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KFO 216: Characterisation of the Oncogenic Signalling Network in Multiple Myeloma: Development of Targeted Therapies

KFO 216: Characterisation of the Oncogenic Signalling Network in Multiple Myeloma: Development of Targeted Therapies
KFO 216:多发性骨髓瘤致癌信号网络的表征:靶向治疗的开发
批准号:
100308792
负责人:
金额:
$0.0万
依托单位国家:
德国
项目类别:
Clinical Research Units
财政年份:
2009
资助国家:
德国
项目状态:
已结题
起止时间:
2008-12-31 至 2015-12-31

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英文摘要
The underlying hypothesis for the Clinical Research Unit is the assumption that in multiple myeloma the malignant phenotype results from deregulation not of a single but of a number of signalling pathways, and that these collectively constitute an oncogenic signalling network. Consequently, we assume that differences in this network may permit functional definition of novel subgroups of this disease. It is therefore the aim of this Clinical Research Unit to attempt an extensive functional characterisation of the oncogenic signalling network to permit the development of novel and effective therapeutic options. This aim will be pursued via two complementing methodical approaches: (1) a combination of functional, molecular and genetic ex vivo characterisations of primary myeloma cells, and (2) the development of different genetic mouse models to study and to verify the oncogenic pathways in primary human myeloma samples in vivo. These animal models will eventually serve in preclinical studies of novel therapeutic approaches. Our previous work has led to the identification of a number of signalling systems that are activated in myeloma cells, such as Ras-, NF-kB- and stress-response-pathways (e.g. the heat shock protein pathway). Our aim is to appraise the functional importance of these pathways in myeloma as accurately as possible and to analyse if and to what extent they cooperate with each other. In a complementary approach we plan to screen for still unknown signalling pathways by using shRNA-based screening techniques. Finally, we will try to identify the genetic lesions that might lead to the activation of these pathways. To this end, we will apply novel genetic technologies such as for example high-throughput sequencing. The results should help to obtain a better understanding of the functional and molecular heterogeneity of this disease. They should also promote identification of novel therapeutically relevant targets and implementation of novel treatment approaches that may be designed to specifically target suitable myeloma subgroups. Within the framework of this Clinical Research Unit, 20 scientists from six different institutes of Wuerzburg University cooperate in six subprojects and three core facilities (z-projects). There is also a close cooperation with physicians and scientists from the department of internal medicine II at the Ulm University.
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