Prabowo, Rianto and Susanto, Hendra and Setiawan, Nurcahya and Sofii, Imam and Barmawi, Agus and Handaya, Adeodatus Yuda (2023) Comparison of Carcinoembryonic Antigen Level and E-Cadherin Expression between Metastatic and Non-Metastatic Colorectal Carcinoma in RSUP, Dr. Sardjito Yogyakarta-Indonesia. Middle East Journal of Cancer, 14 (4). pp. 521-529. ISSN 20086709
Comparison of Carcinoembryonic Antigen Level and E-Cadherin Expression between Metastatic and Non-Metastatic Colorectal Carcinoma in RSUP, Dr. Sardjito Yogyakarta-Indonesia.pdf - Published Version
Restricted to Registered users only
Available under License Creative Commons Attribution.
Download (946kB) | Request a copy
Abstract
Background: WHO has reported 34,189 (8.6) colorectal carcinoma cases out of 396,914 total cancer cases in Indonesia. Accumulated gene mutation and the environment can affect cell regulation, growth, and differentiation, impacting the methylation of tumor suppressor genes. Carcinoembryonic antigen (CEA) is a biomarker used to detect the presence of colorectal carcinoma. Moreover, the E-cadherin gene has an essential role in tissue homeostasis, the adhesion between cells at embryogenesis, tissue morphogenesis, differentiation, and carcinogenesis stages. During instability and dysfunction in its regulation, the E-cadherin gene induces tumor progression. This study aimed to compare the level of CEA and E-cadherin expression in metastatic and non-metastatic sample groups. Method: The present study is descriptive with a quantitative approach using ANOVA one-way, unpaired t-test, and Pearson correlation analysis for the measurement and comparison of the CEA level and relative gene expression value from the reverse transcription-quantitative polymerase chain reaction analysis. Results: The obtained results suggested increasing CEA level and decreasing E-cadherin expression on the metastatic sample. Statistically, E-cadherin proven to show a negative r value or correlation value of CEA, even though it has a significant P-value. In other parameters, alanine transaminase and aspartate aminotransferase indicated a positive r value and a significant P-value. Conclusion: These findings indicated the potential clinical benefit of E-cadherin in detecting tumor progressivity, supported by other significant parameters, such as alanine transaminase and aspartate aminotransferase. Furthermore, E-cadherin was found beneficial in diagnosing the colorectal carcinoma with liver metastatis. Nonetheless, further research is needed to determine the role of E-cadherin regulation in colorectal cancer metastatis. Keywords: Colorectal neoplasms, Neoplasm metastatic, Non-metastatic, Carcinoem-bryonic antigen, E-Cadherin. © 2023, Shiraz University of Medical Sciences. All rights reserved.
Item Type: | Article |
---|---|
Additional Information: | Cited by: 0 |
Uncontrolled Keywords: | alanine aminotransferase; aspartate aminotransferase; cadherin; carcinoembryonic antigen; creatinine; alanine aminotransferase blood level; analysis of variance; Article; body mass; cancer staging; carcinogenesis; cell viability; colorectal carcinoma; correlation analysis; diastolic blood pressure; epithelial mesenchymal transition; erythrocyte count; gene expression; gene mutation; glucose blood level; histogenesis; homeostasis; human; immunohistochemistry; liver metastasis; major clinical study; metastasis; morphogenesis; platelet count; protein expression; protein function; quantitative analysis; real time polymerase chain reaction; real time reverse transcription polymerase chain reaction; receiver operating characteristic; reverse transcription polymerase chain reaction; RNA isolation; sensitivity and specificity; systolic blood pressure; tumor growth; tumor suppressor gene; urea nitrogen blood level |
Subjects: | R Medicine > RC Internal medicine > RC0254 Neoplasms. Tumors. Oncology (including Cancer) |
Divisions: | Faculty of Medicine, Public Health and Nursing > Public Health and Nutrition |
Depositing User: | Ani PURWANDARI |
Date Deposited: | 20 May 2024 06:02 |
Last Modified: | 20 May 2024 06:02 |
URI: | https://ir.lib.ugm.ac.id/id/eprint/1165 |