Literature DB >> 17708250

Intestinal trefoil factor (TFF-3) and extracellular signal-regulated kinase (ERK) in cholangiocarcinoma.

Sikander Ailawadhi1, Hiroki Nagase, Thaer Khoury, Jihnhee Yu, Dongfeng Tan, Jennifer Black, Michael Brattain, Milind Javle.   

Abstract

BACKGROUND/AIMS: The mucin-associated trefoil factor (TFF) peptides are integral to cytoprotection. TFF-3 is aberrantly expressed in colorectal and hepatocellular cancer and associated with an invasive phenotype. TFF-3 is also expressed in normal biliary epithelium. However, its role in biliary cancers is unknown. The biological effects of TFFs may result from EGFR, PI3 kinase, COX-2 and STAT-mediated signaling. We investigated the expression of TFF-3, Erk, Akt, EGFR and COX-2 in biliary cancer.
METHODOLOGY: Twenty-four consecutive cases of cholangiocarcinoma treated from 1996-2002 were studied. Immunohistochemistry was performed using monoclonal antibodies to TFF-3, EGFR, pEGFR, Erk, pErk, Akt, pAkt and COX-2 using validated techniques. Kendall's tau (exact method) and Pearson correlation test were employed to investigate the associations between biomarkers.
RESULTS: Median age was 67 years. Surveillance, Epidemiology and End Results (SEER) stage was local in 1, regional in 15 and distant in 8. TFF-3 expression was detected in 19 cases. There were no significant associations between TFF-3 expression and sex, stage, grade, survival or SEER score. Erk expression in the tumor showed a borderline, negative correlation with TFF-3 (Pearson's p= -0.3988, p = 0.0588).
CONCLUSIONS: TFF-3 is commonly expressed in biliary cancers and may have a negative reciprocal relationship with Erk expression.

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Year:  2007        PMID: 17708250

Source DB:  PubMed          Journal:  Hepatogastroenterology        ISSN: 0172-6390


  3 in total

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Journal:  BMC Cancer       Date:  2014-12-05       Impact factor: 4.430

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Review 3.  The expression and role of trefoil factors in human tumors.

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Journal:  Transl Cancer Res       Date:  2019-08       Impact factor: 1.241

  3 in total

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