Trefoil Factor 1 Stimulates Both Pancreatic Cancer and Stellate Cells and Increases Metastasis

Objectives: Trefoil factor 1 (TFF1) is a stable secretory protein expressed widely in the gastrointestinal mucosa that is also expressed in pancreatic ductal adenocarcinoma (PDAC). In the current study, we documented the extent and timing of TFF1 expression and investigated the effects of TFF1 on PDAC cells and stellate cells, the primary cells of the PDAC stroma. Methods: Trefoil factor 1 expression in pancreatic cancer tissues and cell lines was analyzed using microarray, quantitative reverse transcriptase-polymerase chain reaction, and immunohistochemistry. The effects of recombinant TFF1 on cell growth, migration, and invasion of pancreatic cancer cell lines and immortalized human pancreatic stellate cells (HPSCs) were analyzed using MTS and Matrigel-coated invasion chambers. In vivo studies were also conducted in which Mpanc-96 cells stably expressing TFF1 were implanted orthotopically into nude mice. Results: Trefoil factor 1 was highly increased in preneoplastic lesions. Recombinant TFF1 stimulated motility of both cancer and HPSCs. In contrast, only HPSC cell growth was increased by TFF1. In vivo studies showed that overexpression of TFF1 in PDAC cells did not affect primary tumor growth but greatly increased metastasis. Conclusions: The present data demonstrate that TFF1 influences both PDAC cells and stellate cells and stimulates metastasis.

[1]  Yan Zhao,et al.  Pancreatic Stellate Cells Increase the Invasion of Human Pancreatic Cancer Cells through the Stromal Cell-Derived Factor-1/CXCR4 Axis , 2010, Pancreatology.

[2]  T. Wang,et al.  Secreted Trefoil Factor 2 Activates the CXCR4 Receptor in Epithelial and Lymphocytic Cancer Cell Lines* , 2009, Journal of Biological Chemistry.

[3]  E. Solary,et al.  Trefoil factor TFF1-induced protection of conjunctival cells from apoptosis at premitochondrial and postmitochondrial levels. , 2008, Investigative ophthalmology & visual science.

[4]  A. Lowy,et al.  The chemokine receptor CXCR4 is expressed in pancreatic intraepithelial neoplasia , 2008, Gut.

[5]  M. Mitchell,et al.  Are trefoil factors oncogenic? , 2008, Trends in Endocrinology & Metabolism.

[6]  Douglas B. Evans,et al.  Cancer-associated stromal fibroblasts promote pancreatic tumor progression. , 2008, Cancer research.

[7]  R. Hwang,et al.  Adrenomedullin is expressed in pancreatic cancer and stimulates cell proliferation and invasion in an autocrine manner via the adrenomedullin receptor, ADMR. , 2007, Cancer research.

[8]  T. Arumugam,et al.  Effect of cromolyn on S100P interactions with RAGE and pancreatic cancer growth and invasion in mouse models. , 2006, Journal of the National Cancer Institute.

[9]  H. Grønbæk,et al.  Serum Trefoil Factors in Patients with Inflammatory Bowel Disease , 2006, Digestion.

[10]  A. Jemal,et al.  Cancer Statistics, 2006 , 2006, CA: a cancer journal for clinicians.

[11]  S. Poulsen,et al.  Plasma Levels of Trefoil Factors are Increased in Patients with Advanced Prostate Cancer , 2006, Clinical Cancer Research.

[12]  L. Thim,et al.  Structure of mammalian trefoil factors and functional insights. , 2005, Cellular and molecular life sciences : CMLS.

[13]  F. May,et al.  Interaction between TFF1, a gastric tumor suppressor trefoil protein, and TFIZ1, a brichos domain-containing protein with homology to SP-C. , 2005, Biochemistry.

[14]  Michael Goggins,et al.  Gene expression profiles in pancreatic intraepithelial neoplasia reflect the effects of Hedgehog signaling on pancreatic ductal epithelial cells. , 2005, Cancer research.

[15]  F. Abbas,et al.  Expression of pS2 in prostate cancer correlates with grade and Chromogranin A expression but not with stage , 2004, BMC urology.

[16]  E. Bruyneel,et al.  Trefoil factor family (TFF) peptides and cancer progression , 2004, Peptides.

[17]  Gregory Y. Lauwers,et al.  Hedgehog is an early and late mediator of pancreatic cancer tumorigenesis , 2003, Nature.

[18]  Daniel K. Podolsky,et al.  Trefoil factors: initiators of mucosal healing , 2003, Nature Reviews Molecular Cell Biology.

[19]  M. Katoh Trefoil factors and human gastric cancer (review). , 2003, International journal of molecular medicine.

[20]  Rork Kuick,et al.  Molecular profiling of pancreatic adenocarcinoma and chronic pancreatitis identifies multiple genes differentially regulated in pancreatic cancer. , 2003, Cancer research.

[21]  I. Fidler,et al.  The organ microenvironment and cancer metastasis. , 2002, Differentiation; research in biological diversity.

[22]  L. Thim,et al.  The trefoil factor 1 participates in gastrointestinal cell differentiation by delaying G1-S phase transition and reducing apoptosis , 2002, The Journal of cell biology.

[23]  Tatjana Crnogorac-Jurcevic,et al.  Characterization of gene expression profiles in intraductal papillary-mucinous tumors of the pancreas. , 2002, The American journal of pathology.

[24]  Sara J. Prest,et al.  The estrogen‐regulated protein, TFF1, stimulates migration of human breast cancer cells , 2002, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[25]  F. Bray,et al.  Cancer burden in the year 2000. The global picture. , 2001, European journal of cancer.

[26]  Elise C. Kohn,et al.  The microenvironment of the tumour–host interface , 2001, Nature.

[27]  A. Paradiso,et al.  Association of pS2 (TFF1) release with breast tumour proliferative rate: in vitro and in vivo studies , 1999, Cell proliferation.

[28]  M. Higashiyama,et al.  Estimation of serum level of pS2 protein in patients with lung adenocarcinoma. , 1996, Anticancer research.

[29]  S. Thung,et al.  Trefoil factor-3 expression in human colon cancer liver metastasis , 2008, Clinical & Experimental Metastasis.

[30]  O. Sagol,et al.  Immunohistochemical detection of pS2 protein and heat shock protein-70 in pancreatic adenocarcinomas. Relationship with disease extent and patient survival. , 2002, Pathology, research and practice.

[31]  N. Dubrawsky Cancer statistics , 1989, CA: a cancer journal for clinicians.