Organic anion transporting polypeptide 1B3 (OATP1B3) is overexpressed in colorectal tumors and is a predictor of clinical outcome

Original Research

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Authors: Albert Craig Lockhart, Elizabeth Harris, Bonnie J LaFleur, Nipun B Merchant, Mary Kay Washington, et al

Published Date November 2008 Volume 2008:1 Pages 1 - 7

DOI: http://dx.doi.org/10.2147/CEG.S3743

Albert Craig Lockhart¹, Elizabeth Harris¹, Bonnie J LaFleur¹, Nipun B Merchant¹, Mary Kay Washington¹, Murray B Resnick², Timothy J Yeatman³, Wooin Lee⁴

¹Vanderbilt University Medical Center, Nashville, TN, USA; ²Brown University Medical Center, Providence, RI, USA; ³Moffitt Cancer Center, Tampa, FL, USA; ⁴University of Kentucky, Lexington, KY, USA

Background and aims: OATP1B3 is an organic anion transporting polypeptide (OATP) that functions as a multispecific transporter in the normal liver. We examined the expression and clinical significance of OATP1B3 in colon cancers in tissue microarrays.

Methods: Immunohistochemistry was used to assess OATP1B3 protein expression in paraffinized colon tumor tissue microarrays. OATP1B3 immunostaining was evaluated by location and intensity. Relationships between OATP1B3 expression, known prognostic variables and clinical outcomes were examined.

Results: 278 colon tumor samples of all stages were evaluated for OATP1B3 expression. OATP1B3 immunostaining was detectable in the majority (56%) of the tumor samples. Higher OATP1B3 expression was seen in lower stage tumors (p = 0.003) and lower grade (p = 0.004) tumors, but was not predictive of 5-year survival or tumor recurrence as an independent variable. Within individual tumor grades, OATP1B3 expression was associated with improved 5-year survival, but not recurrence in patients with poorly differentiated tumors.

Conclusion: OATP1B3 expression was seen in the majority of colon tumors and may be a marker of lower grade and lower stage tumors and may predict for improved outcome in certain tumors.

Keywords: tissue array analysis, colon neoplasms, organic anion transporters, tumor markers, immunohistochemistry