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<article xsi:noNamespaceSchemaLocation="http://jats.nlm.nih.gov/publishing/1.1/xsd/JATS-journalpublishing1-mathml3.xsd" dtd-version="1.1" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"><front><journal-meta><journal-id journal-id-type="publisher-id">JCNR</journal-id><journal-title-group><journal-title>Journal of Clinical and Nursing Research</journal-title></journal-title-group><issn>2208-3685</issn><eissn>2208-3693</eissn><publisher><publisher-name>Bio-Byword Scientific Publishing Pty. Ltd.</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.26689/jcnr.v5i4.2271</article-id><article-categories><subj-group subj-group-type="heading"><subject>Article</subject></subj-group></article-categories><title>Significance of EZH2 and BMI-1 Protein Expression in Carcinogenesis of Colon Serrated Adenoma</title><url>https://artdesignp.com/journal/JCNR/5/4/10.26689/jcnr.v5i4.2271</url><author>ZhaoKai</author><pub-date pub-type="publication-year"><year>2021</year></pub-date><volume>5</volume><issue>4</issue><history><date date-type="pub"><published-time>2021-08-02</published-time></date></history><abstract>Objective: To observe the significance of EZH2 and BMI-1 protein expression in the carcinogenesis process of colon serrated adenoma (SSA/P). Methods: Hematoxylin-eosin (HE) staining was used to observe the morphological characteristics of normal tissues, hyperplastic polyp (HP), SSA/P and colon cancer. Immunohistochemical staining was used to detect the expression of EZH2 and BMI-1 protein. The relative expression of EZH2 and BMI-1 was detected by qRT-PCR. Results: Compared with normal tissues, HP and colon cancer tissues, SSA/P showed serrated glandular hyperplasia, glandular dilatation, and deep nuclear staining, which had certain atypia. The positive expression rates of EZH2 and BMI-1 protein were 53.3% and 56%, which were close to those of colon cancer (66.7% and 76.6%) and higher than those of normal group and HP (16% and 8%, P &amp;lt; 0.05). The relative expression of EZH2 and BMI-1 in SSA/P tissue was significantly higher than that in normal group and HP, but lower than that in carcinogenesis group (P&amp;lt;0.05). Conclusion: EZH2 and BMI-1 play an important role in the carcinogenesis of colon serrated adenoma, and can be used as the primary screening index before carcinogenesis.</abstract><keywords/></article-meta></front><body/><back><ref-list><ref id="B1" content-type="article"><label>1</label><element-citation publication-type="journal"><p>Steele JC, Torr EE, Noakes KL, et al., 2006, The Polycomb Group Proteins, BMI-1 and EZH2, are Tumour-Associated Antigens. British Journal of Cancer.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B2" content-type="article"><label>2</label><element-citation publication-type="journal"><p>Bao H, Li J, Xing G, 2014, Expression and Significance of EZH2 and Bmi-1 Genes in Colorectal Cancer Tissues. Heilongjiang Medical Science, 37(1):10-12.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B3" content-type="article"><label>3</label><element-citation publication-type="journal"><p>Brody H., 2015, Colorectal Cancer. Nature. 521(7551): S1.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B4" content-type="article"><label>4</label><element-citation publication-type="journal"><p>Gan L, Yang Y, Li Q, et al., 2018, Epigenetic Regulation of Cancer Progression by EZH2: from Biological Insights to Therapeutic Potential. Biomarker Research, 6(1):10.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B5" content-type="article"><label>5</label><element-citation publication-type="journal"><p>Pourjafar M, Samadi P, Karami M, et al., 2020, Assessment of Clinicopathological and Prognostic Relevance of BMI 1 in Patients with Colorectal Cancer: A Meta Analysis. Biotechnology and Applied Biochemistry.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B6" content-type="article"><label>6</label><element-citation publication-type="journal"><p>Suva ML, Riggi N, Janiszewska M, et al., 2009, EZH2 is Essential for Glioblastoma Cancer Stem Cell Maintenance. Cancer Research, 69(24):9211-9218.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B7" content-type="article"><label>7</label><element-citation publication-type="journal"><p>Yu J, Chen L, Bao Z, et al., 2020, BMI1 Promotes Invasion and Metastasis in Endometrial Adenocarcinoma and is a Poor Prognostic Factor. Oncology Reports.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B8" content-type="article"><label>8</label><element-citation publication-type="journal"><p>Pan H, Hou J, He J, et al., 2010, Expression and Significance of EZH2 and Bmi-1 Genes in Transitional Cell Carcinoma of the Bladder. Chinese Journal of Experimental Surgery, 27(3):292-294.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B9" content-type="article"><label>9</label><element-citation publication-type="journal"><p>Shao G, Zhang G, Pu H, et al., 2015, Expression and Clinical Significance of Bmi-1, NANOG, EZH2 in Colorectal Cancer. Journal of Xinjiang Medical University, 38(3): 350-350.</p><pub-id pub-id-type="doi"/></element-citation></ref></ref-list></back></article>
