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Repression of the transcriptional activity of ERRα with sequence-specific DNA-binding polyamides.
Chen, Chien-Yu; Li, Yang; Jia, Tiezheng; He, Lina; Hare, Alissa A; Silberstein, Amanda; Gallagher, John; Martinez, Thomas F; Stiles, Joseph W; Olenyuk, Bogdan; Dervan, Peter B; Stiles, Bangyan L.
Afiliação
  • Chen CY; Pharmacology and Pharmaceutical Sciences, School of Pharmacy, University of Southern California, Los Angeles, CA 90033, USA.
  • Li Y; Present address: Amgen Inc., One Amgen Center Drive, Thousand Oaks, CA 91320-1799, USA.
  • Jia T; Pharmacology and Pharmaceutical Sciences, School of Pharmacy, University of Southern California, Los Angeles, CA 90033, USA.
  • He L; Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
  • Hare AA; Present address: SUSTECH, 1088 Xueyuan Avenue, Shenzhen, Guangdong Province 518055, P. R. China.
  • Silberstein A; Pharmacology and Pharmaceutical Sciences, School of Pharmacy, University of Southern California, Los Angeles, CA 90033, USA.
  • Gallagher J; Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
  • Martinez TF; Present address: Vanderbilt, Nashville, TN 37240, USA.
  • Stiles JW; Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
  • Olenyuk B; Present address: Westmont College, 955 La Paz Rd, Santa Barbara, CA 93108, USA.
  • Dervan PB; Pharmacology and Pharmaceutical Sciences, School of Pharmacy, University of Southern California, Los Angeles, CA 90033, USA.
  • Stiles BL; Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Med Chem Res ; 29(4): 607-616, 2020 Apr.
Article em En | MEDLINE | ID: mdl-34552311
ABSTRACT
The orphan nuclear receptors estrogen-related receptors (ERRs) bind to the estrogen-related receptor response element (ERRE) to regulate transcriptional programs in cellular metabolism and cancer cell growth. In this study, we evaluated the potential for a pyrrole-imidazole polyamide to block ERRα binding to ERREs to inhibit gene expression. We demonstrated that the ERRE-targeted polyamide 1 blocked the binding of ERRα to the consensus ERRE and reduced the transcriptional activity of ERRα in cell culture. We further showed that inhibiting ERRα transcriptional activity with polyamide 1 led to reduced mitochondrial oxygen consumption, a primary biological effect regulated by ERRα. Finally, our data demonstrated that polyamide 1 is an inhibitor for cancer cell growth.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos