of two of four possible subunits. Administration of bisphosphonates may slow osteolytic lesion progression and stabilize or increase overall bone density, but does not bring about healing [1, 16, 26]. 2008, 3: e3537-10.1371/journal.pone.0003537. Current treatments can improve bone density, decrease skeletal related events and ease bone pain, yet existing bone lesions do not heal. Br J Cancer. In fact, a new drug, denosumab (Prolia), a fully human monoclonal antibody to RANKL, has been approved by the US Food and Drug Administration (FDA) for the treatment of postmenopausal women with high risk of osteoporotic fractures, and is under priority review for patients with bone metastases. Their multifunctionality demonstrates their importance. Clin Exp Metastasis. Article Despite the role of the osteoclasts in this process, the outcome is due in large part to the impact of cancer cells directly and indirectly on osteoblasts. Orthop. TGF- is one of the most prominent. Distant metastasis often Clusters of osteoblasts produce osteoid, composed of collagen, osteonectin, chondroitin sulfate and other non-mineral molecules, which matures and is then mineralized over several months [12]. 2006, 85: 596-607. 2008, 473: 98-105. 2008, Washington, DC: American Society for Bone and Mineral Research, 379-382. full_text. The skeleton is constantly undergoing remodeling. Bone morphogenetic proteins in breast cancer - dual role in tumourigenesis?. Webthyroid carcinoma - solitary metastasis, prostate adenocarcinoma - blastic metastasis, melanoma - lytic metastasis, osteosarcoma - metastasis in children, breast cancer - most common primary source of metastasis in adult females, CAS

Identification of a stimulator or protector of osteoblasts would be a major improvement in treatment for osteolytic breast cancer as well as other diseases of bone loss. It can activate osteoclasts independent of RANKL [21]. Meanwhile, COX-2 produced by breast cancer cells and osteoblasts increases the localized PGE2 concentration, which can directly bind to osteoblasts, promoting RANKL expression and further stimulating osteoclast differentiation. Exp Gerontol. Mercer RR, Mastro AM: Cytokines secreted by bone-metastatic breast cancer cells alter the expression pattern of f-actin and reduce focal adhesion plaques in osteoblasts through PI3K. Vikesa J, Moller AK, Kaczkowski B, Borup R, Winther O, Henao R, et al. Retrieval of the bone at specific times gives a snapshot of the status of metastases. It inhibits the differentiation of osteoclasts by competitive binding with RANKL. 10.1182/blood-2009-08-237628. Current therapeutic targets are indicated in green. Kinder M, Chislock E, Bussard KM, Shuman L, Mastro AM: Metastatic breast cancer induces an osteoblast inflammatory response. Lipton A: Emerging role of bisphosphonates in the clinic--antitumor activity and prevention of metastasis to bone. Clin Oral Investig. Clezardin P, Teti A: Bone metastasis: pathogenesis and therapeutic implications. Both RANKL and VEGF can induce osteoclast formation [48], and MMPs play a role in bone matrix degradation.

2010, 33 (3 Suppl): S1-7. In a study by Mercer and Mastro [59], osteoblasts treated with conditioned media from MDA-MB-231 breast cancer cells displayed disorganized F-actin fibrils and reduced focal adhesion plaques. Among these are the MMPs. CAS Studies with MMP9-null mice indicate its importance in tumor progression in ovarian cancer, prostate cancer and bone metastasis [56]. Klein DC, Raisz LG: Prostaglandins: stimulation of bone resorption in tissue culture. Cells of the osteoblast lineage are derived from mesenchymal stem cells, and are represented in this unit by osteoblasts, bone lining cells and osteocytes. 2005, 310: 270-281. Chronic inflammation has long been considered a risk factor in cancer initiation [68]. The presence of tumor cells in the bone microenvironment perturbs the balance between osteoblasts and osteoclasts, leading to excess bone loss or formation. However, both bone degradation and deposition likely occur early in the metastatic process. Where bone destruction predominates, it appears lytic. There are conflicting reports regarding their effect on osteoblasts. Blood. Zambonin Zallone A, Teti A, Primavera MV: Resorption of vital or devitalized bone by isolated osteoclasts in vitro. It promotes growth and survival of tumor cells [61], and is also involved in osteoclast differentiation. H Singh and JA Neutze (eds. Lung lesions in bone may also be blastic. The mechanisms are thought to be inhibition of tumor cell adhesion as well as osteoclast differentiation. 7. Halpern J, Lynch CC, Fleming J, Hamming D, Martin MD, Schwartz HS, Matrisian LM, Holt GE: The application of a murine bone bioreactor as a model of tumor: bone interaction. Guise TA, Kozlow WM, Heras-Herzig A, Padalecki SS, Yin JJ, Chirgwin JM: Molecular mechanisms of breast cancer metastases to bone. Kingsley LA, Fournier PG, Chirgwin JM, Guise TA: Molecular biology of bone metastasis. It is estimated that 85% of individuals with advanced disease harbor bone metastases [1]. Kang and colleagues [20] found that expression of two MMP genes, MMP1 and ADAMTS1, discriminated between a subline of osteotropic metastatic MDA-MB-231 cells and the parental line. 4. Cortical bone provides strength and protection while trabecular bone is the most metabolically active. In the final stages of metastatic osteolytic breast cancer disease, the cancer cells, fueled by growth factors released from the degraded matrix, expand unchecked. 2010, 3: 572-599. WebBisphosphonates are a class of drugs with a potent bone resorption inhibition activity that have found increasing utility in treating. 1974, 230: 473-475. 10.1016/S1535-6108(03)00132-6. The role of PTHrP in bone metabolism is not fully understood, but it is known to cause upregulation of RANKL and downregulation of OPG [19], thus enhancing osteoclast function leading to bone degradation. 7, Chapter (b) The lesion shows complete sclerotic fill-in 3 months later. Pharmaceuticals. Endocr Relat Cancer. Kang Y, Siegel PM, Shu W, Drobnjak M, Kakonen SM, Cordon-Cardo C, Guise TA, Massague J: A multigenic program mediating breast cancer metastasis to bone. In a series of in vitro, ex vivo and in vivo experiments, Ohshiba and colleagues [45] demonstrated that direct cell-cell contact between breast cancer cells and osteoblasts caused an increase in COX-2 expression in the osteoblasts due to activation of the NFB/mitogen-activated protein (MAP) kinase pathway. Just as osteoblasts are a critical partner in normal bone remodeling, they are vital to the metastatic osteolytic process. In addition, production of inflammatory cytokines (that is, IL-6, TNF-, M-CSF, IL-1) is suppressed by estrogen [64]. Department of Biochemistry and Molecular Cell Biology, The Pennsylvania State University, University Park, PA, 16802, USA, Yu-Chi Chen,Donna M Sosnoski&Andrea M Mastro, You can also search for this author in 2010, 48: 483-495. There is evidence that bisphosphonates also contribute to tumor cell death, especially in combination with chemotherapy [72].

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Lee J, Weber M, Mejia S, Bone E, Watson P, Orr W: A matrix metalloproteinase inhibitor, batimastat, retards the development of osteolytic bone metastases by MDA-MB-231 human breast cancer cells in Balb C nu/nu mice. DMS is a senior research technician with many years experience in the bone field. Under the influence of macrophage colony-stimulating factor (M-CSF) and RANKL (receptor activator for NFB ligand) produced by osteoblasts and other cells in the microenvironment, pre-osteoclasts differentiate into multinuclear, activated osteoclasts that adhere to the bone and begin matrix degradation. J Dent Res. The spreading pathways of metastasis from the starting site to the bones are only partially understood, and some authors propose some bone metastasis via the Batson venous plexus, a two-way, valveless venous pathway that allows cancer cells, infection and emboli to travel freely both to cranial and caudal direction without passing through the main "tumour-catching" places: liver, lung, peritoneum and others. However, both bone Edited by: Rosen CL. Endocrinology. Osteolytic lesions are the end result of osteoclast activity; however, osteoclast differentiation and activation are mediated by osteoblast production of RANKL (receptor activator for NFB ligand) and several osteoclastogenic cytokines. Coleman RE, Lipton A, Roodman GD, Guise TA, Boyce BF, Brufsky AM, Clzardin P, Croucher PI, Gralow JR, Hadji P, Holen I, Mundy GR, Smith MR, Suva LJ: Metastasis and bone loss: Advancing treatment and prevention. 10.1007/s00784-009-0268-2.

Osteomimetic factors include osteopontin (OPN), osteocalcin, osteonectin, bone sialoprotein, RANKL and PTHrP. Commonly, human cancer cells are studied as xenografts in immunodeficient mice, or rodent tumors are studied in syngeneic models. Am J Pathol. The presence of skeletal metastases in patients suffering from cancer leads to a variety of clinical complications. Because osteoblasts secrete both RANKL and OPG, they are major mediators of osteoclastogenesis [25]. 2005, 208: 194-206.

2005, 5 (Suppl): S46-53. At the tissue level, PDGF is involved in bone formation, wound healing, erythropoiesis and angiogenesis as well as tumor growth and lesion development [57]. Other cells of the osteoblastic lineage include bone lining cells and osteocytes. WebAutopsy studies suggest that between 30% and 80% of patients with cancer have evidence of bony metastases.2,3 Although any tumor may metastasize to bone, metastasis is most likely to occur in breast, lung, thyroid, renal, and pros- tate cancers (Table 1). Privacy Ooi LL, Zheng Y, Stalgis-Bilinski K, Dunstan CR: The bone remodeling environment is a factor in breast cancer bone metastasis. Article PubMed At first glance it would seem ideal to pair bisphosphonates or denosumab with teriparatide since the former two block bone resorption and the latter stimulates bone deposition. 2010, 126: 1749-1760.

Yang Y, Ren Y, Ramani VC, Nan L, Suva LJ, Sanderson RD: Heparanase enhances local and systemic osteolysis in multiple myeloma by upregulating the expression and secretion of RANKL. PubMed Webthyroid carcinoma - solitary metastasis, prostate adenocarcinoma - blastic metastasis, melanoma - lytic metastasis, osteosarcoma - metastasis in children, breast cancer - most common primary source of metastasis in adult females, Bone Metastases Share by Noordacom Edit Content Embed More Leaderboard Theme Options Switch template 2010, 363: 2458-2459. 2009, 13: 355-362. At least three essential molecules, TGF-, IGF, and VEGF, need to be activated by MMPs before they can function. PubMed The roentgenogram indicates the net effect of these two processes. In people with breast and prostate cancer, the bone is often the first distant site of cancer spread. 2009, 11: R56-10.1186/bcr2345. The dynamics of this system are interrupted when metastatic breast cancer cells are introduced, adding another layer of active molecules to the bone environment. After your cancer is gone, it is the job of the osteoblasts to rebuild the bone. In the 1960s and 70s it was proposed that bone degradation might result from the physical pressure of the tumor on the bone and/or direct resorption of the bone by tumor cells. Using this device, we have been able to grow osteoblasts into a mineralized tissue. 10.1002/(SICI)1097-0142(19971015)80:8+<1546::AID-CNCR4>3.0.CO;2-I. Ann N Y Acad Sci. The presence of skeletal metastases in patients suffering from cancer leads to a variety of clinical complications. 10.1158/1535-7163.MCT-08-0153. Breast cancer metastasis to the bone: mechanisms of bone loss.

Here we discuss some of the proposed mechanisms that contribute to metastatic breast cancer-induced bone loss. Cackowski FC, Anderson JL, Patrene KD, Choksi RJ, Shapiro SD, Windle JJ, Blair HC, Roodman GD: Osteoclasts are important for bone angiogenesis. Mechanisms of lytic and blastic metastatic disease of bone In the majority of skeletal metastases, new bone develops simultaneously with bone destruction. The roentgenogram indicates the net effect of these two processes. Where the bone formation predominates, the lesion appears sclerotic. {"url":"/signup-modal-props.json?lang=gb"}, Zambon J, Bell D, Di Muzio B, et al. Further stimulation results in large multinuclear cells capable of bone resorption. (a) CT of the T6 vertebra in a patient with breast cancer demonstrates a mixed lytic/blastic metastasis in the anterior aspect of the vertebral body. Anyone you share the following link with will be able to read this content: Sorry, a shareable link is not currently available for this article. Osteoblasts produce macrophage colony stimulating factor (M-CSF) and receptor activator of NFB ligand (RANKL), which bind to their respective receptors, c-fms and RANK, on pre-osteoclasts to bring about osteoclast differentiation and activation. These approaches still rely on animals. Google Scholar, Mundy GR: Bone Remodeling and its Disorders. Morrissey C, Lai JS, Brown LG, Wang YC, Roudiffer MP, Coleman IM, Gulati R, Vakar-Lopez F, True LD, Corey E, Nelson PS, Vessella RL: The expression of osteoclastogenesis-associated factors and osteoblast response to osteolytic prostate cancer cells. This is called osteolytic metastasis. Until recently they were the only FDA approved drugs for metastatic bone disease [71]. Continuing research into the mechanisms of cancer cell dormancy could result in a treatment that would prevent cancer cell proliferation in the bone and the chain of events that leads to osteolysis.

10.1210/er.19.1.18. Osteolytic lesions weaken Of the many prostaglandins, PGE2 is known to play a critical role in cancer progression. Carlsten H: Immune responses and bone loss: the estrogen connection. The most common metastatic lesions of prostate cancer are in bone and can be classified into three distinct pathology subtypes: lytic, blastic, and an indeterminate mixture of both. Osteoblasts and bone stromal cells can respond to a variety of substances that upregulate RANKL. Osteolytic lesions, also called osteoclastic or lytic lesions, are areas of damaged bone that most often occur in people with certain cancers, such as multiple myeloma and breast cancer. (A) The bone remodeling unit consists of osteoblasts, which produce osteoid, bone matrix, and osteoclasts, which degrade mineralized bone.

It is now generally accepted that the bone microenvironment is critical to the colonization and growth or dormancy of metastases. For example, the use of aromatase inhibitors increases the risk for osteoporosis. Podgorski I, Linebaugh BE, Koblinski JE, Rudy DL, Herroon MK, Olive MB, Sloane BF: Bone marrow-derived cathepsin K cleaves SPARC in bone metastasis. Mol Cancer Ther. Exp Cell Res. 2005, 24: 2543-2555. The bone remodeling microenvironment is a complex system in which the cell functions are controlled by multifunctional transcription factors, cytokines and growth factors. Several MMPs (MMP2, 3, 9) can release TGF- from the latent state, allowing it to become active. The roentgenogram indicates the net effect of these two processes. Thus, in the course of the osteolytic process, the osteoblasts are unable to fulfill their role as bone building cells. 1997, 80 (8 Suppl): 1546-1556. WebMetastatic Bone Disease: Treatment Options for Specific Areas of Spread Cancer that begins in an organ, such as the lungs, breast, or prostate, and then spreads to bone is called metastatic bone disease (MBD). 2010;65 (3): 241-5. MMP-9 is important in the cascade leading to activation of VEGFA. WebWhen cancer cells metastasize to the bone, they can cause changes to the bone. In summary, all of these factors contribute to propagating the vicious cycle and increasing osteolysis (Figure 1B). Grey A: Teriparatide for bone loss in the jaw. Curr Opin Support Palliat Care. WebIn the majority of skeletal metastases, new bone develops simultaneously with bone destruction. In the process, growth factors stored in the matrix, such as transforming growth factor (TGF)-, vascular endothelial growth factor (VEGF), insulin-like growth factors (IGFs), bone morphogenic proteins and fibroblast-derived factors, as well as calcium, are released into the bone microenvironment. Even in adults it is estimated that about 10% of the bone is renewed each year [7]. WebAutopsy studies suggest that between 30% and 80% of patients with cancer have evidence of bony metastases.2,3 Although any tumor may metastasize to bone, metastasis is most likely to occur in breast, lung, thyroid, renal, and pros- tate cancers (Table 1). Cell Tissue Res. Edited by: Rosen CL. Mastro AM, Vogler EA: A three-dimensional osteogenic tissue model for the study of metastatic tumor cell interactions with bone. Recently, Roy and colleagues [69] investigated this association in a mouse model of autoimmune arthritis and found that arthritic mice had an increase in both lung and bone metastasis compared to the non-arthritic mice. Several of these molecules are related to the recruitment and differentiation of osteoclasts; some are prominent players in the vicious cycle. Myeloma cells produce factors that upregulate osteoblast production of M-CSF and RANKL and downregulate production of OPG. They also are regulators of other molecules important in the vicious cycle. It is a reservoir of numerous growth factors as well as calcium and phosphorous, which are released from the matrix during bone remodeling. After your cancer is gone, it is the job of the osteoblasts to rebuild the bone. Common treatments for bone metastasis include medications, radiation therapy and surgery. Radiograph shows a destructive expanded osteolytic lesion in the metacarpal of the thumb in a 55-year- old man with lung carcinoma. Osteocytes are terminally differentiated osteoblasts that become embedded in the bone matrix at the end of the deposition phase of remodeling.

Endocrinology. WebBone is the most common site of metastasis for breast cancer. Webthyroid carcinoma - solitary metastasis, prostate adenocarcinoma - blastic metastasis, melanoma - lytic metastasis, osteosarcoma - metastasis in children, breast cancer - However, there is no guarantee that inhibition of osteolytic lesions would prevent the growth of cancer cells in the bone or their spread to other organs. PTHrP is expressed in the primary tumors of about 50% of patients and in more than 90% of breast cancer bone metastasis samples [18].

Distinct histopathology of blastic and lytic prostate cancer in bone. 5. Clarke BL, Khosla S: Physiology of bone loss. The results of an in vivo study showed that OPN-deficient mice showed significantly reduced bone metastasis [38]. 10.1016/j.ctrv.2010.04.003. The cyclooxygenase enzymes COX-1 and COX-2 catalyze the conversion of arachidonic acid to prostaglandins and thromboxanes. The MMP family, composed of more than 20 members, can collectively degrade all components of the extracelluar matrix. Google Scholar. Bone provides support and protects vital organs but also is a metabolically active tissue. Nevertheless, the inaccessibility, opacity and size of the skeleton make it difficult to study even in laboratory animals. Along with colleagues and students she has focused particularly on the fate of osteoblasts in the metastatic bone environment. Runx2 downregulates proliferation and induces p21, RANKL, MMP2, MMP9, MMP13, VEGF, OPN, bone sialoprotein and PTHrP protein expression to promote osteoblast differentiation, bone development and turnover [39]. 2009, 175: 1255-1269.