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The role of non-coding RNAs in metastasis and therapy escape

The role of non-coding RNAs in metastasis and therapy escape
非编码RNA在转移和治疗逃避中的作用
批准号:
257890376
负责人:
Professorin Dr. Christina Elisabeth Hackl
金额:
$0.0万
依托单位国家:
德国
项目类别:
Research Units
财政年份:
2014
资助国家:
德国
项目状态:
已结题
起止时间:
2013-12-31 至 2022-12-31

项目摘要

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Professorin Dr. Christina Elisabeth Hackl的其他基金

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中文摘要
翻译
近年来,几种低剂量节律疗法(LDM)在癌症治疗中取得了成功,特别是对标准大剂量化疗无效的患者、晚期疾病以及大剂量和靶向治疗后的维持治疗。到目前为止,已知的节律治疗机制包括抑制肿瘤血管生成、刺激抗癌细胞毒性T细胞免疫反应、抑制缺氧诱导因子-1α(HIF-1)、直接肿瘤细胞靶向效应和诱导肿瘤休眠。尽管如此,人们对LDM的分子基础知之甚少,例如微RNA(MiRNAs)、环状RNA和长非编码RNA等调控RNA在LDM治疗中的作用。我们项目的总体目标是确定LDM治疗过程中原发肿瘤和转移瘤中非编码RNA的特征。在第一个资助期,我们已经进行了非编码RNA的筛选和数据分析,并开始在分子水平上表征非常有前途的非编码RNA。我们在下一个资助期的工作重点是进一步的功能特征,以及在LDM治疗期间基于非编码RNA的适应效应和治疗逃逸。我们将继续使用BalbNeuT小鼠乳腺癌模型(中心鼠项目)、异种移植瘤HT29.hCG.Luc SCID和同基因CMT93.hCG.Luc C57BL/6结肠癌模型。我们努力的最终目标之一是找到并操纵非编码RNA,并确定对LDM治疗的有益影响。
英文摘要
In recent years, several regimes of low-dose metronomic therapy (LDM) have been successful in cancer therapy especially for patients refractory to standard high-dose chemotherapy, for advanced stage disease and in maintenance therapy following high dose and targeted treatments. So far, known mechanisms of metronomic therapy include suppression of tumor-angiogenesis, stimulation of anticancer cytotoxic T-cell immune responses, inhibition of the hypoxia inducible factor-1 alpha (HIF-1), direct tumor cell targeting effects and the induction of tumor dormancy. Despite this, little is known about the molecular basis of LDM, e.g. the role of regulatory RNAs such as microRNAs (miRNAs), circular RNAs and long non-coding RNAs during LDM therapy. The general goal of our project is to characterize non-coding RNAs in primary tumors and metastasis during LDM therapy. During the first funding period, we have performed non-coding RNA screening and data analysis and started to characterize highly promising non-coding RNAs on a molecular level. The focus of our efforts in the next funding period is on further functional characterization as well as on non-coding RNA-based adaptation effects and therapy escape during LDM therapy. We will continue to use the BalbNeuT mouse model of breast cancer (central mouse project), the xenograft HT29.hCG.Luc SCID and the syngeneic CMT93.hCG.Luc C57BL/6 models of colon cancer. One of the ultimate goals of our endeavor is to find and manipulate a non-coding RNA and identify beneficial effects for LDM therapy.
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Development of innovative preclinical models of orthotopic and metastatic colon and gastric cancer for the translational development of new therapeutic regimens
  • 批准号:
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