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Evaluating the value of Amphiregulin, Phosphatase and Tensin Homologue (PTEN) and P21 Expression for Anti-EGFR Treatment in Metastatic Colorectal Carcinoma

BACKGROUND: Despite the significant progress in target therapy for the treatment of metastatic colorectal carcinoma (mCRC), the overall survival isn’t satisfactory. METHODS: We assessed the expression of Amphiregulin, PTEN, and P21 in sections from 23 paraffin blocks prepared from 23 patients with l...

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Autores principales: Obaya, Ahmed Ali, Mohammed, Amrallah A, Rashied, Hanaa, Morsy, Adel Mahmoud, Osman, Gamal, Allam, Ahmed S, Elsayed, Ahmed M, Harb, Ola A, S H, Walid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: West Asia Organization for Cancer Prevention 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8325139/
https://www.ncbi.nlm.nih.gov/pubmed/33906293
http://dx.doi.org/10.31557/APJCP.2021.22.4.1025
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author Obaya, Ahmed Ali
Mohammed, Amrallah A
Rashied, Hanaa
Morsy, Adel Mahmoud
Osman, Gamal
Allam, Ahmed S
Elsayed, Ahmed M
Harb, Ola A
S H, Walid
author_facet Obaya, Ahmed Ali
Mohammed, Amrallah A
Rashied, Hanaa
Morsy, Adel Mahmoud
Osman, Gamal
Allam, Ahmed S
Elsayed, Ahmed M
Harb, Ola A
S H, Walid
author_sort Obaya, Ahmed Ali
collection PubMed
description BACKGROUND: Despite the significant progress in target therapy for the treatment of metastatic colorectal carcinoma (mCRC), the overall survival isn’t satisfactory. METHODS: We assessed the expression of Amphiregulin, PTEN, and P21 in sections from 23 paraffin blocks prepared from 23 patients with left-sided mCRC using immunohistochemistry (IHC). The relationship between their level of expressions, clinicopathological parameters, response to anti-EGFR, and prognosis were analyzed. RESULTS: High Amphiregulin, PTEN and low P21 expression levels were associated with low tumor grade (p= 0.038 and 0.025 respectively), better response to anti-EGFR treatment (p <0.001), and favorable outcome {progression-free survival (PFS) and overall survival (OS)} (p <0.05). There was a direct relation between Amphiregulin and PTEN expressions (phi coefficient=+0.840), while there was an inverse relation between P21expression and both Amphiregulin (phi coefficient= -0.840) and PTEN expressions (phi coefficient = -1.000), which was statistically significant (P <0.001). CONCLUSION: High Amphiregulin and PTEN expression levels and low P21 expression levels were associated with better response to anti-EGFR therapy and improved survival outcome. They might be considered predictive markers of response to anti-EGFR therapy in mCRC.
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spelling pubmed-83251392021-08-06 Evaluating the value of Amphiregulin, Phosphatase and Tensin Homologue (PTEN) and P21 Expression for Anti-EGFR Treatment in Metastatic Colorectal Carcinoma Obaya, Ahmed Ali Mohammed, Amrallah A Rashied, Hanaa Morsy, Adel Mahmoud Osman, Gamal Allam, Ahmed S Elsayed, Ahmed M Harb, Ola A S H, Walid Asian Pac J Cancer Prev Research Article BACKGROUND: Despite the significant progress in target therapy for the treatment of metastatic colorectal carcinoma (mCRC), the overall survival isn’t satisfactory. METHODS: We assessed the expression of Amphiregulin, PTEN, and P21 in sections from 23 paraffin blocks prepared from 23 patients with left-sided mCRC using immunohistochemistry (IHC). The relationship between their level of expressions, clinicopathological parameters, response to anti-EGFR, and prognosis were analyzed. RESULTS: High Amphiregulin, PTEN and low P21 expression levels were associated with low tumor grade (p= 0.038 and 0.025 respectively), better response to anti-EGFR treatment (p <0.001), and favorable outcome {progression-free survival (PFS) and overall survival (OS)} (p <0.05). There was a direct relation between Amphiregulin and PTEN expressions (phi coefficient=+0.840), while there was an inverse relation between P21expression and both Amphiregulin (phi coefficient= -0.840) and PTEN expressions (phi coefficient = -1.000), which was statistically significant (P <0.001). CONCLUSION: High Amphiregulin and PTEN expression levels and low P21 expression levels were associated with better response to anti-EGFR therapy and improved survival outcome. They might be considered predictive markers of response to anti-EGFR therapy in mCRC. West Asia Organization for Cancer Prevention 2021-04 /pmc/articles/PMC8325139/ /pubmed/33906293 http://dx.doi.org/10.31557/APJCP.2021.22.4.1025 Text en https://creativecommons.org/licenses/by/3.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/) ) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Obaya, Ahmed Ali
Mohammed, Amrallah A
Rashied, Hanaa
Morsy, Adel Mahmoud
Osman, Gamal
Allam, Ahmed S
Elsayed, Ahmed M
Harb, Ola A
S H, Walid
Evaluating the value of Amphiregulin, Phosphatase and Tensin Homologue (PTEN) and P21 Expression for Anti-EGFR Treatment in Metastatic Colorectal Carcinoma
title Evaluating the value of Amphiregulin, Phosphatase and Tensin Homologue (PTEN) and P21 Expression for Anti-EGFR Treatment in Metastatic Colorectal Carcinoma
title_full Evaluating the value of Amphiregulin, Phosphatase and Tensin Homologue (PTEN) and P21 Expression for Anti-EGFR Treatment in Metastatic Colorectal Carcinoma
title_fullStr Evaluating the value of Amphiregulin, Phosphatase and Tensin Homologue (PTEN) and P21 Expression for Anti-EGFR Treatment in Metastatic Colorectal Carcinoma
title_full_unstemmed Evaluating the value of Amphiregulin, Phosphatase and Tensin Homologue (PTEN) and P21 Expression for Anti-EGFR Treatment in Metastatic Colorectal Carcinoma
title_short Evaluating the value of Amphiregulin, Phosphatase and Tensin Homologue (PTEN) and P21 Expression for Anti-EGFR Treatment in Metastatic Colorectal Carcinoma
title_sort evaluating the value of amphiregulin, phosphatase and tensin homologue (pten) and p21 expression for anti-egfr treatment in metastatic colorectal carcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8325139/
https://www.ncbi.nlm.nih.gov/pubmed/33906293
http://dx.doi.org/10.31557/APJCP.2021.22.4.1025
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