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Osteopontin silencing by small interfering RNA suppresses in vitro and in vivo CT26 murine colon adenocarcinoma metastasis.

Publication ,  Journal Article
Wai, PY; Mi, Z; Guo, H; Sarraf-Yazdi, S; Gao, C; Wei, J; Marroquin, CE; Clary, B; Kuo, PC
Published in: Carcinogenesis
April 2005

Hepatic metastasis is a primary cause for failure of locoregional therapy in colorectal cancer. Increased expression of osteopontin (OPN), a ligand for alpha(v)beta3 integrin and CD44 receptors, is associated with metastasis in several types of cancer. However, the mechanism by which OPN mediates metastasis in colorectal cancer remains unknown. We hypothesized that OPN mediates invasion of colon cancer cells through basement membrane and migration through extracellular matrix (ECM). In this study, we used CT26 murine colon adenocarcinoma cells syngeneic to BALB/c mice to generate cell lines (pS-OPN) in which OPN expression was suppressed through small interfering RNA (siRNA) plasmids. CT26 wild-type cells (WT) and CT26 cells stably expressing murine-mismatch siRNA (pS-MM) served as controls. Western blotting quantified OPN protein levels and our most downregulated clone, pS-OPN-A4, demonstrated a mean 3.0-fold decrease in OPN protein expression versus WT. In vitro cell motility and invasiveness were decreased in pS-OPN-A4 by 3.6-fold (P = 0.004 versus WT) and 4.1-fold (P = 0.01 versus WT), but proliferation was similar amongst cell lines. We demonstrated that OPN suppression significantly correlates with MMP-2 downregulation. In vivo hepatic metastasis was assessed by quantifying liver weights and surface tumor nodules in 33 BALB/c mice (11/group) subjected to intrasplenic injection of tumor cells. pS-OPN-A4 resulted in a 50.4% decrease in mean liver weight compared with WT (3.79 +/- 1.49 g versus 1.88 +/- 1.34 g, P = 0.009). Only 18% of pS-OPN-A4 livers had >20 metastatic surface nodules compared with 89% for WT and 75% for pS-MM-V6. This study demonstrates that RNA interference stably reduces CT26 tumor expression of OPN and significantly attenuates CT26 colon cancer metastasis by diminishing tumor cell motility and invasiveness.

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Published In

Carcinogenesis

DOI

ISSN

0143-3334

Publication Date

April 2005

Volume

26

Issue

4

Start / End Page

741 / 751

Location

England

Related Subject Headings

  • Sialoglycoproteins
  • RNA, Small Interfering
  • Osteopontin
  • Organ Size
  • Oncology & Carcinogenesis
  • Mice, Inbred BALB C
  • Mice
  • Matrix Metalloproteinase 2
  • Liver Neoplasms
  • In Vitro Techniques
 

Citation

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Wai, P. Y., Mi, Z., Guo, H., Sarraf-Yazdi, S., Gao, C., Wei, J., … Kuo, P. C. (2005). Osteopontin silencing by small interfering RNA suppresses in vitro and in vivo CT26 murine colon adenocarcinoma metastasis. Carcinogenesis, 26(4), 741–751. https://doi.org/10.1093/carcin/bgi027
Wai, Philip Y., Zhiyong Mi, Hongtao Guo, Shiva Sarraf-Yazdi, Chengjiang Gao, Junping Wei, Carlos E. Marroquin, Bryan Clary, and Paul C. Kuo. “Osteopontin silencing by small interfering RNA suppresses in vitro and in vivo CT26 murine colon adenocarcinoma metastasis.Carcinogenesis 26, no. 4 (April 2005): 741–51. https://doi.org/10.1093/carcin/bgi027.
Wai PY, Mi Z, Guo H, Sarraf-Yazdi S, Gao C, Wei J, et al. Osteopontin silencing by small interfering RNA suppresses in vitro and in vivo CT26 murine colon adenocarcinoma metastasis. Carcinogenesis. 2005 Apr;26(4):741–51.
Wai, Philip Y., et al. “Osteopontin silencing by small interfering RNA suppresses in vitro and in vivo CT26 murine colon adenocarcinoma metastasis.Carcinogenesis, vol. 26, no. 4, Apr. 2005, pp. 741–51. Pubmed, doi:10.1093/carcin/bgi027.
Wai PY, Mi Z, Guo H, Sarraf-Yazdi S, Gao C, Wei J, Marroquin CE, Clary B, Kuo PC. Osteopontin silencing by small interfering RNA suppresses in vitro and in vivo CT26 murine colon adenocarcinoma metastasis. Carcinogenesis. 2005 Apr;26(4):741–751.
Journal cover image

Published In

Carcinogenesis

DOI

ISSN

0143-3334

Publication Date

April 2005

Volume

26

Issue

4

Start / End Page

741 / 751

Location

England

Related Subject Headings

  • Sialoglycoproteins
  • RNA, Small Interfering
  • Osteopontin
  • Organ Size
  • Oncology & Carcinogenesis
  • Mice, Inbred BALB C
  • Mice
  • Matrix Metalloproteinase 2
  • Liver Neoplasms
  • In Vitro Techniques