scholarly journals Effects of Curcumin on Biological Behavior and NF-κB/TNF-α Pathway in Mice with Metastatic Bone Pain of Breast Cancer Induced by Walker 256 Cells

2020 ◽  
Vol 11 (06) ◽  
pp. 339-350
Author(s):  
Aijun Ji ◽  
Mingchen Zhu
2001 ◽  
Vol 66 (2) ◽  
pp. 101-109 ◽  
Author(s):  
Rosa Sciuto ◽  
Anna Festa ◽  
Rosella Pasqualoni ◽  
Alessandro Semprebene ◽  
Sandra Rea ◽  
...  

1998 ◽  
Vol 16 (12) ◽  
pp. 3890-3899 ◽  
Author(s):  
J J Body ◽  
R Bartl ◽  
P Burckhardt ◽  
P D Delmas ◽  
I J Diel ◽  
...  

PURPOSE The purpose of this article is to review the recent data on bisphosphonate use in oncology and to provide some guidelines on the indications for their use in cancer patients. DESIGN The group consensus reached by experts on the rationale for the use of bisphosphonates in cancer patients and their current indications for the treatment of tumor-induced hypercalcemia and metastatic bone pain in advanced disease and for the prevention of the complications of multiple myeloma and of metastatic bone disease are reviewed. RESULTS Bisphosphonates are potent inhibitors of tumor-induced osteoclast-mediated bone resorption. They now constitute the standard treatment for cancer hypercalcemia, for which we recommend a dose of 1,500 mg of clodronate or 90 mg of pamidronate; the latter compound is more potent and has a longer lasting effect. Intravenous bisphosphonates exert clinically relevant analgesic effects in patients with metastatic bone pain. Regular pamidronate infusions can also achieve a partial objective response by conventional International Union Against Cancer criteria and enhance the objective response rate to chemotherapy. In breast cancer, the prolonged administration of oral clodronate 1,600 mg daily reduces the frequency of morbid skeletal events by more than one fourth, whereas monthly pamidronate infusions of 90 mg for only 1 year in addition to chemotherapy reduce by more than one third the frequency of all skeletal-related events. The use of bisphosphonates to prevent bone metastases remains experimental. Last, bisphosphonates in addition to chemotherapy are superior to chemotherapy alone in patients with stages II and III multiple myeloma and can reduce the skeletal morbidity rate by approximately one half. CONCLUSION Bisphosphonate use is a major therapeutic advance in the management of the skeletal morbidity caused by metastatic breast cancer or multiple myeloma, although many questions remain unanswered, notably regarding the optimal selection of patients and the duration of treatment.


2016 ◽  
Vol 7 ◽  
Author(s):  
Priyank A. Shenoy ◽  
Andy Kuo ◽  
Irina Vetter ◽  
Maree T. Smith

Breast Cancer ◽  
2008 ◽  
pp. 257-269
Author(s):  
Marnix G. E. H. Lam ◽  
John M. H. de Klerk ◽  
Peter P. van Rijk

2019 ◽  
Vol 46 (12) ◽  
pp. 1201-1215 ◽  
Author(s):  
Priyank A. Shenoy ◽  
Andy Kuo ◽  
German Leparc ◽  
Tobias Hildebrandt ◽  
Werner Rust ◽  
...  

2021 ◽  
Vol 11 ◽  
Author(s):  
Linjie Ju ◽  
Peipei Hu ◽  
Ping Chen ◽  
Jiejie Wu ◽  
Zhuoqun Li ◽  
...  

Metastatic bone pain is characterized by insufferable bone pain and abnormal bone structure. A major goal of bone cancer treatment is to ameliorate osteolytic lesion induced by tumor cells. Corydalis saxicola Bunting total alkaloids (CSBTA), the alkaloid compounds extracted from the root of C. saxicola Bunting, have been shown to possess anticancer and analgesic properties. In this study, we aimed to verify whether CSBTA could relieve cancer induced bone pain and inhibit osteoclastogenesis. The in vivo results showed that CSBTA ameliorated Walker 256 induced bone pain and osteoporosis in rats. Histopathological changes also supported that CSBTA inhibited Walker 256 cell-mediated osteolysis. Further in vitro analysis confirmed that CSBTA reduced the expression of RANKL and downregulate the level of RANKL/OPG ratio in breast cancer cells. Moreover, CSBTA could inhibit osteoclastogenesis by suppressing RANKL-induced NF-κB and c-Fos/NFATc1 pathways. Collectively, this study demonstrated that CSBTA could attenuate cancer induced bone pain via a novel mechanism. Therefore, CSBTA might be a promising candidate drug for metastatic bone pain patients.


2004 ◽  
Vol 31 (S1) ◽  
pp. S162-S170 ◽  
Author(s):  
Marnix G. E. H. Lam ◽  
John M. H. de Klerk ◽  
Peter P. van Rijk

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