Molecular and Cellular Pathobiology ACombinedArray-BasedComparativeGenomicHybridization and Functional Library Screening Approach Identifies mir-30d As an Oncomir in Cancer

نویسندگان

  • Ning Li
  • Sippy Kaur
  • Joel Greshock
  • Heini Lassus
  • Xiaomin Zhong
  • Yanling Wang
  • Arto Leminen
  • Zhongjun Shao
  • Xiaowen Hu
  • Shun Liang
  • Dionyssios Katsaros
  • Qihong Huang
  • Barbara L. Weber
  • George Coukos
  • Lin Zhang
چکیده

Oncomirs aremicroRNAs (miRNA) that acts as oncogenes or tumor suppressor genes. Efficient identification of oncomirs remains a challenge. Here we report a novel, clinically guided genetic screening approach for the identification of oncomirs, identifying mir-30d through this strategy. mir-30d regulates tumor cell proliferation, apoptosis, senescence, and migration. The chromosomal locus harboring mir-30d was amplified in more than 30% of multiple types of human solid tumors (n 1⁄4 1,283). Importantly, higher levels of mir-30d expression were associated significantly with poor clinical outcomes in ovarian cancer patients (n1⁄4 330, P1⁄4 0.0016). Mechanistic investigations suggested that mir-30d regulates a large number of cancer-associated genes, including the apoptotic caspase CASP3. The guided genetic screening approach validated by this study offers a powerful tool to identify oncomirs that may have utility as biomarkers or targets for drug development. Cancer Res; 72(1);

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A combined array-based comparative genomic hybridization and functional library screening approach identifies mir-30d as an oncomir in cancer.

Oncomirs are microRNAs (miRNA) that acts as oncogenes or tumor suppressor genes. Efficient identification of oncomirs remains a challenge. Here we report a novel, clinically guided genetic screening approach for the identification of oncomirs, identifying mir-30d through this strategy. mir-30d regulates tumor cell proliferation, apoptosis, senescence, and migration. The chromosomal locus harbor...

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تاریخ انتشار 2011