Literature DB >> 26050229

Sam68 promotes cellular proliferation and predicts poor prognosis in esophageal squamous cell carcinoma.

Yayun Wang1, Li Liang2, Jianguo Zhang3, Mei Li2, Junya Zhu1, Chen Gong1, Linlin Yang4, Jia Zhu4, Lingling Chen1, Runzhou Ni5.   

Abstract

Sam68 (Src-associated in mitosis of 68 kD) is a KH domain RNA-binding protein. The expression of Sam68 was correlated with kinds of tumors. Yet, the expression mechanisms and physiological significance of Sam68 in ESCC remains unclear. In this study, we clarified a potential role of Sam68 in the treatment of ESCC. Western blot and immunohistochemistry (IHC) analysis revealed that the protein level of Sam68 was higher in ESCC tumor tissues and cell lines. In addition, IHC stain revealed that Sam68 was positively correlated with clinical pathologic variables such as tumor grade and tumor invasion. In addition, Sam68 could be an independent prognostic indicator for patients' overall survival. In vitro studies such as starvation and refeeding assay along with Sam68-shRNA transfection assay demonstrated that Sam68 expression promoted proliferation of ESCC cells. And Sam68 downregulation caused decreased rate of cell growth and colony formation. Reasons are associated with growth arrest of cell cycle at G1/S phase. Moreover, our results clarified that Sam68 could promote ESCC cell proliferation via the activation of Akt/GSK-3β pathway. This research indicated that Sam68 might accelerate the cell cycle progression and be considered as a new therapy target in ESCC.

Entities:  

Keywords:  Esophageal squamous cell carcinoma (ESCC); Prognosis; Proliferation; Sam68

Mesh:

Substances:

Year:  2015        PMID: 26050229     DOI: 10.1007/s13277-015-3631-8

Source DB:  PubMed          Journal:  Tumour Biol        ISSN: 1010-4283


  26 in total

1.  A role for the GSG domain in localizing Sam68 to novel nuclear structures in cancer cell lines.

Authors:  T Chen; F M Boisvert; D P Bazett-Jones; S Richard
Journal:  Mol Biol Cell       Date:  1999-09       Impact factor: 4.138

2.  Retardation of the G2-M phase progression on gene disruption of RNA binding protein Sam68 in the DT40 cell line.

Authors:  Qing-Hua Li; Izumi Haga; Toshiki Shimizu; Michiyasu Itoh; Tomohiro Kurosaki; Jun-ichi Fujisawa
Journal:  FEBS Lett       Date:  2002-08-14       Impact factor: 4.124

3.  Cell biology. RNA metabolism and oncogenesis.

Authors:  Deborah L Johnson; Sandra A S Johnson
Journal:  Science       Date:  2008-04-25       Impact factor: 47.728

4.  Overexpression of forkhead box J2 can decrease the migration of breast cancer cells.

Authors:  Yingying Wang; Shuyun Yang; Qichao Ni; Song He; Yunhong Zhao; Qin Yuan; Chunmiao Li; Hongwei Chen; Li Zhang; Lin Zou; Aiguo Shen; Chun Cheng
Journal:  J Cell Biochem       Date:  2012-08       Impact factor: 4.429

Review 5.  The RNA-binding protein Sam68 is a multifunctional player in human cancer.

Authors:  Pamela Bielli; Roberta Busà; Maria Paola Paronetto; Claudio Sette
Journal:  Endocr Relat Cancer       Date:  2011-07-01       Impact factor: 5.678

6.  MIF4G domain containing protein regulates cell cycle and hepatic carcinogenesis by antagonizing CDK2-dependent p27 stability.

Authors:  C Wan; S Hou; R Ni; L Lv; Z Ding; X Huang; Q Hang; S He; Y Wang; C Cheng; X X Gu; G Xu; A Shen
Journal:  Oncogene       Date:  2013-12-16       Impact factor: 9.867

Review 7.  Targeting the human EGFR family in esophagogastric cancer.

Authors:  Alicia Okines; David Cunningham; Ian Chau
Journal:  Nat Rev Clin Oncol       Date:  2011-04-05       Impact factor: 66.675

Review 8.  Regulation of gene expression by the RNA-binding protein Sam68 in cancer.

Authors:  Prabhakar Rajan; Luke Gaughan; Caroline Dalgliesh; Amira El-Sherif; Craig N Robson; Hing Y Leung; David J Elliott
Journal:  Biochem Soc Trans       Date:  2008-06       Impact factor: 5.407

Review 9.  Hallmarks of cancer: the next generation.

Authors:  Douglas Hanahan; Robert A Weinberg
Journal:  Cell       Date:  2011-03-04       Impact factor: 41.582

10.  The nuclear RNA-binding protein Sam68 translocates to the cytoplasm and associates with the polysomes in mouse spermatocytes.

Authors:  Maria Paola Paronetto; Francesca Zalfa; Flavia Botti; Raffaele Geremia; Claudia Bagni; Claudio Sette
Journal:  Mol Biol Cell       Date:  2005-10-12       Impact factor: 4.138

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  5 in total

1.  A comprehensive study on genome-wide coexpression network of KHDRBS1/Sam68 reveals its cancer and patient-specific association.

Authors:  B Sumithra; Urmila Saxena; Asim Bikas Das
Journal:  Sci Rep       Date:  2019-07-31       Impact factor: 4.379

2.  High expression of HNRNPR in ESCA combined with 18F-FDG PET/CT metabolic parameters are novel biomarkers for preoperative diagnosis of ESCA.

Authors:  Xiao-Yu Liu; Yan Gao; Xue-Yan Kui; Xu-Sheng Liu; Yao-Hua Zhang; Yu Zhang; Chang-Bin Ke; Zhi-Jun Pei
Journal:  J Transl Med       Date:  2022-10-04       Impact factor: 8.440

3.  High expression of Sam68 in sacral chordomas is associated with worse clinical outcomes.

Authors:  Hai Wen; Pengzhi Li; Hong Ma; Jiaoyun Zheng; Yipin Yu; Guohua Lv
Journal:  Onco Targets Ther       Date:  2017-09-22       Impact factor: 4.147

4.  Sam68 is Overexpressed in Epithelial Ovarian Cancer and Promotes Tumor Cell Proliferation.

Authors:  Lijuan Dong; Hailuo Che; Mingmei Li; Xuepeng Li
Journal:  Med Sci Monit       Date:  2016-09-13

5.  The p53 status can influence the role of Sam68 in tumorigenesis.

Authors:  Naomi Li; Chau Tuan-Anh Ngo; Olga Aleynikova; Nicole Beauchemin; Stéphane Richard
Journal:  Oncotarget       Date:  2016-11-01
  5 in total

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