Increased expression of MAP2 inhibits melanoma cell proliferation, invasion and tumor growth in vitro and in vivo

• Published in: Experimental dermatology 2010-11, Vol.19 (11), p.958-964
• Main Authors: Song, Zhiqi, He, Chun-Di, Sun, Changkai, Xu, Yanni, Jin, Xin, Zhang, Yi, Xiao, Ting, Wang, Yakun, Lu, Ping, Jiang, Yi, Wei, Huachen, Chen, Hong-Duo
• Format: Article
• Language: English
• Subjects: Animals; Apoptosis - physiology; Biological and medical sciences; Cell Cycle - physiology; Cell Differentiation - physiology; Cell Line, Tumor; Cell Proliferation; Cell Shape - physiology; Cell Surface Extensions - pathology; Cell Survival - physiology; Dermatology; Female; Humans; Medical sciences; melanoma cell; Melanoma, Experimental - metabolism; Melanoma, Experimental - pathology; Mice; Mice, Inbred BALB C; Mice, Nude; microtuble-associated protein 2; microtubule; Microtubule-Associated Proteins - genetics; Microtubule-Associated Proteins - metabolism; Microtubules - metabolism; Neoplasm Invasiveness - genetics; Transduction, Genetic; Tumors of the skin and soft tissue. Premalignant lesions
• ISSN: 0906-6705; 1600-0625
• DOI: 10.1111/j.1600-0625.2009.01020.x

Please cite this paper as: Increased expression of MAP2 inhibits melanoma cell proliferation, invasion and tumor growth in vitro and in vivo. Experimental Dermatology 2010; 19: 958–964. :  Malignant melanoma (MM) is characterized by aggressive metastasis and high mortality rate. Microtubule‐associated proteins 2 (MAP2) is expressed abundantly in majority of melanocytic nevi and primary melanomas, but absent in metastatic melanomas. To determine whether MAP2 correlates with tumor progression of MM, we investigated the effects of MAP2 inhibition on the biological behaviour of metastatic melanoma in vitro and in vivo. Our results demonstrated that adenovirus‐mediated MAP2 induced apoptotic cell death and cell cycle arrest in metastatic human and mouse melanoma cell lines in vitro, and substantially inhibited the growth of melanomas in nude mice in vivo. In addition, intracellular expression of MAP2 was found to induce the morphologic alteration, suppress the migration and invasion and affect the assembly, stabilization and bundling of microtubules in melanoma cells. This is the first study that MAP2 expression significantly inhibits the growth of MM in vivo. Our results suggest that MAP2 may serve as a promising molecular target for therapy and chemoprevention of MM in humans.