Literature DB >> 20410808

Fascin expression predicts survival after potentially curative resection of node-positive colon cancer.

Charles Chan1, Lucy Jankova, Caroline L S Fung, Candice Clarke, Graham Robertson, Pierre H Chapuis, Les Bokey, Betty P C Lin, Owen F Dent, Stephen Clarke.   

Abstract

Fascin, an actin-bundling protein, is expressed in many neoplasms including colorectal cancer. It is considered to be a mediator of tumor cell invasion and an indicator of aggressive phenotype; however, there are few reports on the association between fascin and prognosis in colorectal cancer. The aims of this study were to: (a) investigate the expression of fascin in the central part of the tumor and at the invasive front in patients who had a potentially curative resection for node-positive colonic carcinoma; (b) examine the method of scoring fascin expression; and (c) investigate the association between fascin expression and overall survival and other clinicopathologic features. Fascin expression was assessed by immunostaining of microarrays from archived tissue of 470 patients who were followed for a minimum of 5 years after resection. Other clinicopathologic data had been recorded prospectively according to a standardized protocol. Analysis of overall survival was by the Kaplan-Meier method and Cox regression. For both central tumor tissue and the invasive front, it was found that the percentage of stained cells was a sufficient measure of fascin expression in relation to survival, with staining intensity providing no significant additional information. At both levels, there was a significant independent association between high fascin expression and diminished survival, although this association was much stronger in the central region (adjusted hazard ratio 1.6, P<0.001) than at the invasive front (adjusted hazard ratio 1.1, P=0.044). Fascin expression predicted overall survival but did not displace other routinely collected clinicopathologic predictors.

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Year:  2010        PMID: 20410808     DOI: 10.1097/PAS.0b013e3181db36c0

Source DB:  PubMed          Journal:  Am J Surg Pathol        ISSN: 0147-5185            Impact factor:   6.394


  16 in total

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Review 4.  Filopodia and adhesion in cancer cell motility.

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5.  Is availability of anti-EGFR therapy for the colorectal adenocarcinomas showing fascin expression limited?

Authors:  Nazım Emrah Koçer; Fazilet Kayaselçuk
Journal:  Target Oncol       Date:  2013-04-16       Impact factor: 4.493

6.  Overexpression of protein S100A4 is independently associated with overall survival in stage C colonic cancer but only in cytoplasm at the advancing tumour front.

Authors:  P S S Kho; L Jankova; C L-S Fung; C Chan; C Clarke; B P C Lin; G Robertson; M Molloy; P H Chapuis; E L Bokey; O F Dent; S Clarke
Journal:  Int J Colorectal Dis       Date:  2012-05-09       Impact factor: 2.571

7.  Glutathione S-transferase Pi expression predicts response to adjuvant chemotherapy for stage C colon cancer: a matched historical control study.

Authors:  Lucy Jankova; Graham Robertson; Charles Chan; King L Tan; Maija Kohonen-Corish; Caroline L-S Fung; Candice Clarke; Betty P C Lin; Mark Molloy; Pierre H Chapuis; Les Bokey; Owen F Dent; Stephen J Clarke
Journal:  BMC Cancer       Date:  2012-05-28       Impact factor: 4.430

8.  Drosophila Fascin is a novel downstream target of prostaglandin signaling during actin remodeling.

Authors:  Christopher M Groen; Andrew J Spracklen; Tiffany N Fagan; Tina L Tootle
Journal:  Mol Biol Cell       Date:  2012-10-10       Impact factor: 4.138

9.  MicroRNA-133a suppresses colorectal cancer cell invasion by targeting Fascin1.

Authors:  Keyan Zheng; Weicheng Liu; Ye Liu; Congqing Jiang; Qun Qian
Journal:  Oncol Lett       Date:  2014-12-01       Impact factor: 2.967

Review 10.  Association of fascin-1 with mortality, disease progression and metastasis in carcinomas: a systematic review and meta-analysis.

Authors:  Vanessa Y Tan; Sarah J Lewis; Josephine C Adams; Richard M Martin
Journal:  BMC Med       Date:  2013-02-26       Impact factor: 8.775

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