Results published in Blood, the official journal of the American Society of Hematology, confirm that inhibition of the IRE1α-XBP1 pathway impacts the survival of myeloma cells, suggesting a promising therapeutic option in multiple myeloma. The pre-clinical study, conducted by researchers at Dana-Farber Cancer Institute in collaboration with MannKind Corporation (Nasdaq: MNKD), confirm that blocking the XBP1 arm of the unfolded protein response with MannKind's novel, first-in-class IRE1α RNase domain inhibitor, MKC-3946, alone or in combination with bortezomib or 17AAG, inhibited growth in multiple myeloma cells, while leaving normal cells intact.
"Results from this research study demonstrate that biologically based therapies have great potential to advance the treatment of multiple myeloma and extend the lives of patients with this devastating and deadly disease," said Kenneth C. Anderson, M.D., director of the Jerome Lipper Multiple Myeloma Center at Dana-Farber Cancer Institute, Kraft Family Professor of Medicine at Harvard Medical School, and corresponding author of the study. "Our findings show that targeting the XBP1 pathway with a selective IRE1α inhibitor, in this case the small molecule inhibitor MKC-3946, is a promising therapeutic strategy, providing the preclinical basis for future trials evaluating the clinical efficacy of this approach to improve patient outcomes in multiple myeloma."
In healthy individuals, a key signaling process, known as the unfolded protein response, regulates protein folding and facilitates cellular homeostasis. In patients with multiple myeloma, this process is not properly regulated, in part because the IRE1α enzyme activates the XBP1 gene, allowing myeloma cells to escape cell death, grow and/or become resistant to chemotherapy, radiotherapy and certain cancer drugs. Researchers believe that by restoring normal cell regulation and function, myeloma tumor cells no longer continue to multiply, and become more susceptible to common oncology treatments.
Findings from this pre-clinical study show that MKC-3946 inhibited the IRE1α-XBP1 pathway of myeloma cells, successfully blocking XBP1 splicing. Results also showed that the study compound:
- Enhanced cytotoxicity induced by the oncology agents bortezomib or 17AAG, even in the presence of bone marrow stromal cells or exogenous IL-6;
- Contributed to cell death in combination with these agents and as a single agent with fresh bone marrow aspirates from myeloma patients;
- Inhibited growth of multiple myeloma cells in vivo alone and in combination with these agents