Abstract Background and Aim: Doublecortin-like kinase 1 (Dclk1) is known to regulate neuronal differentiation, migration, and neurogenesis (Shu et al., Neuron 2006). Accumulating evidence suggests that the protein is a putative marker for intestinal and pancreatic stem cells, including cancer stem cells (CSCs) of those organs (Gagliardi et al., Pathol Res 2012, Nakanishi et al., Nat Genet 2013, Bailey et al., Gastroenterology 2013). Since carcinoid tumor is defined as a neuroendocrine tumor, we assessed whether or not the Dclk1 protein, a marker of CSC, was expressed in human rectal carcinoid tumor tissues. Patients and Methods: Eighteen patients (9 male, 9 female; mean age, 51) with rectal carcinoid tumors were included in this study. Informed consent was obtained from all of the patients. The tumors were safely resected by endoscopic mucosal resection (EMR) method between 2003 and 2012 in the Kurume University Hospital. Mean diameter of the tumors was 5.4 mm (range, 2.0-8.0 mm). Immunohistochemical staining was performed to examine the Dclk1 protein expression, accompanied by the staining for the commonly-used neuroendocrine markers synaptophysin, chromogranin A, and CD56. The immune-reactivity was evaluated according to the following criteria: the intensity of staining was scored in each specimen on a scale of 0 to 3, in which 0 = negative staining, 1 = weakly positive staining, 2 = moderately positive staining, and 3 = strongly positive staining. The extent to which positive cells were seen in each specimen (‘‘extent of distribution’’ of positive cells) was estimated on a scale of 0 to 2, in which 0 = positive staining in 0% to 20% of cells; 1, in 21% to 60%; and 2, in 61% to 100%. Sum of the scores was calculated for each specimen. Results: The total score for Dclk1, synaptophysin, CD56, and chromogranin A was 87/90, 86/90, 60/90, and 34/90, respectively. Conclusions: Human rectal caricinoid tumor highly expressed Dclk1, and the high expression rate indicated that the protein expression was a novel feature for the neuroendocrine tumor. It is suggested that Dclk1 is a potential marker of not only CSCs but also non-epithelial tumors, such as carcinoid tumor, regulating crucial tumor cell behaviors. Citation Format: Yu Ikezono, Hironori Koga, Mitsuhiko Abe, Takafumi Yoshida, Toru Nakamura, Jun Akiba, Hirohisa Yano, Osamu Tsuruta, Takuji Torimura, Michio Sata. Human rectal carcinoid tumors highly express DCLK1, a putative cancer stem cell marker. [abstract]. In: Proceedings of the 105th Annual Meeting of the American Association for Cancer Research; 2014 Apr 5-9; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2014;74(19 Suppl):Abstract nr 3050. doi:10.1158/1538-7445.AM2014-3050
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