1.Topographic expression of p21WAF1/SDI1/CIP1, bcl2, and p53 is altered at the early stage of colorectal carcinogenesis.
Jeong Hee CHO ; Im Hwan ROE ; Chang Young LIM ; Dong Kook PARK ; Woo Ho KIM ; Yong Il KIM
Journal of Korean Medical Science 2000;15(6):667-674
We analyzed the expression of p21, bcl2, and p53 in normal and different pathologic mucosa of the human colorectum using immunohistochemistry and cold polymerase chain reaction-single strand conformation polymorphism. The topography of normal mucosa showed; bcl2 and p53 expression restricted to basal epithelial cells and p21 expressed only in superficial epithelial cells. This topographic expression was altered in hyperplastic polyps and adenomas. Hyperplastic polyps revealed absence of or weak bcl2 expression and strong p21 expression without topography. In adenomas, whereas bcl2 expression increased and extended to parabasal and superficial dysplastic epithelium, the increase of p21 expression was limited to surface dysplastic epithelium. p53 was weakly expressed throughout the full thickness of dysplastic epithelium. Bcl2 expression in adenomas was stronger than in carcinomas; p53 expression was converse and p21 expression was variable. In carcinomas, this topographic expression was largely abrogated but p53 mutation (36%) was more frequent than in adenomas (2%). In carcinomas, p21 and p53 expression correlated inversely, but there was no relationship with bcl2. These results suggest that there is precisely ordered topographic pattern of p21, bcl2, and wild p53 expression in normal colorectal cells, but this becomes disordered during the early stage of colorectal carcinogenesis.
Colorectal Neoplasms/physiopathology
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Colorectal Neoplasms/pathology
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Colorectal Neoplasms/metabolism*
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Colorectal Neoplasms/genetics
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Cyclins/biosynthesis*
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Human
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Mutagenesis
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Protein p53/genetics
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Protein p53/biosynthesis*
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Proto-Oncogene Proteins c-bcl-2/biosynthesis*
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Time Factors
2.Immunohistochemical Expression of p53, Bcl-2, and Ki-67 Proteins in Traditional Serrated Adenomas of Colon.
Jin Hwan JUNG ; Heon Ju KWON ; Tae Jung KIM ; Hyung Jun CHO ; Hye Kang KIM ; Dae Young CHEUNG ; Jin Il KIM ; Jae Kwang KIM
The Korean Journal of Gastroenterology 2013;62(6):336-343
BACKGROUND/AIMS: Serrated adenomas of the colon show mixed characteristics of both hyperplastic and adenomatous polyps. Serrated adenomas are known to progress via the serrated pathway than the adenoma-carcinoma pathway. The aim of this study was to evaluate the characteristics of traditional serrated adenomas compared to hyperplastic polyps and tubular adenomas by using immunohistochemical staining for p53, Bcl-2, and Ki-67. METHODS: Age, sex, location, size and the immunoexpression of p53, Bcl-2, and Ki-67 were retrospectively analyzed in 20 traditional serrated adenomas, 20 hyperplastic polyps, and 20 tubular adenomas from January 2007 to December 2012 at The Catholic University of Korea, Yeouido St. Mary's Hospital. RESULTS: There was no difference in Bcl-2 and p53 expression between traditional serrated adenomas and hyperplastic polyps. Ki-67 Expression of traditional serrated adenomas was higher than that of hyperplastic polyps (p=0.001). Ki-67 and p53 expression was similar between traditional serrated and tubular adenomas. Bcl-2 expression of traditional serrated adenomas was lower than that of tubular adenomas (p=0.001). Regarding the expression of p53, Bcl-2, and Ki-67 in traditional serrated adenomas, there were no statistical differences among age, sex, location, and size. CONCLUSIONS: Our study suggested that Ki-67 may be helpful in distinguishing traditional serrated adenomas from hyperplastic polyps, and p53 expression may be ineffective in distinguishing between traditional serrated and tubular adenomas. From Bcl-2 expression, it is suggested that the tumorigenesis of traditional serrated adenomas is lower than that of tubular adenomas.
Adenoma/genetics/metabolism/*physiopathology
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Aged
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Colonic Polyps/physiopathology
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Colorectal Neoplasms/genetics/metabolism/*physiopathology
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Female
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*Gene Expression Regulation, Neoplastic
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Humans
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Immunohistochemistry
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Ki-67 Antigen/*genetics/metabolism
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Male
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Middle Aged
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Proto-Oncogene Proteins c-bcl-2/*genetics/metabolism
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Retrospective Studies
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Tumor Suppressor Protein p53/*genetics/metabolism
3.Immunohistochemical Expression of p53, Bcl-2, and Ki-67 Proteins in Traditional Serrated Adenomas of Colon.
Jin Hwan JUNG ; Heon Ju KWON ; Tae Jung KIM ; Hyung Jun CHO ; Hye Kang KIM ; Dae Young CHEUNG ; Jin Il KIM ; Jae Kwang KIM
The Korean Journal of Gastroenterology 2013;62(6):336-343
BACKGROUND/AIMS: Serrated adenomas of the colon show mixed characteristics of both hyperplastic and adenomatous polyps. Serrated adenomas are known to progress via the serrated pathway than the adenoma-carcinoma pathway. The aim of this study was to evaluate the characteristics of traditional serrated adenomas compared to hyperplastic polyps and tubular adenomas by using immunohistochemical staining for p53, Bcl-2, and Ki-67. METHODS: Age, sex, location, size and the immunoexpression of p53, Bcl-2, and Ki-67 were retrospectively analyzed in 20 traditional serrated adenomas, 20 hyperplastic polyps, and 20 tubular adenomas from January 2007 to December 2012 at The Catholic University of Korea, Yeouido St. Mary's Hospital. RESULTS: There was no difference in Bcl-2 and p53 expression between traditional serrated adenomas and hyperplastic polyps. Ki-67 Expression of traditional serrated adenomas was higher than that of hyperplastic polyps (p=0.001). Ki-67 and p53 expression was similar between traditional serrated and tubular adenomas. Bcl-2 expression of traditional serrated adenomas was lower than that of tubular adenomas (p=0.001). Regarding the expression of p53, Bcl-2, and Ki-67 in traditional serrated adenomas, there were no statistical differences among age, sex, location, and size. CONCLUSIONS: Our study suggested that Ki-67 may be helpful in distinguishing traditional serrated adenomas from hyperplastic polyps, and p53 expression may be ineffective in distinguishing between traditional serrated and tubular adenomas. From Bcl-2 expression, it is suggested that the tumorigenesis of traditional serrated adenomas is lower than that of tubular adenomas.
Adenoma/genetics/metabolism/*physiopathology
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Aged
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Colonic Polyps/physiopathology
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Colorectal Neoplasms/genetics/metabolism/*physiopathology
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Female
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*Gene Expression Regulation, Neoplastic
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Humans
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Immunohistochemistry
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Ki-67 Antigen/*genetics/metabolism
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Male
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Middle Aged
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Proto-Oncogene Proteins c-bcl-2/*genetics/metabolism
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Retrospective Studies
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Tumor Suppressor Protein p53/*genetics/metabolism
4.Mesua ferrea stem bark extract induces apoptosis and inhibits metastasis in human colorectal carcinoma HCT 116 cells, through modulation of multiple cell signalling pathways.
Muhammad ASIF ; Armaghan SHAFAEI ; Aman Shah ABDUL MAJID ; Mohammed Oday EZZAT ; Saad S DAHHAM ; Mohamed B Khadeer AHAMED ; Chern Ein OON ; Amin Malik Shah ABDUL MAJID
Chinese Journal of Natural Medicines (English Ed.) 2017;15(7):505-514
Considering the great potential of natural products as anticancer agents, the present study was designed to explore the molecular mechanisms responsible for anticancer activities of Mesua ferrea stem bark extract against human colorectal carcinoma. Based on MTT assay results, bioactive sub-fraction (SF-3) was selected for further studies using HCT 116 cells. Repeated column chromatography resulted in isolation of less active α-amyrin from SF-3, which was identified and characterized by GC-MS and HPLC methods. α-amyrin and betulinic acid contents of SF-3 were measured by HPLC methods. Fluorescent assays revealed characteristic apoptotic features, including cell shrinkage, nuclear condensation, and marked decrease in mitochondrial membrane potential in SF-3 treated cells. In addition, increased levels of caspases-9 and -3/7 levels were also observed in SF-3 treated cells. SF-3 showed promising antimetastatic properties in multiple in vitro assays. Multi-pathway analysis revealed significant down-regulation of WNT, HIF-1α, and EGFR with simultaneous up-regulation of p53, Myc/Max, and TGF-β signalling pathways in SF-3 treated cells. In addition, promising growth inhibitory effects were observed in SF-3 treated HCT 116 tumour spheroids, which give a hint about in vivo antitumor efficacy of SF-3 phytoconstituents. In conclusion, these results demonstrated that anticancer effects of SF-3 towards colon cancer are through modulation of multiple molecular pathways.
Antineoplastic Agents
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pharmacology
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Apoptosis
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drug effects
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Cell Line, Tumor
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Colorectal Neoplasms
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drug therapy
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metabolism
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pathology
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physiopathology
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ErbB Receptors
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genetics
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metabolism
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HCT116 Cells
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Humans
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Hypoxia-Inducible Factor 1, alpha Subunit
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genetics
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metabolism
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Magnoliopsida
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chemistry
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Neoplasm Metastasis
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prevention & control
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Plant Bark
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chemistry
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Plant Extracts
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pharmacology
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Signal Transduction
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drug effects
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Wnt Proteins
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genetics
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metabolism