Liver colonization by human colon cancer cells is reduced by antisense inhibition of MUC2 mucin synthesis

Gastroenterology. 1999 Feb;116(2):363-71. doi: 10.1016/s0016-5085(99)70133-2.

Abstract

Background & aims: Alterations in the production of epithelial mucins have been correlated with advanced tumor stage in the colon, but direct evidence for a role of specific mucin genes in liver metastasis is lacking. The current study was designed to establish more directly the role of MUC2 in colon cancer metastasis.

Methods: MUC2 levels were manipulated in highly metastatic human colon cancer cells using eukaryotic expression constructs designed to express a portion of MUC2 complementary DNA in antisense orientation. To assess the effect of MUC2 levels on metastatic potential, liver colonization was assessed in athymic mice after splenic-portal inoculation.

Results: Stable integration of the MUC2 antisense construct into metastatic colon cancer cells (LS LiM6) resulted in an 80% reduction in MUC2-specific messenger RNA and a concomitant decrease in MUC2 apomucin protein. This reduction was associated with a 50% reduction in synthesis of mature glucosamine-labeled mucin, almost complete inhibition of secretion of sialyl-LeX and sialyl-Tn antigens, and a 40% decrease in binding of colon cancer cells to E-selectin. Reduction in MUC2 levels was associated with a marked decrease in liver colonization.

Conclusions: This study provides direct evidence that MUC2 plays an important role in colon cancer metastasis.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Biomarkers, Tumor / antagonists & inhibitors
  • Biomarkers, Tumor / biosynthesis*
  • Blotting, Western
  • Colonic Neoplasms / genetics
  • Colonic Neoplasms / metabolism*
  • Colonic Neoplasms / pathology
  • DNA Primers
  • DNA, Antisense / metabolism
  • DNA, Complementary / metabolism
  • DNA, Neoplasm / metabolism
  • E-Selectin / metabolism
  • Gene Expression Regulation, Neoplastic*
  • Humans
  • Liver Neoplasms / genetics
  • Liver Neoplasms / metabolism*
  • Liver Neoplasms / secondary
  • Mice
  • Mice, Nude
  • Mucin-2
  • Mucins / antagonists & inhibitors
  • Mucins / biosynthesis*
  • Neoplasm Proteins / antagonists & inhibitors
  • Neoplasm Proteins / biosynthesis*
  • RNA, Messenger / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction

Substances

  • Biomarkers, Tumor
  • DNA Primers
  • DNA, Antisense
  • DNA, Complementary
  • DNA, Neoplasm
  • E-Selectin
  • MUC2 protein, human
  • Muc2 protein, mouse
  • Mucin-2
  • Mucins
  • Neoplasm Proteins
  • RNA, Messenger