利用转移性乳腺癌的临床前模型。

IF 9.7 1区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Diego A. Pedroza , Yang Gao , Xiang H.-F. Zhang , Jeffrey M. Rosen
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引用次数: 0

摘要

已确诊乳腺癌转移的妇女在临床上可选择的治疗方案非常有限。然而,大多数临床前研究实际上并不是针对已确立的转移性疾病开发治疗方案。在这篇综述中,我们将讨论临床前大转移性乳腺癌模型的现状,包括但不限于共生 GEMM、PDX 和异种移植。这些模型中经常被忽视的挑战包括荧光团免疫原性新抗原、实验性转移与自发性转移的差异以及肿瘤异质性。此外,由于转移灶肿瘤免疫微环境(TIME)的细胞可塑性,新批准的免疫检查点阻断剂(ICB)在转移灶的疗效可能与原发局部肿瘤不同。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Leveraging preclinical models of metastatic breast cancer

Women that present to the clinic with established breast cancer metastases have limited treatment options. Yet, the majority of preclinical studies are actually not directed at developing treatment regimens for established metastatic disease. In this review we will discuss the current state of preclinical macro-metastatic breast cancer models, including, but not limited to syngeneic GEMM, PDX and xenografts. Challenges within these models which are often overlooked include fluorophore-immunogenic neoantigens, differences in experimental vs spontaneous metastasis and tumor heterogeneity. Furthermore, due to cell plasticity in the tumor immune microenvironment (TIME) of the metastatic landscape, the treatment efficacy of newly approved immune checkpoint blockade (ICB) may differ in metastatic sites as compared to primary localized tumors.

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来源期刊
Biochimica et biophysica acta. Reviews on cancer
Biochimica et biophysica acta. Reviews on cancer 医学-生化与分子生物学
CiteScore
17.20
自引率
0.00%
发文量
138
审稿时长
33 days
期刊介绍: Biochimica et Biophysica Acta (BBA) - Reviews on Cancer encompasses the entirety of cancer biology and biochemistry, emphasizing oncogenes and tumor suppressor genes, growth-related cell cycle control signaling, carcinogenesis mechanisms, cell transformation, immunologic control mechanisms, genetics of human (mammalian) cancer, control of cell proliferation, genetic and molecular control of organismic development, rational anti-tumor drug design. It publishes mini-reviews and full reviews.
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