Critical role of CDK2 for melanoma growth linked to its melanocyte-specific transcriptional regulation by MITF

Autor: Sridhar Ramaswamy, Emi K. Nishimura, Martin A. Horstmann, Wade E. Huber, Todd R. Golub, Jinyan Du, Hans R. Widlund, David E. Fisher, Kenneth N. Ross
Rok vydání: 2004
Předmět:
Cancer Research
Transcription
Genetic

Gene Expression
S Phase
E-Box Elements
0302 clinical medicine
Genes
Reporter

CDC2-CDC28 Kinases
Transcriptional regulation
RNA
Small Interfering

Melanoma
Oligonucleotide Array Sequence Analysis
0303 health sciences
Membrane Glycoproteins
biology
Reverse Transcriptase Polymerase Chain Reaction
Flow Cytometry
Microphthalmia-associated transcription factor
Cyclin-Dependent Kinases
3. Good health
DNA-Binding Proteins
Gene Expression Regulation
Neoplastic

medicine.anatomical_structure
Proto-Oncogene Proteins c-bcl-2
Oncology
030220 oncology & carcinogenesis
Melanocytes
biological phenomena
cell phenomena
and immunity

gp100 Melanoma Antigen
Chromatin Immunoprecipitation
Cell Survival
Blotting
Western

bcl-X Protein
Melanocyte
Transfection
03 medical and health sciences
Cell Line
Tumor

Roscovitine
medicine
Humans
Kinase activity
Protein Kinase Inhibitors
Transcription factor
Gene
Cell Proliferation
030304 developmental biology
Microphthalmia-Associated Transcription Factor
Cyclin-Dependent Kinase 2
Cyclin-dependent kinase 2
Proteins
Cell Biology
Fibroblasts
medicine.disease
Molecular biology
Purines
Mutation
Cancer research
biology.protein
Transcription Factors
Zdroj: Cancer Cell. 6:565-576
ISSN: 1535-6108
DOI: 10.1016/j.ccr.2004.10.014
Popis: The genomic organization of the CDK2 gene, which overlaps the melanocyte-specific gene SILV/PMEL17, poses an interesting regulatory challenge. We show that, despite its ubiquitous expression, CDK2 exhibits tissue-specific regulation by the essential melanocyte lineage transcription factor MITF. In addition, functional studies revealed this regulation to be critical for maintaining CDK2 kinase activity and growth of melanoma cells. Expression levels of MITF and CDK2 are tightly correlated in primary melanoma specimens and predict susceptibility to the CDK2 inhibitor roscovitine. CDK2 depletion suppressed growth and cell cycle progression in melanoma, but not other cancers, corroborating previous results. Collectively, these data indicate that CDK2 activity in melanoma is largely maintained at the transcriptional level by MITF, and unlike other malignancies, it may be a suitable drug target in melanoma.
Databáze: OpenAIRE