Identification of the cellular origin and "stemness" phenotype of malignant rhabdoid tumours (MRT) may represent a new therapeutic approach in paediatric oncology

introduction: Malignant Rhabdoid Tumours (MRT) arc especially lethal cancers that predominantly occur in infants and young ehildrcn. MRT arc caused by biallelic inactivation of a single gene; SMARCB I which is a component of SWI/S F chromatin remodelling complex. The tumours can be found almost ever...

وصف كامل

محفوظ في:
التفاصيل البيبلوغرافية
المؤلف الرئيسي: Ras Azira Ramli (مؤلف)
التنسيق: أطروحة كتاب
اللغة:English
الموضوعات:
الوسوم: إضافة وسم
لا توجد وسوم, كن أول من يضع وسما على هذه التسجيلة!
جدول المحتويات:
  • 1. Introduction
  • 2. Materials and Methods
  • 3. An analysis of putative cell of origin for malignant rhabdoid tumours (MRT)
  • 4. Somatic CRISPS/CAS9 mediated knockout of SMARCB1 in a putative cell of origin: a system for the development of Malignant Rhabdoid Tumours (MRT) models and identification of potential therapeutic targets
  • 5. Establishing Tumoursphere assay of Malignant Rhabdoid Tumours (MRT) cell lines for self-renewal identification and analysis
  • 6. Therapeutic targeting of the self-renewal machinery as a novel Malignant Rhabdoid Tumour cancer therapy strategy
  • 7. Conclusion
  • 8. Reference