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Increased Expression of ATG10 in Colorectal Cancer Is Associated with Lymphovascular Invasion and Lymph Node Metastasis
Authors:Yoon Kyung Jo  Seung Cheol Kim  In Ja Park  So Jung Park  Dong-Hoon Jin  Seung-Woo Hong  Dong-Hyung Cho  Jin Cheon Kim
Institution:1. Graduate School of East-West Medical Science, Kyung Hee University, Gyeonggi-do, Korea.; 2. Institute for Innovative Cancer Research, Asan Medical Center, Seoul, Korea.; 3. Department of Surgery, University of Ulsan College of Medicine and Asan Medical Center, Seoul, Korea.; 4. Department of Oncology, University of Ulsan College of Medicine and Asan Medical Center, Seoul, Korea.; Klinikum rechts der Isar der TU München, Germany,
Abstract:

Background

Autophagy has paradoxical and complex functions in cancer development, and autophagy-related genes (ATG) are key regulators in autophagy. Until now, more than 30 different ATG proteins have been identified in yeast, and their mammalian counterparts also have been reported. Although the roles of a few ATG proteins in cancer have been characterized, the role of ATG10 is almost completely unknown.

Methodology/Principal Findings

To investigate the clinicopathological role of ATG10 in colorectal cancer, we analyzed ATG10 expression in colorectal cancer tissues and cell lines. Protein expression analysis showed that ATG10 is highly increased in colorectal cancer (tissue - 18/37 cases, 48%; cell line –8/12 cell lines, 66%). Immunohistochemical analysis with clinicopathological features indicated a strong association of the up-regulation of ATG10 with tumor lymph node metastasis (p = 0.005) and invasion (p<0.001). Moreover, both 5-year disease free survival and overall survival rates of patients bearing tumors that did not express ATG10 were significantly higher than those of patients bearing ATG10-expressing tumors (p = 0.012).

Conclusion/Significance

Increased expression of ATG10 in colorectal cancer is associated with lymphovascular invasion and lymph node metastasis indicating that ATG10 may be a potential prognostic maker in colorectal cancer.
Keywords:
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