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同源小鼠乳腺管内(MIND)自发转移模型的建立及其用于三阴性乳腺癌的特征描述。

Development and characterization of mammary intraductal (MIND) spontaneous metastasis models for triple-negative breast cancer in syngeneic mice.

机构信息

Department of Breast Surgery, The Second Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, P.R. China.

Medical College of Nanchang University, Nanchang, Jiangxi, P.R. China.

出版信息

Sci Rep. 2020 Mar 13;10(1):4681. doi: 10.1038/s41598-020-61679-8.

Abstract

Triple-negative breast cancer (TNBC) has a more aggressive phenotype and higher metastasis and recurrence rates than other breast cancer subtypes. TNBC currently lacks a transplantation model that is suitable for clinical simulations of the tumor microenvironment. Intraductal injection of tumor cells into the mammary duct could mimic the occurrence and development of breast cancer. Herein, we injected 4T1 cells into the mammary ducts of BALB/C mice to build a preclinical model of TNBC and optimized the related construction method to observe the occurrence and spontaneous metastasis of tumors. We compared the effects of different cell numbers on tumorigenesis rates, times to tumorigenesis, and metastases to determine the optimal number of cells for modelling. We demonstrated that 4T1-MIND model mice injected with 20,000 cells revealed a suitable tumor formation rate and time, thus indicating a potential treatment time window after distant metastasis. We also injected 20,000 cells directly into the breast fat pad or breast duct for parallel comparison. The results still showed that the 4T1-MIND model provides sufficient treatment time for lung metastases in mice and that it is a more reliable model for early tumor development. The 4T1-MIND model requires continuous improvement and optimization. A suitable and optimized model for translational research and studies on the microenvironment in TNBC should be developed.

摘要

三阴性乳腺癌(TNBC)比其他乳腺癌亚型具有更具侵袭性的表型和更高的转移和复发率。TNBC 目前缺乏适合模拟肿瘤微环境的移植模型。将肿瘤细胞注入乳腺导管内可以模拟乳腺癌的发生和发展。在此,我们将 4T1 细胞注入 BALB/C 小鼠的乳腺导管中,建立了 TNBC 的临床前模型,并优化了相关的构建方法,以观察肿瘤的发生和自发转移。我们比较了不同细胞数量对肿瘤发生率、肿瘤发生时间和转移的影响,以确定建模的最佳细胞数量。我们证明,注射 20,000 个细胞的 4T1-MIND 模型小鼠显示出合适的肿瘤形成率和时间,从而表明在远处转移后存在潜在的治疗时间窗。我们还将 20,000 个细胞直接注入乳腺脂肪垫或乳腺导管进行平行比较。结果仍然表明,4T1-MIND 模型为小鼠的肺转移提供了足够的治疗时间,并且是研究早期肿瘤发展的更可靠模型。4T1-MIND 模型需要不断改进和优化。应该开发适合 TNBC 转化研究和微环境研究的优化模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5129/7070052/4e8cafd20afb/41598_2020_61679_Fig1_HTML.jpg

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