Suppr超能文献

唑来膦酸给药时机对转移性骨肿瘤的影响。

Effect of Zoledronic Acid Administration Timing on Metastatic Bone Tumors.

作者信息

Watanabe Manabu, Tsuchie Hiroyuki, Nagasawa Hiroyuki, Hongo Michio, Kasukawa Yuji, Kudo Daisuke, Kasama Fumihito, Oya Keita, Kawaragi Takashi, Miyakoshi Naohisa

机构信息

Department of Orthopedic Surgery, Akita University Graduate School of Medicine, Akita, Japan;

Department of Orthopedic Surgery, Akita University Graduate School of Medicine, Akita, Japan.

出版信息

In Vivo. 2025 Jul-Aug;39(4):1984-1991. doi: 10.21873/invivo.13995.

Abstract

BACKGROUND/AIM: Breast cancer frequently metastasizes to the bone, reducing quality of life and survival. Zoledronic acid (ZA), is used to treat bone metastasis; however, differences in efficacy depending on the timing of administration are not clear. This study investigated the effects of different timing of ZA administration in a mouse model of breast cancer bone metastasis.

MATERIALS AND METHODS

E0771 cells (1.0×10 cells/10 μl) were injected into the femur of C57BL/6 mice to create a local bone metastasis model. The groups that started ZA administration one week before, at the same time as, one week after, and two weeks after tumor-cell administration were designated as the -1w, 0w, 1w, and 2w groups, respectively. A fifth group that did not receive ZA treatment was created as a control. ZA was administered at a dose of 100 μg/kg, and the same dose was administered once a week from the start of administration. The animals were sacrificed two and five weeks after tumor-cell administration. We evaluated body weight at the time of tumor-cell administration and sacrifice, and after sacrifice, the weight of the affected thigh, tumor volume, and bone destruction rate were determined using micro-computed tomography. Tumor necrosis and tumor growth were measured using histological immunostaining.

RESULTS

Five weeks after tumor-cell administration, bone destruction rate was significantly lower in all groups compared to the control group (<0.05). Additionally, the -1w group exhibited a significantly lower bone destruction rate than 1w and 2w groups (<0.05). There were no significant differences in tumor necrosis, but tumor growth was significantly lower in the -1w and 0w groups (<0.05).

CONCLUSION

The earlier ZA was administered, the more strongly it suppressed bone destruction and tumor cell proliferation.

摘要

背景/目的:乳腺癌常转移至骨骼,降低生活质量并影响生存期。唑来膦酸(ZA)用于治疗骨转移;然而,给药时间不同疗效是否存在差异尚不清楚。本研究在乳腺癌骨转移小鼠模型中探究了不同给药时间的ZA的作用。

材料与方法

将E0771细胞(1.0×10个细胞/10μl)注射到C57BL/6小鼠的股骨中,建立局部骨转移模型。在肿瘤细胞接种前一周、同时、接种后一周和接种后两周开始给予ZA的组分别指定为-1w、0w、1w和2w组。设立未接受ZA治疗的第五组作为对照。ZA以100μg/kg的剂量给药,从给药开始每周给予相同剂量。在肿瘤细胞接种后两周和五周处死动物。我们评估了肿瘤细胞接种时、处死时的体重,处死动物后,使用微型计算机断层扫描确定患侧大腿的重量、肿瘤体积和骨破坏率。使用组织学免疫染色测量肿瘤坏死和肿瘤生长情况。

结果

肿瘤细胞接种后五周,与对照组相比,所有组的骨破坏率均显著降低(<0.05)。此外,-1w组的骨破坏率显著低于1w和2w组(<0.05)。肿瘤坏死方面无显著差异,但-1w和0w组的肿瘤生长显著较低(<0.05)。

结论

ZA给药越早,对骨破坏和肿瘤细胞增殖的抑制作用越强。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec85/12223653/be9f5ab04ef0/in_vivo-39-1986-g0001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验