2016, Number 1
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Ann Hepatol 2016; 15 (1)
Suppression of trophoblast cell surface antigen 2 enhances proliferation and migration in liver fluke-associated cholangiocarcinoma
Sawanyawisuth K, Tantapotinan N, Kraiklang R, Puapairoj A, Wongkham C, Riggins GJ, Wongkham S
Language: English
References: 34
Page: 71-81
PDF size: 433.91 Kb.
ABSTRACT
Background and aim. Trophoblast cell surface antigen 2 (TROP2) or tumor-associated calcium signal transducer 2 (TACSTD2)
is a 36-kDa type I transmembrane glycoprotein and exerts dual functions as an oncogene and tumor suppressor in cancer cells. In
this study, we investigated the expression and functions of TROP2 in liver fluke-associated cholangiocarcinoma (CCA).
Material
and methods. TROP2 expression in 85 CCA tissues was detected by using immunohistochemistry. The methylation status of
TROP2 promoter was studied in 15 matched pairs of normal and CCA formalin fixed paraffin embedded (FFPE) tissues using the bisulfite
genomic sequencing (BGS) method. The functions of TROP2 on cancer cell behavior were investigated using siRNA in CCA
cell lines. Proliferation, migration and invasion assays were performed. A PCR array was used to evaluate the impact of TROP2
knockdown on the gene expression profiles.
Results. TROP2 was highly expressed in all normal bile duct epithelia, but significantly
down-regulated in CCA cells. Sixty percent of CCA revealed promoter hypermethylation compared to the corresponding adjacent
normal tissues. TROP2 knockdown significantly enhanced the proliferation and migration in CCA cell lines, and altered the expressions
of
MARCK, EMP1 and
FILIP1L.
Conclusion. We provide new evidence that TROP2 is epigenetically down-regulated and
operates as a negative regulator of cell proliferation and migration in liver fluke-associated CCA.
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