Polo-like kinase 4 as a potential predictive biomarker of chemoradioresistance in locally advanced rectal cancer
- Author(s)
- Hyunseung Oh; Soon Gu Kim; Sung Uk Bae; Sang Jun Byun; Shin Kim; Jae-Ho Lee; Ilseon Hwang; Sun Young Kwon; Hye Won Lee
- Keimyung Author(s)
- Bae, Sung Uk; Byun, Sang Jun; Kim, Shin; Lee, Jae Ho; Hwang, Il Seon; Kwon, Sun Young; Lee, Hye Won
- Department
- Dept. of Surgery (외과학)
Dept. of Radiation Oncology (방사선종양학)
Dept. of Immunology (면역학)
Dept. of Anatomy (해부학)
Dept. of Pathology (병리학)
- Journal Title
- J Pathol Transl Med
- Issued Date
- 2022
- Volume
- 56
- Issue
- 1
- Keyword
- Polo-like kinase 4; Rectal neoplasms; Chemoradiotherapy; Biomarker
- Abstract
- 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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