Tumor-dependent secretion of close homolog of L1 results in elevation of its circulating level in mouse model for human lung tumor

Biochem Biophys Res Commun. 2018 Jul 2;501(4):982-987. doi: 10.1016/j.bbrc.2018.05.096. Epub 2018 May 22.

Abstract

Close homolog of L1 (CHL1) and its truncated form mainly play crucial roles in mouse brain development and neural functions. Herein, we newly identified that truncated form of CHL1 is produced and released from lung tumor tissue in a mouse model expressing human EML4-ALK fusion gene. Both western blot and direct ELISA analysis revealed that mouse CHL1 level in serum (including serum extracellular vesicles) was significantly elevated in EML4-ALK transgenic mice. The correlation between the tumor size and the amount of CHL1 secretion could be examined in this study, and showed a significant positive correlation in a tumor size-dependent manner. Considering these results, the measurement of circulating CHL1 level may contribute to assess a tumor progression in human lung tumor patients.

Keywords: Adhesion molecule; CHL1; EML4-ALK gene; Lung tumor; Tumor marker.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Adhesion Molecules / blood*
  • Cell Adhesion Molecules / metabolism*
  • Disease Models, Animal
  • Enzyme-Linked Immunosorbent Assay
  • HEK293 Cells
  • Humans
  • Lung Neoplasms / blood*
  • Lung Neoplasms / pathology
  • Mice, Inbred C57BL
  • Tumor Burden

Substances

  • Cell Adhesion Molecules
  • Chl1 protein, mouse