Literature DB >> 26198729

Expression and Significances of MTSS1 in Pancreatic Cancer.

Li Zhou1, Jian Li1, Qian-Qian Shao1, Jun-Chao Guo2, Zhi-Yong Liang3, Wei-Xun Zhou3, Tai-Ping Zhang1, Lei You1, Yu-Pei Zhao4.   

Abstract

Thus far, expression of metastasis suppressor 1 (MTSS1), its clinicopathologic and prognostic significances in pancreatic cancer (PC) remain unknown. Expression of MTSS1 was detected by Western blotting in PC cell lines, and by tissue microarray-based immunohistochemical staining in paired tumor and non-tumor samples from 242 patients with PC. Furthermore, the correlations between MTSS1 expression and clinicopathologic variables as well as overall survival were evaluated. In PC cell lines, MTSS1 was differentially expressed. In addition, MTSS1 expression was significantly lower in tumor than in non-tumor tissues (P < 0.001 in both McNemar and Mann-Whitney U tests). High tumoral expression of MTSS1 was closely associated with absence of lymph node metastasis (P = 0.023). Univariate analysis found that high MTSS1 expression in tumor tissues was a strong predictor of favorable overall survival in the whole cohort (P < 0.001). Besides, its impacts on prognosis were also observed in nine out of fourteen subgroups. Finally, MTSS1 expression was identified as an independent prognostic marker in the whole cohort (P = 0.031) as well as in six subgroups (P < 0.05), as shown by multivariate Cox regression test. Down-regulation of MTSS1 expression is evident in PC, and is associated with lymph node metastasis and poor prognosis.

Entities:  

Keywords:  Lymph node metastasis; Metastasis suppressor 1; Pancreatic cancer; Prognosis

Mesh:

Substances:

Year:  2015        PMID: 26198729     DOI: 10.1007/s12253-015-9963-2

Source DB:  PubMed          Journal:  Pathol Oncol Res        ISSN: 1219-4956            Impact factor:   3.201


  32 in total

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Journal:  J Cell Sci       Date:  2011-03-15       Impact factor: 5.285

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Review 2.  Long Non-Coding RNAs in Pancreatic Cancer: Biologic Functions, Mechanisms, and Clinical Significance.

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3.  Inhibition of miR-15b decreases cell migration and metastasis in colorectal cancer.

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Review 6.  Gene expression changes contribute to stemness and therapy resistance of relapsed acute myeloid leukemia: roles of SOCS2, CALCRL, MTSS1, and KDM6A.

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