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Tissue microarrays in Chinese human rectal cancer: study of expressions of the tumor-associated genes.

AbstractBACKGROUNDS/AIMS:
The cellular basis for rectal cancer development is still unclear. The aim of this study was to evaluate the relationship between the expression of p53, cyclinD1, bcl-2, ß-catenin, c-myc, cyclooxygenase-2 (COX-2) and nm23-H1 and the clinicopathological characteristics of rectal cancer.
METHODOLOGY:
Expressions of p53, cyclinD1, bcl-2, ß-catenin, c-myc, COX-2 and nm23-H1 proteins were detected by immunohistochemical staining to two tissue microarrays containing tissues accumulated from 54 human rectal cancers and 40 para-cancer mucosa.
RESULTS:
Significant differences were demonstrated between the rectal cancers and their benign para-cancer counterparts according to the expressions of p53, cyclinD1, bcl-2, ß-catenin, c-myc, COX-2 and nm23-H1 (p<0.05). Additionally, positive correlations of ß-catenin with cyclinD1 and c-myc (r=0.412, p=0.002; r=0.447, p=0.000) and of p53 with bcl-2 (r=0.332, p=0.001) were found. Cancer tissues with overexpression of ß-catenin or bcl-2 were less likely to differentiate to advanced grade. Expression of cyclinD1 had a correlation with clinical stages (p=0.039). In addition, a negative correlation was found between nm23-H1 expression and the histological grades, distance metastasis and Duke's stages.
CONCLUSIONS:
Aberrant expression of p53, cyclinD1, bcl-2, ß-catenin, c-myc, COX-2 and nm23-H1 might attribute to the carcinogenesis of human rectal cancer. Furthermore, cyclinD1 and nm23-H1 might be involved in rectal cancer progression. This study recommends the application of tissue microarrays in rectal cancer research for its reliable quick throughput.
AuthorsMao Song Lin, Wei Chang Chen, Jun Xing Huang, Heng Jun Gao, Bao Feng Zhang, Jing Fang, Qiong Zhou, Ying Hu
JournalHepato-gastroenterology (Hepatogastroenterology) 2011 Nov-Dec Vol. 58 Issue 112 Pg. 1937-42 ISSN: 0172-6390 [Print] Greece
PMID22024062 (Publication Type: Journal Article)
Chemical References
  • CCND1 protein, human
  • CTNNB1 protein, human
  • MYC protein, human
  • Proto-Oncogene Proteins c-bcl-2
  • Proto-Oncogene Proteins c-myc
  • beta Catenin
  • Cyclin D1
Topics
  • Adult
  • Aged
  • Aged, 80 and over
  • Cyclin D1 (analysis, genetics)
  • Female
  • Genes, p53
  • Humans
  • Immunohistochemistry
  • Intestinal Mucosa (metabolism)
  • Male
  • Middle Aged
  • Proto-Oncogene Proteins c-bcl-2 (analysis, genetics)
  • Proto-Oncogene Proteins c-myc (analysis, genetics)
  • Rectal Neoplasms (chemistry, metabolism, pathology)
  • Tissue Array Analysis (methods)
  • beta Catenin (analysis, genetics)

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