Reg IV regulates normal intestinal and colorectal cancer cell susceptibility to radiation-induced apoptosis

Gastroenterology. 2010 Feb;138(2):616-26, 626.e1-2. doi: 10.1053/j.gastro.2009.10.050. Epub 2009 Nov 10.

Abstract

Background & aims: Regenerating (Reg) gene IV is predominantly expressed in gastrointestinal cells and highly up-regulated in many gastrointestinal malignancies, including colorectal cancer (CRC). Human CRC cells expressing higher levels of Reg IV gene and its protein product (Reg IV) are resistant to conventional therapies, including irradiation (IR). However, the underlying mechanism is not well defined.

Methods: A murine model of IR-induced intestinal injury and in vitro and in vivo models of human CRC were used to determine the role of Reg IV in regulation of normal intestinal and colorectal cancer cell susceptibility to IR-induced apoptosis.

Results: Treatments of recombinant human Reg IV (rhR4) protein protected normal intestinal crypt cells from IR-induced apoptosis by increasing the expression of antiapoptotic genes Bcl-2, Bcl-XL, and survivin. However, overexpression of Reg IV in human CRC cells was associated with increased resistance to IR-induced apoptosis. Therefore, we used antagonism of Reg IV as a tool to increase CRC cell susceptibility to IR-induced cell death. Two complementary approaches using specific monoclonal antibodies and small interfering RNAs were tested in both in vitro and in vivo models of human CRC. Both approaches resulted in increased apoptosis and decreased cell proliferation, leading to decreased tumor growth and increased animal survival. Furthermore, these approaches increased CRC cell susceptibility to IR-induced apoptosis.

Conclusions: These results implicate Reg IV as an important modulator of gastrointestinal cell susceptibility to IR; hence, it is a potential target for adjunctive treatments for human CRC and other gastrointestinal malignancies.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adenocarcinoma / pathology
  • Adenocarcinoma / radiotherapy*
  • Animals
  • Antibodies, Monoclonal / pharmacology
  • Apoptosis / radiation effects*
  • Cell Line, Tumor
  • Cell Proliferation
  • Colon / metabolism*
  • Colon / pathology
  • Colorectal Neoplasms / pathology
  • Colorectal Neoplasms / radiotherapy*
  • Disease Models, Animal
  • Female
  • Humans
  • Inhibitor of Apoptosis Proteins
  • Lectins, C-Type / antagonists & inhibitors
  • Lectins, C-Type / metabolism*
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Mice, Nude
  • Microtubule-Associated Proteins / metabolism
  • Neoplasm Proteins / antagonists & inhibitors
  • Neoplasm Proteins / metabolism*
  • Pancreatitis-Associated Proteins
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • Radiotherapy
  • Repressor Proteins
  • Survivin
  • Transplantation, Heterologous
  • Treatment Outcome
  • bcl-X Protein / metabolism

Substances

  • Antibodies, Monoclonal
  • BIRC5 protein, human
  • Birc5 protein, mouse
  • Inhibitor of Apoptosis Proteins
  • Lectins, C-Type
  • Microtubule-Associated Proteins
  • Neoplasm Proteins
  • Pancreatitis-Associated Proteins
  • Proto-Oncogene Proteins c-bcl-2
  • REG4 protein, human
  • REG4 protein, mouse
  • Repressor Proteins
  • Survivin
  • bcl-X Protein

Associated data

  • RefSeq/NM_032044