Association of DNA methylation status, gene and protein expression of her family in colorectal adenocarcinoma

Colorectal cancer (CRC) is the third most common cancer worldwide and the second leading cancer in Malaysia. Despite advanced therapies, many cases of recurrence and resistance have been reported. Surgery is only applicable for early diagnosed CRC cases. Reliable biomarkers are very crucial for earl...

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Main Author: Othman @ Jaffar, Rosfayati
Format: Thesis
Language:English
Published: 2020
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Online Access:http://psasir.upm.edu.my/id/eprint/98201/1/FPSK%28p%29%202021%209%20IR.pdf
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spelling my-upm-ir.982012022-07-28T04:20:53Z Association of DNA methylation status, gene and protein expression of her family in colorectal adenocarcinoma 2020-10 Othman @ Jaffar, Rosfayati Colorectal cancer (CRC) is the third most common cancer worldwide and the second leading cancer in Malaysia. Despite advanced therapies, many cases of recurrence and resistance have been reported. Surgery is only applicable for early diagnosed CRC cases. Reliable biomarkers are very crucial for early diagnosis, prognosis and therapeutic target. Overexpression of HER family members (EGFR, HER2, HER3 and HER4) has been associated with oncogenic transformation via DNA methylation of the promoter regions. Aberrant DNA methylation of HER family members has been implicated in carcinogenesis of CRC mainly through the regulation of gene expression. This study aimed to determine the DNA methylation status and gene expression of HER family members in CRC cell lines and in formalin-fixed paraffin embedded (FFPE) samples as well as the protein expression of HER family members in FFPE samples. The associations of DNA methylation status, gene and protein expression of these genes in FFPE samples were also determined. Fifty-nine archival FFPE CRC cases with the adjacent normal colon tissues were retrieved. The selected tissues were micro-dissected manually prior to RNA and DNA extraction. Gene expression and DNA methylation status of HER family members were evaluated by qPCR and MSP technique respectively. Protein expression was determined using immunohistochemistry (IHC) technique. Prior to FFPE, the same procedures were performed on CRC cell lines i.e. HT-29, HCT116, Caco-2 and CCD 841 CoN (normal colon) with treatment of 5’-aza-2’-deoxytidine (5-aza-dC) and 5-fluorouracil (5-FU). Upregulation of HER family members were discovered in all CRC cell lines with HER3 recorded significant expression (p<0.0001). EGFR and HER3 were hypomethylated whereas HER4 was hypermethylated in CRC cells. Downregulation of all genes were observed in several CRC cell lines after treatment with only HER3 shows significant result (p<0.001). EGFR, HER2 and HER3 remained unmethylated after being treated with 5-FU and HER4 was unmethylated after treatment with 5-aza-dC. Overexpression of EGFR (54.2%, p-value=0.021), HER2 (52.5%, p-value=0.022), and HER3 (42.4%, p-value=0.077) and hypomethylation of EGFR (81.4%) and HER3 (91.5%) were discovered in FFPE CRC tissues. Positive proteins expressions of EGFR (42.4%), HER2 (11.9%), HER3 (47.5%) and HER4 (57.6%) were seen in FFPE tissues. However, no significant association was found between DNA methylation, mRNA levels and protein expression of HER family members. Aberrant DNA methylation pattern of HER3 showed significant association with tumour differentiation (p-value=0.035) and tumour location (p-value=0.007). Even though our data suggest that there is no significant relationship between DNA methylation and mRNA expression, the aberrant regulation and hypomethylation of these genes strongly suggest the important role of these genes in tumourigenesis of CRC. Hypomethylation facilitates the activation of these genes which promotes oncogenic cell growth, loss of imprinting or genomic instability and subsequently promotes carcinogenesis and progression of CRC. Therefore, HER family has a potential as prognostic factors and therapeutic target for CRC. The genes are very promising candidates for the identification of new biomarkers. However, further investigation on DNA hypomethylation is required. Colorectal Neoplasms Methylation 2020-10 Thesis http://psasir.upm.edu.my/id/eprint/98201/ http://psasir.upm.edu.my/id/eprint/98201/1/FPSK%28p%29%202021%209%20IR.pdf text en public doctoral Universiti Putra Malaysia Colorectal Neoplasms Methylation Mohtarrudin, Norhafizah
institution Universiti Putra Malaysia
collection PSAS Institutional Repository
language English
advisor Mohtarrudin, Norhafizah
topic Colorectal Neoplasms
Methylation

spellingShingle Colorectal Neoplasms
Methylation

Othman @ Jaffar, Rosfayati
Association of DNA methylation status, gene and protein expression of her family in colorectal adenocarcinoma
description Colorectal cancer (CRC) is the third most common cancer worldwide and the second leading cancer in Malaysia. Despite advanced therapies, many cases of recurrence and resistance have been reported. Surgery is only applicable for early diagnosed CRC cases. Reliable biomarkers are very crucial for early diagnosis, prognosis and therapeutic target. Overexpression of HER family members (EGFR, HER2, HER3 and HER4) has been associated with oncogenic transformation via DNA methylation of the promoter regions. Aberrant DNA methylation of HER family members has been implicated in carcinogenesis of CRC mainly through the regulation of gene expression. This study aimed to determine the DNA methylation status and gene expression of HER family members in CRC cell lines and in formalin-fixed paraffin embedded (FFPE) samples as well as the protein expression of HER family members in FFPE samples. The associations of DNA methylation status, gene and protein expression of these genes in FFPE samples were also determined. Fifty-nine archival FFPE CRC cases with the adjacent normal colon tissues were retrieved. The selected tissues were micro-dissected manually prior to RNA and DNA extraction. Gene expression and DNA methylation status of HER family members were evaluated by qPCR and MSP technique respectively. Protein expression was determined using immunohistochemistry (IHC) technique. Prior to FFPE, the same procedures were performed on CRC cell lines i.e. HT-29, HCT116, Caco-2 and CCD 841 CoN (normal colon) with treatment of 5’-aza-2’-deoxytidine (5-aza-dC) and 5-fluorouracil (5-FU). Upregulation of HER family members were discovered in all CRC cell lines with HER3 recorded significant expression (p<0.0001). EGFR and HER3 were hypomethylated whereas HER4 was hypermethylated in CRC cells. Downregulation of all genes were observed in several CRC cell lines after treatment with only HER3 shows significant result (p<0.001). EGFR, HER2 and HER3 remained unmethylated after being treated with 5-FU and HER4 was unmethylated after treatment with 5-aza-dC. Overexpression of EGFR (54.2%, p-value=0.021), HER2 (52.5%, p-value=0.022), and HER3 (42.4%, p-value=0.077) and hypomethylation of EGFR (81.4%) and HER3 (91.5%) were discovered in FFPE CRC tissues. Positive proteins expressions of EGFR (42.4%), HER2 (11.9%), HER3 (47.5%) and HER4 (57.6%) were seen in FFPE tissues. However, no significant association was found between DNA methylation, mRNA levels and protein expression of HER family members. Aberrant DNA methylation pattern of HER3 showed significant association with tumour differentiation (p-value=0.035) and tumour location (p-value=0.007). Even though our data suggest that there is no significant relationship between DNA methylation and mRNA expression, the aberrant regulation and hypomethylation of these genes strongly suggest the important role of these genes in tumourigenesis of CRC. Hypomethylation facilitates the activation of these genes which promotes oncogenic cell growth, loss of imprinting or genomic instability and subsequently promotes carcinogenesis and progression of CRC. Therefore, HER family has a potential as prognostic factors and therapeutic target for CRC. The genes are very promising candidates for the identification of new biomarkers. However, further investigation on DNA hypomethylation is required.
format Thesis
qualification_level Doctorate
author Othman @ Jaffar, Rosfayati
author_facet Othman @ Jaffar, Rosfayati
author_sort Othman @ Jaffar, Rosfayati
title Association of DNA methylation status, gene and protein expression of her family in colorectal adenocarcinoma
title_short Association of DNA methylation status, gene and protein expression of her family in colorectal adenocarcinoma
title_full Association of DNA methylation status, gene and protein expression of her family in colorectal adenocarcinoma
title_fullStr Association of DNA methylation status, gene and protein expression of her family in colorectal adenocarcinoma
title_full_unstemmed Association of DNA methylation status, gene and protein expression of her family in colorectal adenocarcinoma
title_sort association of dna methylation status, gene and protein expression of her family in colorectal adenocarcinoma
granting_institution Universiti Putra Malaysia
publishDate 2020
url http://psasir.upm.edu.my/id/eprint/98201/1/FPSK%28p%29%202021%209%20IR.pdf
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