Blocking the PAH2 domain of Sin3A inhibits tumorigenesis and confers retinoid sensitivity in triple negative breast cancer

Nidhi Bansal, Almudena Bosch, Boris Leibovitch, Lutecia Pereira, Elena Cubedo, Jianshi Yu, Keely Pierzchalski, Jace W. Jones, Melissa Fishel, Maureen Kane, Arthur Zelent, Samuel Waxman, Eduardo Farias

Research output: Contribution to journalArticlepeer-review

5 Scopus citations


Triple negative breast cancer (TNBC) frequently relapses locally, regionally or as systemic metastases. Development of targeted therapy that offers significant survival benefit in TNBC is an unmet clinical need. We have previously reported that blocking interactions between PAH2 domain of chromatin regulator Sin3A and the Sin3 interaction domain (SID) containing proteins by SID decoys result in EMT reversal, and re-expression of genes associated with differentiation. Here we report a novel and therapeutically relevant combinatorial use of SID decoys. SID decoys activate RARa/β pathways that are enhanced in combination with RARa-selective agonist AM80 to induce morphogenesis and inhibit tumorsphere formation. These findings correlate with inhibition of mammary hyperplasia and a significant increase in tumor-free survival in MMTV-Myc oncomice treated with a small molecule mimetic of SID (C16). Further, in two well-established mouse TNBC models we show that treatment with C16-AM80 combination has marked anti-tumor effects, prevents lung metastases and seeding of tumor cells to bone marrow. This correlated to a remarkable 100% increase in diseasefree survival with a possibility of "cure" in mice bearing a TNBC-like tumor. Targeting Sin3A by C16 alone or in combination with AM80 may thus be a promising adjuvant therapy for treating or preventing metastatic TNBC.

Original languageEnglish (US)
Pages (from-to)43689-43702
Number of pages14
Issue number28
StatePublished - 2016


  • Metastases
  • Retinoids
  • SID decoys
  • Sin3A
  • Triple negative breast cancer

ASJC Scopus subject areas

  • Oncology


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