Identification of Down's syndrome critical locus gene SIM2-s as a drug therapy target for solid tumors.

Proc Natl Acad Sci U S A

Center for Molecular Biology and Biotechnology and Department of Biology, Florida Atlantic University, 777 Glades Road, Boca Raton, FL 33431, USA.

Published: April 2003

AI Article Synopsis

  • Researchers identified the Single Minded 2 gene (SIM2), linked to Down's syndrome, as being specifically expressed in certain solid tumors, notably colon, prostate, and pancreatic cancers.
  • Antisense inhibition of SIM2-s in colon cancer cells led to reduced cell growth and increased cell death, indicating its potential as a target for cancer therapy.
  • This study suggests a new direction for cancer drug development and may enhance our understanding of cancer risks in patients with Down's syndrome.

Article Abstract

We report here a cancer drug therapy use of a gene involved in Down's syndrome. Using bioinformatics approaches, we recently predicted Single Minded 2 gene (SIM2) from Down's syndrome critical region to be specific to certain solid tumors. Involvement of SIM2 in solid tumors has not previously been reported. Intrigued by a possible association between a Down's syndrome gene and solid tumors, we monitored SIM2 expression in solid tumors. Isoform-specific expression of SIM2 short-form (SIM2-s) was seen selectively in colon, prostate, and pancreatic carcinomas but not in breast, lung, or ovarian carcinomas nor in most normal tissues. In colon tumors, SIM2-s expression was seen in early stages. Antisense inhibition of SIM2-s expression in a colon cancer cell line caused inhibition of gene expression, growth inhibition, and apoptosis. The administration of the antisense, but not the control, oligonucleotides caused a pronounced inhibition of tumor growth in nude mice with no major toxicity. Our findings provide a strong rationale for the genes-to-drugs paradigm, establish SIM2-s as a molecular target for cancer therapeutics, and may further understanding of the cancer risk of Down's syndrome patients.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC153629PMC
http://dx.doi.org/10.1073/pnas.0831000100DOI Listing

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