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Advances in preclinical therapeutics development using small animal imaging and molecular analyses: the gastrointestinal stromal tumors model

机译:利用小动物成像和分子分析进行临床前治疗开发的进展:胃肠道间质瘤模型

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摘要

The large use of target therapies in the treatment of gastrointestinal stromal tumors (GISTs) highlighted the urgency to integrate new molecular imaging technologies, to develop new criteria for tumor response evaluation and to reach a more comprehensive definition of the molecular target. These aspects, which come from clinical experiences, are not considered enough in preclinical research studies which aim to evaluate the efficacy of new drugs or new combination of drugs with molecular target. We developed a xenograft animal model GIST882 using nude mice. We evaluated both the molecular and functional characterization of the tumor mass. The mutational analysis of KIT receptor of the GIST882 cell lines and tumor mass showed a mutation on exon 13 that was still present after in vivo cell growth. The glucose metabolism and cell proliferation was evaluated with a small animal PET using both FDG and FLT. The experimental development of new therapies for GIST treatment requires sophisticated animal models in order to represent the tumor molecular heterogeneity already demonstrated in the clinical setting and in order to evaluate the efficacy of the treatment also considering the inhibition of tumor metabolism, and not only considering the change in size of tumors. This approach of cancer research on GISTs is crucial and essential for innovative perspectives that could cross over to other types of cancer.
机译:目标疗法在胃肠道间质瘤(GIST)中的大量使用突显了整合新的分子成像技术,开发新的肿瘤反应评估标准以及对分子靶标进行更全面定义的迫切性。这些来自临床经验的方面在旨在评估新药或具有分子靶标的新药功效的临床前研究中还不够充分。我们使用裸鼠开发了异种移植动物模型GIST882。我们评估了肿瘤块的分子和功能特征。对GIST882细胞系的KIT受体和肿瘤块的突变分析显示,第13外显子的突变在体内细胞生长后仍然存在。使用FDG和FLT用小型动物PET评估葡萄糖的代谢和细胞增殖。 GIST治疗新疗法的实验开发需要复杂的动物模型,以代表已经在临床环境中证实的肿瘤分子异质性,并且在评估治疗效果的同时还考虑了肿瘤代谢的抑制作用,而不仅考虑了肿瘤大小的变化。这种对GIST进行癌症研究的方法对于可能跨越其他类型癌症的创新观点至关重要且至关重要。

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