Metabolic Enzyme Sulfotransferase 1A1 Is the Trigger for N-Benzyl Indole Carbinol Tumor Growth Suppression.

نویسندگان

  • Deborah M Rothman
  • Xiaolin Gao
  • Elizabeth George
  • Timothy Rasmusson
  • Diksha Bhatia
  • Irina Alimov
  • Louis Wang
  • Amin Kamel
  • Panagiotis Hatsis
  • Yan Feng
  • Antonin Tutter
  • Gregory Michaud
  • Earl McDonald
  • Kavitha Venkatesan
  • David Farley
  • Mary Ellen Digan
  • Yucheng Ni
  • Fred Harbinski
  • Mithat Gunduz
  • Christopher J Wilson
  • Alan Buckler
  • Mark Labow
  • John Tallarico
  • Vic E Myer
  • Jeffrey A Porter
  • Shaowen Wang
چکیده

In an attempt to identify novel therapeutics and mechanisms to differentially kill tumor cells using phenotypic screening, we identified N-benzyl indole carbinols (N-BICs), synthetic analogs of the natural product indole-3-carbinol (I3C). To understand the mode of action for the molecules we employed Cancer Cell Line Encyclopedia viability profiling and correlative informatics analysis to identify and ultimately confirm the phase II metabolic enzyme sulfotransferase 1A1 (SULT1A1) as the essential factor for compound selectivity. Further studies demonstrate that SULT1A1 activates the N-BICs by rendering the compounds strong electrophiles which can alkylate cellular proteins and thereby induce cell death. This study demonstrates that the selectivity profile for N-BICs is through conversion by SULT1A1 from an inactive prodrug to an active species that induces cell death and tumor suppression.

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عنوان ژورنال:
  • Chemistry & biology

دوره 22 9  شماره 

صفحات  -

تاریخ انتشار 2015