Literature DB >> 23612849

S100 calcium-binding protein A4 is a novel independent prognostic factor for the poor prognosis of gastric carcinomas.

Ying Zhao1, Tianbiao Zhang, Qiang Wang.   

Abstract

Overexpression of the S100 calcium-binding protein A4 (S100A4) is involved in epithelial-to-mesenchymal transition, oncogenic transformation, angiogenesis, cytoskeletal integrity and cancer metastasis. Here, we elucidated the role of S100A4 in tumorigenesis and progression of gastric carcinomas. S100A4 expression in gastric carcinomas, adenomas and adjacent non-neoplastic mucosa was analyzed by immunohistochemical, real-time reverse transcriptase (RT)-polymerase chain reaction (PCR) and western blot analyses, and was correlated with various clinicopathological parameters. S100A4 protein expression was increased gradually in the following order: gastritis (19.2%), intestinal metaplasia (IM; 23.3%), dysplasia (34.9%) and carcinoma (55.2%; P<0.001). S100A4 was positively correlated with tumor size, depth of invasion, lymphatic invasion, lymph node metastasis and tumor-node-metastasis (TNM) staging (P<0.05), but not with the age and gender of the carcinoma patients (P>0.05). Intestinal-type (IT) carcinomas showed a higher S100A4 expression than diffuse-type (DT) carcinomas (P<0.001). S100A4 mRNA expression also increased in the following order: gastritis < IM < dysplasia < carcinoma (P<0.05). S100A4 overexpression was observed in gastric carcinomas with a larger diameter, deeper invasion, lymph node metastasis and in IT carcinoma (P<0.05). Univariate analysis using the Kaplan-Meier method indicated a lower cumulative survival rate for patients with weak or moderate S100A4 expression compared with patients not expressing S100A4 (P<0.001). Multivariate analysis using Cox's proportional hazard model demonstrated that depth of invasion, lymphatic or venous invasion, lymph node metastasis, TNM staging and S100A4 expression were independent factors for poor patient prognosis (P<0.05). In conclusion, S100A4 upregulation is positively associated with the pathogenesis, growth, invasion, metastasis and differentiation of gastric carcinomas. S100A4 may be a promising marker indicative of the aggressive behavior and prognosis of gastric carcinomas.

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Year:  2013        PMID: 23612849     DOI: 10.3892/or.2013.2419

Source DB:  PubMed          Journal:  Oncol Rep        ISSN: 1021-335X            Impact factor:   3.906


  4 in total

1.  Circulating Metastasis Associated in Colon Cancer 1 transcripts in gastric cancer patient plasma as diagnostic and prognostic biomarker.

Authors:  Susen Burock; Pia Herrmann; Ina Wendler; Markus Niederstrasser; Klaus-Dieter Wernecke; Ulrike Stein
Journal:  World J Gastroenterol       Date:  2015-01-07       Impact factor: 5.742

Review 2.  Impact of S100A4 Expression on Clinicopathological Characteristics and Prognosis in Pancreatic Cancer: A Meta-Analysis.

Authors:  Shanshan Huang; Jiawei Zheng; Yufang Huang; Li Song; Yin Yin; Danzhen Ou; Shangxiang He; Xiong Chen; Xuenong Ouyang
Journal:  Dis Markers       Date:  2016-01-19       Impact factor: 3.434

3.  Focal Adhesion Kinase Regulates Fibroblast Migration via Integrin beta-1 and Plays a Central Role in Fibrosis.

Authors:  Xue-Ke Zhao; Yiju Cheng; Ming Liang Cheng; Lei Yu; Mao Mu; Hong Li; Yang Liu; Baofang Zhang; Yumei Yao; Hui Guo; Rong Wang; Quan Zhang
Journal:  Sci Rep       Date:  2016-01-14       Impact factor: 4.379

4.  S100A4 Is a Strong Negative Prognostic Marker and Potential Therapeutic Target in Adenocarcinoma of the Stomach and Esophagus.

Authors:  Christoph Treese; Kimberly Hartl; Michelle Pötzsch; Matthias Dahlmann; Moritz von Winterfeld; Erika Berg; Michael Hummel; Lena Timm; Beate Rau; Wolfgang Walther; Severin Daum; Dennis Kobelt; Ulrike Stein
Journal:  Cells       Date:  2022-03-21       Impact factor: 6.600

  4 in total

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