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Home › Dataset Library › Gene expression profiling of mouse p53-deficient epidermal carcinoma defines molecular determinants of human cancer malignancy (testing...

Dataset: Gene expression profiling of mouse p53-deficient epidermal carcinoma defines molecular determinants of human cancer malignancy (testing dataset)

The epidermal specific ablation of Trp53 gene leads to the spontaneous development of aggressive tumors in mice through a process that is...

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The epidermal specific ablation of Trp53 gene leads to the spontaneous development of aggressive tumors in mice through a process that is accelerated by the simultaneous ablation of Rb gene. Since alterations of p53-dependent pathway are common hallmarks of aggressive, poor prognostic human cancers, these mouse models can recapitulate the molecular features of some of these human malignancies. To evaluate this possibility, gene expression microarray analysis was performed in mouse samples. The mouse tumors display increased expression of cell cycle and chromosomal instability associated genes. Remarkably, they are also enriched in human embryonic stem cell gene signatures, a characteristic feature of human aggressive tumors. Using cross-species comparison and meta-analytical approaches, we also observed that spontaneous mouse tumors display robust similarities with gene expression profiles of human tumors bearing mutated TP53, or displaying poor prognostic outcome, from multiple body tissues. We have obtained a 20-gene signature whose genes are overexpressed in mouse tumors and can identify human tumors with poor outcome from breast cancer, astrocytoma and multiple myeloma. This signature was consistently overexpressed in additional mouse tumors using microarray analysis. Two of the genes of this signature, AURKA and UBE2C, were validated in human breast and cervical cancer as potential biomarkers of malignancy. Our analyses demonstrate that these mouse models are promising preclinical tools aimed to search for malignancy biomarkers and to test targeted therapies of prospective use in human aggressive tumors and/or with p53 mutation or inactivation. Control skin was compared with skin tumors arising in k14Cre;p53loxP/loxP and k14Cre;p53loxP/loxP;pRbloxP/loxP animals, giving a mouse p53-tumor signature

Species:
mouse

Samples:
16

Source:
E-GEOD-19616

PubMed:
20630075

Updated:
Dec.12, 2014

Registered:
Nov.11, 2014


Factors: (via ArrayExpress)
Sample HISTOLOGICAL SUBTYPE TISSUE
GSM489177 not specified skin
GSM489177 not specified skin
GSM489177 not specified skin
GSM489177 not specified skin
GSM489182 mixed squamous cell carcinoma
GSM489183 poorly differentiated squamous cell carcinoma
GSM489184 undifferentiated squamous cell carcinoma
GSM489183 poorly differentiated squamous cell carcinoma
GSM489183 poorly differentiated squamous cell carcinoma
GSM489187 spindle cell carcinoma squamous cell carcinoma
GSM489182 mixed squamous cell carcinoma
GSM489187 spindle cell carcinoma squamous cell carcinoma
GSM489187 spindle cell carcinoma squamous cell carcinoma
GSM489187 spindle cell carcinoma squamous cell carcinoma
GSM489182 mixed squamous cell carcinoma
GSM489187 spindle cell carcinoma squamous cell carcinoma

Tags

  • astrocytoma
  • body
  • breast
  • breast cancer
  • cancer
  • cell
  • cervical cancer
  • embryonic stem cell
  • multiple myeloma
  • myeloma
  • skin
  • stem cell

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