1.Research progress of bisphosphonate and denosumab in bone health management of early breast cancer
Shuqi CHEN ; Minghua CHE ; Wanli ZHANG ; Wenbin ZHOU ; Wei HE
Chinese Journal of Endocrinology and Metabolism 2025;41(1):65-69
Secondary osteoporosis is common in patients with early breast cancer, manifesting as low back pain, bone and joint symptoms, and osteoporotic fractures. Bisphosphonate and denosumab can reduce the incidence of fractures by minimizing bone loss, though they differ in efficacy, treatment course, and side effects. Patients should consider the pros and cons when selecting a drug. Recent studies also focus on decreasing the incidence of bone metastases. This article reviews recent advancements in the use of these two drugs for managing bone health in early breast cancer.
2.Research progress of bisphosphonate and denosumab in bone health management of early breast cancer
Shuqi CHEN ; Minghua CHE ; Wanli ZHANG ; Wenbin ZHOU ; Wei HE
Chinese Journal of Endocrinology and Metabolism 2025;41(1):65-69
Secondary osteoporosis is common in patients with early breast cancer, manifesting as low back pain, bone and joint symptoms, and osteoporotic fractures. Bisphosphonate and denosumab can reduce the incidence of fractures by minimizing bone loss, though they differ in efficacy, treatment course, and side effects. Patients should consider the pros and cons when selecting a drug. Recent studies also focus on decreasing the incidence of bone metastases. This article reviews recent advancements in the use of these two drugs for managing bone health in early breast cancer.
3.Research on influence of repair with tissue engineered tendon of vitreous cryopreservation on ultrastructure of Achilles tendon defect.
Minghua ZHU ; Lin WANG ; Chengjun LIN ; Yi ZENG ; Tingwu QIN ; Rui WANG ; Rui ZHU ; Jun YANG ; Qian CHE
Journal of Biomedical Engineering 2010;27(3):590-594
By observations of the features of ultrastructure changes in the tissue engineered artificial tendon of vitreous cryopreservation, we investigated the repairing effect of tendon after an in-vivo implantation and hence we provided an important theoretical and experimental basis for the vitreous cryopreservation and application of tissue engineered artificial tendon. After vitreous cryopreservation, the implantation materials of tissue engineered artificial tendon dynamically constructed in vitro were implanted in rats for reparation of the tendon defect. A scanning electron microscope was used. At the 2nd week, the materials presented a reticular formation and there were juvenile tendon cells among materials. At the 6th week, materials were already degraded and absorbed, and then were substituted by neonatal tendon cells and collagen fibers. At the 8th week, dense tendon tissues containing uniform tendon cells and collagen fibers were found already formed; the density of collagen fibers significantly increased with time. Using a transmission electron microscope at the 2nd week, we found active proliferation of tendon cells; most of them were immature cells with a complete nuclear membrane, clear nucleolus and little collagen fibers. At the 6th week, tendon cells were more mature with a little-sized, deep-stained nucleolus surrounded by plenty of collagen fibers with complete fiber structure and clear cross striation. There was no significant difference between the two groups. Using an electron microscope, we found a very good agreement in observation of the tissue engineered artificial tendon after the in-vivo implantation in two groups. Neonatal tendon cells and collagen fiber tissues grew well and are in a similar form and order when compared versus normal tendon tissues. This proved that vitreous cryopreservation has no significant influence on the function of tendon cells. The neonatal tissue-engineered tendon exerts good function of growth and repair.
Achilles Tendon
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injuries
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surgery
;
ultrastructure
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Animals
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Cryopreservation
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Female
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Male
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Random Allocation
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Rats
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Rats, Sprague-Dawley
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Tendons
;
cytology
;
transplantation
;
Tissue Engineering
;
methods
;
Tissue Preservation
;
methods
;
Tissue Scaffolds
;
Vitrification

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