Literature DB >> 28913972

Significance of histone methyltransferase SETDB1 expression in colon adenocarcinoma.

Yi-Jung Ho1,2, Yueh-Min Lin3,4, Yen-Chi Huang5, Jungshan Chang6, Kun-Tu Yeh3,7, Liang-In Lin8,9, Zhiyuan Gong10, Tsai-Yu Tzeng11, Jeng-Wei Lu9,10.   

Abstract

This study investigated the clinical implications of SETDB1 (also known as KMT1E) in human colon adenocarcinoma. Expression levels of SETDB1 proteins were analyzed by immunohistochemistry staining, and tissue microarrays were used to examine expression profiles in human patients. Our results revealed that SETDB1 protein expression was significantly higher in tumor tissue than in normal tissue for the breast, colon, liver, and lung (p < 0.05). Moreover, an analysis with SurvExpress software suggested that elevated expression of SETDB1 mRNA was significantly associated with the overall survival of colon adenocarcinoma patients (p < 0.05); and additional analysis involving 90 paired samples of colon adenocarcinoma tissue and normal tissue revealed that SETDB1 protein expression was 82% higher in cancerous cells (p < 0.001). High SETDB1 expression was also found to be significantly correlated with histological grade (p = 0.005), TNM stage (p = 0.003), T-class/primary tumor (p = 0.001), and N-class/regional lymph nodes (p = 0.017); and Kaplan-Meier survival curves indicated that SETDB1 protein expression was significantly associated with poor survival. Finally, univariate analysis demonstrated that SETDB1 protein expression was related to TNM stage (p = 0.004) and SETDB1 score (p = 0.001), whereas multivariate analysis showed that the influence of SETDB1 on overall colon adenocarcinoma survival was independent from other risk factors. Taken together, our results suggest that the SETDB1 protein could serve as a clinical prognostic indicator for colon adenocarcinoma.
© 2017 APMIS. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  Colorectal cancer; SETDB1; colon adenocarcinoma; immunohistochemistry; prognosis

Mesh:

Substances:

Year:  2017        PMID: 28913972     DOI: 10.1111/apm.12745

Source DB:  PubMed          Journal:  APMIS        ISSN: 0903-4641            Impact factor:   3.205


  8 in total

1.  Homeostatic balance of histone acetylation and deconstruction of repressive chromatin marker H3K9me3 during adipocyte differentiation of 3T3-L1 cells.

Authors:  Han-Heom Na; Keun-Cheol Kim
Journal:  Genes Genomics       Date:  2018-08-09       Impact factor: 1.839

2.  The SETDB1-TRIM28 Complex Suppresses Antitumor Immunity.

Authors:  Jianhuang Lin; Dajiang Guo; Heng Liu; Wei Zhou; Chen Wang; Iris Müller; Andrew V Kossenkov; Ronny Drapkin; Benjamin G Bitler; Kristian Helin; Rugang Zhang
Journal:  Cancer Immunol Res       Date:  2021-12       Impact factor: 12.020

Review 3.  Insight into the multi-faceted role of the SUV family of H3K9 methyltransferases in carcinogenesis and cancer progression.

Authors:  Nirmalya Saha; Andrew G Muntean
Journal:  Biochim Biophys Acta Rev Cancer       Date:  2020-12-26       Impact factor: 10.680

4.  Assessment of copy number in protooncogenes are predictive of poor survival in advanced gastric cancer.

Authors:  Meihui Li; Younghoon Kim; Tae-Shin Kim; Nam-Yun Cho; Jeong Mo Bae; Woo Ho Kim; Gyeong Hoon Kang
Journal:  Sci Rep       Date:  2021-06-09       Impact factor: 4.379

5.  Histone Methyltransferase SETDB1 Promotes Immune Evasion in Colorectal Cancer via FOSB-Mediated Downregulation of MicroRNA-22 through BATF3/PD-L1 Pathway.

Authors:  Jiale Tian; Weiwei Wang; Jichao Zhu; Yun Zhuang; Chunrun Qi; Zhengxin Cai; Wenhui Yan; Wenying Lu; Anquan Shang
Journal:  J Immunol Res       Date:  2022-04-20       Impact factor: 4.493

Review 6.  SETDB1 in cancer: overexpression and its therapeutic implications.

Authors:  Vanessa J Lazaro-Camp; Kiarash Salari; Xiangbing Meng; Shujie Yang
Journal:  Am J Cancer Res       Date:  2021-05-15       Impact factor: 6.166

7.  SETDB1 promotes the progression of colorectal cancer via epigenetically silencing p21 expression.

Authors:  Nan Cao; Yali Yu; Hua Zhu; Meng Chen; Ping Chen; Mingxing Zhuo; Yujuan Mao; Lianyun Li; Qiu Zhao; Min Wu; Mei Ye
Journal:  Cell Death Dis       Date:  2020-05-11       Impact factor: 8.469

Review 8.  Clinicopathologic significance of protein lysine methyltransferases in cancer.

Authors:  Theodore Vougiouklakis; Benjamin J Bernard; Nupur Nigam; Kyunghee Burkitt; Yusuke Nakamura; Vassiliki Saloura
Journal:  Clin Epigenetics       Date:  2020-10-13       Impact factor: 6.551

  8 in total

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