Cytoplasmic accumulation of activated leukocyte cell adhesion molecule is a predictor of disease progression and reduced survival in oral cancer patients

阿尔坎 细胞质 病理 细胞 癌症 免疫组织化学 增生 生物 细胞粘附分子 癌症研究 医学 内科学 免疫学 细胞生物学 遗传学
作者
Meenakshi Sawhney,Ajay Matta,Muzafar A. Macha,Jasleen Kaur,S Dattagupta,Nootan Kumar Shukla,Ranju Ralhan
出处
期刊:International Journal of Cancer [Wiley]
卷期号:124 (9): 2098-2105 被引量:42
标识
DOI:10.1002/ijc.24192
摘要

Abstract Activated leukocyte cell adhesion molecule (ALCAM) has been proposed to function as a cell surface sensor for cell density, controlling the transition between local cell proliferation and tissue invasion in cancer progression. Herein, we determined ALCAM expression in 107 oral squamous cell carcinomas (OSCCs), 78 oral lesions (58 hyperplasias and 20 dysplasias) and 30 histologically normal oral tissues using immunohistochemistry and correlated with clinicopathological parameters. Significant increase in ALCAM immunopositivity was observed from normal oral mucosa, hyperplasia, dysplasia to OSCCs ( p trend < 0.001). Increased ALCAM expression was observed in cytoplasm of epithelial cells as early as in hyperplasia ( p = 0.001, OR = 3.8). Sixty‐five of 107 (61%) OSCCs showed significant overexpression of ALCAM protein in cytoplasm/membrane of tumor cells ( p = 0.043; OR = 3.3) in comparison with the normal oral tissues. Among OSCCs, cytoplasmic ALCAM was associated with advanced tumor size, tumor stage and tobacco consumption. Importantly, cytoplasmic ALCAM was an independent predictor of poor prognosis of OSCCs in multivariate analysis ( p = 0.012, OR = 6.2). In an attempt to understand the molecular basis of cytoplasmic localization of ALCAM, 14‐3‐3ζ and 14‐3‐3σ were identified as its novel binding partners in oral cancer cells. In conclusion, increased expression of ALCAM is an early event in oral tumorigenesis; its cytoplasmic accumulation in tumor cells is a predictor of poor prognosis of OSCCs, underscoring its potential as a candidate prognostic marker for oral cancer. © 2008 Wiley‐Liss, Inc.
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