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. 2015 Oct 14;7(4):2037–2053. doi: 10.3390/cancers7040875

Table 1.

Areas for future work.

  • Quantify the tipping point, where physiological Hh signaling becomes oncogenic

  • Identify small molecules that selectively inhibit Hh cholesterolysis in vivo

  • Develop optical Hh cholesterolysis assays for cell studies and deep tissue imaging

  • Determine Hh precursor protein structure at atomic resolution

  • Understand the mechanism of deregulated Hh biosynthesis in transformed cells