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Polo-like kinase 4 as a potential predictive biomarker of chemoradioresistance in locally advanced rectal cancer

BACKGROUND: Polo-like kinase 4 (PLK4) is a serine/threonine protein kinase located in the centriole of the chromosome during the cell cycle. PLK4 overexpression has been described in a variety of many common human epithelial tumors. Conversely, PLK4 acts as a haploinsufficient tumor suppressor in so...

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Autores principales: Oh, Hyunseung, Kim, Soon Gu, Bae, Sung Uk, Byun, Sang Jun, Kim, Shin, Lee, Jae-Ho, Hwang, Ilseon, Kwon, Sun Young, Lee, Hye Won
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Pathologists/The Korean Society for Cytopathology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8743804/
https://www.ncbi.nlm.nih.gov/pubmed/34775733
http://dx.doi.org/10.4132/jptm.2021.10.07
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author Oh, Hyunseung
Kim, Soon Gu
Bae, Sung Uk
Byun, Sang Jun
Kim, Shin
Lee, Jae-Ho
Hwang, Ilseon
Kwon, Sun Young
Lee, Hye Won
author_facet Oh, Hyunseung
Kim, Soon Gu
Bae, Sung Uk
Byun, Sang Jun
Kim, Shin
Lee, Jae-Ho
Hwang, Ilseon
Kwon, Sun Young
Lee, Hye Won
author_sort Oh, Hyunseung
collection PubMed
description BACKGROUND: Polo-like kinase 4 (PLK4) is a serine/threonine protein kinase located in the centriole of the chromosome during the cell cycle. PLK4 overexpression has been described in a variety of many common human epithelial tumors. Conversely, PLK4 acts as a haploinsufficient tumor suppressor in some situations, highlighting the importance of strict regulation of PLK4 expression, activity, and function. Meanwhile, the importance of chemoradiation resistance in rectal cancer is being emphasized more than ever. We aimed to analyze PLK4 expression and the tumor regression grade (TRG) in patients with rectal cancer, treated with chemoradiotherapy (CRT). METHODS: A retrospective study was conducted on 102 patients with rectal cancer who received preoperative CRT. Immunohistochemistry for PLK4 in paraffin-embedded tissue was performed from the biopsy and surgical specimens. RESULTS: We found significant association between high expression of PLK4 and poor response to neoadjuvant CRT (according to both Mandard and The Korean Society of Pathologists TRG systems) in the pre-CRT specimens. Other clinicopathologic parameters did not reveal any correlation with PLK4 expression. CONCLUSIONS: This study revealed an association between high expression of PLK4 in the pre-CRT specimens and TRG. Our results indicated that PLK4 could potentially be a new predictor for CRT effect in patients with rectal cancer.
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spelling pubmed-87438042022-01-18 Polo-like kinase 4 as a potential predictive biomarker of chemoradioresistance in locally advanced rectal cancer Oh, Hyunseung Kim, Soon Gu Bae, Sung Uk Byun, Sang Jun Kim, Shin Lee, Jae-Ho Hwang, Ilseon Kwon, Sun Young Lee, Hye Won J Pathol Transl Med Original Article BACKGROUND: Polo-like kinase 4 (PLK4) is a serine/threonine protein kinase located in the centriole of the chromosome during the cell cycle. PLK4 overexpression has been described in a variety of many common human epithelial tumors. Conversely, PLK4 acts as a haploinsufficient tumor suppressor in some situations, highlighting the importance of strict regulation of PLK4 expression, activity, and function. Meanwhile, the importance of chemoradiation resistance in rectal cancer is being emphasized more than ever. We aimed to analyze PLK4 expression and the tumor regression grade (TRG) in patients with rectal cancer, treated with chemoradiotherapy (CRT). METHODS: A retrospective study was conducted on 102 patients with rectal cancer who received preoperative CRT. Immunohistochemistry for PLK4 in paraffin-embedded tissue was performed from the biopsy and surgical specimens. RESULTS: We found significant association between high expression of PLK4 and poor response to neoadjuvant CRT (according to both Mandard and The Korean Society of Pathologists TRG systems) in the pre-CRT specimens. Other clinicopathologic parameters did not reveal any correlation with PLK4 expression. CONCLUSIONS: This study revealed an association between high expression of PLK4 in the pre-CRT specimens and TRG. Our results indicated that PLK4 could potentially be a new predictor for CRT effect in patients with rectal cancer. The Korean Society of Pathologists/The Korean Society for Cytopathology 2022-01 2021-11-16 /pmc/articles/PMC8743804/ /pubmed/34775733 http://dx.doi.org/10.4132/jptm.2021.10.07 Text en © 2022 The Korean Society of Pathologists/The Korean Society for Cytopathology https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Oh, Hyunseung
Kim, Soon Gu
Bae, Sung Uk
Byun, Sang Jun
Kim, Shin
Lee, Jae-Ho
Hwang, Ilseon
Kwon, Sun Young
Lee, Hye Won
Polo-like kinase 4 as a potential predictive biomarker of chemoradioresistance in locally advanced rectal cancer
title Polo-like kinase 4 as a potential predictive biomarker of chemoradioresistance in locally advanced rectal cancer
title_full Polo-like kinase 4 as a potential predictive biomarker of chemoradioresistance in locally advanced rectal cancer
title_fullStr Polo-like kinase 4 as a potential predictive biomarker of chemoradioresistance in locally advanced rectal cancer
title_full_unstemmed Polo-like kinase 4 as a potential predictive biomarker of chemoradioresistance in locally advanced rectal cancer
title_short Polo-like kinase 4 as a potential predictive biomarker of chemoradioresistance in locally advanced rectal cancer
title_sort polo-like kinase 4 as a potential predictive biomarker of chemoradioresistance in locally advanced rectal cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8743804/
https://www.ncbi.nlm.nih.gov/pubmed/34775733
http://dx.doi.org/10.4132/jptm.2021.10.07
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