Ribosomal Protein Rpl22 Controls the Dissemination of T-cell Lymphoma

Abstract

Mutations in ribosomal proteins cause bone marrow failure syndromes associated with increased cancer risk, but the basis by which they do so remains unclear. We reported previously that the ribosomal protein Rpl22 is a tumor suppressor in T-cell acute lymphoblastic leukemia/lymphoma (T-ALL), and that loss of just one Rpl22 allele accelerates T-cell lymphomagenesis by activating NF-κB and inducing the stem cell factor Lin28B. Here, we show that, paradoxically, loss of both alleles of Rpl22 restricts lymphoma progression through a distinct effect on migration of malignant cells out of the thymus. Lymphoma-prone AKT2-transgenic or PTEN-deficient mice on an Rpl22−/− background developed significantly larger and markedly more vascularized thymic tumors than those observed in Rpl22+/+ control mice. But, unlike Rpl22+/+ or Rpl22+/− tumors, Rpl22−/− lymphomas did not disseminate to the periphery and were retained in the thymus. We traced the defect in the Rpl22−/− lymphoma migratory capacity to downregulation of the KLF2 transcription factor and its targets, including the key migratory factor sphingosine 1-phosphate receptor 1 (S1PR1). Indeed, reexpression of S1PR1 in Rpl22-deficient tumor cells restores their migratory capacity in vitro. The regulation of KLF2 and S1PR1 by Rpl22 appears to be proximal as Rpl22 reexpression in Rpl22-deficient lymphoma cells restores expression of KLF2 and S1P1R, while Rpl22 knockdown in Rpl22-sufficient lymphomas attenuates their expression. Collectively, these data reveal that, while loss of one copy of Rpl22 promotes lymphomagenesis and disseminated disease, loss of both copies impairs responsiveness to migratory cues and restricts malignant cells to the thymus. Cancer Res; 76(11); 3387–96. ©2016 AACR.

Document Details

Document Type
Pub Defense Publication
Publication Date
May 31, 2016
Source ID
10.1158/0008-5472.can-15-2698

Entities

People

  • David L. Wiest
  • Jason E Stadanlick
  • Joseph R. Testa
  • Kathy Q. Cai
  • Nehal Solanki-patel
  • Noa Greenberg-kushnir
  • Sang-yun Lee
  • Shawn P. Fahl
  • Shuyun Rao

Organizations

  • Fox Chase Cancer Center
  • Leukemia & Lymphoma Society
  • National Institutes of Health
  • United States Department of Defense

Tags

Fields of Study

  • Biology
  • Medicine

Readers

  • Immunology
  • Oncology
  • Underwater engineering and Marine Technology.

Technology Areas

  • Biotechnology
  • Biotechnology - Cancer Biotech