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成骨细胞系细胞在他莫昔芬存在时的行为:骨整合的体外和体内研究

Behavior of Osteoblastic Lineage Cells When in the Presence of Tamoxifen: In Vitro and In Vivo Studies on Osseointegration.

作者信息

Fiorin Luiz Guilherme, Galliera Emanuela, Matheus Henrique R, Henin Dolaji, Ervolino Edilson, Simionato Gabriela Carrara, de Almeida Juliano Milanezi, Dellavia Claudia

机构信息

Department of Diagnosis and Surgery, Division of Periodontics, São Paulo State University "Júlio de Mesquita Filho"-UNESP, Araçatuba 16015-050, Brazil.

Thin Section Laboratory, Department of Biomedical, Surgical and Dental Sciences, Università degli Studi di Milano Statale (UNIMI), 7-20122 Milan, Italy.

出版信息

Dent J (Basel). 2025 Aug 1;13(8):351. doi: 10.3390/dj13080351.

Abstract

Tamoxifen, a selective estrogen receptor modulator widely used as an adjunct in the treatment of breast cancer, has known effects on bone metabolism, although its impact on osseointegration and cellular responses during early bone healing remains unclear. Understanding these effects is essential given the increasing use of dental implants in cancer survivors. The study aimed to observe the influence of tamoxifen on human osteosarcoma (SAOS-2) cells lines, as well on the osseointegration of titanium implants in ovariectomized female rats. SAOS-2 cells were incubated with Dulbecco's modified growth medium. Six titanium (Ti) disks were used at each time point. The samples were divided into groups with the presence (TAM, = 36) or not (CTR, = 36) of tamoxifen in a concentration of 2 μM. In vivo, 72 animals were divided in groups with bilateral ovariectomy or SHAM and tamoxifen administration or not (15 mg/kg). Cell viability, mineralization rate, and collagen synthesis were assessed, as well as bone/implant contact (BIC) and bone ingrowth (BIN). Tamoxifen caused a decrease in SAOS-2 viability, although an increase in the mineralization rate was observed. In vivo, the TAM groups presented higher BIC and BIN when compared to their control, but a lower percentage of mature collagen cells. Based on our findings, in vitro, the therapy with TAM slightly reduced the viability of SAOS-2 cells while significantly increasing the mineralization rate. In vivo, the therapy positively influenced BIC and BIN during the osseointegration phase.

摘要

他莫昔芬是一种广泛用作乳腺癌辅助治疗药物的选择性雌激素受体调节剂,已知其对骨代谢有影响,但其对早期骨愈合过程中骨整合和细胞反应的影响仍不清楚。鉴于癌症幸存者中牙种植体的使用越来越多,了解这些影响至关重要。该研究旨在观察他莫昔芬对人骨肉瘤(SAOS-2)细胞系的影响,以及对去卵巢雌性大鼠钛种植体骨整合的影响。SAOS-2细胞用杜尔贝科改良生长培养基培养。每个时间点使用6个钛(Ti)盘。将样品分为两组,一组含有浓度为2μM的他莫昔芬(TAM,n = 36),另一组不含他莫昔芬(CTR,n = 36)。在体内,将72只动物分为双侧卵巢切除组或假手术组,并分别给予或不给予他莫昔芬(15mg/kg)。评估细胞活力、矿化率和胶原蛋白合成,以及骨/种植体接触(BIC)和骨长入(BIN)。他莫昔芬导致SAOS-2细胞活力下降,尽管观察到矿化率有所增加。在体内,与对照组相比,TAM组的BIC和BIN更高,但成熟胶原细胞的百分比更低。根据我们的研究结果,在体外,TAM治疗略微降低了SAOS-2细胞的活力,同时显著提高了矿化率。在体内,该治疗在骨整合阶段对BIC和BIN产生了积极影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5df/12384849/c10a8a8ac949/dentistry-13-00351-g001.jpg

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