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Tight Junction Protein 1 May Identify Sensitivity to Proteasome Inhibitors in Patients With Multiple Myeloma

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Key Points

  • TJP1 modulated signaling through a pathway involving EGFR, JAK1, and STAT3. The study findings supported the hypothesis that plasma cells that express low TJP1 levels have both high EGFR/JAK1/STAT3 activity and proteasome content.
  • The team observed that patients whose myeloma cells expressed low TJP1 levels were significantly less likely to achieve a response or benefit from bortezomib.
  • Researchers suggested that patients with high signaling through EGFR/JAK1/STAT3 pathway may benefit from combination therapies such as bortezomib with either the EGFR inhibitor erlotinib, or a JAK1 inhibitor such as ruxolitinib. 

A gene known as TJP1 (tight junction protein 1) could help determine which multiple myeloma patients would best benefit from proteasome inhibitors such as bortezomib, as well as combination approaches to enhance proteasome inhibitor sensitivity, according to a study led by researchers from The University of Texas MD Anderson Cancer Center. Their findings were published by Zhang et al in Cancer Cell.

“Proteasome inhibitors form the cornerstone of our standard therapy for multiple myeloma. However, no biomarkers have been clinically validated that can identify patients most likely to respond to this treatment,” said Robert Orlowski, MD, PhD, Chair ad Interim of Lymphoma/Myeloma at MD Anderson. “Our findings provide a rationale for use of TJP1 as the first biomarker to select patients who are most and least likely to benefit from proteasome inhibitors.”

Study Findings

TJP1 has not previously been known to play any role as a mediator of proteasome inhibitor sensitivity in multiple myeloma. Dr. Orlowski’s group showed that TJP1 modulated signaling through a pathway involving EGFR, JAK1, and STAT3. The study findings supported the hypothesis that plasma cells that express low TJP1 levels have both high EGFR/JAK1/STAT3 activity and proteasome content.

“Therefore, these plasma cells were resistant to proteasome inhibitors,” said Dr. Orlowski. “Moreover, they demonstrated a previously unknown role for EGFR signaling in myeloma, and for STAT3 in controlling the level of proteasomes in cells, and therefore the cell’s ability to break down proteins.”

The team observed that patients whose myeloma cells expressed low TJP1 levels were significantly less likely to achieve a response or benefit from bortezomib.

“This study allows us to identify promising future directions to overcome proteasome inhibitor resistance in patients with high signaling through EGFR/JAK1/STAT3 pathway by offering combination therapies such as bortezomib with either the EGFR inhibitor erlotinib, or a JAK1 inhibitor such as ruxolitinib,” said Dr. Orlowski.

The content in this post has not been reviewed by the American Society of Clinical Oncology, Inc. (ASCO®) and does not necessarily reflect the ideas and opinions of ASCO®.


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