Rapid screen of human genes for relevance to cancer using fission yeast

Kyung-Sook Chung1, Young-Joo Jang, Nam-Soon Kim

  • 1Laboratory of Human Genome, KRIBB, Daejeon, Korea.

Insights

This study used fission yeast to screen human genes for cancer relevance. Researchers identified 16 genes that, when overexpressed, showed cancer-like effects in yeast and increased cell proliferation in mice, suggesting potential cancer markers and therapeutic targets.

Area of Science:

  • Molecular Biology
  • Genetics
  • Cancer Research

Background:

  • Cancer research involves identifying genes that contribute to disease development.
  • Screening large numbers of human genes for cancer relevance is challenging.
  • Fission yeast (Schizosaccharomyces pombe) offers a model system for functional genomics.

Purpose of the Study:

  • To evaluate the utility of fission yeast for rapid screening of human cancer-related genes.
  • To identify novel human genes with oncogenic properties.
  • To validate identified genes as potential diagnostic markers and therapeutic targets for liver and gastric cancers.

Main Methods:

  • Microarray analysis identified 437 human full-length cDNAs from liver and gastric cancer tissues.
  • Overexpression of cDNAs in Schizosaccharomyces pombe assessed for cancer-related phenotypes (growth inhibition, morphological changes).
  • Sixteen candidate genes were further validated by expression analysis in cancer cell lines and proliferation assays in NIH3T3 cells.

Main Results:

  • Overexpression of 161 human cDNAs in S. pombe induced cancer-related phenotypes.
  • Sixteen genes consistently caused growth defects and morphological changes.
  • These 16 genes were highly expressed in cancer cell lines and increased NIH3T3 cell proliferation by 32-120%.

Conclusions:

  • Fission yeast serves as a powerful and advantageous tool for rapid screening of human cancer-related genes.
  • The identified genes represent potential diagnostic markers and therapeutic targets for liver and stomach cancers.
  • Further studies can elucidate the mechanisms of carcinogenesis involving these genes.